dsaid,accession,platform,deg_count,disease,diseaseid,tissue,data_source,library_strategy,organism,control_case_sample_count,definition DSA00001,GSE224398,GPL21103,1000,Alzheimer's Disease,C0002395,Hippocampus,GEO,scRNA-Seq,Mus musculus,1|1,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA00002,GSE224398,GPL21103,1000,Alzheimer's Disease,C0002395,Hippocampus,GEO,scRNA-Seq,Mus musculus,1|1,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA00003,GSE224398,GPL21103,1000,Alzheimer's Disease,C0002395,Hippocampus,GEO,scRNA-Seq,Mus musculus,1|1,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA00004,GSE224022,GPL16791,1000,Retinoblastoma,C0035335,Retina,GEO,RNA-Seq,Homo sapiens,4|5,DO:A retinal cell cancer and malignant neoplasm of retina and neuroblastoma and neuroendocrine tumors that derives_from the tissues of the retina. DSA00005,GSE126342,GPL11154,1000,Congenital Myotonic Dystrophy,C0410226,Skeletal muscle,GEO,RNA-Seq,Homo sapiens,9|11,"MONDO:An inherited progressive disorder affecting the muscles. It is characterized by muscle wasting and hypotonia, cataracts, heart conduction defects and endocrinopathies." DSA00006,GSE126342,GPL11154,1000,Myotonic Dystrophy Type 1,C0027126,Skeletal muscle,GEO,RNA-Seq,Homo sapiens,6|16,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA00007,GSE224253,GPL17692,0,Allergic Disorder of Respiratory System,C1504369,,GEO,Microarray,Homo sapiens,7|9, DSA00008,GSE224253,GPL17692,1000,Allergic Disorder of Respiratory System,C1504369,,GEO,Microarray,Homo sapiens,7|7, DSA00009,GSE223245,GPL33038,0,Brain Damage,C0006109,Whole blood,GEO,Microarray,Homo sapiens,4|4,MONDO:Chronic form of encephalitis. DSA00010,GSE223245,GPL33038,0,Brain Damage,C0006109,Whole blood,GEO,Microarray,Homo sapiens,4|4,MONDO:Chronic form of encephalitis. DSA00011,GSE223245,GPL33038,171,Brain Damage,C0006109,Whole blood,GEO,Microarray,Homo sapiens,4|4,MONDO:Chronic form of encephalitis. DSA00012,GSE220612,GPL17021,1000,Myocardial Ischemia,C0151744,Heart,GEO,RNA-Seq,Mus musculus,4|4,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA00013,GSE220612,GPL17021,1000,Myocardial Ischemia,C0151744,Heart,GEO,RNA-Seq,Mus musculus,4|3,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA00014,GSE220612,GPL17021,1000,Myocardial Ischemia,C0151744,Heart,GEO,RNA-Seq,Mus musculus,4|4,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA00015,GSE224056,GPL24676,1000,Gastric Cancer,C0699791,Stomach,GEO,RNA-Seq,Homo sapiens,4|5,DO:A gastrointestinal system cancer that is located_in the stomach. DSA00016,GSE224056,GPL24676,112,Gastric Cancer,C0699791,Stomach,GEO,RNA-Seq,Homo sapiens,5|5,DO:A gastrointestinal system cancer that is located_in the stomach. DSA00017,GSE223964,GPL20301,1000,Diabetes,C0011847,Skin,GEO,scRNA-Seq,Homo sapiens,3|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00018,GSE223885,GPL24106,1000,COVID-19,D8888888,Venous blood,GEO,RNA-Seq,Homo sapiens,10|10,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA00019,GSE6344,GPL97,1000,Clear Cell Ependymoma,C1384403,Kidney,GEO,Microarray,Homo sapiens,5|5,"EFO:A WHO grade II, slow growing tumor of children and young adults, usually located intraventricularly. It is the most common ependymal neoplasm. It often causes clinical symptoms by blocking cerebrospinal fluid pathways. Key histological features include perivascular pseudorosettes and ependymal rosettes. (WHO)" DSA00020,GSE223561,GPL24247,1000,Acute Liver Failure;Post Operative Delirium,,Liver,GEO,scRNA-Seq,Mus musculus,3|2, DSA00021,GSE223561,GPL24247,1000,Acute Liver Failure;Post Operative Delirium,,Liver,GEO,scRNA-Seq,Mus musculus,3|2, DSA00022,GSE223561,GPL24247,1000,Acute Liver Failure;Post Operative Delirium,,Liver,GEO,scRNA-Seq,Mus musculus,3|4, DSA00023,GSE223561,GPL24676,1000,Acute Liver Failure,C0162557,Liver,GEO,scRNA-Seq,Homo sapiens,3|3,"HPO:Hepatic failure refers to the inability of the liver to perform its normal synthetic and metabolic functions, which can result in coagulopathy and alteration in the mental status of a previously healthy individual. Hepatic failure is defined as fulminant if there is onset of encephalopathy within 4 weeks of the onset of symptoms in a patient with a previously healthy liver." DSA00024,GSE221789,GPL24247,1000,Aortic Aneurysm,C0003486,Abdominal aorta,GEO,scRNA-Seq,Mus musculus,2|2,DO:An aortic disease that is characterized by an enlargement (dilation) of the aorta to greater than 1.5 times normal size. DSA00025,GSE221606,GPL13112,410,Angioimmunoblastic T-Cell Lymphoma,C0023493,Spleen;lymph node,GEO,RNA-Seq,Mus musculus,4|4,"DO:A T-cell acute leukemia that results_in abnormal increase of lymphocytes, derives_from T-cells, has_material_basis_in Human T-lymphotropic virus 1 (HTLV-1), which is transmitted_by sexual contact, transmitted_by contaminated needles used by intravenous-drug users, and transmitted_by breast feeding. The infection results_in_formation_of skin lesions." DSA00026,GSE221606,GPL13112,729,Angioimmunoblastic T-Cell Lymphoma,C0023493,Lymph node,GEO,RNA-Seq,Mus musculus,4|4,"DO:A T-cell acute leukemia that results_in abnormal increase of lymphocytes, derives_from T-cells, has_material_basis_in Human T-lymphotropic virus 1 (HTLV-1), which is transmitted_by sexual contact, transmitted_by contaminated needles used by intravenous-drug users, and transmitted_by breast feeding. The infection results_in_formation_of skin lesions." DSA00027,GSE221598,GPL24247,1000,Chronic Kidney Disease,C1561643,Kidney,GEO,RNA-Seq,Mus musculus,3|3,DO:A kidney failure that is characterized by the gradual loss of kidney function. DSA00028,GSE217153,GPL17021,1000,Diabetic Kidney Disease,C0011881,Kidney,GEO,RNA-Seq,Mus musculus,3|4,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA00029,GSE217153,GPL17021,1000,Diabetic Kidney Disease,C0011881,Kidney,GEO,RNA-Seq,Mus musculus,3|4,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA00030,GSE215424,GPL24676,1000,Amyotrophic Lateral Sclerosis,C0002736,Muscle,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA00031,GSE6344,GPL97,999,Clear Cell Ependymoma,C1384403,Kidney,GEO,Microarray,Homo sapiens,5|5,"EFO:A WHO grade II, slow growing tumor of children and young adults, usually located intraventricularly. It is the most common ependymal neoplasm. It often causes clinical symptoms by blocking cerebrospinal fluid pathways. Key histological features include perivascular pseudorosettes and ependymal rosettes. (WHO)" DSA00032,GSE199899,GPL17021,1000,Liver Cancer,C2239176,Liver,GEO,RNA-Seq,Mus musculus,3|4,DO:A hepatobiliary system cancer that is located_in the liver. DSA00033,GSE199899,GPL17021,1000,Liver Cancer,C2239176,Liver,GEO,RNA-Seq,Mus musculus,4|6,DO:A hepatobiliary system cancer that is located_in the liver. DSA00034,GSE196481,GPL23038,1000,Acute Pancreatitis,C0001339,,GEO,Microarray,Mus musculus,4|4,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA00035,GSE196481,GPL23038,1000,Acute Pancreatitis,C0001339,Duodenum,GEO,Microarray,Mus musculus,4|4,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA00036,GSE196454,GPL24247,969,Classic Galactosemia,C0268151,Ovary,GEO,RNA-Seq,Mus musculus,3|3,DO:A galactosemia that has_material_basis_in homozygous or compund heterozygous mutation in GALT on chromosome 9p13.3. DSA00037,GSE194174,GPL17021,1000,Chronic Pain,C0150055,Dorsal root ganglion,GEO,RNA-Seq,Mus musculus,1|1,"HPO:Persistent pain, usually defined as pain that has lasted longer than 3 to 6 months." DSA00038,GSE194174,GPL17021,1000,Chronic Pain,C0150055,Dorsal root ganglion,GEO,RNA-Seq,Mus musculus,1|1,"HPO:Persistent pain, usually defined as pain that has lasted longer than 3 to 6 months." DSA00039,GSE194174,GPL17021,490,Chronic Pain,C0150055,Dorsal root ganglion,GEO,RNA-Seq,Mus musculus,1|1,"HPO:Persistent pain, usually defined as pain that has lasted longer than 3 to 6 months." DSA00040,GSE6613,GPL96,0,Neurodegenerative Diseases,C0524851,Whole blood,GEO,Microarray,Homo sapiens,22|33,DO:A central nervous system disease that results in the progressive deterioration of function or structure of neurons. DSA00041,GSE68468,GPL96,604,Colon Cancer,C0699790,Colon,GEO,Microarray,Homo sapiens,1|300,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA00042,GSE7670,GPL96,1000,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Homo sapiens,30|27,DO:A respiratory system cancer that is located_in the lung. DSA00043,GSE7670,GPL96,1000,Lung Cancer,C0684249,Lung,GEO,Microarray,Homo sapiens,30|1,DO:A respiratory system cancer that is located_in the lung. DSA00044,GSE223972,GPL21290,1000,Multiple Myeloma,C0026764,,GEO,scRNA-Seq,Homo sapiens,2|4,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA00045,GSE223405,GPL16791,1000,Prostate Cancer,C0600139,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA00046,GSE223405,GPL16791,1000,Prostate Cancer,C0600139,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA00047,GSE218276,GPL16791,0,Cardiomyopathy,C0878544,Whole blood,GEO,RNA-Seq,Homo sapiens,8|8,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA00048,GSE218276,GPL24676,121,Cardiomyopathy,C0878544,Whole blood,GEO,RNA-Seq,Homo sapiens,36|6,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA00049,GSE215979,GPL24247,1000,Diabetic Cardiomyopathy,C0853897,Myocardium,GEO,RNA-Seq,Mus musculus,3|3,"MSH:Diabetes complications in which VENTRICULAR REMODELING in the absence of CORONARY ATHEROSCLEROSIS and hypertension results in cardiac dysfunctions, typically LEFT VENTRICULAR DYSFUNCTION. The changes also result in myocardial hypertrophy, myocardial necrosis and fibrosis, and collagen deposition due to impaired glucose tolerance." DSA00050,GSE214376,GPL18573,1000,Sporadic Creutzfeldt-Jakob Disease,C1852467,Frontal cortex,GEO,RNA-Seq,Homo sapiens,9|5,"MONDO:Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease characterized by typical CJD features (rapidly progressive dementia, personality/behavioral changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia." DSA00051,GSE213337,GPL24247,1000,Diabetes,C0011847,Heart,GEO,scRNA-Seq,Mus musculus,1|1,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00052,GSE213080,GPL19057,1000,Ischemic Insult,,Left ventricle,GEO,scRNA-Seq,Mus musculus,1|1, DSA00053,GSE77953,GPL96,1000,Colorectal Adenoma,C1302401,Colorectum,GEO,Microarray,Homo sapiens,13|17,"EFO:An adenoma that arises from the colon or rectum. The group of colorectal adenomas includes tubular, villous, and tubulovillous adenomas, traditional serrated adenomas, sessile serrated adenomas/polyps, and familial adenomatous polyposis." DSA00054,GSE208719,GPL23479,1000,Leukemia,C0023418,Bone marrow,GEO,RNA-Seq,Mus musculus,2|2,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA00055,GSE208076,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,3|7,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA00056,GSE207854,GPL24247,83,Social Defeat Stress,,Brain,GEO,RNA-Seq,Mus musculus,3|3, DSA00057,GSE77953,GPL96,1000,Colorectal Carcinoma,C0009402,Colorectum,GEO,Microarray,Homo sapiens,13|17,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA00058,GSE7803,GPL96,1000,Squamous Cell Carcinoma of Cervix,C0279671,Cervix,GEO,Microarray,Homo sapiens,10|3,DO:A cervix carcinoma that has_material_basis_in squamous cells of the cervix. DSA00059,GSE9006,GPL96,236,Type 1 Diabetes,C0011854,Blood,GEO,Microarray,Homo sapiens,24|81,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA00060,GSE9006,GPL96,348,Type 2 Diabetes,C0011860,Blood,GEO,Microarray,Homo sapiens,24|12,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00061,GSE9006,GPL97,121,Type 1 Diabetes,C0011854,Blood,GEO,Microarray,Homo sapiens,24|81,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA00062,GSE9006,GPL97,143,Type 2 Diabetes,C0011860,Blood,GEO,Microarray,Homo sapiens,24|12,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00063,GSE9476,GPL96,1000,Acute Myeloid Leukemia,C0023467,,GEO,Microarray,Homo sapiens,18|26,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA00064,GSE9476,GPL96,1000,Acute Myeloid Leukemia,C0023467,,GEO,Microarray,Homo sapiens,10|26,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA00065,GSE196008,GPL13112,1000,Liver Cancer,C2239176,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA00066,GSE186027,GPL25526,1000,Hepatoblastoma,C0206624,Liver,GEO,scRNA-Seq,Homo sapiens,1|1,DO:A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver. DSA00067,GSE186027,GPL25526,566,Hepatoblastoma,C0206624,Liver,GEO,scRNA-Seq,Homo sapiens,1|1,DO:A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver. DSA00068,GSE223718,GPL24676,1000,Adenocarcinoma,C0001418,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A carcinoma that has_material_basis_in abnormally proliferating cells, derives_from epithelial cells, which originate in glandular tissue." DSA00069,GSE223718,GPL24676,1000,Adenocarcinoma,C0001418,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A carcinoma that has_material_basis_in abnormally proliferating cells, derives_from epithelial cells, which originate in glandular tissue." DSA00070,GSE217948,GPL24676,1000,COVID-19,D8888888,Whole blood,GEO,RNA-Seq,Homo sapiens,64|202,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA00071,GSE214987,GPL24676,1000,Osteoarthritis,C0157946,,GEO,RNA-Seq,Homo sapiens,3|3,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA00072,GSE214987,GPL24676,142,Osteoarthritis,C0157946,,GEO,RNA-Seq,Homo sapiens,3|3,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA00073,GSE206510,GPL16791,2,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA00074,GSE206510,GPL16791,1,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,4|5,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA00075,GSE197392,GPL19057,151,Type 2 Diabetes,C0011860,Adductor muscle,GEO,RNA-Seq,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00076,GSE197392,GPL19057,115,Type 2 Diabetes,C0011860,Adductor muscle,GEO,RNA-Seq,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00077,GSE197392,GPL19057,75,Type 2 Diabetes,C0011860,Adductor muscle,GEO,RNA-Seq,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00078,GSE197392,GPL19057,5,Type 2 Diabetes,C0011860,Adductor muscle,GEO,RNA-Seq,Mus musculus,3|4,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00079,GSE197392,GPL19057,67,Type 2 Diabetes,C0011860,Gastrocnemius muscle,GEO,RNA-Seq,Mus musculus,3|4,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00080,GSE197392,GPL19057,16,Type 2 Diabetes,C0011860,Gastrocnemius muscle,GEO,RNA-Seq,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00081,GSE197392,GPL19057,108,Type 2 Diabetes,C0011860,Gastrocnemius muscle,GEO,RNA-Seq,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00082,GSE197392,GPL19057,1,Type 2 Diabetes,C0011860,Gastrocnemius muscle,GEO,RNA-Seq,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00083,GSE9750,GPL96,1000,Cervical Cancer,C4048328,Cervix,GEO,Microarray,Homo sapiens,21|33,DO:A female reproductive organ cancer that is located_in the cervix. DSA00084,GSE9750,GPL96,1000,Cervical Cancer,C4048328,,GEO,Microarray,Homo sapiens,3|9,DO:A female reproductive organ cancer that is located_in the cervix. DSA00085,GSE9874,GPL96,0,Atherosclerosis,C0004153,,GEO,Microarray,Homo sapiens,15|13,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA00086,GSE9874,GPL96,0,Atherosclerosis,C0004153,,GEO,Microarray,Homo sapiens,15|14,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA00087,GSE9574,GPL96,21,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,15|14,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA00088,GSE94237,GPL19057,1000,Alopecia Areata,C0002171,Skin,GEO,RNA-Seq,Mus musculus,6|6,DO:An autoimmune disease resulting in the loss of hair on the scalp and elsewhere on the body initially causing bald spots. DSA00089,GSE69123,GPL13112,20,Type 2 Diabetes,C0011860,Adductor muscle,GEO,RNA-Seq,Mus musculus,6|6,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00090,GSE69123,GPL13112,6,Type 2 Diabetes,C0011860,Gastrocnemius muscle,GEO,RNA-Seq,Mus musculus,6|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00091,GSE5090,GPL96,0,Polycystic Ovary Syndrome,C0032460,Omental adipose tissue,GEO,Microarray,Homo sapiens,8|9,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA00092,GSE6710,GPL96,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,13|12,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA00093,GSE136757,GPL570,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,30|30,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA00094,GSE136757,GPL570,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,30|25,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA00095,GSE214701,GPL24247,7,Brain Damage,C0006109,Hippocampus,GEO,RNA-Seq,Mus musculus,3|3,MONDO:Chronic form of encephalitis. DSA00096,GSE202010,GPL24247,1000,Polycystic Liver Disease,C0158683,,GEO,RNA-Seq,Mus musculus,3|3,MONDO:An autosomal dominant inherited condition characterized by many cysts of various sizes scattered throughout the liver. DSA00097,GSE202010,GPL24247,1000,Polycystic Liver Disease,C0158683,,GEO,RNA-Seq,Mus musculus,3|3,MONDO:An autosomal dominant inherited condition characterized by many cysts of various sizes scattered throughout the liver. DSA00098,GSE202010,GPL24247,1000,Polycystic Liver Disease,C0158683,,GEO,RNA-Seq,Mus musculus,3|3,MONDO:An autosomal dominant inherited condition characterized by many cysts of various sizes scattered throughout the liver. DSA00099,GSE184986,GPL24247,1000,Myocardial Infarction,C0027051,,GEO,RNA-Seq,Mus musculus,2|4,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA00100,GSE222095,GPL19057,1000,Pancreatic Cancer,C0235974,Spleen,GEO,RNA-Seq,Mus musculus,3|3,DO:An endocrine gland cancer located_in the pancreas. DSA00101,GSE222095,GPL19057,1000,Pancreatic Cancer,C0235974,Spleen,GEO,RNA-Seq,Mus musculus,3|3,DO:An endocrine gland cancer located_in the pancreas. DSA00102,GSE222095,GPL19057,1000,Pancreatic Cancer,C0235974,Spleen,GEO,RNA-Seq,Mus musculus,3|3,DO:An endocrine gland cancer located_in the pancreas. DSA00103,GSE222095,GPL19057,1000,Pancreatic Cancer,C0235974,Spleen,GEO,RNA-Seq,Mus musculus,3|3,DO:An endocrine gland cancer located_in the pancreas. DSA00104,GSE218618,GPL18573,1000,Conjunctival Melanoma,C0346360,,GEO,RNA-Seq,Homo sapiens,8|10,EFO:A malignant melanoma within the conjunctiva of the eye. DSA00105,GSE217798,GPL16791,1000,Renal Cell Carcinoma,C0007134,,GEO,RNA-Seq,Homo sapiens,6|6,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA00106,GSE217430,GPL17021,43,Alzheimer's Disease,C0002395,Hippocampus,GEO,RNA-Seq,Mus musculus,4|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA00107,GSE217430,GPL17021,156,Alzheimer's Disease,C0002395,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA00108,GSE136757,GPL570,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,30|20,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA00109,GSE67223,GPL6244,0,Ovarian Fibroma,C0149951,Ovary,GEO,Microarray,Homo sapiens,3|8,HPO:The presence of a fibroma of the ovary. DSA00110,GSE195658,GPL17021,1000,Eosinophilic Esophagitis,C0341106,Esophagus,GEO,RNA-Seq,Mus musculus,5|5,DO:An esophagitis characterized by inflammation involving eosinophils located_in esophagus. DSA00111,GSE183218,GPL20301,1000,Dilated Cardiomyopathy,C0007193,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA00112,GSE183218,GPL20301,1000,Dilated Cardiomyopathy,C0007193,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA00113,GSE183218,GPL20301,1000,Dilated Cardiomyopathy,C0007193,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA00114,GSE67223,GPL6244,0,Ovarian Serous Adenocarcinoma,C1335177,Ovary,GEO,Microarray,Homo sapiens,3|1,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA00115,GSE211993,GPL28038,1000,Alzheimer's Disease,C0002395,,GEO,RNA-Seq,Homo sapiens,5|5,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA00116,GSE211993,GPL28038,1000,Alzheimer's Disease,C0002395,,GEO,RNA-Seq,Homo sapiens,5|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA00117,GSE211993,GPL28038,1000,Alzheimer's Disease,C0002395,,GEO,RNA-Seq,Homo sapiens,5|5,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA00118,GSE211993,GPL28038,1000,Alzheimer's Disease,C0002395,,GEO,RNA-Seq,Homo sapiens,5|5,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA00119,GSE203151,GPL21103,1000,Obesity,C0028754,Pancreatic islet,GEO,scRNA-Seq,Mus musculus,1|1,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA00120,GSE202667,GPL20844,1000,Parkinson's Disease,C0030567,,GEO,Microarray,Homo sapiens,30|11,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA00121,GSE202667,GPL20844,1000,Parkinson's Disease,C0030567,,GEO,Microarray,Homo sapiens,30|6,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA00122,GSE202667,GPL20844,1000,Parkinson's Disease,C0030567,,GEO,Microarray,Homo sapiens,30|12,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA00123,GSE67223,GPL6244,0,Ovarian Serous Cystadenoma,C0346170,Ovary,GEO,Microarray,Homo sapiens,3|8,"HPO:A cystic tumor of the ovary, containing thin, clear, yellow serous fluid and varying amounts of solid tissue." DSA00124,GSE67223,GPL6244,0,Ovarian Serous Cystadenoma,C0346170,Ovary,GEO,Microarray,Homo sapiens,3|5,"HPO:A cystic tumor of the ovary, containing thin, clear, yellow serous fluid and varying amounts of solid tissue." DSA00125,GSE135917,GPL6244,0,Obstructive Sleep Apnea,C4237227,Subcutaneous fat,GEO,Microarray,Homo sapiens,8|10,"DO:A sleep apnea that is characterized by repeated collapse and obstruction of the upper airway during sleep, which results in reduced airflow (hypopnea) or complete airflow cessation (apnea), oxygen desaturation, and arousals from sleep." DSA00126,GSE131738,GPL570,87,Sezary Syndrome,C0036920,Blood,GEO,Microarray,Homo sapiens,3|3,"MONDO:Sezary syndrome (SS) is an aggressive form of cutaneous T-cell lymphoma characterized by a triad of erythroderma, lymphadenopathy and circulating atypical lymphocytes (Sezary cells)." DSA00127,GSE131738,GPL570,571,Sezary Syndrome,C0036920,Blood,GEO,Microarray,Homo sapiens,3|3,"MONDO:Sezary syndrome (SS) is an aggressive form of cutaneous T-cell lymphoma characterized by a triad of erythroderma, lymphadenopathy and circulating atypical lymphocytes (Sezary cells)." DSA00128,GSE131738,GPL570,52,Sezary Syndrome,C0036920,Blood,GEO,Microarray,Homo sapiens,3|2,"MONDO:Sezary syndrome (SS) is an aggressive form of cutaneous T-cell lymphoma characterized by a triad of erythroderma, lymphadenopathy and circulating atypical lymphocytes (Sezary cells)." DSA00129,GSE189670,GPL24676,515,Human Papilloma Virus Infection,C0343641,,GEO,scRNA-Seq,Homo sapiens,1|1,"DO:A viral infectious disease that results_in infection located_in skin, has_material_basis_in human papillomavirus (types 2 and 4). This infection is characterized by a raised wart with roughened surface, most common on hands, but can grow anywhere on the body." DSA00130,GSE185383,GPL21103,1000,Ischemia Reperfusion Injury,C0035126,Kidney,GEO,RNA-Seq,Mus musculus,3|3,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA00131,GSE223120,GPL20301,1000,Colorectal Carcinoma,C0009402,Colorectum,GEO,RNA-Seq,Homo sapiens,20|20,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA00132,GSE222982,GPL23227,480,Metastatic Ovarian Cancer,C1140680,Ovary,GEO,RNA-Seq,Homo sapiens,5|5,DO:A female reproductive organ cancer that is located_in the ovary. DSA00133,GSE222957,GPL23479,1000,Ischemia Reperfusion Injury,C0035126,Lung,GEO,RNA-Seq,Mus musculus,3|4,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA00134,GSE222935,GPL13112,1000,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA00135,GSE218492,GPL24676,1000,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA00136,GSE203307,GPL17021,1000,Melanoma,C0025202,Ear,GEO,RNA-Seq,Mus musculus,3|4,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA00137,GSE201330,GPL24247,118,Bile Duct Disease,C0004943,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis." DSA00138,GSE194032,GPL23038,974,Breast Cancer,C0678222,Bone marrow,GEO,Microarray,Mus musculus,5|5,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA00139,GSE194032,GPL23038,1,Breast Cancer,C0678222,Bone marrow,GEO,Microarray,Mus musculus,4|4,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA00140,GSE223208,GPL21163,1000,Myocardial Infarction,C0027051,Heart,GEO,Microarray,Mus musculus,3|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA00141,GSE223208,GPL21163,97,Myocardial Infarction,C0027051,Heart,GEO,Microarray,Mus musculus,3|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA00142,GSE221480,GPL24247,1000,Spinal And Bulbar Muscular Atrophy,C1839259,Quadriceps,GEO,RNA-Seq,Mus musculus,4|4,DO:A spinal muscular dystrophy that has_material_basis_in an X-linked recessive expansion of CAG triplet repeats (glutamine) in exon 1 of AR gene encoding the androgen receptor. DSA00143,GSE221480,GPL24247,1000,Spinal And Bulbar Muscular Atrophy,C1839259,Quadriceps,GEO,RNA-Seq,Mus musculus,3|4,DO:A spinal muscular dystrophy that has_material_basis_in an X-linked recessive expansion of CAG triplet repeats (glutamine) in exon 1 of AR gene encoding the androgen receptor. DSA00144,GSE220939,GPL11154,1000,Type 2 Diabetes,C0011860,Kidney cortex,GEO,scRNA-Seq,Homo sapiens,6|6,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00145,GSE220080,GPL11202,1000,Spinal And Bulbar Muscular Atrophy,C1839259,Quadriceps,GEO,Microarray,Mus musculus,4|3,DO:A spinal muscular dystrophy that has_material_basis_in an X-linked recessive expansion of CAG triplet repeats (glutamine) in exon 1 of AR gene encoding the androgen receptor. DSA00146,GSE219210,GPL24676,1000,Tonsillar Cancer,C0558355,Tonsil,GEO,scRNA-Seq,Homo sapiens,1|5,MONDO:A carcinoma that involves the tonsil. DSA00147,GSE211398,GPL18573,1000,Pancreatic Adenocarcinoma,C0281361,Pancreas,GEO,RNA-Seq,Homo sapiens,5|3,DO:A pancreatic carcinoma that derives_from epithelial cells of glandular origin. DSA00148,GSE211398,GPL18573,1000,Pancreatic Adenocarcinoma,C0281361,Pancreas,GEO,RNA-Seq,Homo sapiens,11|9,DO:A pancreatic carcinoma that derives_from epithelial cells of glandular origin. DSA00149,GSE138206,GPL570,1000,Oral Squamous Cell Carcinoma,C0585362,Tongue,GEO,Microarray,Homo sapiens,6|6,"EFO:A squamous cell carcinoma arising from the oral cavity. It affects predominantly adults in their fifth and sixth decades of life and is associated with alcohol and tobacco use. Human papillomavirus is present in approximately half of the cases. It is characterized by a tendency to metastasize early to the lymph nodes. When the tumor is small, patients are often asymptomatic. Physical examination may reveal erythematous or white lesions or plaques. The majority of patients present with signs and symptoms of locally advanced disease including mucosal ulceration, pain, difficulty with speaking, chewing, and swallowing, bleeding, weight loss, and neck swelling. Patients may also present with swollen neck lymph nodes without any symptoms from the oropharyngeal tumor. The most significant prognostic factors are the size of the tumor and the lymph nodes status." DSA00150,GSE197120,GPL24676,164,Xfe Progeroid Syndrome,C1970416,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A progeroid syndrome that is characterized by aged bird-like facies, lack of subcutaneous fat, dwarfism, cachexia and microcephaly and that has_material_basis_in homozygous mutation in the ERCC4 gene on chromosome 16p13." DSA00151,GSE168496,GPL18573,26,Parkinson's Disease,C0030567,Substantia nigra,GEO,RNA-Seq,Homo sapiens,8|8,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA00152,GSE222807,GPL13112,1000,Fatty Liver Disease,C0400966,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA00153,GSE138206,GPL570,775,Oral Squamous Cell Carcinoma,C0585362,Tongue,GEO,Microarray,Homo sapiens,6|6,"EFO:A squamous cell carcinoma arising from the oral cavity. It affects predominantly adults in their fifth and sixth decades of life and is associated with alcohol and tobacco use. Human papillomavirus is present in approximately half of the cases. It is characterized by a tendency to metastasize early to the lymph nodes. When the tumor is small, patients are often asymptomatic. Physical examination may reveal erythematous or white lesions or plaques. The majority of patients present with signs and symptoms of locally advanced disease including mucosal ulceration, pain, difficulty with speaking, chewing, and swallowing, bleeding, weight loss, and neck swelling. Patients may also present with swollen neck lymph nodes without any symptoms from the oropharyngeal tumor. The most significant prognostic factors are the size of the tumor and the lymph nodes status." DSA00154,GSE88839,GPL570,49,Hepatocellular Adenoma,C0206669,Liver,GEO,Microarray,Homo sapiens,3|35,"EFO:A benign epithelial neoplasm arising from the hepatocytes. Grossly, it appears as a soft, round mass which often contains areas of hemorrhage and necrosis. Morphologically, the neoplastic cells resemble normal hepatocytes and form plates separated by sinusoids. Most patients have a history of contraceptive or anabolic steroids use." DSA00155,GSE198551,GPL24676,1000,Limb-Girdle Muscular Dystrophy Type 2A,C1869123,Muscle,GEO,RNA-Seq,Homo sapiens,3|3,DO:An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding the proteolytic enzyme calpain-3 (CAPN3) on chromosome 15q15. DSA00156,GSE197016,GPL24676,7,Bladder Cancer,C0699885,Urothelium,GEO,RNA-Seq,Mus musculus,3|4,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA00157,GSE197016,GPL24676,706,Bladder Cancer,C0699885,Urothelium,GEO,RNA-Seq,Mus musculus,3|4,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA00158,GSE197016,GPL24676,1000,Bladder Cancer,C0699885,Urothelium,GEO,RNA-Seq,Mus musculus,3|3,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA00159,GSE197016,GPL24676,1000,Bladder Cancer,C0699885,Urothelium,GEO,RNA-Seq,Mus musculus,3|5,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA00160,GSE197016,GPL24676,1000,Bladder Cancer,C0699885,Urothelium,GEO,RNA-Seq,Mus musculus,3|7,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA00161,GSE197016,GPL24676,1000,Bladder Cancer,C0699885,Urothelium,GEO,RNA-Seq,Mus musculus,3|5,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA00162,GSE223060,GPL20301,1000,Multiple Myeloma,C0026764,Bone marrow,GEO,scRNA-Seq,Homo sapiens,7|18,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA00163,GSE221005,GPL17021,1000,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA00164,GSE221005,GPL17021,1000,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA00165,GSE199792,GPL19057,1000,Retinopathy,C0035309,Retina,GEO,scRNA-Seq,Mus musculus,1|1,DO:An eye disease that is located_in the retina. DSA00166,GSE186821,GPL24247,1000,Diabetes,C0011847,Skin,GEO,scRNA-Seq,Mus musculus,4|4,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00167,GSE220969,GPL24676,1000,Dengue Disease,C0011311,Blood,GEO,scRNA-Seq,Homo sapiens,4|8,"DO:A viral infectious disease that results in infection, has_material_basis_in Dengue virus" DSA00168,GSE220969,GPL24676,1000,Dengue Disease,C0011311,Blood,GEO,scRNA-Seq,Homo sapiens,4|8,"DO:A viral infectious disease that results in infection, has_material_basis_in Dengue virus" DSA00169,GSE185764,GPL17586,0,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,4|7,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA00170,GSE185764,GPL17586,0,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,4|4,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA00171,GSE185764,GPL17586,0,Atopic Dermatitis,C0011615,Skin,GEO,Microarray,Homo sapiens,4|4,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA00172,GSE143789,GPL16791,980,Thyroid Associated Opthalmopathies,C0339143,Adipose tissue,GEO,RNA-Seq,Homo sapiens,3|3,"MSH:An autoimmune disorder of the EYE, occurring in patients with Graves disease. Subtypes include congestive (inflammation of the orbital connective tissue), myopathic (swelling and dysfunction of the extraocular muscles), and mixed congestive-myopathic ophthalmopathy." DSA00173,GSE220264,GPL16558,1000,Juvenile Idiopathic Arthritis,C3890205,Synovial fluid,GEO,RNA-Seq,Homo sapiens,3|4,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA00174,GSE220264,GPL16558,1000,Juvenile Idiopathic Arthritis,C3890205,Synovial fluid,GEO,RNA-Seq,Homo sapiens,4|4,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA00175,GSE211700,GPL20795,1000,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,9|10,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA00176,GSE211700,GPL20795,1000,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,9|10,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA00177,GSE184773,GPL21103,8,Obsessive-Compulsive Disorder,C0028768,Brain,GEO,RNA-Seq,Mus musculus,4|4,"DO:An anxiety disorder that involves unwanted and repeated thoughts, feelings, ideas, sensations (obsessions), or behaviors that make them feel driven to do something (compulsions)." DSA00178,GSE184773,GPL21103,11,Obsessive-Compulsive Disorder,C0028768,Brain,GEO,RNA-Seq,Mus musculus,4|4,"DO:An anxiety disorder that involves unwanted and repeated thoughts, feelings, ideas, sensations (obsessions), or behaviors that make them feel driven to do something (compulsions)." DSA00179,GSE184773,GPL21103,14,Obsessive-Compulsive Disorder,C0028768,Brain,GEO,RNA-Seq,Mus musculus,4|4,"DO:An anxiety disorder that involves unwanted and repeated thoughts, feelings, ideas, sensations (obsessions), or behaviors that make them feel driven to do something (compulsions)." DSA00180,GSE207912,GPL18573,1000,Hepatoblastoma,C0206624,,GEO,RNA-Seq,Homo sapiens,2|2,DO:A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver. DSA00181,GSE207912,GPL18573,1000,Hepatocellular Carcinoma,C0334287,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA00182,GSE219084,GPL23038,0,Diabetes,C0011847,Retina,GEO,Microarray,Mus musculus,10|9,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00183,GSE217155,GPL23479,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,3|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA00184,GSE130856,GPL570,1000,Villitis of Unknown Etiology,C1300128,Placenta,GEO,Microarray,Homo sapiens,9|10,"NCI:T-cell immune response with diffuse perivillous fibrin deposition associated with intrauterine growth restriction, pre-term birth and recurrent fetal loss." DSA00185,GSE211682,GPL21103,1000,Anterior Cruciate Ligament Tear,,Skeletal muscle,GEO,RNA-Seq,Mus musculus,3|3, DSA00186,GSE211681,GPL20301,9,Anterior Cruciate Ligament Tear,,Skeletal muscle,GEO,RNA-Seq,Homo sapiens,16|16, DSA00187,GSE207094,GPL21697,568,Granulosa Cell Tumor,C0018206,Ovary,GEO,RNA-Seq,Homo sapiens,3|3,DO:A sex cord-gonadal stromal tumor that has_material_basis_in granulosa cells and arises from the sex cord stroma. DSA00188,GSE207094,GPL21697,83,Granulosa Cell Tumor,C0018206,Ovary,GEO,RNA-Seq,Homo sapiens,3|3,DO:A sex cord-gonadal stromal tumor that has_material_basis_in granulosa cells and arises from the sex cord stroma. DSA00189,GSE199001,GPL24247,1,COVID-19,D8888888,Spleen,GEO,RNA-Seq,Mus musculus,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA00190,GSE199001,GPL24247,13,COVID-19,D8888888,Lung,GEO,RNA-Seq,Mus musculus,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA00191,GSE197925,GPL16791,1000,Facial Anomaly,C0266617,,GEO,RNA-Seq,Homo sapiens,3|2,HPO:An abnormality of the face. DSA00192,GSE197925,GPL16791,1000,Facial Anomaly,C0266617,,GEO,RNA-Seq,Homo sapiens,3|2,HPO:An abnormality of the face. DSA00193,GSE130856,GPL570,1000,Villitis of Unknown Etiology,C1300128,Placenta,GEO,Microarray,Homo sapiens,9|10,"NCI:T-cell immune response with diffuse perivillous fibrin deposition associated with intrauterine growth restriction, pre-term birth and recurrent fetal loss." DSA00194,GSE128470,GPL96,879,Dermatomyositis,C0011633,Muscle,GEO,Microarray,Homo sapiens,12|12,DO:A myositis that results_in inflammation located_in muscle or located_in skin where a skin rash is often seen prior to the onset of muscle weakness. The disease may result from either a viral infection or an autoimmune reaction. DSA00195,GSE128470,GPL96,1000,Inclusion Body Myositis,C0238190,Muscle,GEO,Microarray,Homo sapiens,12|26,"DO:A myositis that is characterized by late onset of skeletal muscle inflammation, weakness, and atrophy with cytoplasmic granules and vacuoles in the muscle." DSA00196,GSE128470,GPL96,950,Necrotizing Myopathy,C4024608,Muscle,GEO,Microarray,Homo sapiens,12|6, DSA00197,GSE189983,GPL24676,1000,Rett Syndrome,C0035372,,GEO,RNA-Seq,Homo sapiens,1|1,"DO:A pervasive developmental disease that is characterized by normal early growth and development followed by a slowing of development, loss of purposeful use of the hands, distinctive hand movements, slowed brain and head growth, problems with walking, seizures, and intellectual disability." DSA00198,GSE189888,GPL21103,105,Ischemia Reperfusion Injury,C0035126,Myocardium,GEO,RNA-Seq,Mus musculus,4|4,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA00199,GSE188864,GPL21103,1000,Obesity,C0028754,Spleen,GEO,RNA-Seq,Mus musculus,3|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA00200,GSE178557,GPL13497,0,Osteoarthritis,C0157946,Cartilage,GEO,Microarray,Homo sapiens,4|4,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA00201,GSE197854,GPL21103,1000,Pancreatic Neuroendocrine Tumor,C0496784,Spleen,GEO,scRNA-Seq,Mus musculus,2|2,DO:An islet cell tumor that has_material_basis_in epithelial cells. DSA00202,GSE197854,GPL21103,1000,Pancreatic Neuroendocrine Tumor,C0496784,Spleen,GEO,scRNA-Seq,Mus musculus,2|2,DO:An islet cell tumor that has_material_basis_in epithelial cells. DSA00203,GSE197854,GPL21103,1000,Pancreatic Neuroendocrine Tumor,C0496784,Spleen,GEO,scRNA-Seq,Mus musculus,2|2,DO:An islet cell tumor that has_material_basis_in epithelial cells. DSA00204,GSE197854,GPL21103,1000,Pancreatic Neuroendocrine Tumor,C0496784,Spleen,GEO,scRNA-Seq,Mus musculus,2|2,DO:An islet cell tumor that has_material_basis_in epithelial cells. DSA00205,GSE186257,GPL24676,338,Pre-Eclampsia,C0032914,Placenta,GEO,RNA-Seq,Homo sapiens,18|25,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA00206,GSE222300,GPL24676,1000,Rectal Cancer,C0007113,Rectum,GEO,scRNA-Seq,Homo sapiens,1|1,DO:A colorectal cancer that is located_in the rectum. DSA00207,GSE218047,GPL24247,1000,Type 2 Diabetes,C0011860,,GEO,RNA-Seq,Mus musculus,3|2,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00208,GSE128470,GPL96,191,Non specific Myopathy,,Muscle,GEO,Microarray,Homo sapiens,12|14, DSA00209,GSE101685,GPL570,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,8|8,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA00210,GSE222144,GPL24676,1000,Heart Failure,C0018801,Heart,GEO,scRNA-Seq,Homo sapiens,1|1,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA00211,GSE101685,GPL570,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,8|8,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA00212,GSE213519,GPL18573,1000,Metastatic Melanoma,C0025202,Brain,GEO,scRNA-Seq,Homo sapiens,2|2,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA00213,GSE211702,GPL24247,63,Retina Degeneration,C0035304,Retina,GEO,scRNA-Seq,Mus musculus,3|3,DO:A retinal disease that is characterized by deterioration of the retina caused by the progressive and eventual death of the cells of the retina. DSA00214,GSE211702,GPL24247,38,Retina Degeneration,C0035304,Retina,GEO,scRNA-Seq,Mus musculus,3|3,DO:A retinal disease that is characterized by deterioration of the retina caused by the progressive and eventual death of the cells of the retina. DSA00215,GSE211489,GPL18460,747,Head And Neck Cancer,C0018671,,GEO,RNA-Seq,Homo sapiens,2|4,"DO:An organ system cancer that arises in the head or neck region. This region includes the nasal cavity, sinuses, lips, mouth, salivary glands, throat, or larynx." DSA00216,GSE211489,GPL18460,163,Head And Neck Cancer,C0018671,,GEO,RNA-Seq,Homo sapiens,2|4,"DO:An organ system cancer that arises in the head or neck region. This region includes the nasal cavity, sinuses, lips, mouth, salivary glands, throat, or larynx." DSA00217,GSE164359,GPL20301,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,RNA-Seq,Homo sapiens,9|18,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA00218,GSE222188,,1000,Neurodevelopmental Disorder,C1535926,,GEO,RNA-Seq,Mus musculus,3|3,"MSH:These are a group of conditions with onset in the developmental period. The disorders typically manifest early in development, often before the child enters grade school, and are characterized by developmental deficits that produce impairments of personal, social, academic, or occupational functioning. (From DSM-5)." DSA00219,GSE100026,GPL18573,1000,Chronic Myeloid Leukemia,C0023473,Peripheral blood,GEO,RNA-Seq,Homo sapiens,5|5,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA00220,GSE100026,GPL18573,1000,Chronic Myeloid Leukemia,C0023473,Peripheral blood,GEO,RNA-Seq,Homo sapiens,5|5,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA00221,GSE100026,GPL18573,1000,Progressive Chronic Myeloid Leukemia,C0023473,Peripheral blood,GEO,RNA-Seq,Homo sapiens,5|5,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA00222,GSE100050,GPL570,1000,Melanoma,C0025202,,GEO,Microarray,Homo sapiens,6|6,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA00223,GSE100054,GPL23126,1,Parkinson's Disease,C0030567,Peripheral blood,GEO,Microarray,Homo sapiens,9|10,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA00224,GSE100080,GPL570,1000,Metastatic Colorectal Cancer,C4721579,,GEO,Microarray,Homo sapiens,1|5, DSA00225,GSE100080,GPL570,1000,Metastatic Colorectal Cancer,C4721579,,GEO,Microarray,Homo sapiens,1|5, DSA00226,GSE100150,GPL6884,1000,Juvenile Dermatomyositis,C0263666,Blood,GEO,Microarray,Homo sapiens,9|40,EFO:Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness. DSA00227,GSE100150,GPL6884,50,Chronic Obstructive Pulmonary Disease,C0024117,Blood,GEO,Microarray,Homo sapiens,24|19,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA00228,GSE100150,GPL6884,1000,Kawasaki Disease,C0026691,Blood,GEO,Microarray,Homo sapiens,23|21,"DO:A lymphadenitis characterized by swelling of cervical lymph nodes in infants and young children and inflammation of medium-sized blood vessels located_in body, has_symptom fever, has_symptom congestion of ocular conjunctivae, has_symptom reddening of lips, has_symptom reddening of oral cavity, has_symptom protuberance of tongue papillae and has_symptom edema of extremities." DSA00229,GSE100150,GPL6884,0,Melanoma,C0025202,Blood,GEO,Microarray,Homo sapiens,5|22,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA00230,GSE100150,GPL6884,1000,Sepsis,C0243026,Blood,GEO,Microarray,Homo sapiens,12|18,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA00231,GSE100150,GPL6884,1000,Sepsis,C0243026,Blood,GEO,Microarray,Homo sapiens,12|15,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA00232,GSE100150,GPL6884,924,Influenza,C0021400,Blood,GEO,Microarray,Homo sapiens,14|25,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA00233,GSE100150,GPL6884,1000,Multiple Sclerosis,C0026769,Blood,GEO,Microarray,Homo sapiens,22|34,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA00234,GSE100150,GPL6884,1000,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,14|55,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA00235,GSE100150,GPL6884,1000,Systemic-Onset Juvenile Idiopathic Arthritis,C0087031,Blood,GEO,Microarray,Homo sapiens,23|62,"MONDO:Systemic-onset juvenile idiopathic arthritis is marked by the severity of the extra-articular manifestations (fever, cutaneous eruptions) and by an equal sex ratio." DSA00236,GSE100150,GPL6884,1000,Tuberculosis,C0041296,Blood,GEO,Microarray,Homo sapiens,11|23,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA00237,GSE100179,GPL17586,1000,Colorectal Adenoma,C1302401,Colon,GEO,Microarray,Homo sapiens,20|20,"EFO:An adenoma that arises from the colon or rectum. The group of colorectal adenomas includes tubular, villous, and tubulovillous adenomas, traditional serrated adenomas, sessile serrated adenomas/polyps, and familial adenomatous polyposis." DSA00238,GSE100179,GPL17586,1000,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,20|20,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA00239,GSE100179,GPL17586,1000,Progressive Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,17|20,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA00240,GSE100179,GPL17586,25,High Grade Colorectal Adenoma,C1302401,Colon,GEO,Microarray,Homo sapiens,8|2,"EFO:An adenoma that arises from the colon or rectum. The group of colorectal adenomas includes tubular, villous, and tubulovillous adenomas, traditional serrated adenomas, sessile serrated adenomas/polyps, and familial adenomatous polyposis." DSA00241,GSE100191,GPL13497,0,Rheumatoid Arthritis,C0003873,Blood,GEO,Microarray,Homo sapiens,5|5,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA00242,GSE100191,GPL13497,6,Rheumatoid Arthritis,C0003873,Blood,GEO,Microarray,Homo sapiens,7|5,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA00243,GSE100281,GPL11532,1000,Chronic Obstructive Pulmonary Disease,C0024117,Quadriceps,GEO,Microarray,Homo sapiens,16|79,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA00244,GSE100297,GPL21290,1000,Multiple Sclerosis,C0026769,Optic chiasm,GEO,RNA-Seq,Homo sapiens,5|5,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA00245,GSE100581,GPL19057,1000,Breast Cancer,C0678222,,GEO,RNA-Seq,Mus musculus,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA00246,GSE100609,GPL16699,0,Osteoporosis,C0029456,,GEO,Microarray,Homo sapiens,4|4,DO:A bone resorption disease characterized by decreased density of normally mineralized bone which results_in the thinning of bone tissue and decreased mechanical strength. DSA00247,GSE100624,GPL17303,1000,Asthma,C0004096,Peripheral blood,GEO,RNA-Seq,Homo sapiens,1|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA00248,GSE100624,GPL17303,1000,Asthma,C0004096,Peripheral blood,GEO,RNA-Seq,Homo sapiens,1|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA00249,GSE100624,GPL17303,1000,Asthma,C0004096,Peripheral blood,GEO,RNA-Seq,Homo sapiens,1|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA00250,GSE100624,GPL17303,1000,Asthma,C0004096,Peripheral blood,GEO,RNA-Seq,Homo sapiens,1|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA00251,GSE100663,GPL7202,103,Demyelination,C0011304,Corpus callosum,GEO,Microarray,Mus musculus,3|6,"MSH:The first region-restricted episode of CNS inflammatory demyelination in a patient. It is usually characterized by an acute monosymptomatic presentation of the optic nerves, brainstem, or spinal cord. It may not reoccur (isolated), or it may progress to MULTIPLE SCLEROSIS." DSA00252,GSE100684,GPL16791,1000,Kaposi Sarcoma,C0036220,,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A connective tissue cancer that derives_from lymphatic endothelium, and derives_from spindle cells, results_in_formation_of vascular channels that fill with blood cells, has_material_basis_in Human herpesvirus 8 (HHV8)." DSA00253,GSE100785,GPL11154,1000,Colon Tumor,C0009375,Colon,GEO,RNA-Seq,Homo sapiens,6|6,DO:A colorectal cancer that is located_in the colon. DSA00254,GSE100882,GPL16791,1000,T-Cell Prolymphocytic Leukemia,C2363142,Peripheral blood,GEO,RNA-Seq,Homo sapiens,5|10,EFO:A slow-growing type of leukemia (blood cancer) in which too many lymphocytes are found in the bone marrow and/or blood. The T-cell is specified as the defective cell line. DSA00255,GSE101112,GPL17021,1000,Alzheimer's Disease,C0002395,Hippocampus,GEO,RNA-Seq,Mus musculus,5|6,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA00256,GSE101141,GPL570,43,Myelomeningocele,C0086664,,GEO,Microarray,Homo sapiens,10|10,"DO:A spina bifida characterized by protrusion of the spinal cord through an opening, covered by meningeal membranes." DSA00257,GSE101176,GPL2895,0,Endometriosis,C0014175,,GEO,Microarray,Homo sapiens,3|3,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA00258,GSE101176,GPL2895,0,Endometriosis,C0014175,,GEO,Microarray,Homo sapiens,3|3,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA00259,GSE101176,GPL2895,0,Endometriosis,C0014175,,GEO,Microarray,Homo sapiens,3|3,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA00260,GSE101685,GPL570,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,8|8,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA00261,GSE131329,GPL6244,1000,Hepatoblastoma,C0206624,Liver,GEO,Microarray,Homo sapiens,14|53,DO:A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver. DSA00262,GSE10123,GPL2895,196,Premature Aging,C0231341,,GEO,Microarray,Homo sapiens,6|6,"MONDO:Changes in the organism associated with senescence, occurring at an accelerated rate." DSA00263,GSE101286,GPL6947,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,3|4,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA00264,GSE101286,GPL6947,1000,Non-Specific Interstitial Pneumonia,C1290344,Lung,GEO,Microarray,Homo sapiens,3|8,"DO:An idiopathic interstitial pneumonia that occurs mainly in women, people who do not smoke, and people younger than 50 years with no known cause or risk factors. Lung biopsies may show predominantly interstitial inflammation or fibrosis or a combination of inflammation and fibrosis. A dry cough and shortness of breath develop over 6 to 18 months. Low-grade fever and a feeling of illness (malaise) may occur." DSA00265,GSE101288,GPL6947,0,Spinocerebellar Ataxia Type 12,,Peripheral blood,GEO,Microarray,Homo sapiens,9|15, DSA00266,GSE101425,GPL570,88,B-Cell Acute Lymphoblastic Leukemia,C0862030,,GEO,Microarray,Homo sapiens,16|35,DO:A precursor lymphoblastic lymphoma/leukemia that is characterized by the presence of too many B-cell lymphoblasts in the blood and bone marrow. DSA00267,GSE101425,GPL570,0,B-Cell Acute Lymphoblastic Leukemia,C0862030,,GEO,Microarray,Homo sapiens,16|6,DO:A precursor lymphoblastic lymphoma/leukemia that is characterized by the presence of too many B-cell lymphoblasts in the blood and bone marrow. DSA00268,GSE101425,GPL570,0,B-Cell Acute Lymphoblastic Leukemia,C0862030,,GEO,Microarray,Homo sapiens,16|29,DO:A precursor lymphoblastic lymphoma/leukemia that is characterized by the presence of too many B-cell lymphoblasts in the blood and bone marrow. DSA00269,GSE101451,GPL20795,226,Androgenetic Alopecia,C0162311,Hair follicle,GEO,RNA-Seq,Homo sapiens,1|2,DO:An alopecia that is characterized by M-shaped hair line recession and thinning of hair at the crown of the head in males. DSA00270,GSE101451,GPL20795,854,Androgenetic Alopecia,C0162311,Hair follicle,GEO,RNA-Seq,Homo sapiens,1|2,DO:An alopecia that is characterized by M-shaped hair line recession and thinning of hair at the crown of the head in males. DSA00271,GSE101474,GPL16686,19,Sebaceous Gland Carcinoma,C0206684,,GEO,Microarray,Homo sapiens,4|4,"HPO:A carcinoma that arises in a sebaseous gland (an exocrine gland of the skin that secretes sebum, a waxy substance)" DSA00272,GSE101474,GPL16686,15,Sebaceous Gland Carcinoma,C0206684,,GEO,Microarray,Homo sapiens,4|4,"HPO:A carcinoma that arises in a sebaseous gland (an exocrine gland of the skin that secretes sebum, a waxy substance)" DSA00273,GSE101534,GPL16686,6,Parkinson's Disease,C0030567,,GEO,Microarray,Homo sapiens,18|18,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA00274,GSE101534,GPL16686,0,Parkinson's Disease,C0030567,,GEO,Microarray,Homo sapiens,18|6,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA00275,GSE101548,GPL11154,3,Parkinson's Disease,C0030567,Skin,GEO,RNA-Seq,Homo sapiens,2|2,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA00276,GSE101548,GPL11154,23,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,4|4,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA00277,GSE101548,GPL11154,6,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,3|4,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA00278,GSE101548,GPL11154,5,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,4|4,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA00279,GSE101585,GPL20301,125,Dilated Cardiomyopathy,C0007193,Peripheral blood,GEO,RNA-Seq,Homo sapiens,7|8,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA00280,GSE101621,GPL21103,1000,T-Cell Acute Lymphoblastic Leukemia,C1961099,Spleen,GEO,RNA-Seq,Mus musculus,3|3,DO:An acute lymphoblastic leukemia that is characterized by too many T-cell lymphoblasts found in the bone marrow and blood. DSA00281,GSE101702,GPL21185,1000,Influenza,C0021400,Blood,GEO,Microarray,Homo sapiens,52|107,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA00282,GSE101720,GPL18573,1,Rhinitis,C0035455,Bronchus,GEO,RNA-Seq,Homo sapiens,8|10,"DO:A upper respiratory infectious disease which involves irritation and inflammation of the mucous membrane of the nose due to viruses, bacteria or irritants. The inflammation results in generation of excessive amounts of mucus leading to runny nose, as well as nasal congestion and post-nasal drip." DSA00283,GSE101720,GPL18573,13,Rhinitis,C0035455,Nasal,GEO,RNA-Seq,Homo sapiens,9|10,"DO:A upper respiratory infectious disease which involves irritation and inflammation of the mucous membrane of the nose due to viruses, bacteria or irritants. The inflammation results in generation of excessive amounts of mucus leading to runny nose, as well as nasal congestion and post-nasal drip." DSA00284,GSE101720,GPL18573,807,Asthma;Rhinitis,,Bronchus,GEO,RNA-Seq,Homo sapiens,8|7, DSA00285,GSE101720,GPL18573,285,Asthma;Rhinitis,,Nasal,GEO,RNA-Seq,Homo sapiens,9|7, DSA00286,GSE101756,GPL18573,1000,B-Cell Expansion With Nfkb And T-Cell Anergy,C4551967,Blood,GEO,RNA-Seq,Homo sapiens,8|8,"MONDO:BENTA disease (B cell Expansion with N F-N:B and T cell Anergy) is a very rare congenital immune deficiency disorder. The main symptoms include spleen enlargement (splenomegalia) and frequent ear, sinus, and lung infections early in life. Some patients can present with molluscum contagiosum or chronic Epstein-Barr virus (EBV) infection. Blood exams show alterations of several immune cells with very high numbers of polyclonal B cell lymphocytos (above 2200/N20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA00751,GSE113469,GPL10558,1000,Coeliac Disease,C0007570,,GEO,Microarray,Homo sapiens,20|17,"DO:An autoimmune disease of gastrointestinal tract that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite." DSA00752,GSE113524,GPL16791,0,Alzheimer's Disease,C0002395,Olfactory bulb,GEO,RNA-Seq,Homo sapiens,20|19,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA00753,GSE138134,GPL13112,1000,Acute Pancreatitis,C0001339,,GEO,RNA-Seq,Mus musculus,1|1,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA00754,GSE138134,GPL13112,1000,Acute Pancreatitis,C0001339,,GEO,RNA-Seq,Mus musculus,1|1,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA00755,GSE138182,GPL19057,1,Malnutrition,C0162429,Cortex,GEO,RNA-Seq,Mus musculus,4|5,"DO:A nutritional deficiency disease that is characterized by inadequate dietary protein and calories, which can have profound systemic effects including decreased metabolism, altered tissue distribution, compromised immunity, and impaired growth, and has_material_basis_in dietary deprivation." DSA00756,GSE125521,GPL6885,1000,Chronic Obstructive Pulmonary Disease,C0024117,Lung,GEO,Microarray,Mus musculus,9|9,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA00757,GSE125592,GPL16791,875,Complete Hydatidiform Mole,C0678213,,GEO,RNA-Seq,Homo sapiens,2|2,"EFO:A gestational trophoblastic disorder characterized by marked enlargement of the chorionic villi, hyperplasia of the villous trophoblastic cells and hydropic changes." DSA00758,GSE125592,GPL16791,1000,Complete Hydatidiform Mole,C0678213,,GEO,RNA-Seq,Homo sapiens,10|10,"EFO:A gestational trophoblastic disorder characterized by marked enlargement of the chorionic villi, hyperplasia of the villous trophoblastic cells and hydropic changes." DSA00759,GSE125638,GPL20301,491,Myotonic Dystrophy,C0027126,,GEO,RNA-Seq,Homo sapiens,2|4,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA00760,GSE125745,GPL6887,0,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Mus musculus,2|2,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA00761,GSE125769,GPL20301,308,Type 2 Diabetes Mellitus,C0011847,Pancreas,GEO,RNA-Seq,Homo sapiens,2|12,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00762,GSE125769,GPL20301,782,Type 2 Diabetes Mellitus,C0011847,,GEO,RNA-Seq,Homo sapiens,2|11,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00763,GSE125769,GPL20301,861,Type 2 Diabetes Mellitus,C0011847,,GEO,RNA-Seq,Homo sapiens,2|12,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00764,GSE125779,GPL17586,1000,Focal Segmental Glomerulosclerosis,C0017668,Kidney tubules,GEO,Microarray,Homo sapiens,8|8,"EFO:A renal disorder characterized by sclerotic lesions in the glomeruli. Causes include drugs, viruses, and malignancies (lymphomas), or it may be idiopathic. It presents with asymptomatic proteinuria or nephritic syndrome and it may lead to renal failure." DSA00765,GSE125805,GPL21697,0,Schizophrenia,C0036341,,GEO,RNA-Seq,Homo sapiens,9|9,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA00766,GSE125818,GPL10558,0,IgA Nephropathy,C0017661,,GEO,Microarray,Homo sapiens,4|5,DO:A glomerulonephritis characterized by build up of IgA antibody in the glomerulus. DSA00767,GSE125873,GPL16791,1000,Bronchopulmonary Dysplasia,C0006287,Peripheral blood,GEO,RNA-Seq,Homo sapiens,10|21,"MONDO:Bronchopulmonary dysplasia is a chronic respiratory disease that results from complications related to lung injury during the treatment of infant acute respiratory distress syndrome in low-birth-weight premature infants or from abnormal lung development in older infants. Clinical signs are tachypnea, tachycardia and signs of respiratory distress such as intercostal recession, grunting and nasal flaring." DSA00768,GSE138250,GPL9052,1000,Complete Hydatidiform Mole,C0678213,Placenta,GEO,RNA-Seq,Homo sapiens,1|4,"EFO:A gestational trophoblastic disorder characterized by marked enlargement of the chorionic villi, hyperplasia of the villous trophoblastic cells and hydropic changes." DSA00769,GSE125991,GPL10558,975,Visceral Leishmaniasis,C0023290,Blood,GEO,Microarray,Homo sapiens,6|10,"DO:A leishmaniasis that is the most severe form of the disease caused by protozoan parasites of the Leishmania genus, resulting in the infection of the internal organs such as liver, spleen and bone marrow. The symptoms include fever, weight loss, and an enlarged spleen and liver." DSA00770,GSE125999,GPL21697,0,Schizophrenia,C0036341,,GEO,RNA-Seq,Homo sapiens,30|30,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA00771,GSE126009,GPL11154,85,Azoospermia,C0004509,,GEO,RNA-Seq,Homo sapiens,2|4,DO:A male infertility disease characterized by the absence of any measurable level of sperm in semen. DSA00772,GSE126009,GPL11154,1,Azoospermia,C0004509,,GEO,RNA-Seq,Homo sapiens,2|4,DO:A male infertility disease characterized by the absence of any measurable level of sperm in semen. DSA00773,GSE126009,GPL11154,16,Azoospermia,C0004509,,GEO,RNA-Seq,Homo sapiens,2|4,DO:A male infertility disease characterized by the absence of any measurable level of sperm in semen. DSA00774,GSE126027,GPL18573,1000,Kabuki Syndrome 1,C0796004,,GEO,scRNA-Seq,Homo sapiens,2|1,"DO:A syndrome characterized by multiple congenital anomalies and mental retardation. Other characteristics include a peculiar facial gestalt, short stature, skeletal and visceral abnormalities, cardiac anomalies, and immunological defects." DSA00775,GSE126027,GPL18573,1000,Kabuki Syndrome 1,C0796004,,GEO,scRNA-Seq,Homo sapiens,1|2,"DO:A syndrome characterized by multiple congenital anomalies and mental retardation. Other characteristics include a peculiar facial gestalt, short stature, skeletal and visceral abnormalities, cardiac anomalies, and immunological defects." DSA00776,GSE126124,GPL6244,1000,Crohn's Disease,C0010346,Colon,GEO,Microarray,Homo sapiens,19|37,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA00777,GSE126124,GPL6244,1000,Crohn's Disease,C0010346,Peripheral blood,GEO,Microarray,Homo sapiens,32|39,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA00778,GSE126124,GPL6244,0,Uc - L Colitis,,Colon,GEO,Microarray,Homo sapiens,19|4, DSA00779,GSE126124,GPL6244,1000,Uc - L Colitis,,Peripheral blood,GEO,Microarray,Homo sapiens,32|4, DSA00780,GSE126124,GPL6244,1000,Uc - Pancolitis,,Peripheral blood,GEO,Microarray,Homo sapiens,32|14, DSA00781,GSE126124,GPL6244,1000,Uc - Pancolitis,,Colon,GEO,Microarray,Homo sapiens,19|13, DSA00782,GSE126169,GPL18573,1000,Obesity,C0028754,,GEO,RNA-Seq,Homo sapiens,5|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA00783,GSE126307,GPL13369,4,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,9|31,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA00784,GSE126352,GPL18573,48,Hypercholesterolemia,C0020443,,GEO,RNA-Seq,Homo sapiens,5|5,HPO:An increased concentration of cholesterol in the blood. DSA00785,GSE126427,GPL24676,28,Multiple Sclerosis,C0026769,Whole blood,GEO,RNA-Seq,Homo sapiens,3|3,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA00786,GSE126487,GPL21290,1000,Posterior Polymorphous Corneal Dystrophy,C0339284,,GEO,RNA-Seq,Homo sapiens,1|1,DO:A corneal dystrophy that is characterised by changes in Descemet's membrane and endothelial layer. DSA00787,GSE126512,GPL11154,35,Depression,C0011581,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A mood disorder that involves the presence of a low mood almost daily over a span of at least two years. DSA00788,GSE126547,GPL17021,1000,Leukemia,C0023418,Bone marrow,GEO,RNA-Seq,Mus musculus,4|4,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA00789,GSE126547,GPL17021,1000,Leukemia,C0023418,Bone marrow,GEO,RNA-Seq,Mus musculus,4|4,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA00790,GSE126547,GPL17021,1000,Leukemia,C0023418,Bone marrow,GEO,RNA-Seq,Mus musculus,4|4,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA00791,GSE126547,GPL17021,1000,Leukemia,C0023418,Bone marrow,GEO,RNA-Seq,Mus musculus,4|4,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA00792,GSE126553,GPL24247,1000,Type 1 Diabetes,C0011854,,GEO,RNA-Seq,Mus musculus,1|1,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA00793,GSE126569,GPL16791|GPL20301,1000,Idiopathic Dilated Cardiomyopathy,C1449563,Left ventricle,GEO,RNA-Seq,Homo sapiens,17|15,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LMNA gene on chromosome 1q21. DSA00794,GSE126614,GPL11154,1000,Tuberculosis,C0041296,Blood,GEO,RNA-Seq,Homo sapiens,19|20,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA00795,GSE126614,GPL11154,1000,Tuberculosis,C0041296,Blood,GEO,RNA-Seq,Homo sapiens,19|20,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA00796,GSE126783,GPL21103,1000,Retina Degeneration,C0035304,Retina,GEO,scRNA-Seq,Mus musculus,1|1,DO:A retinal disease that is characterized by deterioration of the retina caused by the progressive and eventual death of the cells of the retina. DSA00797,GSE126795,GPL18635,1000,Metabolic Myopathy,C0270984,Gastrocnemius muscle,GEO,RNA-Seq,Mus musculus,3|3,MONDO:A group of rare inherited disorders characterized by a deficiency of enzymes that are involved in metabolic pathways that affect muscles. The disorders are characterized by muscle dysfunction. DSA00798,GSE126802,GPL13497,0,Multiple Sclerosis,C0026769,Subcortical white matter,GEO,Microarray,Homo sapiens,9|18,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA00799,GSE126848,GPL18573,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Homo sapiens,14|16,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA00800,GSE126848,GPL18573,243,Obesity,C0028754,Liver,GEO,RNA-Seq,Homo sapiens,14|12,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA00801,GSE126848,GPL18573,1000,Steatosis,C2711227,Liver,GEO,RNA-Seq,Homo sapiens,14|15,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA00802,GSE126887,GPL13112,324,Obesity,C0028754,,GEO,RNA-Seq,Mus musculus,2|2,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA00803,GSE126923,GPL21847,36,Acute Liver Inflammation,C0267797,,GEO,Microarray,Homo sapiens,4|4,"HPO:Acute hepatic injury resulting from inflammation typically accompanied by increased serum alanine transaminase activity. Etiologies include viral hepatitis, drugs, toxins, and autoimmune disorders." DSA00804,GSE126923,GPL21847,106,Acute Liver Inflammation,C0267797,,GEO,Microarray,Homo sapiens,3|3,"HPO:Acute hepatic injury resulting from inflammation typically accompanied by increased serum alanine transaminase activity. Etiologies include viral hepatitis, drugs, toxins, and autoimmune disorders." DSA00805,GSE126923,GPL21847,81,Acute Liver Inflammation,C0267797,,GEO,Microarray,Homo sapiens,4|7,"HPO:Acute hepatic injury resulting from inflammation typically accompanied by increased serum alanine transaminase activity. Etiologies include viral hepatitis, drugs, toxins, and autoimmune disorders." DSA00806,GSE127190,GPL21493,1000,Experimental Autoimmune Encephalomyelitis,C0014072,Colon,GEO,RNA-Seq,Mus musculus,10|9,"EFO:An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)" DSA00807,GSE127255,GPL6246,1000,Muscular Dystrophy,C0026850,Plantaris muscle,GEO,Microarray,Mus musculus,6|6,"DO:A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted." DSA00808,GSE127255,GPL6246,1000,Muscular Dystrophy,C0026850,Plantaris muscle,GEO,Microarray,Mus musculus,6|6,"DO:A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted." DSA00809,GSE127265,GPL23126,540,Cervical Cancer,C4048328,,GEO,Microarray,Homo sapiens,3|7,DO:A female reproductive organ cancer that is located_in the cervix. DSA00810,GSE138480,GPL17021,1,Axon Injury,,Embryonic dorsal root ganglia,GEO,RNA-Seq,Mus musculus,3|3, DSA00811,GSE127435,GPL1261,228,Defective Skin Barrier Function,,Epidermis,GEO,Microarray,Mus musculus,5|4, DSA00812,GSE138480,GPL17021,1,Axon Injury,,Embryonic dorsal root ganglia,GEO,RNA-Seq,Mus musculus,3|3, DSA00813,GSE127468,GPL18573,1000,HIV-1 Infection,C1836231,,GEO,RNA-Seq,Homo sapiens,4|4,EFO:The type species of lentivirus and the etiologic agent of acquired immunodeficiency syndrome (AIDS). It is characterized by its cytopathic effect and affinity for the T4-lymphocyte. DSA00814,GSE127468,GPL18573,632,HIV-1 Infection,C1836231,,GEO,RNA-Seq,Homo sapiens,4|4,EFO:The type species of lentivirus and the etiologic agent of acquired immunodeficiency syndrome (AIDS). It is characterized by its cytopathic effect and affinity for the T4-lymphocyte. DSA00815,GSE127468,GPL18573,542,HIV-1 Infection,C1836231,,GEO,RNA-Seq,Homo sapiens,4|4,EFO:The type species of lentivirus and the etiologic agent of acquired immunodeficiency syndrome (AIDS). It is characterized by its cytopathic effect and affinity for the T4-lymphocyte. DSA00816,GSE127478,GPL20301,1000,Mitochondrial Myopathy; Encephalopathy; Lactic Acidosis; And Stroke-Like Episodes,C0162671,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A mitochondrial encephalomyopathy that is characterized by mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes, has_symptom myalgia, motor weakness, headaches, seizures, and stroke-like episodes with acute hemiparesis and severe headaches, and develops_from mutation in mitochondrial genes including MT-TL1, which encodes tRNA proteins." DSA00817,GSE127696,GPL20301,191,Cystic Fibrosis,C0010674,Bronchus,GEO,RNA-Seq,Homo sapiens,6|7,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA00818,GSE127696,GPL20301,219,Cystic Fibrosis,C0010674,Bronchus,GEO,RNA-Seq,Homo sapiens,6|7,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA00819,GSE127831,GPL18573,1000,Cutaneous Leishmaniasis,C0023283,Skin,GEO,RNA-Seq,Homo sapiens,7|21,"DO:A leishmaniasis that involves skin infection caused by Leishmania species, resulting in one or more cutaneous lesions." DSA00820,GSE127853,GPL20795,0,Myocardial Infarction,C0027051,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA00821,GSE127854,GPL19057,361,Hypertrophic Cardiomyopathy,C0007194,,GEO,RNA-Seq,Mus musculus,3|4,DO:A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations. DSA00822,GSE127873,GPL16791,28,Ovarian Cancer,C1140680,Ovary,GEO,RNA-Seq,Homo sapiens,9|22,DO:A female reproductive organ cancer that is located_in the ovary. DSA00823,GSE127903,GPL20795,1000,Intrahepatic Cholangiocarcinoma,C0345905,,GEO,RNA-Seq,Homo sapiens,2|2,DO:A cholangiocarcinoma that arises from the intrahepatic bile duct epithelium in any site of the intrahepatic biliary tree. DSA00824,GSE127952,GPL20995,3,Primary Sjogren Syndrome,C0151449,Salivary gland,GEO,Microarray,Homo sapiens,6|8,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA00825,GSE128027,GPL16791,1000,Asthma,C0004096,Venous blood,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA00826,GSE128027,GPL16791,1000,Asthma,C0004096,Venous blood,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA00827,GSE128027,GPL16791,1000,Asthma,C0004096,Venous blood,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA00828,GSE128033,GPL18573,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,scRNA-Seq,Homo sapiens,1|5,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA00829,GSE128033,GPL18573,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,scRNA-Seq,Homo sapiens,1|3,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA00830,GSE128040,GPL18573,1000,Mitochondrial Abnormalities,C4020732,,GEO,RNA-Seq,Homo sapiens,1|1,"HPO:An anomaly of the mitochondrion, the membranous cytoplasmic organelle the interior of which is subdivided by cristae. The mitochondrion is a self replicating organelle that is the site of tissue respiration." DSA00831,GSE128044,GPL22598,2,Liver Tumor,C0345904,Liver,GEO,Microarray,Mus musculus,3|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA00832,GSE128044,GPL22598,641,Liver Tumor,C0345904,Liver,GEO,Microarray,Mus musculus,3|4,DO:A hepatobiliary system cancer that is located_in the liver. DSA00833,GSE128044,GPL22598,522,Liver Tumor,C0345904,Liver,GEO,Microarray,Mus musculus,3|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA00834,GSE128044,GPL22598,1000,Liver Tumor,C0345904,Liver,GEO,Microarray,Mus musculus,3|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA00835,GSE128045,GPL23092,1000,Liver Tumor,C0345904,,GEO,Microarray,Mus musculus,4|4,DO:A hepatobiliary system cancer that is located_in the liver. DSA00836,GSE128046,GPL23092,1000,Liver Tumor,C0345904,,GEO,Microarray,Mus musculus,3|4,DO:A hepatobiliary system cancer that is located_in the liver. DSA00837,GSE128046,GPL23092,1000,Liver Tumor,C0345904,,GEO,Microarray,Mus musculus,3|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA00838,GSE138480,GPL17021,57,Axon Injury,,Embryonic dorsal root ganglia,GEO,RNA-Seq,Mus musculus,3|3, DSA00839,GSE128101,GPL20301|GPL21103,27,Marfan Syndrome,C0024796,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A connective tissue disease that is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens." DSA00840,GSE128169,GPL18573,1000,Systemic Sclerosis With Lung Involvement,C0339904,Lung,GEO,scRNA-Seq,Homo sapiens,1|4,HPO:It is a bilateral reticular pattern of linear or lineonodular densities that are most pronounced in basilar portions of the lungs on standard chest x-ray. It is the third minor criterion for scleroderma diagnosis. DSA00841,GSE128169,GPL18573,1000,Systemic Sclerosis With Lung Involvement,C0339904,Lung,GEO,scRNA-Seq,Homo sapiens,3|2,HPO:It is a bilateral reticular pattern of linear or lineonodular densities that are most pronounced in basilar portions of the lungs on standard chest x-ray. It is the third minor criterion for scleroderma diagnosis. DSA00842,GSE138480,GPL17021,504,Axon Injury,,Embryonic dorsal root ganglia,GEO,RNA-Seq,Mus musculus,3|3, DSA00843,GSE128185,GPL26290,178,Rett Syndrome,C0035372,Forebrain,GEO,Microarray,Mus musculus,10|10,"DO:A pervasive developmental disease that is characterized by normal early growth and development followed by a slowing of development, loss of purposeful use of the hands, distinctive hand movements, slowed brain and head growth, problems with walking, seizures, and intellectual disability." DSA00844,GSE128212,GPL11002,1000,T-Cell Acute Lymphoblastic Leukemia,C1961099,Thymus,GEO,RNA-Seq,Mus musculus,3|9,DO:An acute lymphoblastic leukemia that is characterized by too many T-cell lymphoblasts found in the bone marrow and blood. DSA00845,GSE128270,GPL16699,50,Chagas Disease,C0041234,,GEO,Microarray,Homo sapiens,3|2,DO:A parasitic protozoa infectious disease that involves infection caused by parasitic protozoan of the genus Trypanosoma in animals and humans. DSA00846,GSE128303,GPL10558,396,Sepsis,C0243026,,GEO,Microarray,Homo sapiens,4|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA00847,GSE128303,GPL10558,1000,Sepsis,C0243026,,GEO,Microarray,Homo sapiens,4|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA00848,GSE128303,GPL10558,0,Sepsis,C0243026,,GEO,Microarray,Homo sapiens,4|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA00849,GSE128303,GPL10558,0,Sepsis,C0243026,,GEO,Microarray,Homo sapiens,4|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA00850,GSE128314,GPL17586,1000,Dermatomyositis,C0011633,Skin,GEO,Microarray,Homo sapiens,5|4,DO:A myositis that results_in inflammation located_in muscle or located_in skin where a skin rash is often seen prior to the onset of muscle weakness. The disease may result from either a viral infection or an autoimmune reaction. DSA00851,GSE128334,GPL17021,1000,Non-Alcoholic Steatohepatitis,C3241937,,GEO,scRNA-Seq,Mus musculus,2|2,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA00852,GSE128337,GPL19057|GPL21103,1000,Non-Alcoholic Steatohepatitis,C3241937,,GEO,RNA-Seq,Mus musculus,5|15,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA00853,GSE128342,GPL18573,1000,Mixed Lineage Leukemia,C3888194,,GEO,RNA-Seq,Homo sapiens,2|2, DSA00854,GSE128375,GPL16570,1,Diabetes,C0011847,Bone marrow,GEO,Microarray,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA00855,GSE128496,GPL13112,1000,Gne Myopathy,C1833373,Kidney,GEO,RNA-Seq,Mus musculus,4|4,"MONDO:Nonaka distal myopathy (described in Japan) and the quadriceps-sparing autosomal recessive inclusion body myopathy type 2 (IBM2; independently described in Iranian Jews and later in other Jewish and non-Jewish populations) constitute the same pathological entity, distinguished by the sparing of quadriceps." DSA00856,GSE128531,GPL18573,1000,Cutaneous T Cell Lymphoma,C0079773,Skin,GEO,scRNA-Seq,Homo sapiens,4|5,DO:A non-Hodgkin's lymphoma that has_material_basis_in a mutation of T cells. DSA00857,GSE138480,GPL17021,145,Axon Injury,,Embryonic dorsal root ganglia,GEO,RNA-Seq,Mus musculus,3|3, DSA00858,GSE128626,GPL18573,157,Tuberculosis,C0041296,,GEO,RNA-Seq,Homo sapiens,4|4,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA00859,GSE138841,GPL18460,1000,West Nile Virus Infection,C0043124,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A viral infectious disease that results in inflammation located in brain, has_material_basis_in West Nile virus, which is transmitted_by Culex, Aedes, or Anopheles species of mosquitoes. The infection has_symptom high fever, has_symptom headache, has_symptom neck stiffness, has_symptom stupor, has_symptom disorientation, has_symptom coma, has_symptom tremors, has_symptom convulsions, has_symptom muscle weakness, has_symptom vision loss, has_symptom numbness, and has_symptom paralysis." DSA00860,GSE138841,GPL18460,1000,West Nile Virus Infection,C0043124,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A viral infectious disease that results in inflammation located in brain, has_material_basis_in West Nile virus, which is transmitted_by Culex, Aedes, or Anopheles species of mosquitoes. The infection has_symptom high fever, has_symptom headache, has_symptom neck stiffness, has_symptom stupor, has_symptom disorientation, has_symptom coma, has_symptom tremors, has_symptom convulsions, has_symptom muscle weakness, has_symptom vision loss, has_symptom numbness, and has_symptom paralysis." DSA00861,GSE128637,GPL10558,1000,Hidradenitis Suppurativa,C0162836,Skin,GEO,Microarray,Homo sapiens,11|10,"DO:A hidradenitis that is characterized by chronic inflammation of the apocrine sweat glands, has_symptom painful nodules, abscesses, sinus tract formation, scarring, erythema, pruritis, and pain, and has_material_basis_in chronic inflammation of the apocrine sweat glands leading to recurrent folliculitis and an accompanying immune response that worsens inflammation." DSA00862,GSE12865,GPL6244,1000,Pediatric Osteosarcoma,C1332986,,GEO,Microarray,Homo sapiens,2|12,MONDO:An osteosarcoma occurring in childhood. DSA00863,GSE128682,GPL21697,1000,Ulcerative Colitis,C0009324,Stomach,GEO,RNA-Seq,Homo sapiens,16|14,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA00864,GSE128682,GPL21697,1000,Ulcerative Colitis,C0009324,Stomach,GEO,RNA-Seq,Homo sapiens,16|14,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA00865,GSE139171,GPL19057,444,Acute Kidney Injury,C2609414,Kidney,GEO,RNA-Seq,Mus musculus,3|3,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA00866,GSE139171,GPL19057,134,Acute Kidney Injury,C2609414,Kidney,GEO,RNA-Seq,Mus musculus,3|3,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA00867,GSE139899,GPL21103,24,Injury of Liver,C0160390,Liver,GEO,RNA-Seq,Mus musculus,3|3,NCI:Damage to liver structure or function due to trauma or toxicity. DSA00868,GSE128726,GPL21185,1000,Hepatocellular Carcinoma,C0334287,,GEO,Microarray,Homo sapiens,9|10,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA00869,GSE128726,GPL21185,247,Hepatocellular Carcinoma,C0334287,,GEO,Microarray,Homo sapiens,9|14,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA00870,GSE128740,GPL18573,508,Lymphatic Malformation 3,C4747646,Whole blood,GEO,RNA-Seq,Homo sapiens,9|10,DO:A hereditary lymphedema characterized by autosomal dominant inheritance that has_material_basis_in mutation in the GJC2 gene on chromosome 1q42. DSA00871,GSE128818,GPL17021|GPL19057|GPL21103|GPL21476,438,Developmental Disability,C0008073,Limb bud,GEO,scRNA-Seq,Mus musculus,1|1,"EFO:Disorders in which there is a delay in development based on that expected for a given age level or stage of development. These impairments or disabilities originate before age 18, may be expected to continue indefinitely, and constitute a substantial impairment. Biological and nonbiological factors are involved in these disorders. (From American Psychiatric Glossary, 6th ed)" DSA00872,GSE128838,GPL13112,20,Williams Syndrome,C0175702,Cortex,GEO,RNA-Seq,Mus musculus,3|3,"DO:A syndrome that is characterized by mild to moderate intellectual disability, a broad forehead, a short nose with a broad tip, full cheeks, and a wide mouth with full lips and difficulty with visual-spatial tasks and has_material_basis_in hemizygous deletion of 1.5 to 1.8 Mb on chromosome 7q11.23." DSA00873,GSE128839,GPL13112,47,Williams Syndrome,C0175702,Cortex,GEO,RNA-Seq,Mus musculus,3|3,"DO:A syndrome that is characterized by mild to moderate intellectual disability, a broad forehead, a short nose with a broad tip, full cheeks, and a wide mouth with full lips and difficulty with visual-spatial tasks and has_material_basis_in hemizygous deletion of 1.5 to 1.8 Mb on chromosome 7q11.23." DSA00874,GSE128840,GPL11154,255,Williams Syndrome,C0175702,Frontal cortex,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A syndrome that is characterized by mild to moderate intellectual disability, a broad forehead, a short nose with a broad tip, full cheeks, and a wide mouth with full lips and difficulty with visual-spatial tasks and has_material_basis_in hemizygous deletion of 1.5 to 1.8 Mb on chromosome 7q11.23." DSA00875,GSE128844,GPL21697,1000,Myotonic Dystrophy Type 1,C0027126,Skin,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA00876,GSE128850,GPL15523,1000,Pure Total Flavonoids From Citrus,,Liver,GEO,Microarray,Mus musculus,3|3, DSA00877,GSE129006,GPL11002|GPL17021,164,Respiratory Failure,C1145670,Lung,GEO,RNA-Seq,Mus musculus,2|2,"EFO:The significant impairment of gas exchange within the lungs resulting in hypoxia, hypercarbia, or both, to the extent that organ tissue perfusion is severely compromised. Causes include chronic obstructive pulmonary disease, asthma, emphysema, acute respiratory distress syndrome, pneumonia, pulmonary edema, pneumothorax, and congestive heart failure. Treatment requires intubation and mechanical ventilation until the time the lungs recover sufficient function." DSA00878,GSE129006,GPL11002|GPL17021,224,Respiratory Failure,C1145670,Lung,GEO,RNA-Seq,Mus musculus,2|2,"EFO:The significant impairment of gas exchange within the lungs resulting in hypoxia, hypercarbia, or both, to the extent that organ tissue perfusion is severely compromised. Causes include chronic obstructive pulmonary disease, asthma, emphysema, acute respiratory distress syndrome, pneumonia, pulmonary edema, pneumothorax, and congestive heart failure. Treatment requires intubation and mechanical ventilation until the time the lungs recover sufficient function." DSA00879,GSE129033,GPL16791,1000,Leprosy,C0023343,Blood,GEO,RNA-Seq,Homo sapiens,3|9,"DO:A primary bacterial infectious disease that results_in infection located_in superficial peripheral nerves, located_in skin, located_in mucous membranes of the upper respiratory tract, located_in anterior chamber of the eyes, or located_in testes, has_material_basis_in Mycobacterium leprae, which is transmitted_by aerosol spread from infected nasal secretions to exposed nasal and oral mucosa. The infection has_symptom skin lesions, has_symptom sensory loss, has_symptom motor loss and has_symptom eye damage." DSA00880,GSE139947,GPL16791,1000,Pathological Retinal Angiogenesis,,,GEO,RNA-Seq,Homo sapiens,3|1, DSA00881,GSE140013,GPL13112,0,Obesity,C0028754,Placenta,GEO,RNA-Seq,Mus musculus,4|8,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA00882,GSE140929,GPL21493,18,Colorectal Carcinoma,C0009402,Colon,GEO,RNA-Seq,Mus musculus,4|6,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA00883,GSE140972,GPL18635,0,Inflammatory Responses Driven By The High Fat Diet,,Small intestine,GEO,RNA-Seq,Mus musculus,3|3, DSA00884,GSE140972,GPL18635,4,Inflammatory Responses Driven By The High Fat Diet,,Small intestine,GEO,RNA-Seq,Mus musculus,3|3, DSA00885,GSE140972,GPL18635,0,Inflammatory Responses Driven By The High Fat Diet,,Small intestine,GEO,RNA-Seq,Mus musculus,3|3, DSA00886,GSE141027,GPL16791,14,Lipomas,C0023798,Subcutaneous adipose tissue,GEO,RNA-Seq,Homo sapiens,4|4,DO:A lipoma that is characterized by floret giant cells with overlapping nuclei. DSA00887,GSE141027,GPL16791,22,Lipomas,C0023798,Subcutaneous adipose tissue,GEO,RNA-Seq,Homo sapiens,4|4,DO:A lipoma that is characterized by floret giant cells with overlapping nuclei. DSA00888,GSE129296,GPL23038,1000,Alzheimer's Disease,C0002395,Cortex and hippocampus,GEO,Microarray,Mus musculus,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA00889,GSE129296,GPL23038,1000,Alzheimer's Disease,C0002395,Cortex and hippocampus,GEO,Microarray,Mus musculus,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA00890,GSE129296,GPL23038,10,Alzheimer's Disease,C0002395,Cortex and hippocampus,GEO,Microarray,Mus musculus,4|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA00891,GSE129296,GPL23038,0,Alzheimer's Disease,C0002395,Cortex and hippocampus,GEO,Microarray,Mus musculus,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA00892,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,2|2,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA00893,GSE129310,GPL16791,113,Lowe Syndrome,C0028860,,GEO,RNA-Seq,Homo sapiens,6|6,"DO:A syndrome that has_material_basis_in mutation in the OCRL gene on chromosome Xq26 and that is characterized by hydrophthalmia, cataract, mental retardation, vitamin D-resistant rickets, amino aciduria, and reduced ammonia production by the kidney." DSA00894,GSE129473,GPL11154,43,Huntington's Disease,C0020179,Brain,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA00895,GSE129473,GPL11154,3,Huntington's Disease,C0020179,Brain,GEO,RNA-Seq,Homo sapiens,3|43,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA00896,GSE129482,GPL17021,1000,Lung Squamous Cell Carcinoma,C0149782,Lung,GEO,RNA-Seq,Mus musculus,5|5,DO:A non-small cell lung carcinoma that has_material_basis_in the squamous cell. DSA00897,GSE129516,GPL19057|GPL21103|GPL24247,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,scRNA-Seq,Mus musculus,3|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA00898,GSE129573,GPL17021,1000,Obesity,C0028754,Adipose tissue,GEO,RNA-Seq,Mus musculus,2|2,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA00899,GSE129573,GPL17021,1000,Obesity,C0028754,Adipose tissue,GEO,RNA-Seq,Mus musculus,2|2,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA00900,GSE129666,GPL21290,1000,Diabetic Kidney Disease,C0011881,,GEO,RNA-Seq,Homo sapiens,3|3,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA00901,GSE129784,GPL19057,1000,Endometrial Cancer,C0476089,Endometrial epithelium,GEO,RNA-Seq,Mus musculus,6|4,DO:A uterine cancer that is located_in tissues lining the uterus. DSA00902,GSE129784,GPL19057,1000,Endometrial Cancer,C0476089,Endometrial epithelium,GEO,RNA-Seq,Mus musculus,6|4,DO:A uterine cancer that is located_in tissues lining the uterus. DSA00903,GSE129784,GPL19057,1000,Endometrial Cancer,C0476089,Endometrial epithelium,GEO,RNA-Seq,Mus musculus,6|4,DO:A uterine cancer that is located_in tissues lining the uterus. DSA00904,GSE129808,GPL16791,1000,Autism Spectrum Disorder,C1510586,,GEO,RNA-Seq,Homo sapiens,1|3,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA00905,GSE129811,GPL23227,135,Mitochondrial Myopathy,C0162670,Muscle,GEO,RNA-Seq,Homo sapiens,8|4,DO:A myopathy that is characterized by mitochondrial dysfunction. DSA00906,GSE129811,GPL23227,147,Mitochondrial Myopathy,C0162670,Muscle,GEO,RNA-Seq,Homo sapiens,8|5,DO:A myopathy that is characterized by mitochondrial dysfunction. DSA00907,GSE129881,GPL17021,1000,Abdominal Aortic Aneurysm,C0162871,,GEO,RNA-Seq,Mus musculus,1|3,DO:An aortic aneurysm that is located_in the abdominal aorta. DSA00908,GSE129881,GPL17021,1000,Abdominal Aortic Aneurysm,C0162871,,GEO,RNA-Seq,Mus musculus,1|3,DO:An aortic aneurysm that is located_in the abdominal aorta. DSA00909,GSE129881,GPL17021,146,Abdominal Aortic Aneurysm,C0162871,,GEO,RNA-Seq,Mus musculus,2|3,DO:An aortic aneurysm that is located_in the abdominal aorta. DSA00910,GSE129881,GPL17021,30,Abdominal Aortic Aneurysm,C0162871,,GEO,RNA-Seq,Mus musculus,2|3,DO:An aortic aneurysm that is located_in the abdominal aorta. DSA00911,GSE129881,GPL17021,283,Abdominal Aortic Aneurysm,C0162871,,GEO,RNA-Seq,Mus musculus,2|4,DO:An aortic aneurysm that is located_in the abdominal aorta. DSA00912,GSE129881,GPL17021,203,Abdominal Aortic Aneurysm,C0162871,,GEO,RNA-Seq,Mus musculus,2|4,DO:An aortic aneurysm that is located_in the abdominal aorta. DSA00913,GSE129881,GPL17021,32,Abdominal Aortic Aneurysm,C0162871,,GEO,RNA-Seq,Mus musculus,3|4,DO:An aortic aneurysm that is located_in the abdominal aorta. DSA00914,GSE129881,GPL17021,1,Abdominal Aortic Aneurysm,C0162871,,GEO,RNA-Seq,Mus musculus,3|4,DO:An aortic aneurysm that is located_in the abdominal aorta. DSA00915,GSE129943,GPL16791,1000,Kidney Disease,C0022658,Kidney,GEO,RNA-Seq,Homo sapiens,3|3,DO:A kidney disease that is characterized by an inflammation of the kidneys. DSA00916,GSE130049,GPL11154,69,Renal Cell Carcinoma,C0007134,,GEO,RNA-Seq,Homo sapiens,2|2,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA00917,GSE130070,GPL20301,1000,Inflammatory Bowel Disease,C0021390,Peripheral blood,GEO,scRNA-Seq,Homo sapiens,1|1,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA00918,GSE130116,GPL20301,1000,Acute Lymphoblastic Leukemia,C0023449,Bone marrow,GEO,scRNA-Seq,Homo sapiens,4|7,DO:A acute leukemia that is characterized by over production of lymphoblasts. DSA00919,GSE130147,GPL21103,236,Obesity,C0028754,White adipose tissue,GEO,RNA-Seq,Mus musculus,3|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA00920,GSE130174,GPL20301,561,Cavernous Angioma With Symptomatic Hemorrhage,,,GEO,RNA-Seq,Homo sapiens,3|5, DSA00921,GSE130180,GPL21626,1000,Steatohepatitis,C2711227,,GEO,RNA-Seq,Mus musculus,6|3,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA00922,GSE130180,GPL21626,1000,Steatohepatitis,C2711227,,GEO,RNA-Seq,Mus musculus,3|3,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA00923,GSE130244,GPL570,57,Melanoma,C0025202,Skin,GEO,Microarray,Homo sapiens,2|4,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA00924,GSE130244,GPL570,447,Melanoma,C0025202,Skin,GEO,Microarray,Homo sapiens,2|4,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA00925,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,2|2,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA00926,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,2|2,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA00927,GSE130313,GPL11154,76,Systemic Sclerosis,C0036421,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies." DSA00928,GSE130313,GPL11154,70,Systemic Sclerosis,C0036421,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies." DSA00929,GSE130313,GPL11154,207,Systemic Sclerosis,C0036421,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies." DSA00930,GSE13034,GPL339,1,Progressive Extrapyramidal Movement Disorder,C2748610,,GEO,Microarray,Mus musculus,3|3, DSA00931,GSE13034,GPL339,0,Progressive Extrapyramidal Movement Disorder,C2748610,,GEO,Microarray,Mus musculus,3|3, DSA00932,GSE130353,GPL18573,7,Chronic Fatigue Syndrome,C0015674,Peripheral blood,GEO,RNA-Seq,Homo sapiens,10|10,"DO:A syndrome that involves prolonged and severe tiredness or weariness that is unrelated to exertion, is not relieved by rest and for a minimum of six months and is not directly caused by other conditions." DSA00933,GSE130353,GPL18573,389,Q Fever,C0034362,Peripheral blood,GEO,RNA-Seq,Homo sapiens,10|10,"DO:A primary bacterial infectious disease that is a zoonotic infectious disease affecting multiple organs, has_material_basis_in Coxiella burnetii, which is transmitted_by inhalation of air contaminated by barnyard dust containing dried placental material, birth fluids, or excreta of infected herd animals, transmitted_by ingestion of contaminated milk, transmitted_by tick bites and transmitted_by contact with infected person. The infection has_symptom fever, has_symptom headache, has_symptom cough, has_symptom pleuritic chest pain, has_symptom myalgia and has_symptom arthralgia." DSA00934,GSE130353,GPL18573,28,Q Fever,C0034362,Peripheral blood,GEO,RNA-Seq,Homo sapiens,10|10,"DO:A primary bacterial infectious disease that is a zoonotic infectious disease affecting multiple organs, has_material_basis_in Coxiella burnetii, which is transmitted_by inhalation of air contaminated by barnyard dust containing dried placental material, birth fluids, or excreta of infected herd animals, transmitted_by ingestion of contaminated milk, transmitted_by tick bites and transmitted_by contact with infected person. The infection has_symptom fever, has_symptom headache, has_symptom cough, has_symptom pleuritic chest pain, has_symptom myalgia and has_symptom arthralgia." DSA00935,GSE130435,GPL20301,1000,Endometriosis,C0014175,,GEO,RNA-Seq,Homo sapiens,4|6,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA00936,GSE130444,GPL20795,1000,Cockayne Syndrome,C0009207,,GEO,RNA-Seq,Homo sapiens,1|1,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA00937,GSE130444,GPL20795,1000,Cockayne Syndrome,C0009207,,GEO,RNA-Seq,Homo sapiens,1|1,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA00938,GSE130465,GPL16791,1000,Prostate Cancer,C0600139,,GEO,RNA-Seq,Homo sapiens,5|10,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA00939,GSE130465,GPL16791,1000,Prostate Cancer,C0600139,,GEO,RNA-Seq,Homo sapiens,5|10,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA00940,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,2|2,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA00941,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,2|1,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA00942,GSE130563,GPL17930,0,Pancreatic Ductal Adenocarcinoma,C1335302,Rectus abdominis muscle,GEO,Microarray,Homo sapiens,16|8,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA00943,GSE130563,GPL17930,0,Pancreatic Ductal Adenocarcinoma,C1335302,Rectus abdominis muscle,GEO,Microarray,Homo sapiens,16|17,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA00944,GSE130626,GPL24247,273,Demyelination,C0011304,Brain,GEO,scRNA-Seq,Mus musculus,1|1,"MSH:The first region-restricted episode of CNS inflammatory demyelination in a patient. It is usually characterized by an acute monosymptomatic presentation of the optic nerves, brainstem, or spinal cord. It may not reoccur (isolated), or it may progress to MULTIPLE SCLEROSIS." DSA00945,GSE130883,GPL17021,10,Angelman Syndrome,C0162635,Hippocampus,GEO,RNA-Seq,Mus musculus,6|6,"DO:A syndrome that is characterized by delayed development, intellectual disability, severe speech impairment, and problems with movement and balance." DSA00946,GSE130921,GPL9185,1000,Mammary Tumor,C1512981,Mammary gland,GEO,RNA-Seq,Mus musculus,3|10,NCI:Production of a new growth or growths in the mammary gland. DSA00947,GSE130928,GPL570,1000,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,42|22,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA00948,GSE130953,GPL10558,1000,Diffuse Cutaneous Systemic Sclerosis,C1258104,Whole blood,GEO,Microarray,Homo sapiens,62|62,"EFO:A variant of systemic scleroderma characterized by sclerosis of the skin, Raynaud phenomenon, and organ involvement, including pulmonary fibrosis, renal disease, and gastrointestinal tract involvement." DSA00949,GSE130955,GPL16791,1000,Systemic Sclerosis [Scleroderma],C2364016,Skin,GEO,RNA-Seq,Homo sapiens,33|58, DSA00950,GSE131031,GPL18573,1000,Tuberculosis,C0041296,Lung,GEO,RNA-Seq,Homo sapiens,4|17,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA00951,GSE131113,GPL570,0,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,Microarray,Homo sapiens,2|2,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA00952,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,2|2,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA00953,GSE131284,GPL21103,32,Hypertriglyceridemia,C0020557,Liver,GEO,RNA-Seq,Mus musculus,4|5,EFO:A laboratory test result indicating elevated triglyceride concentration in the blood. DSA00954,GSE131293,GPL570,0,Moyamoya Disease,C0026654,,GEO,Microarray,Homo sapiens,3|3,DO:A cerebral arterial disease characterized by constriction of certain arteries at the base of the brain. Blood flow is blocked by the constriction and also by blood clots. DSA00955,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,2|2,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA00956,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,2|2,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA00957,GSE131486,GPL24247,424,Damaged Optic Nerve,C3887709,Retina,GEO,RNA-Seq,Mus musculus,3|3,"DO:An optic neuritis that is characterized by nutritional deficiency causing optic nerve dysfunction, has_symptom painless bilateral progressive decrease in visual acuity and color perception, and has_material_basis_in nuritional deficits, especially of folate and vitamin B, which can be associated with restrictive diets and alcohol abuse." DSA00958,GSE131526,GPL16791,1000,Type 1 Diabetes,C0011854,Whole blood,GEO,RNA-Seq,Homo sapiens,3|12,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA00959,GSE131568,GPL20301,1000,Oral Leukoplakia,C0023532,Oral mucosa,GEO,RNA-Seq,Homo sapiens,6|6,DO:A skin disease characterized by a defect in the normal process of keratinization of the mucosa. DSA00960,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,2|2,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA00961,GSE131705,GPL16791,1000,Coeliac Disease,C0007570,Duodenum,GEO,RNA-Seq,Homo sapiens,21|33,"DO:An autoimmune disease of gastrointestinal tract that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite." DSA00962,GSE131793,GPL6244,0,Pulmonary Arterial Hypertension,C2973725,,GEO,Microarray,Homo sapiens,10|10,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA00963,GSE131819,GPL22121,0,Obesity,C0028754,Visceral adipose tissue,GEO,Microarray,Homo sapiens,3|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA00964,GSE131835,GPL26710,0,Esophageal Adenocarcinoma,C0279628,Subcutaneous adipose tissue,GEO,Microarray,Homo sapiens,8|8,DO:An esophageal carcinoma that derives_from epithelial cells of glandular origin. DSA00965,GSE131835,GPL26710,1000,Esophageal Adenocarcinoma,C0279628,Visceral adipose tissue,GEO,Microarray,Homo sapiens,8|8,DO:An esophageal carcinoma that derives_from epithelial cells of glandular origin. DSA00966,GSE131877,GPL16791,1000,AIPL1-Leber Congenital Amaurosis,,Retina,GEO,RNA-Seq,Homo sapiens,5|3, DSA00967,GSE131877,GPL16791,1000,AIPL1-Leber Congenital Amaurosis,,Retina,GEO,RNA-Seq,Homo sapiens,7|4, DSA00968,GSE131877,GPL16791,203,AIPL1-Leber Congenital Amaurosis,,Retina,GEO,RNA-Seq,Homo sapiens,3|2, DSA00969,GSE131877,GPL16791,417,AIPL1-Leber Congenital Amaurosis,,Retina,GEO,RNA-Seq,Homo sapiens,3|3, DSA00970,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,2|2,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA00971,GSE131963,GPL20775,1000,Allergic Contact Dermatitis,C0162820,Skin,GEO,Microarray,Mus musculus,3|3,"DO:A contact dermatitis that is an allergic skin reaction to foreign chemical or substances leading to red, itchy, weepy reaction where the skin has come into contact with a substance that the immune system recognizes as foreign." DSA00972,GSE131963,GPL20775,1000,Allergic Contact Dermatitis,C0162820,Skin,GEO,Microarray,Mus musculus,3|3,"DO:A contact dermatitis that is an allergic skin reaction to foreign chemical or substances leading to red, itchy, weepy reaction where the skin has come into contact with a substance that the immune system recognizes as foreign." DSA00973,GSE132006,GPL19965,0,Allergic Asthma,C0155877,,GEO,Microarray,Homo sapiens,5|5,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA00974,GSE132006,GPL19965,1,Allergic Asthma,C0155877,Whole blood,GEO,Microarray,Homo sapiens,5|5,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA00975,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,2|2,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA00976,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,2|2,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA00977,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,2|2,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA00978,GSE132215,GPL18460,1000,Squamous Cell Carcinoma,C0007137,Skin,GEO,RNA-Seq,Homo sapiens,3|3,DO:A carcinoma that derives_from squamous epithelial cells. DSA00979,GSE132267,GPL16570,1000,Lymphoma,C0024299,Bone marrow,GEO,Microarray,Mus musculus,3|15,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA00980,GSE132326,GPL17021,1000,Pancreatic Cancer,C0235974,Pancreas,GEO,RNA-Seq,Mus musculus,5|4,DO:An endocrine gland cancer located_in the pancreas. DSA00981,GSE132326,GPL17021,1000,Pancreatic Cancer,C0235974,Pancreas,GEO,RNA-Seq,Mus musculus,4|3,DO:An endocrine gland cancer located_in the pancreas. DSA00982,GSE141259,GPL21103,890,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,2|1,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA00983,GSE132401,GPL24676,1000,Single Ventricle,C0152424,,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A heart septal defect characterized by an opening in the interventricular septum, causing a shunt between ventricles." DSA00984,GSE132401,GPL24676,720,Tetralogy of Fallot,C0039685,,GEO,RNA-Seq,Homo sapiens,5|5,"HPO:A congenital cardiac malformation comprising pulmonary stenosis, overriding aorta, ventricular septum defect, and right ventricular hypertrophy. The diagnosis of TOF is made if at least three of the four above mentioned features are present." DSA00985,GSE132509,GPL20301,1000,Acute Lymphoblastic Leukemia,C0023449,,GEO,scRNA-Seq,Homo sapiens,2|4,DO:A acute leukemia that is characterized by over production of lymphoblasts. DSA00986,GSE132509,GPL20301,1000,Acute Lymphoblastic Leukemia,C0023449,,GEO,scRNA-Seq,Homo sapiens,2|2,DO:A acute leukemia that is characterized by over production of lymphoblasts. DSA00987,GSE132509,GPL20301,1000,Acute Lymphoblastic Leukemia,C0023449,,GEO,scRNA-Seq,Homo sapiens,2|2,DO:A acute leukemia that is characterized by over production of lymphoblasts. DSA00988,GSE132550,GPL18281,1000,Peripheral T-Cell Lymphoma,C0079774,,GEO,Microarray,Homo sapiens,10|80,DO:A mature T-cell and NK-cell lymphoma includes a group of T-cell lymphomas that develop away from the thymus. DSA00989,GSE132651,GPL96,0,Coronary Atherosclerosis,C0010054,,GEO,Microarray,Homo sapiens,6|13,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA00990,GSE132666,GPL4133,240,HTLV-1-Associated Myelopathy/Tropical Spastic Paraparesis,,,GEO,Microarray,Homo sapiens,4|4, DSA00991,GSE132666,GPL4133,1000,HTLV-1-Associated Myelopathy/Tropical Spastic Paraparesis,,,GEO,Microarray,Homo sapiens,4|4, DSA00992,GSE132689,GPL18573,74,Schizophrenia,C0036341,,GEO,RNA-Seq,Homo sapiens,12|12,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA00993,GSE132699,GPL20301,1000,Allergic Asthma,C0155877,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA00994,GSE132699,GPL20301,0,Allergic Asthma,C0155877,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA00995,GSE132701,GPL17021,41,Chronic Heart Failure,C0018801,,GEO,RNA-Seq,Mus musculus,5|5,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA00996,GSE132731,GPL15103,1000,Retinopathy,C0035309,,GEO,RNA-Seq,Mus musculus,8|8,DO:An eye disease that is located_in the retina. DSA00997,GSE132771,GPL21103|GPL24676,7,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,scRNA-Seq,Mus musculus,3|2,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA00998,GSE132771,GPL21103|GPL24676,6,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,scRNA-Seq,Mus musculus,3|3,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA00999,GSE132790,GPL16791,8,Tuberculosis Infection,C1609538,Peripheral blood,GEO,RNA-Seq,Homo sapiens,2|5,"MONDO:Mycobacterium tuberculosis infection that does not induce infectious expression of the disease in the affected person, although it can cause continuous immune response generated towards TB antigens; person having LTBI are asymptomatic and acting as a reservoir of active tuberculosis tuberculosis cases and Mycobacterium tuberculosis and run a 5-10% risk of reactivating tuberculosis throughout their lives." DSA01000,GSE132790,GPL16791,1,Tuberculosis Infection,C1609538,Peripheral blood,GEO,RNA-Seq,Homo sapiens,12|10,"MONDO:Mycobacterium tuberculosis infection that does not induce infectious expression of the disease in the affected person, although it can cause continuous immune response generated towards TB antigens; person having LTBI are asymptomatic and acting as a reservoir of active tuberculosis tuberculosis cases and Mycobacterium tuberculosis and run a 5-10% risk of reactivating tuberculosis throughout their lives." DSA01001,GSE132790,GPL16791,0,Tuberculosis Infection,C1609538,Peripheral blood,GEO,RNA-Seq,Homo sapiens,2|2,"MONDO:Mycobacterium tuberculosis infection that does not induce infectious expression of the disease in the affected person, although it can cause continuous immune response generated towards TB antigens; person having LTBI are asymptomatic and acting as a reservoir of active tuberculosis tuberculosis cases and Mycobacterium tuberculosis and run a 5-10% risk of reactivating tuberculosis throughout their lives." DSA01002,GSE132790,GPL16791,0,Tuberculosis Infection,C1609538,Peripheral blood,GEO,RNA-Seq,Homo sapiens,13|14,"MONDO:Mycobacterium tuberculosis infection that does not induce infectious expression of the disease in the affected person, although it can cause continuous immune response generated towards TB antigens; person having LTBI are asymptomatic and acting as a reservoir of active tuberculosis tuberculosis cases and Mycobacterium tuberculosis and run a 5-10% risk of reactivating tuberculosis throughout their lives." DSA01003,GSE132802,GPL21290,1000,Drug Hypersensitivity Syndrome,C3541994,,GEO,scRNA-Seq,Homo sapiens,1|5,"MONDO:DRESS syndrome (Drug Rash with Eosinophilia and Systemic Symptoms) is a hypersensitivity reaction characterized by a generalized skin rash, fever, eosinophilia, lymphocytosis and visceral involvement (hepatitis, nephritis, pneumonitis, pericarditis and myocarditis) and, in some patients, reactivation of human herpes virus 6." DSA01004,GSE132802,GPL21290,1000,Drug Hypersensitivity Syndrome,C3541994,Skin,GEO,scRNA-Seq,Homo sapiens,6|1,"MONDO:DRESS syndrome (Drug Rash with Eosinophilia and Systemic Symptoms) is a hypersensitivity reaction characterized by a generalized skin rash, fever, eosinophilia, lymphocytosis and visceral involvement (hepatitis, nephritis, pneumonitis, pericarditis and myocarditis) and, in some patients, reactivation of human herpes virus 6." DSA01005,GSE132819,GPL6246,1,Depression,C0011581,Dentate gyrus,GEO,Microarray,Mus musculus,3|3,DO:A mood disorder that involves the presence of a low mood almost daily over a span of at least two years. DSA01006,GSE132836,GPL16791,1000,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,RNA-Seq,Homo sapiens,5|6,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA01007,GSE13284,GPL570,14,Sickle Cell-Beta-Thalassemia Disease Syndrome,C0221019,,GEO,Microarray,Homo sapiens,6|6,"MONDO:Sickle beta thalassemia is an inherited condition that affects hemoglobin, the protein in red blood cells that carries oxygen to different parts of the body.It is a type of sickle cell disease. Affected people havea differentchange (mutation) in each copy of their HBB gene: onethat causes red blood cells to form a 'sickle' or crescent shape and a second that is associated with beta thalassemia, a blood disorder that reduces the production of hemoglobin. Depending on the beta thalassemia mutation, people may have no normal hemoglobin (called sickle beta zero thalassemia) or a reduced amount of normal hemoglobin (called sickle beta plus thalassemia). The presence of sickle-shaped red blood cells, which often breakdown prematurely and can get stuck in blood vessels, combined with the reduction or absence of mature redblood cells leadsto the many signs and symptoms of sickle beta thalassemia. Features, which may include anemia (low levels of red blood cells), repeated infections, and frequent episodes of pain, generally develop in early childhood and vary in severity depending on the amount of normal hemoglobin made. Sickle beta thalassemia is inherited in an autosomal recessive manner. Treatment is supportive and depends on the signs and symptoms present in each person." DSA01008,GSE132880,GPL21103,1000,Myocardial Infarction,C0027051,Heart,GEO,scRNA-Seq,Mus musculus,4|4,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA01009,GSE132910,GPL24247,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,scRNA-Seq,Mus musculus,1|1,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA01010,GSE132910,GPL24247,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,scRNA-Seq,Mus musculus,1|1,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA01011,GSE132914,GPL24676,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,scRNA-Seq,Homo sapiens,3|3,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA01012,GSE133084,GPL16699,2,Xeroderma Pigmentosum,C0043346,,GEO,Microarray,Homo sapiens,3|3,DO:A syndrome that is characterized by a deficiency in the ability to repair ultraviolet damage that has_material_basis_in autosomal recessive inheritance of DNA repair. DSA01013,GSE133100,GPL17021,0,Polycystic Ovary Syndrome,C0032460,,GEO,RNA-Seq,Mus musculus,15|15,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA01014,GSE133101,GPL18573,2,Parkinson's Disease,C0030567,Amygdala,GEO,RNA-Seq,Homo sapiens,8|15,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01015,GSE133101,GPL18573,3,Parkinson's Disease,C0030567,Medil temporal gyrus,GEO,RNA-Seq,Homo sapiens,8|13,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01016,GSE133101,GPL18573,0,Parkinson's Disease,C0030567,Substantia nigra,GEO,RNA-Seq,Homo sapiens,10|15,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01017,GSE133137,GPL24014,61,Neuroblastoma,C0027819,,GEO,RNA-Seq,Homo sapiens,5|4,DO:An autonomic nervous system neoplasm that derives_from immature nerve cells. DSA01018,GSE133180,GPL17021,1000,Brain Inflammation,C0014038,Spinal cord,GEO,RNA-Seq,Mus musculus,2|2,DO:A brain disease that is characterized as an acute inflammation of the brain with flu-like symptoms. DSA01019,GSE133180,GPL17021,1000,Brain Inflammation,C0014038,Spinal cord,GEO,RNA-Seq,Mus musculus,2|1,DO:A brain disease that is characterized as an acute inflammation of the brain with flu-like symptoms. DSA01020,GSE133180,GPL17021,1000,Brain Inflammation,C0014038,Spinal cord,GEO,RNA-Seq,Mus musculus,2|2,DO:A brain disease that is characterized as an acute inflammation of the brain with flu-like symptoms. DSA01021,GSE133247,GPL17303,1000,Bardet-Biedl Syndrome,C0752166,,GEO,RNA-Seq,Homo sapiens,8|2,"DO:A Cowden syndrome that is characterized by macrocephaly, multiple noncancerous tumors and hamartomas, and dark freckles on the penis, and has_material_basis_in heterozygous germline mutation in the PTEN gene on chromosome 10q23." DSA01022,GSE133247,GPL17303,1000,Meckel Syndrome,C3714506,,GEO,RNA-Seq,Homo sapiens,8|4,DO:A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of MKS1 on chromosome 17q22. DSA01023,GSE133264,GPL20301,143,Microcephaly,C0025958,Skin,GEO,RNA-Seq,Homo sapiens,3|2,DO:A congenital nervous system abnormality that is characterized by a significantly smaller than normal head in infants. DSA01024,GSE133317,GPL16791,525,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,3|6,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01025,GSE133317,GPL16791,1000,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,3|6,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01026,GSE133346,GPL570,351,Multiple Myeloma,C0026764,Adipose tissue,GEO,Microarray,Homo sapiens,12|12,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA01027,GSE133369,GPL17021,1,Fetal Alcohol Spectrum Disorder,C2985290,Hippocampus,GEO,RNA-Seq,Mus musculus,3|3,"MONDO:A group of disorders caused by a prenatal exposure to maternal consumption of alcohol leading to a range of behavioral, cognitive and neurological deficits in the offspring. It is characterized by physical growth problems, distinct facies, and varying psycho-neurological issues." DSA01028,GSE133369,GPL17021,2,Fetal Alcohol Spectrum Disorder,C2985290,Hippocampus,GEO,RNA-Seq,Mus musculus,3|3,"MONDO:A group of disorders caused by a prenatal exposure to maternal consumption of alcohol leading to a range of behavioral, cognitive and neurological deficits in the offspring. It is characterized by physical growth problems, distinct facies, and varying psycho-neurological issues." DSA01029,GSE133518,GPL16791,1000,Non-Small Cell Lung Cancer,C0007131,,GEO,RNA-Seq,Homo sapiens,1|1,DO:A respiratory system cancer that is located_in the lung. DSA01030,GSE133518,GPL16791,1000,Non-Small Cell Lung Cancer,C0007131,,GEO,RNA-Seq,Homo sapiens,1|1,DO:A respiratory system cancer that is located_in the lung. DSA01031,GSE141259,GPL21103,29,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,2|1,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA01032,GSE141259,GPL21103,734,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,2|2,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA01033,GSE141259,GPL21103,773,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,2|1,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA01034,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,7|3,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA01035,GSE133534,GPL24676,1000,Schizophrenia,C0036341,,GEO,RNA-Seq,Homo sapiens,11|10,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA01036,GSE133554,GPL21493,0,Epilepsy,C0014544,Brain,GEO,RNA-Seq,Mus musculus,5|6,"DO:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions." DSA01037,GSE133577,GPL11202,208,Obesity,C0028754,Pancreatic islet,GEO,Microarray,Mus musculus,3|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA01038,GSE133603,GPL18573|GPL19057,64,Autoimmune Polyendocrinopathy,C4316913,Oral mucosal gingival tissue,GEO,RNA-Seq,Homo sapiens,2|4,"MONDO:A group of diverse conditions that are characterized by spontaneous, multi-organ autoimmunity, which target both endocrine (adrenal, gonad, pancreatic islet cells, parathyroid, pituitary, thyroid) and non-endocrine (gastrointestinal, integumentary, lymphatic) tissues." DSA01039,GSE133642,GPL17021,0,Leukemia,C0023418,,GEO,RNA-Seq,Mus musculus,6|17,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA01040,GSE133642,GPL17021,1000,Leukemia,C0023418,,GEO,RNA-Seq,Mus musculus,6|17,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA01041,GSE133642,GPL17021,382,Leukemia,C0023418,,GEO,RNA-Seq,Mus musculus,5|17,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA01042,GSE133642,GPL17021,1000,Leukemia,C0023418,,GEO,RNA-Seq,Mus musculus,6|16,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA01043,GSE133642,GPL17021,1000,Leukemia,C0023418,,GEO,RNA-Seq,Mus musculus,6|12,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA01044,GSE133642,GPL17021,1000,Leukemia,C0023418,,GEO,RNA-Seq,Mus musculus,6|10,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA01045,GSE133642,GPL17021,1000,Leukemia,C0023418,,GEO,RNA-Seq,Mus musculus,6|11,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA01046,GSE133684,GPL20795,1000,Pancreatic Ductal Adenocarcinoma,C1335302,Plasma,GEO,RNA-Seq,Homo sapiens,117|282,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA01047,GSE133754,GPL9052,270,Dilated Cardiomyopathy With Ataxia,C1857776,,GEO,RNA-Seq,Homo sapiens,4|4,DO:A 3-methylglutaconic aciduria that has_material_basis_in homozygous mutation in the DNAJC19 gene on chromosome 3q26. DSA01048,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,7|5,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA01049,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,7|3,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA01050,GSE133914,GPL18480,920,Obesity,C0028754,,GEO,RNA-Seq,Mus musculus,6|6,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA01051,GSE133915,GPL18480,48,Obesity,C0028754,,GEO,RNA-Seq,Mus musculus,8|8,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA01052,GSE133932,GPL19127,34,Autism Spectrum Disorder,C1510586,Forebrain,GEO,Microarray,Mus musculus,3|3,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA01053,GSE133969,GPL11180,66,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Mus musculus,5|6,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA01054,GSE133969,GPL11180,571,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Mus musculus,5|10,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA01055,GSE133979,GPL17303,257,Pancreatic Ductal Adenocarcinoma,C1335302,Rectus abdominis muscle,GEO,RNA-Seq,Homo sapiens,11|23,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA01056,GSE134011,GPL18573,1000,Alport Syndrome,C1567741,,GEO,RNA-Seq,Homo sapiens,3|9,"DO:A syndrome disease that is characterized by glomerulonephritis, endstage kidney disease, and hearing loss." DSA01057,GSE134025,GPL20115,18,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,3|3,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA01058,GSE134056,GPL18573,71,Endometriosis,C0014175,Endometrium,GEO,RNA-Seq,Homo sapiens,22|16,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA01059,GSE134185,GPL1261,0,Type 2 Diabetes,C0011860,Liver,GEO,Microarray,Mus musculus,8|8,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA01060,GSE134290,GPL570,108,Ankylosing Spondylitis,C0038013,,GEO,Microarray,Homo sapiens,3|3,"DO:A bone inflammation disease that results_in inflammation in the joints of the spine and pelvis. The disease has_symptom pain, has_symptom stiffness in the spine, has_symptom stiffness in the neck, has_symptom stiffness in the hips, has_symptom stiffness in the jaw and has_symptom stiffness in the rib cage." DSA01061,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,7|4,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA01062,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,7|4,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA01063,GSE134383,GPL17021|GPL21103,1000,Acute Lung Injury,C0242488,Lung,GEO,RNA-Seq,Mus musculus,3|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA01064,GSE134497,GPL24676,1000,Bipolar Disorder,C0005586,,GEO,RNA-Seq,Homo sapiens,11|11,DO:A mood disorder that involves alternating periods of mania and depression. DSA01065,GSE134520,GPL20795,1000,Chronic Atrophic Gastritis,C0017154,Stomach,GEO,scRNA-Seq,Homo sapiens,9|9,"HPO:Atrophic gastritis (AG) is a histopathological entity that is characterized by chronic inflammation of the gastric mucosa with loss of gastric glandular cells and replacement by intestinal-type epithelium, pyloric-type glands, and fibrous tissue." DSA01066,GSE134520,GPL20795,1000,Early Gastric Cancer,C0349530,Stomach,GEO,scRNA-Seq,Homo sapiens,9|4,"MONDO:An invasive adenocarcinoma confined to the mucosa or mucosa and submucosa of the gastric wall. The regional lymph nodes may or may not be involved. It usually occurs in the lesser curvature. The 5-year survival rate following resection is between 80 percent and 95 percent, and remains high even when lymph node metastases are present." DSA01067,GSE134520,GPL20795,1000,Gastric Metaplastic Polyp,C0878649,Stomach,GEO,scRNA-Seq,Homo sapiens,9|16,"NCI:A non-neoplastic polyp that arises from the stomach and is characterized by the presence of dilated gastric foveoli, edematous changes, and inflammation." DSA01068,GSE134520,GPL20795,1000,Gastric Metaplastic Polyp,C0878649,Stomach,GEO,scRNA-Seq,Homo sapiens,9|12,"NCI:A non-neoplastic polyp that arises from the stomach and is characterized by the presence of dilated gastric foveoli, edematous changes, and inflammation." DSA01069,GSE141259,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,scRNA-Seq,Mus musculus,7|2,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA01070,GSE141308,GPL17021,30,Synovitis,C0039103,Bone marrow,GEO,RNA-Seq,Mus musculus,3|3,DO:A connective tissue disease that results_in inflammation located_in synovial membrane that lines a synovial joint which causes pain and swelling. DSA01071,GSE141511,GPL21103,1000,Cholangiocarcinoma,C0206698,Bile duct,GEO,RNA-Seq,Mus musculus,3|3,DO:A bile duct carcinoma that derives_from epithelial cells of glandular origin. DSA01072,GSE141511,GPL21103,1000,Cholangiocarcinoma,C0206698,Bile duct,GEO,RNA-Seq,Mus musculus,3|3,DO:A bile duct carcinoma that derives_from epithelial cells of glandular origin. DSA01073,GSE141511,GPL21103,1000,Cholangiocarcinoma,C0206698,Bile duct,GEO,RNA-Seq,Mus musculus,3|3,DO:A bile duct carcinoma that derives_from epithelial cells of glandular origin. DSA01074,GSE141729,GPL21273,1000,Baumannii Infection,,Lung,GEO,RNA-Seq,Mus musculus,3|3, DSA01075,GSE134580,GPL16791,0,Obesity,C0028754,Sperm,GEO,RNA-Seq,Homo sapiens,8|13,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA01076,GSE134580,GPL16791,0,Obesity,C0028754,Sperm,GEO,RNA-Seq,Homo sapiens,8|11,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA01077,GSE134636,GPL19057|GPL24247,0,Parkinson's Disease,C0030567,Midbrain,GEO,RNA-Seq,Mus musculus,12|12,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01078,GSE134644,GPL23934,1000,Acute Megakaryoblastic Leukemia,C0023462,,GEO,RNA-Seq,Homo sapiens,7|3,DO:An acute myeloid leukemia that derives from blood-forming tissue in which megakaryocytes proliferate in the bone marrow and circulate in the blood in large numbers. DSA01079,GSE134649,GPL20301,1000,Ulcerative Colitis,C0009324,Colon,GEO,scRNA-Seq,Homo sapiens,3|3,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA01080,GSE134662,GPL16791,1000,Intestinal Graft Versus Host Disease,C1334228,Colon,GEO,RNA-Seq,Homo sapiens,10|44, DSA01081,GSE141736,GPL24247,1000,Myelofibrosis,C0026987,Bone marrow,GEO,scRNA-Seq,Mus musculus,2|2,DO:A myeloid neoplasm that is located in the bone marrow which results in bone marrow being replaced by fibrous (scar) tissue. DSA01082,GSE141736,GPL24247,1000,Myelofibrosis,C0026987,Bone marrow,GEO,scRNA-Seq,Mus musculus,2|2,DO:A myeloid neoplasm that is located in the bone marrow which results in bone marrow being replaced by fibrous (scar) tissue. DSA01083,GSE142107,GPL21103,593,Sciatic Nerve Lesion,C0154748,Sciatic nerve axoplasm,GEO,RNA-Seq,Mus musculus,3|3,MONDO:A peripheral nerve lesion that involves the sciatic nerve. DSA01084,GSE134976,GPL13112,101,Obesity,C0028754,Liver,GEO,RNA-Seq,Mus musculus,3|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA01085,GSE134976,GPL13112,350,Obesity,C0028754,Liver,GEO,RNA-Seq,Mus musculus,3|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA01086,GSE142107,GPL21103,214,Sciatic Nerve Lesion,C0154748,Sciatic nerve axoplasm,GEO,RNA-Seq,Mus musculus,3|3,MONDO:A peripheral nerve lesion that involves the sciatic nerve. DSA01087,GSE142107,GPL21103,1000,Sciatic Nerve Lesion,C0154748,Sciatic nerve axoplasm,GEO,RNA-Seq,Mus musculus,3|3,MONDO:A peripheral nerve lesion that involves the sciatic nerve. DSA01088,GSE135004,GPL17586,0,Pemphigus,C0030807,,GEO,Microarray,Homo sapiens,3|3,DO:A pemphigus characterized by autosomal dominant blisters and erosions on the skin and mucous membranes erosions cause by autoantibodies to intercellular cement substance. DSA01089,GSE13501,GPL570,13,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,59|28,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA01090,GSE13501,GPL570,183,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,59|42,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA01091,GSE13501,GPL570,49,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,59|45,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA01092,GSE13501,GPL570,1000,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,59|21,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA01093,GSE135026,GPL16791|GPL18573,1000,Leukemia,C0023418,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA01094,GSE135065,GPL15207,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,3|3,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA01095,GSE135065,GPL15207,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,3|3,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA01096,GSE135065,GPL15207,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,3|3,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA01097,GSE135092,GPL16791,1000,Age Related Macular Degeneration,C0242383,Retina,GEO,RNA-Seq,Homo sapiens,101|27,DO:A degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision. DSA01098,GSE135092,GPL16791,1,Age Related Macular Degeneration,C0242383,Retina,GEO,RNA-Seq,Homo sapiens,115|28,DO:A degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision. DSA01099,GSE135092,GPL16791,454,Age Related Macular Degeneration,C0242383,,GEO,RNA-Seq,Homo sapiens,105|26,DO:A degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision. DSA01100,GSE135092,GPL16791,136,Age Related Macular Degeneration,C0242383,,GEO,RNA-Seq,Homo sapiens,112|23,DO:A degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision. DSA01101,GSE135173,GPL16791,1000,Persistent Polyclonal B-Cell Lymphocytosis,C1847973,Blood,GEO,RNA-Seq,Homo sapiens,4|3,"MONDO:Persistent polyclonal B-cell lymphocytosis (PPBL) is a rare, generally benign, lymphoproliferative hematological disease characterized by: chronic, stable, persistent, polyclonal lymphocytosis of memory B-cell origin, the presence of binucleated lymphocytes in the peripheral blood, and a polyclonal increase in serum immunoglobulin M (IgM). Patients are most frequently asymptomatic or may present with mild splenomegaly." DSA01102,GSE135186,GPL21103|GPL24247,1000,Experimental Autoimmune Encephalomyelitis,C0014072,Spinal cord,GEO,RNA-Seq,Mus musculus,1|1,"EFO:An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)" DSA01103,GSE135223,GPL24676,1000,Crohn's Disease,C0010346,,GEO,RNA-Seq,Homo sapiens,5|5,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA01104,GSE135223,GPL24676,1000,Ulcerative Colitis,C0009324,,GEO,RNA-Seq,Homo sapiens,5|5,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA01105,GSE135251,GPL18573,1000,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,RNA-Seq,Homo sapiens,10|205,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA01106,GSE135285,GPL24676,824,Acute-On-Chronic Liver Failure,C3850141,Peripheral blood,GEO,RNA-Seq,Homo sapiens,6|4,"EFO:Acute-on-chronic liver failure (ACLF) is an extreme condition during the natural history of chronic HBV infection, with a relatively high short-term mortality." DSA01107,GSE135285,GPL24676,1000,Alcoholic Hepatitis,C0019187,Peripheral blood,GEO,RNA-Seq,Homo sapiens,6|4,MONDO:Acute hepatitis resulting from ingestion of alcohol. DSA01108,GSE135287,GPL18573,2,Rubinstein-Taybi Syndrome,C0035934,,GEO,RNA-Seq,Homo sapiens,8|10,DO:A syndrome characterized by congenital anomalies located_in heart and located_in upper limb. DSA01109,GSE142107,GPL21103,443,Sciatic Nerve Lesion,C0154748,Sciatic nerve axoplasm,GEO,RNA-Seq,Mus musculus,3|3,MONDO:A peripheral nerve lesion that involves the sciatic nerve. DSA01110,GSE135437,GPL21290,956,Glioblastoma Multiforme,C1621958,Brain,GEO,RNA-Seq,Homo sapiens,40|10,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA01111,GSE135442,GPL21103,1000,Alport Syndrome,C1567741,,GEO,RNA-Seq,Mus musculus,3|3,"DO:A syndrome disease that is characterized by glomerulonephritis, endstage kidney disease, and hearing loss." DSA01112,GSE135442,GPL21103,1000,Alport Syndrome,C1567741,,GEO,RNA-Seq,Mus musculus,3|3,"DO:A syndrome disease that is characterized by glomerulonephritis, endstage kidney disease, and hearing loss." DSA01113,GSE135485,GPL21290,74,Endometriosis,C0014175,Endometrium,GEO,RNA-Seq,Homo sapiens,4|54,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA01114,GSE135501,GPL13667,1,Chronic Hepatitis,C0019189,Peripheral blood,GEO,Microarray,Homo sapiens,14|41,"EFO:An active inflammatory process affecting the liver for more than six months. Causes include viral infections, autoimmune disorders, drugs, and metabolic disorders." DSA01115,GSE135511,GPL6883,1000,Multiple Sclerosis,C0026769,Motor cortex,GEO,Microarray,Homo sapiens,10|20,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA01116,GSE135511,GPL6883,1000,Multiple Sclerosis,C0026769,Motor cortex,GEO,Microarray,Homo sapiens,10|20,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA01117,GSE135589,GPL570,0,Huntington's Disease,C0020179,Whole blood,GEO,Microarray,Homo sapiens,24|18,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01118,GSE135589,GPL570,0,Huntington's Disease,C0020179,Whole blood,GEO,Microarray,Homo sapiens,24|18,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01119,GSE135589,GPL570,0,Huntington's Disease,C0020179,Whole blood,GEO,Microarray,Homo sapiens,24|19,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01120,GSE135589,GPL570,0,Huntington's Disease,C0020179,Whole blood,GEO,Microarray,Homo sapiens,24|17,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01121,GSE135589,GPL570,0,Huntington's Disease,C0020179,Whole blood,GEO,Microarray,Homo sapiens,20|15,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01122,GSE135589,GPL570,0,Huntington's Disease,C0020179,Whole blood,GEO,Microarray,Homo sapiens,20|15,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01123,GSE135589,GPL570,0,Huntington's Disease,C0020179,Whole blood,GEO,Microarray,Homo sapiens,20|16,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01124,GSE135589,GPL570,0,Huntington's Disease,C0020179,Whole blood,GEO,Microarray,Homo sapiens,20|16,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01125,GSE135635,GPL18573|GPL20301,1000,Non-Sjogren's sicca,,,GEO,RNA-Seq,Homo sapiens,8|14, DSA01126,GSE135635,GPL18573|GPL20301,815,Non-Sjogren's sicca,,,GEO,RNA-Seq,Homo sapiens,9|11, DSA01127,GSE135635,GPL18573|GPL20301,360,Primary Sjogren Syndrome,C0151449,,GEO,RNA-Seq,Homo sapiens,8|9,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA01128,GSE135635,GPL18573|GPL20301,19,Primary Sjogren Syndrome,C0151449,,GEO,RNA-Seq,Homo sapiens,9|11,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA01129,GSE135652,GPL17077,314,Aicardi Goutieres Syndrome,C0393591,Skin,GEO,Microarray,Homo sapiens,4|12,"DO:A syndrome that is a genetically heterogeneous encephalopathy characterized in its most severe form by cerebral atrophy, leukodystrophy, intracranial calcifications, chronic cerebrospinal fluid lymphocytosis, increased CSF alpha-interferon, and negative serologic investigations for common prenatal infections." DSA01130,GSE142107,GPL21103,1000,Sciatic Nerve Lesion,C0154748,Sciatic nerve axoplasm,GEO,RNA-Seq,Mus musculus,3|3,MONDO:A peripheral nerve lesion that involves the sciatic nerve. DSA01131,GSE142279,GPL20795,1000,Colorectal Tumor,C0699790,Colorectum,GEO,RNA-Seq,Homo sapiens,20|20,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA01132,GSE135743,GPL18573,1000,Parkinson's Disease,C0030567,Appendix,GEO,RNA-Seq,Homo sapiens,29|12,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01133,GSE135773,GPL21290,189,Koolen De Vries Syndrome,C1864871,,GEO,RNA-Seq,Homo sapiens,4|3,"DO:A syndrome that is characterized by developmental delay, intellectual disability, muscle weakness (hypotonia), epilepsy, distinctive facial features and congenital malformations of the heart, urogenital tract and the central nervous system, and has_material_basis_in either a chromosome 17 (17q21.31) microdeletion or a mutation in the KANSL1-gene." DSA01134,GSE69428,GPL570,1000,Ovarian Serous Carcinoma,C1335177,Oviduct,GEO,Microarray,Homo sapiens,10|10,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA01135,GSE7014,GPL570,411,Myotonic Dystrophy Type 1,C0027126,Skeletal muscle,GEO,Microarray,Homo sapiens,6|5,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA01136,GSE135786,GPL13112|GPL21103,367,Myeloma,C0026764,,GEO,RNA-Seq,Mus musculus,5|5,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA01137,GSE135786,GPL13112|GPL21103,282,Myeloma,C0026764,,GEO,RNA-Seq,Mus musculus,4|4,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA01138,GSE135786,GPL13112|GPL21103,352,Myeloma,C0026764,,GEO,RNA-Seq,Mus musculus,5|5,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA01139,GSE135805,GPL18573,1000,Dilated Cardiomyopathy,C0007193,Myocardium,GEO,RNA-Seq,Homo sapiens,1|1,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA01140,GSE135805,GPL18573,1000,Hypertrophic Cardiomyopathy,C0007194,Myocardium,GEO,RNA-Seq,Homo sapiens,1|1,DO:A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations. DSA01141,GSE135805,GPL18573,1000,Ischemic Cardiomyopathy,C0349782,Myocardium,GEO,RNA-Seq,Homo sapiens,1|1,EFO:Ischemic cardiomyopathy is a cardiomyopathy in which a weakness in the muscle of the heart due to inadequate oxygen delivery to the myocardium with coronary artery disease being the most common cause. DSA01142,GSE7014,GPL570,1000,Myotonic Dystrophy Type 2,C2931689,Skeletal muscle,GEO,Microarray,Homo sapiens,6|8,"DO:A myotonic disease that is characterized by myotonia and progressive, proximal muscle wasting and weakness affecting the skeletal and smooth muscles of the neck, shoulders, elbows and hips and has_material_basis_in the autosomal dominant inheritance of the CNBP (ZNF9) gene containing an expansion of a CCTG repeat in intron one." DSA01143,GSE71989,GPL570,1000,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,Microarray,Homo sapiens,8|13,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA01144,GSE72140,GPL570,0,Melasma,C0025218,Face,GEO,Microarray,Homo sapiens,22|22,EFO:Disorders of increased melanin pigmentation that develop without preceding inflammatory disease. DSA01145,GSE7345,GPL570,0,Autoimmune Lymphoproliferative Syndrome,C1328840,,GEO,Microarray,Homo sapiens,2|1,"DO:A hypersensitivity reaction type IV disease that is an inherited disorder in which the body cannot properly regulate the number of immune system cells (lymphocytes). It is characterized by the production of an abnormally large number of lymphocytes. Accumulation of excess lymphocytes results in enlargement of the lymph nodes, the liver, and the spleen." DSA01146,GSE135902,GPL16791,1000,Chronic Myelomonocytic Leukemia,C1333043,Blood,GEO,RNA-Seq,Homo sapiens,28|12,NCI:A chronic myelomonocytic leukemia characterized by the presence of less than 10 percent blasts in the bone marrow and less than 5 percent blasts in the peripheral blood. DSA01147,GSE13597,GPL96,9,Nasopharyngeal Carcinoma,C2931822,Nasopharynx,GEO,Microarray,Homo sapiens,3|25,"DO:A pharynx cancer that is located in the nasopharynx, the uppermost region of the pharynx or throat, where the nasal passages and auditory tubes join the remainder of the upper respiratory tract." DSA01148,GSE7345,GPL570,0,Autoimmune Lymphoproliferative Syndrome,C1328840,,GEO,Microarray,Homo sapiens,2|1,"DO:A hypersensitivity reaction type IV disease that is an inherited disorder in which the body cannot properly regulate the number of immune system cells (lymphocytes). It is characterized by the production of an abnormally large number of lymphocytes. Accumulation of excess lymphocytes results in enlargement of the lymph nodes, the liver, and the spleen." DSA01149,GSE73613,GPL570,0,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,2|2,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA01150,GSE136048,GPL17586,0,Placenta Accreta Spectrum,,Placenta,GEO,Microarray,Homo sapiens,3|6, DSA01151,GSE136053,GPL16791,90,Latent Autoimmune Diabetes In Adults,C1739108,,GEO,RNA-Seq,Homo sapiens,5|4,"EFO:Latent autoimmune diabetes in adults (LADA) is a form of diabetes mellitus type 1 that occurs in adulthood, often with a slower course of onset than type 1 diabetes diagnosed in juveniles." DSA01152,GSE7392,GPL570,0,Intraabdominal Fibromatosis,C0206646,Kidney,GEO,Microarray,Homo sapiens,7|8,"MSH:A relatively large mass of unusually firm scarlike connective tissue resulting from active participation of fibroblasts, occurring most frequently in the abdominal muscles of women who have borne children. The fibroblasts infiltrate surrounding muscle and fascia. (Stedman, 25th ed)" DSA01153,GSE7392,GPL570,0,Intraabdominal Fibromatosis,C0206646,Kidney,GEO,Microarray,Homo sapiens,7|8,"MSH:A relatively large mass of unusually firm scarlike connective tissue resulting from active participation of fibroblasts, occurring most frequently in the abdominal muscles of women who have borne children. The fibroblasts infiltrate surrounding muscle and fascia. (Stedman, 25th ed)" DSA01154,GSE136129,GPL11154,1000,Prostate Cancer,C0600139,Prostate,GEO,RNA-Seq,Homo sapiens,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA01155,GSE136200,GPL16791,85,Sepsis,C0243026,Blood,GEO,RNA-Seq,Homo sapiens,16|24,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA01156,GSE7451,GPL570,9,Sjogren's Syndrome,C1527336,Saliva,GEO,Microarray,Homo sapiens,10|10,DO:An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. DSA01157,GSE75271,GPL570,1000,Hepatoblastoma,C0206624,Liver,GEO,Microarray,Homo sapiens,5|50,DO:A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver. DSA01158,GSE7553,GPL570,3,Melanoma In Situ,C0025202,Skin,GEO,Microarray,Homo sapiens,4|2,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA01159,GSE136309,GPL17021,2,Hypoglycemia,C0020615,Liver,GEO,RNA-Seq,Mus musculus,8|8,DO:A glucose metabolism disease that is characterized by abnormally low levels of blood glucose. DSA01160,GSE136309,GPL17021,2,Hypoglycemia,C0020615,Liver,GEO,RNA-Seq,Mus musculus,8|8,DO:A glucose metabolism disease that is characterized by abnormally low levels of blood glucose. DSA01161,GSE136335,GPL17586,860,Polycythemia Vera,C0032463,Peripheral blood,GEO,Microarray,Homo sapiens,6|3,"DO:A myeloproliferative neoplasm characterized by erythroid hyperplasia, myeloid leukocytosis, thrombocytosis, and splenomegaly." DSA01162,GSE136335,GPL17586,606,Post Polycythaemia Vera Myelofibrosis,C3805232,Peripheral blood,GEO,Microarray,Homo sapiens,6|1,"NCI:Progression of polycythemia vera characterized by decreased erythropoiesis and granulopoiesis, reticulin and collagen fibrosis of the bone marrow, leucoerythroblastic reaction in the peripheral blood, poikilocytosis, tear-drop shaped red blood cells, and splenomegaly." DSA01163,GSE136344,GPL5175,1,Metabolic Syndrome,C0524620,Vastus lateralis,GEO,Microarray,Homo sapiens,12|7,"DO:An abdominal obesity-metabolic syndrome characterized by insulin resistance and hyperinsulinemia, dyslipidemia, essential hypertension, abdominal obesity, glucose intolerance or noninsulin-dependent diabetes mellitus and an increased risk of cardiovascular events." DSA01164,GSE7553,GPL570,1000,Metastatic Melanoma,C0278883,Skin,GEO,Microarray,Homo sapiens,4|40,"EFO:A melanoma that has spread from its primary site to another anatomic site. Melanomas frequently metastasize to lymph nodes, liver, lungs, and brain." DSA01165,GSE7553,GPL570,45,Melanoma,C0025202,Skin,GEO,Microarray,Homo sapiens,4|14,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA01166,GSE7553,GPL570,1000,Squamous Cell Carcinoma,C0007137,Skin,GEO,Microarray,Homo sapiens,4|11,DO:A carcinoma that derives_from squamous epithelial cells. DSA01167,GSE136358,GPL17021,287,Encephalomyelitis,C0014070,Hindbrain,GEO,RNA-Seq,Mus musculus,16|10,EFO:Inflammation of the brain and the spinal cord. DSA01168,GSE136358,GPL17021,1000,Encephalomyelitis,C0014070,Hindbrain,GEO,RNA-Seq,Mus musculus,8|6,EFO:Inflammation of the brain and the spinal cord. DSA01169,GSE136358,GPL17021,581,Encephalomyelitis,C0014070,Hindbrain,GEO,RNA-Seq,Mus musculus,16|13,EFO:Inflammation of the brain and the spinal cord. DSA01170,GSE136358,GPL17021,949,Encephalomyelitis,C0014070,Hindbrain,GEO,RNA-Seq,Mus musculus,8|4,EFO:Inflammation of the brain and the spinal cord. DSA01171,GSE136358,GPL17021,621,Encephalomyelitis,C0014070,Hindbrain,GEO,RNA-Seq,Mus musculus,16|12,EFO:Inflammation of the brain and the spinal cord. DSA01172,GSE136358,GPL17021,1000,Encephalomyelitis,C0014070,Hindbrain,GEO,RNA-Seq,Mus musculus,8|6,EFO:Inflammation of the brain and the spinal cord. DSA01173,GSE136371,GPL20301,1000,Cystic Fibrosis,C0010674,Whole blood,GEO,RNA-Seq,Homo sapiens,16|33,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA01174,GSE7553,GPL570,1000,Basal Cell Carcinoma,C0007117,Skin,GEO,Microarray,Homo sapiens,4|15,DO:A skin carcinoma affecting basal cells. DSA01175,GSE136587,GPL18573,1,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,3|12,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01176,GSE136587,GPL18573,15,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,3|12,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01177,GSE136666,GPL11154,0,Parkinson's Disease,C0030567,Putamen,GEO,RNA-Seq,Homo sapiens,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01178,GSE136666,GPL11154,131,Parkinson's Disease,C0030567,Substantia nigra,GEO,RNA-Seq,Homo sapiens,5|5,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01179,GSE136682,GPL21273,5,Colorectal Carcinoma,C0009402,Intestine,GEO,RNA-Seq,Mus musculus,4|3,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA01180,GSE136731,GPL20301,134,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,11|8,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01181,GSE136731,GPL20301,108,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,11|17,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01182,GSE136731,GPL20301,76,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,11|11,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01183,GSE136781,GPL17303,1000,Non-Functioning Pituitary Adenoma,C0338078,Pituitary gland,GEO,RNA-Seq,Homo sapiens,4|23,EFO:A hormone producing or non-producing pituitary gland adenoma not associated with a hormonal syndrome. DSA01184,GSE136781,GPL17303,1000,Non-Functioning Pituitary Adenoma,C0338078,Pituitary gland,GEO,RNA-Seq,Homo sapiens,4|19,EFO:A hormone producing or non-producing pituitary gland adenoma not associated with a hormonal syndrome. DSA01185,GSE136792,GPL13912,17,Familial Hypercholesterolemia,C0020445,,GEO,Microarray,Mus musculus,3|3,DO:A familial hyperlipidemia characterized by very high levels of low-density lipoprotein (LDL) and early cardiovascular disease. DSA01186,GSE136809,GPL13112,1000,Erythroleukemia,C4520840,Bone marrow,GEO,RNA-Seq,Mus musculus,3|5,NCI:Acute erythroid leukemia characterised by the presence of at least 50% erythroid precursors and at least 20% myeloblasts in the bone marrow. DSA01187,GSE7753,GPL570,1000,Systemic Juvenile Idiopathic Arthritis,C1384600,,GEO,Microarray,Homo sapiens,17|30,"EFO:Juvenile idiopathic arthritis (JIA), also known as juvenile rheumatoid arthritis (JRA), is the most common form of arthritis in children and adolescents. (Juvenile in this context refers to an onset before age 16, idiopathic refers to a condition with no defined cause, and arthritis is the inflammation of the synovium of a joint.) JIA is an autoimmune, non-infective, inflammatory joint disease of more than 6 weeks duration in children less than 16 years of age. The disease commonly occurs in children from the ages of 7 to 12, but it may occur in adolescents as old as 15 years of age, as well as in infants. It is a subset of arthritis seen in childhood, which may be transient and self-limited or chronic. It differs significantly from arthritis commonly seen in adults (osteoarthritis, rheumatoid arthritis), and other types of arthritis that can present in childhood which are chronic conditions (e.g. psoriatic arthritis and ankylosing spondylitis). Aetiopathology is similar to rheumatoid arthritis but with less marked cartilage erosion, and joint instability and absent rheumatoid factor. JIA affects approximately 1 in 1,000 children in any given year, with about 1 in 10,000 having a more severe form." DSA01188,GSE7904,GPL570,1000,Sporadic Basal-Like Cancers,,Breast,GEO,Microarray,Homo sapiens,7|18, DSA01189,GSE136893,GPL21103,1000,Typhoid Fever,C0041466,Gall bladder,GEO,RNA-Seq,Mus musculus,4|3,"DO:A primary bacterial infectious disease that is a communicable systemic illness, has_material_basis_in Salmonella enterica subsp enterica serovar Typhi, which is transmitted_by ingestion of food or water contaminated with the feces of an infected person. The infection has_symptom fever, has_symptom diarrhea, has_symptom prostration, has_symptom headache, has_symptom splenomegaly, has_symptom liver enlargement, has_symptom eruption of rose-colored spots, and has_symptom leukopenia." DSA01190,GSE136893,GPL21103,1000,Typhoid Fever,C0041466,Gall bladder,GEO,RNA-Seq,Mus musculus,3|3,"DO:A primary bacterial infectious disease that is a communicable systemic illness, has_material_basis_in Salmonella enterica subsp enterica serovar Typhi, which is transmitted_by ingestion of food or water contaminated with the feces of an infected person. The infection has_symptom fever, has_symptom diarrhea, has_symptom prostration, has_symptom headache, has_symptom splenomegaly, has_symptom liver enlargement, has_symptom eruption of rose-colored spots, and has_symptom leukopenia." DSA01191,GSE136948,GPL17021,653,Diabetes,C0011847,Muscle,GEO,RNA-Seq,Mus musculus,4|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA01192,GSE79973,GPL570,1000,Gastric Cancer,C0699791,Stomach,GEO,Microarray,Homo sapiens,10|10,DO:A gastrointestinal system cancer that is located_in the stomach. DSA01193,GSE8050,GPL570,0,Renal Cell Carcinoma,C0007134,Kidney,GEO,Microarray,Homo sapiens,2|2,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA01194,GSE137085,GPL16791|GPL21290,1000,Hutchinson-Gilford Progeria Syndrome,C0033300,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA01195,GSE137085,GPL16791|GPL21290,1000,Hutchinson-Gilford Progeria Syndrome,C0033300,,GEO,RNA-Seq,Homo sapiens,2|3,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA01196,GSE137107,GPL16686,450,Chronic Mucocutaneous Candidiasis,C0006845,Dermis,GEO,Microarray,Homo sapiens,2|2,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA01197,GSE137107,GPL16686,188,Chronic Mucocutaneous Candidiasis,C0006845,Dermis,GEO,Microarray,Homo sapiens,2|2,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA01198,GSE137107,GPL16686,501,Chronic Mucocutaneous Candidiasis,C0006845,Dermis,GEO,Microarray,Homo sapiens,2|2,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA01199,GSE137107,GPL16686,453,Chronic Mucocutaneous Candidiasis,C0006845,Dermis,GEO,Microarray,Homo sapiens,2|2,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA01200,GSE8545,GPL570,1000,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,18|18,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA01201,GSE85457,GPL570,351,Anaplastic Thyroid Carcinoma,C0238461,Thyroid,GEO,Microarray,Homo sapiens,3|4,DO:A thyroid gland carcinoma that is composed of undifferentiated cells. DSA01202,GSE8671,GPL570,1000,Colorectal Adenoma,C1302401,Colon,GEO,Microarray,Homo sapiens,4|4,"EFO:An adenoma that arises from the colon or rectum. The group of colorectal adenomas includes tubular, villous, and tubulovillous adenomas, traditional serrated adenomas, sessile serrated adenomas/polyps, and familial adenomatous polyposis." DSA01203,GSE8671,GPL570,972,Colorectal Adenoma,C1302401,Colon,GEO,Microarray,Homo sapiens,4|4,"EFO:An adenoma that arises from the colon or rectum. The group of colorectal adenomas includes tubular, villous, and tubulovillous adenomas, traditional serrated adenomas, sessile serrated adenomas/polyps, and familial adenomatous polyposis." DSA01204,GSE8671,GPL570,1000,Colorectal Adenoma,C1302401,Colon,GEO,Microarray,Homo sapiens,7|7,"EFO:An adenoma that arises from the colon or rectum. The group of colorectal adenomas includes tubular, villous, and tubulovillous adenomas, traditional serrated adenomas, sessile serrated adenomas/polyps, and familial adenomatous polyposis." DSA01205,GSE8671,GPL570,1000,Colorectal Adenoma,C1302401,Colon,GEO,Microarray,Homo sapiens,16|16,"EFO:An adenoma that arises from the colon or rectum. The group of colorectal adenomas includes tubular, villous, and tubulovillous adenomas, traditional serrated adenomas, sessile serrated adenomas/polyps, and familial adenomatous polyposis." DSA01206,GSE87385,GPL570,0,Amyotrophic Lateral Sclerosis,C0002736,,GEO,Microarray,Homo sapiens,2|2,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA01207,GSE87385,GPL570,13,Amyotrophic Lateral Sclerosis,C0002736,,GEO,Microarray,Homo sapiens,2|2,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA01208,GSE8762,GPL570,0,Huntington's Disease,C0020179,Blood,GEO,Microarray,Homo sapiens,5|8,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01209,GSE8762,GPL570,0,Huntington's Disease,C0020179,Blood,GEO,Microarray,Homo sapiens,5|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01210,GSE8977,GPL570,1000,Invasive Ductal Carcinoma,C1134719,,GEO,Microarray,Homo sapiens,15|7,DO:A breast ductal carcinoma that is characterized by infiltration into the fibrous or fatty tissue of the breast outside of the duct where it originated. DSA01211,GSE9452,GPL570,72,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,3|1,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA01212,GSE9511,GPL80,496,Uterine Leiomyosarcoma,C0280631,Myometrium,GEO,Microarray,Homo sapiens,4|1,DO:A uterine Corpus sarcoma and leiomyosarcoma and uterine Corpus smooth muscle neoplasm that is located_in the smooth muscle of the uterus. DSA01213,GSE9511,GPL80,2,Uterine Leiomyoma,C0042133,Myometrium,GEO,Microarray,Homo sapiens,4|7,DO:An uterine benign neoplasm derived from the smooth muscle layer of the uterus. DSA01214,GSE9511,GPL80,33,Uterine Leiomyosarcoma,C0280631,Myometrium,GEO,Microarray,Homo sapiens,4|8,DO:A uterine Corpus sarcoma and leiomyosarcoma and uterine Corpus smooth muscle neoplasm that is located_in the smooth muscle of the uterus. DSA01215,GSE9511,GPL80,48,Primary Leiomyosarcoma,C0855057,Myometrium,GEO,Microarray,Homo sapiens,4|4,NCI:Leiomyosarcoma that is confined to a specific site without evidence of spread to other anatomic sites. DSA01216,GSE9511,GPL80,316,Leiomyoma,C0042133,Myometrium,GEO,Microarray,Homo sapiens,4|1,DO:An uterine benign neoplasm derived from the smooth muscle layer of the uterus. DSA01217,GSE9511,GPL80,316,Leiomyoma,C0042133,Myometrium,GEO,Microarray,Homo sapiens,4|1,DO:An uterine benign neoplasm derived from the smooth muscle layer of the uterus. DSA01218,GSE9576,GPL570,1000,Primary Carcinoma,C1335475,Ileum,GEO,Microarray,Homo sapiens,3|3,NCI:Carcinoma that is confined to the site in which it initially manifested. DSA01219,GSE98421,GPL570,0,Polycystic Ovary Syndrome,C0032460,Adipose tissue,GEO,Microarray,Homo sapiens,4|4,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA01220,GSE24369,GPL6244,1000,Desmoid Fibromatosis,C0079218,Soft tissue,GEO,Microarray,Homo sapiens,2|6,"EFO:A desmoid tumor (DT) is a benign, locally invasive soft tissue tumor associated with a high recurrence rate but with no metastatic potential." DSA01221,GSE24369,GPL6244,1000,Extraskeletal Myxoid Chondrosarcoma,C1275278,Soft tissue,GEO,Microarray,Homo sapiens,2|6,DO:An extraosseous chondrosarcoma that has_material_basis_in cells derived from transformed cells that produce cartilage and is characterized by a marked abundance of extracellular mucoid (myxoid) matrix. DSA01222,GSE137141,GPL16699,1000,Hidradenitis Suppurativa,C0162836,Skin,GEO,Microarray,Homo sapiens,8|8,"DO:A hidradenitis that is characterized by chronic inflammation of the apocrine sweat glands, has_symptom painful nodules, abscesses, sinus tract formation, scarring, erythema, pruritis, and pain, and has_material_basis_in chronic inflammation of the apocrine sweat glands leading to recurrent folliculitis and an accompanying immune response that worsens inflammation." DSA01223,GSE137141,GPL16699,3,Hidradenitis Suppurativa,C0162836,Skin,GEO,Microarray,Homo sapiens,8|8,"DO:A hidradenitis that is characterized by chronic inflammation of the apocrine sweat glands, has_symptom painful nodules, abscesses, sinus tract formation, scarring, erythema, pruritis, and pain, and has_material_basis_in chronic inflammation of the apocrine sweat glands leading to recurrent folliculitis and an accompanying immune response that worsens inflammation." DSA01224,GSE137143,GPL24676,1000,Multiple Sclerosis,C0026769,,GEO,RNA-Seq,Homo sapiens,21|115,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA01225,GSE137143,GPL24676,1000,Multiple Sclerosis,C0026769,,GEO,RNA-Seq,Homo sapiens,20|108,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA01226,GSE137143,GPL24676,150,Multiple Sclerosis,C0026769,,GEO,RNA-Seq,Homo sapiens,20|113,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA01227,GSE137152,GPL21493,1000,Juvenile Myelomonocytic Leukemia,C0349639,,GEO,RNA-Seq,Mus musculus,3|3,DO:A myelodysplastic/myeloproliferative neoplasm that is characterized by the uncontrolled growth of monocytes. DSA01228,GSE137213,GPL19057,0,Parkinson's Disease,C0030567,Colon,GEO,RNA-Seq,Mus musculus,5|5,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01229,GSE137213,GPL19057,3,Parkinson's Disease,C0030567,Colon,GEO,RNA-Seq,Mus musculus,4|5,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01230,GSE137268,GPL6104,240,Asthma,C0004096,Sputum,GEO,Microarray,Homo sapiens,15|21,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01231,GSE137268,GPL6104,574,Asthma,C0004096,Sputum,GEO,Microarray,Homo sapiens,15|33,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01232,GSE148778,GPL6246,0,Hypoxia,C0242184,Kidney,GEO,Microarray,Mus musculus,3|3,"EFO:A decrease in the amount of oxygen in the body. Symptoms range from mild (impaired judgment, memory loss, impaired motor coordination) to severe (seizures and coma)." DSA01233,GSE148784,GPL19057,3,Parkinson's Disease,C0030567,Brain,GEO,RNA-Seq,Mus musculus,5|5,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01234,GSE148810,GPL28426,138,Juvenile Polymyositis,C3826988,Skin,GEO,Microarray,Homo sapiens,8|9,MONDO:An idiopathic inflammatory myopathy of childhood resulting in muscle weakness. DSA01235,GSE148810,GPL28426,662,Juvenile Polymyositis,C3826988,Skin,GEO,Microarray,Homo sapiens,8|6,MONDO:An idiopathic inflammatory myopathy of childhood resulting in muscle weakness. DSA01236,GSE148810,GPL28426,589,Childhood Onset,C1837352,Skin,GEO,Microarray,Homo sapiens,8|7,HPO:Onset of disease at the age of between 1 and 5 years. DSA01237,GSE148821,GPL17021,71,Thrombocytopenia,C0040034,Spleen,GEO,RNA-Seq,Mus musculus,5|6,DO:A blood platelet disease that is characterized by low a platelet count in the blood. DSA01238,GSE148821,GPL17021,581,Thrombocytopenia,C0040034,Bone marrow,GEO,RNA-Seq,Mus musculus,6|5,DO:A blood platelet disease that is characterized by low a platelet count in the blood. DSA01239,GSE148821,GPL17021,123,Thrombocytopenia,C0040034,Spleen,GEO,RNA-Seq,Mus musculus,3|7,DO:A blood platelet disease that is characterized by low a platelet count in the blood. DSA01240,GSE148821,GPL17021,0,Thrombocytopenia,C0040034,Bone marrow,GEO,RNA-Seq,Mus musculus,6|5,DO:A blood platelet disease that is characterized by low a platelet count in the blood. DSA01241,GSE148821,GPL17021,4,Thrombocytopenia,C0040034,Spleen,GEO,RNA-Seq,Mus musculus,3|7,DO:A blood platelet disease that is characterized by low a platelet count in the blood. DSA01242,GSE148821,GPL17021,68,Thrombocytopenia,C0040034,Bone marrow,GEO,RNA-Seq,Mus musculus,5|6,DO:A blood platelet disease that is characterized by low a platelet count in the blood. DSA01243,GSE24369,GPL6244,1000,Low-Grade Fibromyxoid Sarcoma,C1275282,Soft tissue,GEO,Microarray,Homo sapiens,2|17,"EFO:A low grade, late-metastasizing variant of fibrosarcoma characterized by alternating fibrous and myxoid areas and a whorling growth pattern. The neoplastic cells have a spindle morphology, and lack hyperchromasia or significant nuclear atypia. Approximately 40% of cases show the focal presence of collagen rosettes. A t(7;16)(q33;p11) translocation has been identified in the majority of cases, associated with the presence of FUS-CREB3L2 fusion protein. Rare cases carry the t(11;16)(p11;p11) translocation which is associated with the presence of the FUS-CREB3L1 fusion protein." DSA01244,GSE148851,GPL15207,1000,Hepatocellular Carcinoma,C0334287,,GEO,Microarray,Homo sapiens,3|3,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA01245,GSE148944,GPL28285,267,Tongue Squamous Cell Carcinoma,C0349566,Oral tongue,GEO,Microarray,Homo sapiens,6|28,DO:A head and neck squamous cell carcinoma that is located_in the tongue. DSA01246,GSE148944,GPL28285,234,Tongue Squamous Cell Carcinoma,C0349566,Oral tongue,GEO,Microarray,Homo sapiens,6|10,DO:A head and neck squamous cell carcinoma that is located_in the tongue. DSA01247,GSE148952,GPL20795,5,Placenta Accreta,C0032044,Placenta,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A placenta disease that is characterized by an abnormally deep attachment of the placenta, through the endometrium and into the myometrium." DSA01248,GSE148991,GPL16791,1000,Metastatic Prostate Cancer,C0936223,Plasma,GEO,RNA-Seq,Homo sapiens,5|6,EFO:A carcinoma that arises from the prostate gland and has spread to other anatomic sites. DSA01249,GSE149050,GPL16791,35,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,10|24,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01250,GSE149050,GPL16791,368,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,11|20,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01251,GSE149050,GPL16791,407,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,12|24,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01252,GSE149050,GPL16791,933,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,12|20,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01253,GSE149050,GPL16791,1000,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,11|115,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01254,GSE149050,GPL16791,121,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,26|93,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01255,GSE149084,GPL20795,1000,Cryptorchidism,C0010417,,GEO,RNA-Seq,Homo sapiens,3|6,"EFO:The failure of one or both testes of a male fetus to descend from the abdomen into the scrotum during the late part of pregnancy. If not surgically corrected in early childhood, males may be at increased risk for testicular cancer later in life." DSA01256,GSE149135,GPL13112,1000,Experimental Autoimmune Encephalomyelitis,C0014072,Central nervous system,GEO,RNA-Seq,Mus musculus,2|5,"EFO:An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)" DSA01257,GSE149135,GPL13112,1000,Experimental Autoimmune Encephalomyelitis,C0014072,Central nervous system,GEO,RNA-Seq,Mus musculus,2|5,"EFO:An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)" DSA01258,GSE149206,GPL21290,1000,Colorectal Carcinoma,C0009402,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|3,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA01259,GSE24369,GPL6244,1000,Myxofibrosarcoma,C3714524,Soft tissue,GEO,Microarray,Homo sapiens,2|6,"DO:A sarcoma that arises from the soft tissue and is characterized by the presence of spindle-shaped cells, cellular pleomorphism, thin-walled blood vessels, fibrous septa, and myxoid stroma." DSA01260,GSE149313,GPL20301,1000,Severe Fever With Thrombocytopenia Syndrome Banyangvirus,,Blood,GEO,scRNA-Seq,Homo sapiens,3|2, DSA01261,GSE149313,GPL20301,1000,Severe Fever With Thrombocytopenia Syndrome Banyangvirus,,Blood,GEO,scRNA-Seq,Homo sapiens,3|2, DSA01262,GSE149313,GPL20301,1000,Severe Fever With Thrombocytopenia Syndrome Banyangvirus,,Blood,GEO,scRNA-Seq,Homo sapiens,3|3, DSA01263,GSE149369,GPL11154,1000,Burn-Mckeown Syndrome,C1837822,,GEO,RNA-Seq,Homo sapiens,6|6,"MONDO:Choanal atresia - deafness - cardiac defects - dysmorphism syndrome, also known as Burn-McKeown syndrome, is an extremely rare multiple congenital anomaly syndrome characterized by bilateral choanal atresia associated with a characteristic cranio-facial dysmorphism (hypertelorism with narrow palpebral fissures, coloboma of inferior eyelid with presence of eyelashes medial to the defect, prominent nasal bridge, thin lips, prominent ears), that can be accompanied by hearing loss, unilateral cleft lip, preauricular tags, cardiac septal defects and anomalies of the kidneys. The features of this syndrome overlaps considerably with those of the CHARGE syndrome." DSA01264,GSE149369,GPL11154,1000,Burn-Mckeown Syndrome,C1837822,,GEO,RNA-Seq,Homo sapiens,6|6,"MONDO:Choanal atresia - deafness - cardiac defects - dysmorphism syndrome, also known as Burn-McKeown syndrome, is an extremely rare multiple congenital anomaly syndrome characterized by bilateral choanal atresia associated with a characteristic cranio-facial dysmorphism (hypertelorism with narrow palpebral fissures, coloboma of inferior eyelid with presence of eyelashes medial to the defect, prominent nasal bridge, thin lips, prominent ears), that can be accompanied by hearing loss, unilateral cleft lip, preauricular tags, cardiac septal defects and anomalies of the kidneys. The features of this syndrome overlaps considerably with those of the CHARGE syndrome." DSA01265,GSE149599,GPL23126,773,Alzheimer's Disease,C0002395,,GEO,Microarray,Homo sapiens,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01266,GSE149599,GPL23126,396,Alzheimer's Disease,C0002395,,GEO,Microarray,Homo sapiens,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01267,GSE149602,GPL20301,74,Autosomal Dominant Hyper-Ige Syndrome,C2936739,,GEO,RNA-Seq,Homo sapiens,6|3,DO:A hyper IgE syndrome that has_material_basis_in heterozygous mutation in the STAT3 gene on chromosome 17q21. DSA01268,GSE24369,GPL6244,1000,Solitary Fibrous Tumor,C1266119,Soft tissue,GEO,Microarray,Homo sapiens,2|5,"MONDO:Solitary fibrous tumor (SFT) represents a diverse group of ubiquitous rare spindle cell neoplasms that may be benign or malignant and that most frequently arises from the pleura and peritoneum and rarely from other sites such as head and neck, liver and skeletal muscle. SFT may be clinically asymptomatic or may present with enlarging mass, compressive effects depending on the site involved and rarely with paraneoplastic manifestations (osteoarthropathy or hypoglycemia)." DSA01269,GSE25401,GPL6244,774,Obesity,C0028754,White adipose tissue,GEO,Microarray,Homo sapiens,26|30,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA01270,GSE28735,GPL6244,1000,Pancreatic Tumor,C0030297,Pancreas,GEO,Microarray,Homo sapiens,45|45,DO:An endocrine gland cancer located_in the pancreas. DSA01271,GSE31552,GPL6244,262,Adenocarcinoid Tumor,C0334302,,GEO,Microarray,Homo sapiens,11|12,MONDO:A malignant epithelial neoplasm composed of a mixture of neuroendocrine cells with morphologic and immunohistochemical characteristics of carcinoid tumor and malignant glandular cells. DSA01272,GSE149863,GPL19057,71,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA01273,GSE149863,GPL19057,152,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA01274,GSE149894,GPL20258,0,Malaria,C0024530,,GEO,Microarray,Mus musculus,5|4,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA01275,GSE149894,GPL20258,0,Malaria,C0024530,,GEO,Microarray,Mus musculus,5|3,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA01276,GSE149921,GPL28485,552,Glioblastoma,C0017636,,GEO,Microarray,Homo sapiens,11|50,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA01277,GSE149980,GPL17077,15,Unipolar Depression,C0041696,,GEO,Microarray,Homo sapiens,18|16,DO:A major depressive disorder characterized by near-complete absence of pleasure. DSA01278,GSE150047,GPL21626,1000,Malaria,C0024530,,GEO,RNA-Seq,Mus musculus,7|5,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA01279,GSE150047,GPL21626,1000,Malaria,C0024530,,GEO,RNA-Seq,Mus musculus,7|5,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA01280,GSE150047,GPL21626,324,Malaria,C0024530,,GEO,RNA-Seq,Mus musculus,7|5,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA01281,GSE150047,GPL21626,104,Malaria,C0024530,,GEO,RNA-Seq,Mus musculus,7|6,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA01282,GSE150061,GPL17021,1000,Pancreatic Cancer,C0235974,Blood,GEO,RNA-Seq,Mus musculus,3|4,DO:An endocrine gland cancer located_in the pancreas. DSA01283,GSE150061,GPL17021,1000,Pancreatic Cancer,C0235974,,GEO,RNA-Seq,Mus musculus,3|4,DO:An endocrine gland cancer located_in the pancreas. DSA01284,GSE150061,GPL17021,1000,Pancreatic Cancer,C0235974,Brain,GEO,RNA-Seq,Mus musculus,3|3,DO:An endocrine gland cancer located_in the pancreas. DSA01285,GSE150061,GPL17021,1000,Pancreatic Cancer,C0235974,Liver,GEO,RNA-Seq,Mus musculus,3|4,DO:An endocrine gland cancer located_in the pancreas. DSA01286,GSE150073,GPL18480,1000,Obesity,C0028754,Liver,GEO,RNA-Seq,Mus musculus,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA01287,GSE150073,GPL18480,1000,Obesity,C0028754,Liver,GEO,RNA-Seq,Mus musculus,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA01288,GSE150117,GPL16791,1000,Cornelia De Lange Syndrome,C0270972,Prefrontal cortex,GEO,RNA-Seq,Homo sapiens,6|3,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA01289,GSE150118,GPL16791,215,Cornelia De Lange Syndrome,C0270972,Prefrontal cortex,GEO,RNA-Seq,Homo sapiens,6|4,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA01290,GSE150137,GPL11154,486,Hutchinson-Gilford Progeria Syndrome,C0033300,,GEO,RNA-Seq,Homo sapiens,3|6,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA01291,GSE150290,GPL16791,1000,Gastric Cancer,C0699791,Stomach,GEO,RNA-Seq,Homo sapiens,17|8,DO:A gastrointestinal system cancer that is located_in the stomach. DSA01292,GSE150290,GPL16791,1000,Gastric Cancer,C0699791,Stomach,GEO,RNA-Seq,Homo sapiens,17|15,DO:A gastrointestinal system cancer that is located_in the stomach. DSA01293,GSE150337,GPL23227,1000,Relapsing-Remitting Multiple Sclerosis,C0751967,Whole blood,GEO,RNA-Seq,Homo sapiens,3|2,"DO:A multiple sclerosis that is characterized by relapse (attacks of symptom flare-ups) followed by remission (periods of recovery). Symptoms may vary from mild to severe, and relapses and remissions may last for days or months. More than 80 percent of people who have MS begin with relapsing-remitting cycles." DSA01294,GSE150337,GPL23227,1000,Relapsing-Remitting Multiple Sclerosis,C0751967,Whole blood,GEO,RNA-Seq,Homo sapiens,3|7,"DO:A multiple sclerosis that is characterized by relapse (attacks of symptom flare-ups) followed by remission (periods of recovery). Symptoms may vary from mild to severe, and relapses and remissions may last for days or months. More than 80 percent of people who have MS begin with relapsing-remitting cycles." DSA01295,GSE150394,GPL21103,798,Familial Danish Dementia,C1861735,Brain,GEO,RNA-Seq,Mus musculus,3|3,"DO:A cerebral amyloid angiopathy characterized by ataxia, intention tremor, psychosis and dementia that has_material_basis_in an autosomal dominant mutation of ITM2B on chromosome 13q14.2." DSA01296,GSE150408,GPL21185,0,Intervertebral Disc Degeneration,C0158266,Whole blood,GEO,Microarray,Homo sapiens,17|17,DO:A bone deterioration disease that has_material_basis_in gradual dehydration and tears located_in intervertebral disc. DSA01297,GSE31552,GPL6244,0,Adenoid Squamous Cell Carcinoma,C0334250,,GEO,Microarray,Homo sapiens,2|7,DO:A squamous cell carcinoma that is characterized by a tubular microscopic pattern and keratinocyte acantholysis. DSA01298,GSE150453,GPL23159,1,Episodic Vestibular Syndrome With Hyperventilation-Induced Downbeat Nystagmus,,Whole blood,GEO,Microarray,Homo sapiens,7|7, DSA01299,GSE150510,GPL21103,1000,Spinal Muscular Atrophy,C0026847,Skeletal muscle,GEO,RNA-Seq,Mus musculus,3|3,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA01300,GSE150510,GPL21103,1000,Spinal Muscular Atrophy,C0026847,Skeletal muscle,GEO,RNA-Seq,Mus musculus,3|3,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA01301,GSE150621,GPL16791,61,Gestational Diabetes,C0085207,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A diabetes mellitus that manifests during pregnancy. DSA01302,GSE150621,GPL16791,52,Gestational Diabetes,C0085207,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A diabetes mellitus that manifests during pregnancy. DSA01303,GSE150641,GPL23480,49,Toxic Nephropathy,C1404837,Kidney,GEO,RNA-Seq,Mus musculus,3|3,NCI:Kidney damage resulting from exposure to drugs. DSA01304,GSE150641,GPL23480,1000,Toxic Nephropathy,C1404837,Kidney,GEO,RNA-Seq,Mus musculus,3|3,NCI:Kidney damage resulting from exposure to drugs. DSA01305,GSE150696,GPL17585,1000,Alzheimer's Disease,C0002395,Prefrontal cortex,GEO,Microarray,Homo sapiens,9|9,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01306,GSE150696,GPL17585,511,Dementia With Lewy Bodies,C0752347,Prefrontal cortex,GEO,Microarray,Homo sapiens,9|12,"DO:A dementia that is characterized by the development of abnormal proteinaceous (alpha-synuclein) cytoplasmic inclusions, called Lewy bodies, throughout the brain that results in progressive decline in mental abilities." DSA01307,GSE150728,GPL24676,53,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,2|7,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA01308,GSE31552,GPL6244,1000,Squamous Cell Carcinoma,C0007137,,GEO,Microarray,Homo sapiens,7|8,DO:A carcinoma that derives_from squamous epithelial cells. DSA01309,GSE150819,GPL24676,56,COVID-19,D8888888,Bronchus,GEO,RNA-Seq,Homo sapiens,3|11,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA01310,GSE150819,GPL18573,1000,Lung Tumor,C0242379,Lung,GEO,RNA-Seq,Homo sapiens,3|3,DO:A lung cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells and is located_in the lungs and has_symptom cough and has_symptom chest discomfort or pain and has_symptom weight loss and has_symptom hemoptysis. DSA01311,GSE31552,GPL6244,1000,Adenocarcinoid Tumor,C0334302,,GEO,Microarray,Homo sapiens,20|19,MONDO:A malignant epithelial neoplasm composed of a mixture of neuroendocrine cells with morphologic and immunohistochemical characteristics of carcinoid tumor and malignant glandular cells. DSA01312,GSE150838,GPL13112,645,C3 Glomerulopathy,C4087273,Liver,GEO,RNA-Seq,Mus musculus,3|3,"ORDO:A form of primary membranoproliferative glomerulonephritis characterized by the presence in renal biopsy samples of a glomerulonephritis with sole (or at least dominant) glomerular immunofluorescence staining for C3. Non-specific alterations or proliferative patterns with C3-dominant glomerular staining are also possible. Based upon electron microscopic findings, C3 glomerulopathy (C3G) may be further classified as C3 glomerulonephritis (C3GN) or Dense deposit disease (DDD)." DSA01313,GSE150838,GPL13112,1000,C3 Glomerulopathy,C4087273,Kidney,GEO,RNA-Seq,Mus musculus,3|6,"ORDO:A form of primary membranoproliferative glomerulonephritis characterized by the presence in renal biopsy samples of a glomerulonephritis with sole (or at least dominant) glomerular immunofluorescence staining for C3. Non-specific alterations or proliferative patterns with C3-dominant glomerular staining are also possible. Based upon electron microscopic findings, C3 glomerulopathy (C3G) may be further classified as C3 glomerulonephritis (C3GN) or Dense deposit disease (DDD)." DSA01314,GSE150846,GPL23126,602,Respiratory System Disease,C0035204,Nasal polyp,GEO,Microarray,Homo sapiens,3|3,"EFO:A non-neoplastic or neoplastic disorder that affects the respiratory system. Representative examples include pneumonia, chronic obstructive pulmonary disease, pulmonary failure, lung adenoma, lung carcinoma, and tracheal carcinoma." DSA01315,GSE150851,GPL20301,0,Psoriasis,C0033860,Sigmoideum,GEO,RNA-Seq,Homo sapiens,15|23,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA01316,GSE150996,GPL23227,1000,Adult-Onset Still Disease,C0085253,,GEO,RNA-Seq,Homo sapiens,6|6,"DO:A rheumatoid arthritis that is characterized by high fevers, rash, sore throat and joint pain." DSA01317,GSE151092,GPL19057,864,Obesity,C0028754,,GEO,RNA-Seq,Mus musculus,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA01318,GSE151092,GPL19057,375,Obesity,C0028754,,GEO,RNA-Seq,Mus musculus,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA01319,GSE151177,GPL18573,1000,Psoriasis,C0033860,Skin,GEO,scRNA-Seq,Homo sapiens,6|17,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA01320,GSE151195,GPL23227,181,Nasopharyngeal Carcinoma,C2931822,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A pharynx cancer that is located in the nasopharynx, the uppermost region of the pharynx or throat, where the nasal passages and auditory tubes join the remainder of the upper respiratory tract." DSA01321,GSE151250,GPL21290,1000,Hepatic Fibrosis,C0239946,,GEO,RNA-Seq,Homo sapiens,3|3,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA01322,GSE31552,GPL6244,290,Adenoid Squamous Cell Carcinoma,C0334250,,GEO,Microarray,Homo sapiens,2|2,DO:A squamous cell carcinoma that is characterized by a tubular microscopic pattern and keratinocyte acantholysis. DSA01323,GSE151268,GPL16570,1000,Metabolic Diseases,C0025517,White adipose tissue,GEO,Microarray,Mus musculus,10|10,DO:A disease that involving errors in metabolic processes of building or degradation of molecules. DSA01324,GSE151306,GPL10558,733,Secondary Progressive Multiple Sclerosis,C0751965,,GEO,Microarray,Homo sapiens,4|6,"DO:A multiple sclerosis that is characterised by a worsening of disability, rather than by relapses followed by recovery, which progressively worsens until a steady progression of disability replaces the cycles of attacks." DSA01325,GSE151316,GPL23227,1000,Ovarian Serous Carcinoma,C1335177,,GEO,RNA-Seq,Homo sapiens,14|14,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA01326,GSE151371,GPL20301,1000,Spinal Cord Disorder,C0037928,,GEO,RNA-Seq,Homo sapiens,10|38,EFO:A disease involving the spinal cord. DSA01327,GSE151371,GPL20301,1000,Spinal Cord Disorder,C0037928,,GEO,RNA-Seq,Homo sapiens,10|38,EFO:A disease involving the spinal cord. DSA01328,GSE44076,GPL13667,1000,Colon Tumor,C0009375,Colon,GEO,Microarray,Homo sapiens,98|98,DO:A colorectal cancer that is located_in the colon. DSA01329,GSE151495,GPL20301,1000,Diabetic Gastroenteropathy,,Duodenum,GEO,RNA-Seq,Homo sapiens,19|39, DSA01330,GSE151513,GPL16791,318,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,15|18,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA01331,GSE151594,GPL24676,140,Acute Myeloid Leukemia,C0023467,Bone marrow,GEO,RNA-Seq,Homo sapiens,2|6,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA01332,GSE151631,GPL16791,1000,Keratoconus,C0022578,Cornea,GEO,RNA-Seq,Homo sapiens,7|19,"DO:A corneal disease characterized by structural changes within the cornea causing it to thin and change, leading to a protruding conical shape." DSA01333,GSE151673,GPL18573,574,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,RNA-Seq,Homo sapiens,5|5,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA01334,GSE151713,GPL20795,286,Langerhans Cell Histiocytosis,C0019621,Peripheral blood,GEO,RNA-Seq,Homo sapiens,6|3,DO:A histiocytosis that is characterized by clonal proliferation of Langerhans cells. DSA01335,GSE151760,GPL20301,78,Obesity,C0028754,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA01336,GSE151801,GPL24676,104,Acute Lymphoblastic Leukemia,C0023449,Blood,GEO,RNA-Seq,Homo sapiens,3|3,DO:A acute leukemia that is characterized by over production of lymphoblasts. DSA01337,GSE151818,GPL11154,1000,Alzheimer's Disease,C0002395,Organoid,GEO,RNA-Seq,Homo sapiens,26|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01338,GSE31552,GPL6244,0,Squamous Cell Carcinoma,C0007137,,GEO,Microarray,Homo sapiens,10|11,DO:A carcinoma that derives_from squamous epithelial cells. DSA01339,GSE151897,GPL18573,56,Rheumatoid Arthritis,C0003873,,GEO,RNA-Seq,Homo sapiens,3|3,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA01340,GSE151927,GPL17021,1000,Acute Pancreatitis,C0001339,Liver,GEO,RNA-Seq,Mus musculus,8|8,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA01341,GSE151927,GPL17021,1000,Acute Pancreatitis,C0001339,Liver,GEO,RNA-Seq,Mus musculus,8|8,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA01342,GSE151966,GPL24247,1,Prenatal Stress,,Ileum,GEO,RNA-Seq,Mus musculus,3|3, DSA01343,GSE151966,GPL24247,3,Prenatal Stress,,Ileum,GEO,RNA-Seq,Mus musculus,3|3, DSA01344,GSE152004,GPL11154,1000,Asthma,C0004096,Nasal airway epithelium,GEO,RNA-Seq,Homo sapiens,253|440,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01345,GSE152042,GPL16791,1000,Periodontitis,C0031099,Gingiva,GEO,scRNA-Seq,Homo sapiens,2|2,"EFO:Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology)" DSA01346,GSE152061,GPL21103,3,Aortic Valve Stenosis,C0003507,Aortic valve,GEO,RNA-Seq,Mus musculus,6|6,DO:A bicuspid aortic valve disease that has_material_basis_in heterozygous mutation in the SMAD6 gene on chromosome 15q22. DSA01347,GSE152061,GPL21103,3,Aortic Valve Stenosis,C0003507,Aortic valve,GEO,RNA-Seq,Mus musculus,5|3,DO:A bicuspid aortic valve disease that has_material_basis_in heterozygous mutation in the SMAD6 gene on chromosome 15q22. DSA01348,GSE15222,GPL2700,1000,Alzheimer's Disease,C0002395,Cortex,GEO,Microarray,Homo sapiens,187|176,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01349,GSE152286,GPL21810,0,Ataxia Telangiectasia,C0004135,Cerebellum,GEO,Microarray,Mus musculus,4|4,"DO:An autosomal recessive cerebellar ataxia that is characterized by cerebellar ataxia, telangiectases, immune defects, and a predisposition to malignancy and that has_material_basis_in homozygous or compound heterozygous mutation in the ATM gene on chromosome 11q22." DSA01350,GSE152286,GPL21810,7,Ataxia Telangiectasia,C0004135,Cerebellum,GEO,Microarray,Mus musculus,4|4,"DO:An autosomal recessive cerebellar ataxia that is characterized by cerebellar ataxia, telangiectases, immune defects, and a predisposition to malignancy and that has_material_basis_in homozygous or compound heterozygous mutation in the ATM gene on chromosome 11q22." DSA01351,GSE152287,GPL20844,0,Ataxia Telangiectasia,C0004135,,GEO,Microarray,Homo sapiens,5|5,"DO:An autosomal recessive cerebellar ataxia that is characterized by cerebellar ataxia, telangiectases, immune defects, and a predisposition to malignancy and that has_material_basis_in homozygous or compound heterozygous mutation in the ATM gene on chromosome 11q22." DSA01352,GSE152418,GPL24676,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,17|16,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA01353,GSE152446,GPL18573,0,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,RNA-Seq,Homo sapiens,4|4,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA01354,GSE152446,GPL18573,3,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,RNA-Seq,Homo sapiens,4|4,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA01355,GSE152498,GPL16791,17,Coronary Artery Disease,C1956346,Plasma,GEO,RNA-Seq,Homo sapiens,3|3,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA01356,GSE152508,GPL20844,607,Colorectal Carcinoma,C0009402,Peripheral blood,GEO,Microarray,Homo sapiens,3|2,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA01357,GSE152508,GPL20844,1000,Colorectal Carcinoma,C0009402,Peripheral blood,GEO,Microarray,Homo sapiens,3|3,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA01358,GSE152539,GPL16570,0,Alzheimer's Disease,C0002395,Hippocampus,GEO,Microarray,Mus musculus,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01359,GSE152539,GPL16570,0,Alzheimer's Disease,C0002395,Hippocampus,GEO,Microarray,Mus musculus,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01360,GSE37751,GPL6244,1000,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,47|61,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA01361,GSE152600,GPL16791,1000,Metabolic Diseases,C0025517,,GEO,RNA-Seq,Homo sapiens,2|2,DO:A disease that involving errors in metabolic processes of building or degradation of molecules. DSA01362,GSE152618,GPL24247,1000,Lung Metastases,C0153676,Lung,GEO,scRNA-Seq,Mus musculus,2|2,"NCI:The spread of a malignant neoplasm to the lung. This may be from a primary lung malignant neoplasm, or from a malignant neoplasm at a distant site." DSA01363,GSE152618,GPL24247,1000,Myxoid Subcutaneous Tumors,C1834421,,GEO,scRNA-Seq,Mus musculus,2|2, DSA01364,GSE152641,GPL24676,1000,COVID-19,D8888888,Whole blood,GEO,RNA-Seq,Homo sapiens,18|62,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA01365,GSE152740,GPL18573,1000,Myeloid Leukemia,C0023470,,GEO,RNA-Seq,Homo sapiens,2|4,DO:A myelodysplastic myeloproliferative neoplasm characterized by the principal involvement of the neutrophil series with leukocytosis and multilineage dysplasia. The neoplastic cells do not have a Philadelphia chromosome or the BCR/ABL fusion gene. DSA01366,GSE152740,GPL18573,1000,Myeloid Leukemia,C0023470,,GEO,RNA-Seq,Homo sapiens,2|2,DO:A myelodysplastic myeloproliferative neoplasm characterized by the principal involvement of the neutrophil series with leukocytosis and multilineage dysplasia. The neoplastic cells do not have a Philadelphia chromosome or the BCR/ABL fusion gene. DSA01367,GSE152795,GPL28716,61,Metastatic Cancer To The Breast,C0346993,Breast,GEO,Microarray,Mus musculus,5|5,"NCI:The spread of a malignant neoplasm to the breast. This may be from a primary breast malignant neoplasm on the opposite side, or from a malignant neoplasm at a distant site." DSA01368,GSE152795,GPL28716,224,Metastatic Cancer To The Breast,C0346993,Breast,GEO,Microarray,Mus musculus,5|4,"NCI:The spread of a malignant neoplasm to the breast. This may be from a primary breast malignant neoplasm on the opposite side, or from a malignant neoplasm at a distant site." DSA01369,GSE152915,GPL18573,1000,Leigh Syndrome,C0023264,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A mitochondrial metabolism disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity." DSA01370,GSE152938,GPL20795,1000,Chromophobe Renal Cell Carcinoma,C1266042,,GEO,scRNA-Seq,Homo sapiens,1|1,"DO:A renal cell carcinoma that has_material_basis_in chromophobe cell that appear pale when viewed under microscope, but that are larger and display different features than clear cells." DSA01371,GSE152938,GPL20795,1000,Clear Cell Renal Cell Carcinoma,C0007134,,GEO,scRNA-Seq,Homo sapiens,1|2,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA01372,GSE152938,GPL20795,1000,Papillary Renal Cell Carcinoma,C1306837,,GEO,scRNA-Seq,Homo sapiens,1|1,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA01373,GSE38264,GPL6244,1000,Bladder Cancer,C0699885,Bladder,GEO,Microarray,Homo sapiens,10|28,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA01374,GSE38264,GPL6246,1000,Bladder Cancer,C0699885,Bladder,GEO,Microarray,Mus musculus,6|7,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA01375,GSE40888,GPL6244,0,Nonallergic Asthma,C0004096,Peripheral blood,GEO,Microarray,Homo sapiens,13|8,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01376,GSE40888,GPL6244,48,Allergic Asthma,C0155877,Peripheral blood,GEO,Microarray,Homo sapiens,14|13,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01377,GSE153315,GPL17303,1000,Type 2 Diabetes,C0011860,Whole blood,GEO,RNA-Seq,Homo sapiens,10|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA01378,GSE153315,GPL17303,1000,Type 2 Diabetes,C0011860,Whole blood,GEO,RNA-Seq,Homo sapiens,10|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA01379,GSE153413,GPL20301,366,High Grade Intraepithelial Neoplasia,C1334015,Plasma,GEO,RNA-Seq,Homo sapiens,5|5,"NCI:A precancerous neoplastic process that affects the squamous, glandular, or transitional cell epithelium without evidence of invasion. According to the degree of nuclear atypia, number of mitotic figures, and presence of architectural distortion, it is classified as grade II (moderate dysplasia) or grade III (severe dysplasia)." DSA01380,GSE153514,GPL10332,1,Metastatic Castration-Resistant Prostate Carcinoma,C1328504,Peripheral blood,GEO,Microarray,Homo sapiens,6|18,NCI:Prostate carcinoma that grows and continues to spread despite the surgical removal of the testes or medical intervention to block androgen production. DSA01381,GSE43458,GPL6244,1000,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Homo sapiens,30|40,DO:A respiratory system cancer that is located_in the lung. DSA01382,GSE44077,GPL6244,1000,Non-Small Cell Lung Cancer,C0007131,Lung,GEO,Microarray,Homo sapiens,22|18,DO:A respiratory system cancer that is located_in the lung. DSA01383,GSE153547,GPL21273,1000,Lupus Nephritis,C0024143,Kidney,GEO,RNA-Seq,Mus musculus,3|3,DO:A glomerulonephritis that is characterized by inflammation of the kidneys resulting from systemic lupus erythematosus. DSA01384,GSE153555,GPL16791,1000,Aortic Stenosis,C0003507,Bicuspid aortic valve,GEO,RNA-Seq,Homo sapiens,10|10,DO:A bicuspid aortic valve disease that has_material_basis_in heterozygous mutation in the SMAD6 gene on chromosome 15q22. DSA01385,GSE153555,GPL16791,1000,Aortic Insufficiency,C0003504,Tricuspid aortic valve leaflets,GEO,RNA-Seq,Homo sapiens,10|10,"DO:An aortic valve disease that is characterized by leaking of the aortic valve of the heart causes blood to flow in the reverse direction during ventricular diastole, from the aorta into the left ventricle." DSA01386,GSE153559,GPL21290,1000,Metastatic Head And Neck Squamous Cell Carcinoma,C1168401,Lymph node,GEO,scRNA-Seq,Homo sapiens,3|3,"DO:A head and neck carcinoma that has_material_basis_in squamous cells that line the moist, mucosal surfaces inside the head and neck." DSA01387,GSE153580,GPL17021,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,RNA-Seq,Mus musculus,9|9,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA01388,GSE153684,GPL24676,344,COVID-19,D8888888,Stomach,GEO,RNA-Seq,Homo sapiens,9|9,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA01389,GSE153713,GPL11154,1000,Ovarian Cancer Stage I,C0278685,,GEO,RNA-Seq,Homo sapiens,6|6,"NCI:Stage I includes: T1, N0, M0. T1: Tumor limited to ovaries (one or both). N0: No regional lymph node metastasis. M0: No distant metastasis. (AJCC 6th and 7th eds.)" DSA01390,GSE153713,GPL11154,1000,Ovarian Cancer Stage I,C0278685,,GEO,RNA-Seq,Homo sapiens,6|12,"NCI:Stage I includes: T1, N0, M0. T1: Tumor limited to ovaries (one or both). N0: No regional lymph node metastasis. M0: No distant metastasis. (AJCC 6th and 7th eds.)" DSA01391,GSE153715,GPL11154,10,Crohn's Disease,C0010346,Jejunum,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA01392,GSE153715,GPL11154,32,Crohn's Disease,C0010346,Ileum,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA01393,GSE153715,GPL11154,9,Crohn's Disease,C0010346,Jejunum,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA01394,GSE153715,GPL11154,27,Crohn's Disease,C0010346,Ileum,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA01395,GSE153739,GPL18573,53,Uterine Endometriosis,C0341858,Endometrium,GEO,RNA-Seq,Homo sapiens,3|2,"DO:A uterine disease that is characterized by the presence of endometrial tissue grows outside of the endometrium, such as into the myometrium." DSA01396,GSE153739,GPL18573,1000,Ovarian Endometriosis,C0156344,Endometrium,GEO,RNA-Seq,Homo sapiens,3|1,DO:A female reproductive system disease characterized by the growth of endometrial tissue that is located_in the ovary. DSA01397,GSE153739,GPL18573,1000,Ovarian Endometriosis,C0156344,Endometrium,GEO,RNA-Seq,Homo sapiens,3|1,DO:A female reproductive system disease characterized by the growth of endometrial tissue that is located_in the ovary. DSA01398,GSE44077,GPL6244,1000,Lung Carcinoid Tumor,C0280089,Lung,GEO,Microarray,Homo sapiens,22|3,EFO:A neuroendocrine neoplasm that arises from the lung. It is characterized by the presence of uniform polygonal cells with small or moderate amount of cytoplasm and inconspicuous nucleoli. The cells are usually arranged in organoid and trabecular patterns. It is classified as typical or atypical carcinoid tumor based on the number of mitotic figures and the absence or presence of necrosis. Atypical carcinoid tumors have a worse prognosis. DSA01399,GSE47927,GPL6244,223,Chronic Myeloid Leukemia,C0023473,Peripheral blood,GEO,Microarray,Homo sapiens,3|6,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA01400,GSE153761,GPL22120,0,Cervical Spondylosis With Myelopathy,C0158242,Cartilage endplate,GEO,Microarray,Homo sapiens,3|3, DSA01401,GSE153781,GPL20795,1000,Systemic Lupus Erythematosus,C0024141,Blood,GEO,RNA-Seq,Homo sapiens,6|6,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01402,GSE153802,GPL20795,1000,Crohn's Disease,C0010346,Small intestine,GEO,scRNA-Seq,Homo sapiens,1|1,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA01403,GSE153802,GPL20795,1000,Crohn's Disease,C0010346,Small intestine,GEO,scRNA-Seq,Homo sapiens,1|1,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA01404,GSE153829,GPL20115,0,Ossification of The Posterior Longitudinal Ligament of Spine,C1865343,Bone marrow,GEO,Microarray,Homo sapiens,3|3,"DO:A connective tissue disease characterized by ectopic ossification of the posterior longitudinal spinal ligament resulting in spinal cord compression, myelopathy and hyperreflexia." DSA01405,GSE153837,GPL10558,0,Prediabetes,C0362046,Peripheral blood,GEO,Microarray,Homo sapiens,12|16,"DO:A glucose metabolism disease that is characterized by blood glucose levels are high, but not high enough to be classified as type 2 diabetes." DSA01406,GSE47927,GPL6244,6,Chronic Myeloid Leukemia,C0023473,Peripheral blood,GEO,Microarray,Homo sapiens,3|4,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA01407,GSE153873,GPL18573,1000,Alzheimer's Disease,C0002395,Lateral temporal lobe,GEO,RNA-Seq,Homo sapiens,8|10,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01408,GSE153880,GPL16791,251,Systemic Sclerosis [Scleroderma],C2364016,Skin,GEO,RNA-Seq,Homo sapiens,12|11, DSA01409,GSE153881,GPL16791,61,Alzheimer's Disease,C0002395,,GEO,RNA-Seq,Homo sapiens,5|5,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01410,GSE153881,GPL16791,46,Cognitive Impairment,C0338656,,GEO,RNA-Seq,Homo sapiens,5|5,"HPO:Abnormal cognition with deficits in thinking, reasoning, or remembering." DSA01411,GSE47927,GPL6244,81,Chronic Myeloid Leukemia,C0023473,Peripheral blood,GEO,Microarray,Homo sapiens,3|2,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA01412,GSE47927,GPL6244,30,Chronic Myeloid Leukemia,C0023473,Peripheral blood,GEO,Microarray,Homo sapiens,3|6,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA01413,GSE113619,GPL16791,58,Keloid,C0022548,Skin,GEO,RNA-Seq,Homo sapiens,5|8,"EFO:An irregularly shaped, elevated mark on the skin caused by deposits of excessive amounts of collagen during wound healing. It extends beyond the original boundaries of the wound and may enlarge progressively." DSA01414,GSE113619,GPL16791,59,Keloid,C0022548,Skin,GEO,RNA-Seq,Homo sapiens,6|8,"EFO:An irregularly shaped, elevated mark on the skin caused by deposits of excessive amounts of collagen during wound healing. It extends beyond the original boundaries of the wound and may enlarge progressively." DSA01415,GSE113625,GPL17692,72,Metastatic Uveal Melanoma,C4725091,Peripheral blood,GEO,Microarray,Homo sapiens,2|3,NCI:Uveal melanoma that has spread from its primary site to another anatomic site. DSA01416,GSE113625,GPL17692,966,Metastatic Uveal Melanoma,C4725091,Peripheral blood,GEO,Microarray,Homo sapiens,2|3,NCI:Uveal melanoma that has spread from its primary site to another anatomic site. DSA01417,GSE113648,GPL18460,1000,Hutchinson-Gilford Progeria Syndrome,C0033300,Skin,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA01418,GSE113798,GPL20301,15,Major Depressive Disorder,C1269683,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA01419,GSE113798,GPL20301,10,Major Depressive Disorder,C1269683,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA01420,GSE47927,GPL6244,40,Chronic Myeloid Leukemia,C0023473,,GEO,Microarray,Homo sapiens,3|4,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA01421,GSE47927,GPL6244,306,Chronic Myeloid Leukemia,C0023473,Peripheral blood,GEO,Microarray,Homo sapiens,3|2,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA01422,GSE113843,GPL15523,1000,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,Microarray,Mus musculus,2|3,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA01423,GSE113866,GPL10558,1000,Fever,C0015967,Whole blood,GEO,Microarray,Homo sapiens,47|31,HPO:Body temperature elevated above the normal range. DSA01424,GSE113871,GPL16791,1000,Myocardial Infarction,C0027051,Heart,GEO,RNA-Seq,Homo sapiens,3|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA01425,GSE113873,GPL15207,1,Peripheral Artery Disease,C4025272,Gastrocnemius muscle,GEO,Microarray,Homo sapiens,10|12,"HPO:Narrowing of peripheral arteries with reduction of blood flow to the limbs. This feature may be quantified as an ankle-brachial index of less than 0.9, and may be manifested clinically as claudication." DSA01426,GSE113928,GPL10787,0,Huntington's Disease,C0020179,,GEO,Microarray,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01427,GSE113930,GPL10787,175,Huntington's Disease,C0020179,Striatum,GEO,Microarray,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01428,GSE113942,GPL11154,1000,Cervical Cancer,C4048328,Cervix,GEO,RNA-Seq,Homo sapiens,7|7,DO:A female reproductive organ cancer that is located_in the cervix. DSA01429,GSE114076,GPL20844,1000,Plasmodium Falciparum Malaria,C0024535,,GEO,Microarray,Homo sapiens,4|4,"DO:A malaria described as a severe form of the disease caused by a parasite Plasmodium falciparum, which is marked by irrregular recurrence of paroxysms and prolonged or continuous fever." DSA01430,GSE114132,GPL18635,1000,Ventilator-Induced Lung Injury,,Lung,GEO,RNA-Seq,Mus musculus,5|5, DSA01431,GSE114192,GPL18573,1000,Tuberculosis/Hyperglycaemia And Diabetes,,Lung,GEO,RNA-Seq,Homo sapiens,12|19, DSA01432,GSE114192,GPL18573,1000,Tuberculosis/Hyperglycaemia And Diabetes,,Lung,GEO,RNA-Seq,Homo sapiens,12|15, DSA01433,GSE114192,GPL18573,1000,Tuberculosis/Hyperglycaemia And Diabetes,,Lung,GEO,RNA-Seq,Homo sapiens,12|14, DSA01434,GSE114192,GPL18573,1000,Tuberculosis/Hyperglycaemia And Diabetes,,Lung,GEO,RNA-Seq,Homo sapiens,12|10, DSA01435,GSE114192,GPL18573,453,Tuberculosis/Hyperglycaemia And Diabetes,,Lung,GEO,RNA-Seq,Homo sapiens,24|33, DSA01436,GSE114192,GPL18573,1000,Tuberculosis/Hyperglycaemia And Diabetes,,Lung,GEO,RNA-Seq,Homo sapiens,24|15, DSA01437,GSE114192,GPL18573,1000,Tuberculosis/Hyperglycaemia And Diabetes,,Lung,GEO,RNA-Seq,Homo sapiens,24|26, DSA01438,GSE114192,GPL18573,590,Tuberculosis/Hyperglycaemia And Diabetes,,Lung,GEO,RNA-Seq,Homo sapiens,24|11, DSA01439,GSE114245,GPL16791,1000,Prostate Adenocarcinoma,C0007112,Prostate,GEO,RNA-Seq,Homo sapiens,3|6,DO:A prostate carcinoma that derives_from epithelial cells of glandular origin. DSA01440,GSE114245,GPL16791,1000,Prostate Adenocarcinoma,C0007112,Prostate,GEO,RNA-Seq,Homo sapiens,3|6,DO:A prostate carcinoma that derives_from epithelial cells of glandular origin. DSA01441,GSE114245,GPL16791,1000,Prostate Adenocarcinoma,C0007112,Prostate,GEO,RNA-Seq,Homo sapiens,3|6,DO:A prostate carcinoma that derives_from epithelial cells of glandular origin. DSA01442,GSE47927,GPL6244,1000,Chronic Myeloid Leukemia,C0023473,Peripheral blood,GEO,Microarray,Homo sapiens,3|6,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA01443,GSE114286,GPL17303,1000,Psoriasis Vulgaris,C0263361,Skin,GEO,RNA-Seq,Homo sapiens,9|16, DSA01444,GSE47927,GPL6244,256,Chronic Myeloid Leukemia,C0023473,Peripheral blood,GEO,Microarray,Homo sapiens,3|4,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA01445,GSE47927,GPL6244,160,Chronic Myeloid Leukemia,C0023473,Peripheral blood,GEO,Microarray,Homo sapiens,3|2,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA01446,GSE114419,GPL17586,0,Polycystic Ovary Syndrome,C0032460,Ovary,GEO,Microarray,Homo sapiens,3|3,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA01447,GSE114517,GPL18573,0,Parkinson's Disease,C0030567,Brain,GEO,RNA-Seq,Homo sapiens,8|15,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01448,GSE114517,GPL18573,0,Parkinson's Disease,C0030567,Brain,GEO,RNA-Seq,Homo sapiens,9|14,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01449,GSE114517,GPL18573,10,Parkinson's Disease,C0030567,Brain,GEO,RNA-Seq,Homo sapiens,12|17,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01450,GSE114691,GPL11154,1000,Pre-Eclampsia,C0032914,Placenta,GEO,RNA-Seq,Homo sapiens,21|20,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA01451,GSE114691,GPL11154,1000,Pre-Eclampsia;Intrauterine Growth Restriction,,Placenta,GEO,RNA-Seq,Homo sapiens,21|20, DSA01452,GSE114691,GPL11154,1000,Intrauterine Growth Restriction,C1386048,Placenta,GEO,RNA-Seq,Homo sapiens,21|18,HPO:An abnormal restriction of fetal growth with fetal weight below the tenth percentile for gestational age. DSA01453,GSE114709,GPL20775,801,Sickle Cell Disease,C0002895,Lung,GEO,Microarray,Mus musculus,2|2,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA01454,GSE114783,GPL15491,0,Hepatitis B,C0019163,Liver,GEO,Microarray,Homo sapiens,3|10,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus, which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice." DSA01455,GSE114783,GPL15491,1,Liver Cirrhosis,C0023890,Liver,GEO,Microarray,Homo sapiens,3|10,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA01456,GSE114783,GPL15491,0,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,3|10,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA01457,GSE114786,GPL10558,1000,Ataxia With Oculomotor Apraxia Type 1,C1859598,,GEO,Microarray,Homo sapiens,3|3,"DO:An autosomal recessive cerebellar ataxia that is characterized by progressive cerebellar ataxia including oculomotor apraxia, severe neuropathy and hypoalbuminemia, has_material_basis_in autosomal recessive inheritance of mutation in the APTX gene." DSA01458,GSE114852,GPL10558,0,Depression,C0011581,Umbilical cord blood,GEO,Microarray,Homo sapiens,62|31,DO:A mood disorder that involves the presence of a low mood almost daily over a span of at least two years. DSA01459,GSE114852,GPL10558,0,Post-Traumatic Stress Disorder,C0038436,Umbilical cord blood,GEO,Microarray,Homo sapiens,62|13,DO:An anxiety disorder which results from a traumatic experience that results in psychological trauma. DSA01460,GSE114852,GPL10558,0,Post-Traumatic Stress Disorder,C0038436,Umbilical cord blood,GEO,Microarray,Homo sapiens,62|20,DO:An anxiety disorder which results from a traumatic experience that results in psychological trauma. DSA01461,GSE114868,GPL17586,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,20|194,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA01462,GSE114869,GPL17586,1000,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,20|300,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA01463,GSE115018,GPL20115,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,12|12,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA01464,GSE47927,GPL6244,52,Chronic Myeloid Leukemia,C0023473,Peripheral blood,GEO,Microarray,Homo sapiens,3|6,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA01465,GSE115031,GPL16791,1000,Myocardial Infarction,C0027051,Heart,GEO,RNA-Seq,Homo sapiens,3|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA01466,GSE115099,GPL20795,1000,Acne Inversa,C0162836,Skin,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A hidradenitis that is characterized by chronic inflammation of the apocrine sweat glands, has_symptom painful nodules, abscesses, sinus tract formation, scarring, erythema, pruritis, and pain, and has_material_basis_in chronic inflammation of the apocrine sweat glands leading to recurrent folliculitis and an accompanying immune response that worsens inflammation." DSA01467,GSE115193,GPL16791,57,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,RNA-Seq,Homo sapiens,3|3,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA01468,GSE115193,GPL16791,167,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Homo sapiens,3|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA01469,GSE115259,GPL18573,1000,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,3|4,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA01470,GSE115262,GPL18573,1000,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,2|11,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA01471,GSE115262,GPL18573,237,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA01472,GSE115262,GPL18573,40,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA01473,GSE115262,GPL18573,72,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA01474,GSE115503,GPL17021,1000,Systemic Sclerosis [Scleroderma],C2364016,Skin,GEO,RNA-Seq,Mus musculus,2|2, DSA01475,GSE115621,GPL16791,1000,Cardiomyopathy,C0878544,Myocardium,GEO,RNA-Seq,Homo sapiens,2|2,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA01476,GSE115621,GPL16791,1000,Cardiomyopathy,C0878544,Myocardium,GEO,RNA-Seq,Homo sapiens,2|2,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA01477,GSE115650,GPL16791,1000,Facioscapulohumeral Muscular Dystrophy,C0238288,Muscle,GEO,RNA-Seq,Homo sapiens,9|34,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA01478,GSE115857,GPL14951,32,Idiopathic Iga Nephopathy,,Kidney,GEO,Microarray,Homo sapiens,7|55, DSA01479,GSE115906,GPL13112,1000,Malaria,C0024530,Liver,GEO,RNA-Seq,Mus musculus,3|3,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA01480,GSE115906,GPL13112,466,Malaria,C0024530,Lung,GEO,RNA-Seq,Mus musculus,3|3,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA01481,GSE115906,GPL13112,987,Malaria,C0024530,Spleen,GEO,RNA-Seq,Mus musculus,3|3,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA01482,GSE116086,GPL18573,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,RNA-Seq,Homo sapiens,2|2,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA01483,GSE116094,GPL17021,199,Renal Artery Stenosis,C0035067,Kidney,GEO,RNA-Seq,Mus musculus,3|4,HPO:The presence of stenosis of the renal artery. DSA01484,GSE116094,GPL17021,108,Renal Artery Stenosis,C0035067,Kidney,GEO,RNA-Seq,Mus musculus,3|4,HPO:The presence of stenosis of the renal artery. DSA01485,GSE116094,GPL17021,1000,Renal Artery Stenosis,C0035067,Kidney,GEO,RNA-Seq,Mus musculus,4|3,HPO:The presence of stenosis of the renal artery. DSA01486,GSE116111,GPL11154,1000,Melanoma,C0025202,Skin,GEO,RNA-Seq,Homo sapiens,1|3,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA01487,GSE116222,GPL24676,873,Ulcerative Colitis,C0009324,Colon,GEO,RNA-Seq,Homo sapiens,3|3,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA01488,GSE116222,GPL24676,58,Ulcerative Colitis,C0009324,Colon,GEO,RNA-Seq,Homo sapiens,3|3,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA01489,GSE47927,GPL6244,5,Chronic Myeloid Leukemia,C0023473,,GEO,Microarray,Homo sapiens,3|4,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA01490,GSE116294,GPL25249,1000,Multiple Myeloma,C0026764,Bone marrow,GEO,Microarray,Homo sapiens,4|50,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA01491,GSE116294,GPL25249,1000,Plasma Cell Leukemia,C0023484,Bone marrow,GEO,Microarray,Homo sapiens,4|15,DO:A plasma cell neoplasm that is characterized by the presence of a circulating clonal plasma cell count that exceeds 2x10^9/L or is 20% of the leukocyte differential count. DSA01492,GSE47927,GPL6244,129,Chronic Myeloid Leukemia,C0023473,Peripheral blood,GEO,Microarray,Homo sapiens,3|2,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA01493,GSE47927,GPL6244,122,Chronic Myeloid Leukemia,C0023473,Peripheral blood,GEO,Microarray,Homo sapiens,3|2,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA01494,GSE47927,GPL6244,495,Chronic Myeloid Leukemia,C0023473,Peripheral blood,GEO,Microarray,Homo sapiens,3|2,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA01495,GSE48761,GPL6244,1000,Werner Syndrome,C0043119,,GEO,Microarray,Homo sapiens,10|2,"DO:A progeroid syndrome characterized by premature aging and age-related phenotypes such as atherosclerosis, arteriosclerosis, cataracts, osteoporosis, soft tissue calcification, premature thinning, graying, and loss of hair, as well as a high incidence of some types of cancers and that has_material_basis_in mutations in the WRN gene, on chromosome 8." DSA01496,GSE48761,GPL6244,1000,Werner Syndrome,C0043119,,GEO,Microarray,Homo sapiens,10|2,"DO:A progeroid syndrome characterized by premature aging and age-related phenotypes such as atherosclerosis, arteriosclerosis, cataracts, osteoporosis, soft tissue calcification, premature thinning, graying, and loss of hair, as well as a high incidence of some types of cancers and that has_material_basis_in mutations in the WRN gene, on chromosome 8." DSA01497,GSE53000,GPL6244,1000,Clear Cell Renal Cell Carcinoma,C0007134,Kidney,GEO,Microarray,Homo sapiens,6|53,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA01498,GSE62452,GPL6244,0,Pancreatic Tumor,C0030297,Pancreas,GEO,Microarray,Homo sapiens,1|1,DO:An endocrine gland cancer located_in the pancreas. DSA01499,GSE62452,GPL6244,0,Pancreatic Tumor,C0030297,Pancreas,GEO,Microarray,Homo sapiens,3|4,DO:An endocrine gland cancer located_in the pancreas. DSA01500,GSE62452,GPL6244,0,Pancreatic Tumor,C0030297,Pancreas,GEO,Microarray,Homo sapiens,8|10,DO:An endocrine gland cancer located_in the pancreas. DSA01501,GSE116327,GPL16791,1000,Alexander Disease,C0270726,Brain,GEO,RNA-Seq,Homo sapiens,3|5,DO:A leukodystrophy that is characterized by the destruction of white matter and the formation of Rosenthal fibers consisting of abnormal clumps of protein that accumulate in astrocytes. DSA01502,GSE116486,GPL570,317,Atopic Dermatitis,C0011615,Blood,GEO,Microarray,Homo sapiens,18|28,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA01503,GSE116520,GPL10558,1000,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,8|17,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA01504,GSE116616,GPL13497,1000,Acute Myeloblastic Leukemia,C2854122,Bone marrow,GEO,Microarray,Homo sapiens,4|4,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA01505,GSE116616,GPL13497,5,Acute Myeloblastic Leukemia,C2854122,Bone marrow,GEO,Microarray,Homo sapiens,4|4,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA01506,GSE62452,GPL6244,1000,Pancreatic Tumor,C0030297,Pancreas,GEO,Microarray,Homo sapiens,29|35,DO:An endocrine gland cancer located_in the pancreas. DSA01507,GSE62452,GPL6244,1000,Pancreatic Tumor,C0030297,Pancreas,GEO,Microarray,Homo sapiens,13|13,DO:An endocrine gland cancer located_in the pancreas. DSA01508,GSE62452,GPL6244,0,Pancreatic Tumor,C0030297,Pancreas,GEO,Microarray,Homo sapiens,4|3,DO:An endocrine gland cancer located_in the pancreas. DSA01509,GSE116820,GPL23159,0,Bipolar Disorder,C0005586,,GEO,Microarray,Homo sapiens,2|2,DO:A mood disorder that involves alternating periods of mania and depression. DSA01510,GSE116820,GPL23159,1000,Schizophrenia,C0036341,,GEO,Microarray,Homo sapiens,2|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA01511,GSE116820,GPL23159,0,Bipolar Disorder,C0005586,,GEO,Microarray,Homo sapiens,2|2,DO:A mood disorder that involves alternating periods of mania and depression. DSA01512,GSE116820,GPL23159,33,Schizophrenia,C0036341,,GEO,Microarray,Homo sapiens,2|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA01513,GSE116899,GPL11154,368,Rheumatoid Arthritis,C0003873,Blood,GEO,RNA-Seq,Homo sapiens,10|14,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA01514,GSE116934,GPL18573,1000,Spondylocostal Dysostosis,C4083048,,GEO,RNA-Seq,Homo sapiens,3|2,"DO:A dysostosis that results_in abnormal development located_in vertebrae or located_in ribs. The bones of the spine do not develop properly, which causes them to be misshapen and abnormally joined together." DSA01515,GSE116934,GPL18573,683,Spondylocostal Dysostosis,C4083048,,GEO,RNA-Seq,Homo sapiens,3|2,"DO:A dysostosis that results_in abnormal development located_in vertebrae or located_in ribs. The bones of the spine do not develop properly, which causes them to be misshapen and abnormally joined together." DSA01516,GSE116934,GPL18573,1000,Spondylocostal Dysostosis,C4083048,,GEO,RNA-Seq,Homo sapiens,3|1,"DO:A dysostosis that results_in abnormal development located_in vertebrae or located_in ribs. The bones of the spine do not develop properly, which causes them to be misshapen and abnormally joined together." DSA01517,GSE116934,GPL18573,580,Spondylocostal Dysostosis,C4083048,,GEO,RNA-Seq,Homo sapiens,3|2,"DO:A dysostosis that results_in abnormal development located_in vertebrae or located_in ribs. The bones of the spine do not develop properly, which causes them to be misshapen and abnormally joined together." DSA01518,GSE116934,GPL18573,928,Spondylocostal Dysostosis,C4083048,,GEO,RNA-Seq,Homo sapiens,3|2,"DO:A dysostosis that results_in abnormal development located_in vertebrae or located_in ribs. The bones of the spine do not develop properly, which causes them to be misshapen and abnormally joined together." DSA01519,GSE116934,GPL18573,1000,Spondylocostal Dysostosis,C4083048,,GEO,RNA-Seq,Homo sapiens,3|2,"DO:A dysostosis that results_in abnormal development located_in vertebrae or located_in ribs. The bones of the spine do not develop properly, which causes them to be misshapen and abnormally joined together." DSA01520,GSE62452,GPL6244,0,Pancreatic Tumor,C0030297,Pancreas,GEO,Microarray,Homo sapiens,2|2,DO:An endocrine gland cancer located_in the pancreas. DSA01521,GSE117038,GPL16791,1000,Asthma,C0004096,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01522,GSE117038,GPL16791,8,Asthma,C0004096,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|6,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01523,GSE117062,GPL21273,1000,Chronic Colitis,C0267375,Colon,GEO,RNA-Seq,Mus musculus,3|3,"HPO:A chronic inflammatory disease of the large intestine (colon, cecum and rectum)." DSA01524,GSE117090,GPL17586,80,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,Microarray,Homo sapiens,7|28,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA01525,GSE117090,GPL17586,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,Microarray,Homo sapiens,7|30,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA01526,GSE117090,GPL17586,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,Microarray,Homo sapiens,7|30,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA01527,GSE117168,GPL21290,1000,Pyogenic Arthritis; Pyoderma Gangrenosum; And Acne Syndrome [Papa],C1861303,,GEO,RNA-Seq,Homo sapiens,1|1,"DO:A syndrome characterized by familial granulomatous arthritis, uveitis and skin granulomas. It has_material_basis_in heterozygous mutations in the NOD2 gene." DSA01528,GSE117168,GPL21290,1000,Pyogenic Arthritis; Pyoderma Gangrenosum; And Acne Syndrome [Papa],C1861303,Skin,GEO,RNA-Seq,Homo sapiens,1|1,"DO:A syndrome characterized by familial granulomatous arthritis, uveitis and skin granulomas. It has_material_basis_in heterozygous mutations in the NOD2 gene." DSA01529,GSE117221,GPL11154,53,Thalassaemia,C0039730,Peripheral blood,GEO,RNA-Seq,Homo sapiens,17|15,DO:A hemolytic anemia characterized by decreased synthesis of one or more hemoglobin polypeptide chains. DSA01530,GSE117221,GPL11154,1000,Thalassaemia,C0039730,Peripheral blood,GEO,RNA-Seq,Homo sapiens,17|17,DO:A hemolytic anemia characterized by decreased synthesis of one or more hemoglobin polypeptide chains. DSA01531,GSE117230,GPL17586,0,Clear Cell Renal Cell Carcinoma,C0007134,Peripheral blood,GEO,Microarray,Homo sapiens,5|5,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA01532,GSE117230,GPL17586,215,Clear Cell Renal Cell Carcinoma,C0007134,Peripheral blood,GEO,Microarray,Homo sapiens,5|5,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA01533,GSE117249,GPL13112,1000,Kidney Injury,C2609414,Kidney,GEO,RNA-Seq,Mus musculus,4|4,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA01534,GSE117261,GPL6244,1000,Pulmonary Arterial Hypertension,C2973725,Lung,GEO,Microarray,Homo sapiens,25|58,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA01535,GSE117285,GPL17077,1000,Extramammary Paget Disease,C0030186,Skin,GEO,Microarray,Homo sapiens,4|4,DO:A skin carcinoma that is characterized by infiltration of the skin by neoplastic large cells with abundant pale cytoplasm and large nuclei with prominent nucleoli. DSA01536,GSE117405,GPL11154|GPL20301,1000,Psoriasis,C0033860,Skin,GEO,RNA-Seq,Homo sapiens,9|3,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA01537,GSE117405,GPL11154|GPL20301,1000,Psoriasis,C0033860,Skin,GEO,RNA-Seq,Homo sapiens,9|8,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA01538,GSE117405,GPL11154|GPL20301,1000,Psoriasis,C0033860,Skin,GEO,RNA-Seq,Homo sapiens,9|8,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA01539,GSE117489,GPL16791,219,Asthma,C0004096,Tracheobronchial,GEO,RNA-Seq,Homo sapiens,3|6,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01540,GSE117489,GPL16791,185,Asthma,C0004096,Tracheobronchial,GEO,RNA-Seq,Homo sapiens,4|6,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01541,GSE117489,GPL16791,148,Asthma,C0004096,Tracheobronchial,GEO,RNA-Seq,Homo sapiens,4|6,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01542,GSE117489,GPL16791,302,Asthma,C0004096,Tracheobronchial,GEO,RNA-Seq,Homo sapiens,4|6,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01543,GSE117557,GPL13112,1000,Papilloma,C0030354,Epidermis,GEO,RNA-Seq,Mus musculus,3|3,DO:A cell type benign neoplam that is composed of epithelial tissue on papillae of vascularized connective tissue. DSA01544,GSE117557,GPL13112,1000,Papilloma,C0030354,Epidermis,GEO,RNA-Seq,Mus musculus,3|2,DO:A cell type benign neoplam that is composed of epithelial tissue on papillae of vascularized connective tissue. DSA01545,GSE117627,GPL20301,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA01546,GSE117627,GPL20301,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA01547,GSE117647,GPL96,0,Adrenomyeloneuropathy,C1527231,,GEO,Microarray,Homo sapiens,2|2,"DO:A leukodystrophy that disrupts the breakdown of very-long-chain fatty acids resulting in progressive brain damage, failure of the adrenal glands and eventually death." DSA01548,GSE117647,GPL96,25,Cerebral Adrenoleukodystrophy,C4684865,,GEO,Microarray,Homo sapiens,2|2,"NCI:A subtype of adrenoleukodystrophy (ALD) occurring in approximately 40 percent of boys with ALD, primarily affecting the cerebrum, resulting in rapidly declining neurocognitive function and in most patients, premature death." DSA01549,GSE117647,GPL96,0,Adrenomyeloneuropathy,C1527231,,GEO,Microarray,Homo sapiens,2|2,"DO:A leukodystrophy that disrupts the breakdown of very-long-chain fatty acids resulting in progressive brain damage, failure of the adrenal glands and eventually death." DSA01550,GSE117647,GPL96,0,Cerebral Adrenoleukodystrophy,C4684865,,GEO,Microarray,Homo sapiens,2|2,"NCI:A subtype of adrenoleukodystrophy (ALD) occurring in approximately 40 percent of boys with ALD, primarily affecting the cerebrum, resulting in rapidly declining neurocognitive function and in most patients, premature death." DSA01551,GSE117647,GPL96,0,Adrenomyeloneuropathy,C1527231,,GEO,Microarray,Homo sapiens,2|2,"DO:A leukodystrophy that disrupts the breakdown of very-long-chain fatty acids resulting in progressive brain damage, failure of the adrenal glands and eventually death." DSA01552,GSE117647,GPL96,0,Cerebral Adrenoleukodystrophy,C4684865,,GEO,Microarray,Homo sapiens,2|2,"NCI:A subtype of adrenoleukodystrophy (ALD) occurring in approximately 40 percent of boys with ALD, primarily affecting the cerebrum, resulting in rapidly declining neurocognitive function and in most patients, premature death." DSA01553,GSE117647,GPL96,0,Adrenomyeloneuropathy,C1527231,,GEO,Microarray,Homo sapiens,2|2,"DO:A leukodystrophy that disrupts the breakdown of very-long-chain fatty acids resulting in progressive brain damage, failure of the adrenal glands and eventually death." DSA01554,GSE117647,GPL96,20,Cerebral Adrenoleukodystrophy,C4684865,,GEO,Microarray,Homo sapiens,2|2,"NCI:A subtype of adrenoleukodystrophy (ALD) occurring in approximately 40 percent of boys with ALD, primarily affecting the cerebrum, resulting in rapidly declining neurocognitive function and in most patients, premature death." DSA01555,GSE117668,GPL25381,233,Malignant Pleural Mesothelioma,C0812413,,GEO,Microarray,Homo sapiens,1|12,DO:A pleural cancer that has_material_basis_in mesothelium cells. DSA01556,GSE117668,GPL25381,193,Malignant Pleural Mesothelioma,C0812413,,GEO,Microarray,Homo sapiens,1|12,DO:A pleural cancer that has_material_basis_in mesothelium cells. DSA01557,GSE117668,GPL25381,151,Malignant Pleural Mesothelioma,C0812413,,GEO,Microarray,Homo sapiens,1|12,DO:A pleural cancer that has_material_basis_in mesothelium cells. DSA01558,GSE62452,GPL6244,0,Pancreatic Tumor,C0030297,Pancreas,GEO,Microarray,Homo sapiens,1|1,DO:An endocrine gland cancer located_in the pancreas. DSA01559,GSE117680,GPL6244,212,Classical Ehlers-Danlos Syndrome,C4552122,Skin,GEO,Microarray,Homo sapiens,9|4,"DO:An Ehlers-Danlos syndrome that is characterized by loose-jointedness and fragile, bruisable skin that heals with peculiar 'cigarette-paper' scars and that has_material_basis_in heterozygous mutation in the collagen alpha-1(V) gene (COL5A1) on chromosome 9q34." DSA01560,GSE117710,GPL13112,292,Tubulointerstitial Nephropathy,C4025732,Kidney,GEO,RNA-Seq,Mus musculus,2|2,HPO:An abnormality that involves the tubules and interstitial tissue of the kidney. DSA01561,GSE117769,GPL16791,1000,Rheumatoid Arthritis,C0003873,Blood,GEO,RNA-Seq,Homo sapiens,50|70,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA01562,GSE117875,GPL16791,136,Crohn's Disease,C0010346,Ileum,GEO,RNA-Seq,Homo sapiens,7|6,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA01563,GSE117925,GPL25407,0,Alcohol Use Disorder,C0001973,Prefrontal cortex,GEO,Microarray,Mus musculus,4|5,"DO:A substance dependence that is characterized by tolerance, withdrawal symptoms, increasing use, persistent desire to decrease consumption, time spent obtaining or recovering from alcohol caused by a physical and psychological dependence on alcohol." DSA01564,GSE117925,GPL25408,0,Alcohol Use Disorder,C0001973,Prefrontal cortex,GEO,Microarray,Mus musculus,4|5,"DO:A substance dependence that is characterized by tolerance, withdrawal symptoms, increasing use, persistent desire to decrease consumption, time spent obtaining or recovering from alcohol caused by a physical and psychological dependence on alcohol." DSA01565,GSE117928,GPL14951,617,Systemic Sclerosis [Scleroderma],C2364016,Blood,GEO,Microarray,Homo sapiens,19|18, DSA01566,GSE117935,GPL5175,0,Multiple Sclerosis,C0026769,Peripheral blood,GEO,Microarray,Homo sapiens,10|10,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA01567,GSE117993,GPL16791,1000,Crohn's Disease,C0010346,Rectum,GEO,RNA-Seq,Homo sapiens,55|32,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA01568,GSE117993,GPL16791,1000,Crohn's Disease,C0010346,Rectum,GEO,RNA-Seq,Homo sapiens,55|60,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA01569,GSE117993,GPL16791,1000,Ulcerative Colitis,C0009324,Rectum,GEO,RNA-Seq,Homo sapiens,55|43,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA01570,GSE117999,GPL20844,1000,Osteoarthritis,C0157946,Knee,GEO,Microarray,Homo sapiens,10|10,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA01571,GSE118243,GPL21185,0,Allergic Rhinitis,C2607914,Nasal,GEO,Microarray,Homo sapiens,3|5,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA01572,GSE118254,GPL16791,1000,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,37|44,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01573,GSE68417,GPL6244,1000,Clear Cell Renal Cell Carcinoma,C0007134,Kidney,GEO,Microarray,Homo sapiens,14|13,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA01574,GSE118259,GPL10558,1000,Venous Thromboembolism,C1861172,,GEO,Microarray,Homo sapiens,5|8,DO:A blood coagulation disease that is characterized by an increased tendency to form clots. DSA01575,GSE118313,GPL18573,69,Schizophrenia,C0036341,,GEO,RNA-Seq,Homo sapiens,12|12,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA01576,GSE118366,GPL17021,831,Acute Lymphoblastic Leukemia,C0023449,Bone marrow,GEO,RNA-Seq,Mus musculus,2|2,DO:A acute leukemia that is characterized by over production of lymphoblasts. DSA01577,GSE118366,GPL17021,1000,Acute Lymphoblastic Leukemia,C0023449,Bone marrow,GEO,RNA-Seq,Mus musculus,2|2,DO:A acute leukemia that is characterized by over production of lymphoblasts. DSA01578,GSE118476,GPL16791,1000,Myelodysplastic Syndromes,C3463824,Bone,GEO,RNA-Seq,Homo sapiens,4|5,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA01579,GSE118481,GPL10558,0,Diabetes,C0011847,,GEO,Microarray,Homo sapiens,6|6,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA01580,GSE118481,GPL10558,1,Diabetes,C0011847,,GEO,Microarray,Homo sapiens,10|2,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA01581,GSE68417,GPL6244,1000,Clear Cell Renal Cell Carcinoma,C0007134,Kidney,GEO,Microarray,Homo sapiens,14|16,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA01582,GSE118553,GPL10558,211,Alzheimer's Disease,C0002395,Cerebellum,GEO,Microarray,Homo sapiens,22|38,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01583,GSE118553,GPL10558,7,Alzheimer's Disease,C0002395,Cerebellum,GEO,Microarray,Homo sapiens,22|32,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01584,GSE118553,GPL10558,1000,Alzheimer's Disease,C0002395,Entorhinal cortex,GEO,Microarray,Homo sapiens,24|37,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01585,GSE118553,GPL10558,47,Alzheimer's Disease,C0002395,Entorhinal cortex,GEO,Microarray,Homo sapiens,24|37,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01586,GSE118553,GPL10558,611,Alzheimer's Disease,C0002395,Frontal cortex,GEO,Microarray,Homo sapiens,23|40,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01587,GSE118553,GPL10558,344,Alzheimer's Disease,C0002395,Frontal cortex,GEO,Microarray,Homo sapiens,23|33,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01588,GSE118553,GPL10558,1000,Alzheimer's Disease,C0002395,Temporal cortex,GEO,Microarray,Homo sapiens,31|52,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01589,GSE118553,GPL10558,1000,Alzheimer's Disease,C0002395,Temporal cortex,GEO,Microarray,Homo sapiens,31|32,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01590,GSE118633,GPL16791,164,Hutchinson-Gilford Progeria Syndrome,C0033300,Skin,GEO,RNA-Seq,Homo sapiens,2|3,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA01591,GSE118646,GPL21847,1,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,11|7,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA01592,GSE118719,GPL20301,1000,Nasopharyngeal Carcinoma,C2931822,Nasopharynx,GEO,RNA-Seq,Homo sapiens,4|7,"DO:A pharynx cancer that is located in the nasopharynx, the uppermost region of the pharynx or throat, where the nasal passages and auditory tubes join the remainder of the upper respiratory tract." DSA01593,GSE118829,GPL17303,8,Rheumatoid Arthritis,C0003873,Blood,GEO,RNA-Seq,Homo sapiens,10|10,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA01594,GSE118829,GPL17303,17,Rheumatoid Arthritis,C0003873,Blood,GEO,RNA-Seq,Homo sapiens,10|9,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA01595,GSE118829,GPL17303,40,Rheumatoid Arthritis,C0003873,Blood,GEO,RNA-Seq,Homo sapiens,10|10,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA01596,GSE118829,GPL17303,0,Rheumatoid Arthritis,C0003873,Blood,GEO,RNA-Seq,Homo sapiens,10|8,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA01597,GSE118829,GPL17303,400,Rheumatoid Arthritis,C0003873,Blood,GEO,RNA-Seq,Homo sapiens,10|8,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA01598,GSE118829,GPL17303,146,Rheumatoid Arthritis,C0003873,Blood,GEO,RNA-Seq,Homo sapiens,9|9,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA01599,GSE118829,GPL17303,6,Rheumatoid Arthritis,C0003873,Blood,GEO,RNA-Seq,Homo sapiens,10|10,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA01600,GSE118963,GPL11154,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,RNA-Seq,Homo sapiens,1|3,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA01601,GSE119007,GPL20301,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,RNA-Seq,Homo sapiens,3|3,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA01602,GSE119007,GPL20301,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,RNA-Seq,Homo sapiens,3|2,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA01603,GSE119027,GPL16791,1000,Limb-Girdle Muscular Dystrophy Type 2A,C1869123,Skeletal muscle,GEO,RNA-Seq,Homo sapiens,2|2,DO:An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding the proteolytic enzyme calpain-3 (CAPN3) on chromosome 15q15. DSA01604,GSE119102,GPL16791,1000,Glioblastoma,C0017636,,GEO,RNA-Seq,Homo sapiens,1|2,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA01605,GSE119103,GPL16791,1000,Chronic Lymphocytic Leukemia,C0023434,Peripheral blood,GEO,RNA-Seq,Homo sapiens,2|22,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA01606,GSE119136,GPL24532,8,Granulomatosis With Polyangiitis,C3495801,Nasal,GEO,Microarray,Homo sapiens,31|32,"DO:An autoimmune disease that is characterized by necrotizing granulomatous inflammation of the upper and lower respiratory tract, glomerulonephritis, vasculitis, and the presence of antineutrophil cytoplasmatic autoantibodies (ANCAs) in patient sera, and is located_in lung, located_in kidney, located_in skin resulting from an autoimmune attack by antineutrophil cytoplasmic antibodies against small and medium-size blood vessels." DSA01607,GSE119143,GPL17586,0,Pulmonary Tuberculosis,C0041327,Whole blood,GEO,Microarray,Homo sapiens,5|7,"DO:A tuberculosis that is a contagious disease located_in lungs. The infection has_symptom fever, has_symptom cough, has_symptom difficulty in breathing, has_symptom inflammatory infiltrations, has_symptom formation of tubercles, has_symptom caseation, has_symptom pleural effusion, and has_symptom fibrosis." DSA01608,GSE119150,GPL15207,340,Falciparum Malaria,C0024535,Blood,GEO,Microarray,Homo sapiens,6|6,"DO:A malaria described as a severe form of the disease caused by a parasite Plasmodium falciparum, which is marked by irrregular recurrence of paroxysms and prolonged or continuous fever." DSA01609,GSE119207,GPL16686,110,Discoid Lupus Erythematosus,C0024138,Hair follicle,GEO,Microarray,Homo sapiens,4|7,"DO:An autoimmune disease that is characterized by a constellation of findings that include elevated antibodies to nuclear antigens, antiphospholipids, low complement levels, ulcers, non-scarring alopecia, renal or neurologic damage, and low white blood cell and platelet counts, has_symptom rashes, fatigue, arthritis, hair loss, seizures, and symptoms related to affected organs." DSA01610,GSE119207,GPL16686,0,Discoid Lupus Erythematosus,C0024138,Hair follicle,GEO,Microarray,Homo sapiens,7|7,"DO:An autoimmune disease that is characterized by a constellation of findings that include elevated antibodies to nuclear antigens, antiphospholipids, low complement levels, ulcers, non-scarring alopecia, renal or neurologic damage, and low white blood cell and platelet counts, has_symptom rashes, fatigue, arthritis, hair loss, seizures, and symptoms related to affected organs." DSA01611,GSE119322,GPL570,0,Hepatitis B,C0019163,Blood,GEO,Microarray,Homo sapiens,7|7,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus, which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice." DSA01612,GSE119322,GPL570,0,Chronic Hepatitis,C0019189,Blood,GEO,Microarray,Homo sapiens,7|6,"EFO:An active inflammatory process affecting the liver for more than six months. Causes include viral infections, autoimmune disorders, drugs, and metabolic disorders." DSA01613,GSE223060,GPL20301,1000,Multiple Myeloma,C0026764,Bone marrow,GEO,scRNA-Seq,Homo sapiens,7|13,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA01614,GSE119340,GPL23479,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,3|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA01615,GSE119360,GPL9115,1000,Wilms Tumor; Aniridia; Genitourinary Anomalies; And Mental Retardation Syndrome,C0206115,,GEO,RNA-Seq,Homo sapiens,1|3,"DO:A chromosomal deletion syndrome that is a nephroblastoma that results_in a rare genetic syndrome in which affected children are predisposed to develop Wilms tumor, Aniridia (absence of the colored part of the eye, the iris), genitourinary anomalies, and mental retardation. The condition results from a deletion on chromosome 11 resulting in the loss of several genes. As such, it is one of the best studied examples of a condition caused by loss of neighbouring (contiguous) genes." DSA01616,GSE119441,GPL23479,1000,Liver Steatosis,C2711227,Liver,GEO,RNA-Seq,Mus musculus,4|4,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA01617,GSE119441,GPL23479,417,Liver Steatosis,C2711227,Liver,GEO,RNA-Seq,Mus musculus,4|4,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA01618,GSE119501,GPL11154,1000,Recessive Dystrophic Epidermolysis Bullosa,C0079294,Skin,GEO,RNA-Seq,Homo sapiens,3|9,DO:An epidermolysis bullosa dystrophica characterized by recurrent blistering at the level of the sublamina densa beneath the cutaneous basement membrane; it has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding type VII collagen (COL7A1) on chromosome 3p21. DSA01619,GSE119501,GPL11154,1000,Kindler Syndrome,C0406557,Skin,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A skin disease characterized by congenital blistering, skin atrophy, photosensitivity, skin fragility, and scaling." DSA01620,GSE119501,GPL11154,1000,Xeroderma Pigmentosum,C0043346,Skin,GEO,RNA-Seq,Homo sapiens,3|3,DO:A syndrome that is characterized by a deficiency in the ability to repair ultraviolet damage that has_material_basis_in autosomal recessive inheritance of DNA repair. DSA01621,GSE158951,GPL23479,0,Fibrosis; Liver,C0239946,Liver,GEO,RNA-Seq,Mus musculus,2|1,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA01622,GSE119574,GPL24557,0,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Mus musculus,4|3,DO:A respiratory system cancer that is located_in the lung. DSA01623,GSE119600,GPL10558,1000,Crohn's Disease,C0010346,Whole blood,GEO,Microarray,Homo sapiens,47|95,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA01624,GSE119600,GPL10558,1000,Primary Biliary Cholangitis,C0008312,Whole blood,GEO,Microarray,Homo sapiens,47|90,DO:A liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts. DSA01625,GSE119600,GPL10558,1000,Primary Sclerosing Cholangitis,C0566602,Whole blood,GEO,Microarray,Homo sapiens,47|45,"DO:A sclerosing cholangitis characterized by fibroobliterative inflammation of the biliary tract, leading to cirrhosis and portal hypertension." DSA01626,GSE119600,GPL10558,1000,Ulcerative Colitis,C0009324,Whole blood,GEO,Microarray,Homo sapiens,47|93,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA01627,GSE11971,GPL96,1000,Juvenile Dermatomyositis,C0263666,Skeletal muscle,GEO,Microarray,Homo sapiens,4|19,EFO:Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness. DSA01628,GSE119762,GPL17021,1000,Psoriasis-Like Disease,,Skin,GEO,RNA-Seq,Mus musculus,3|3, DSA01629,GSE119762,GPL17021,1000,Psoriasis-Like Disease,,Skin,GEO,RNA-Seq,Mus musculus,3|3, DSA01630,GSE119762,GPL17021,1000,Psoriasis-Like Disease,,Skin,GEO,RNA-Seq,Mus musculus,3|3, DSA01631,GSE119762,GPL17021,1000,Psoriasis-Like Disease,,Skin,GEO,RNA-Seq,Mus musculus,3|3, DSA01632,GSE119828,GPL16791,1000,Cornelia De Lange Syndrome,C0270972,,GEO,RNA-Seq,Homo sapiens,12|9,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA01633,GSE119828,GPL16791,1000,Cornelia De Lange Syndrome,C0270972,,GEO,RNA-Seq,Homo sapiens,12|9,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA01634,GSE119913,GPL10558,1000,Cd46 Deficiency,,,GEO,Microarray,Homo sapiens,3|3, DSA01635,GSE148381,GPL24676,1000,Esophagitis,C0014868,Esophagus,GEO,RNA-Seq,Homo sapiens,7|10,"EFO:Eosinophilic esophagitis (EoE) is a chronic, allergic disease of the esophagus characterized clinically by symptoms of esophageal dysfunction (including vomiting, dysphagia, feeding disorders, food impaction and abdominal pain) which persist after treatment with proton pump inhibitors (PPIs)." DSA01636,GSE120080,GPL21103,1000,Lung Injury,C0273115,Lung,GEO,RNA-Seq,Mus musculus,3|6,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA01637,GSE120123,GPL6480,0,Liver Cancer,C2239176,,GEO,Microarray,Homo sapiens,2|2,DO:A hepatobiliary system cancer that is located_in the liver. DSA01638,GSE120123,GPL6480,0,Liver Cancer,C2239176,,GEO,Microarray,Homo sapiens,2|2,DO:A hepatobiliary system cancer that is located_in the liver. DSA01639,GSE120123,GPL6480,0,Liver Cancer,C2239176,Blood,GEO,Microarray,Homo sapiens,2|2,DO:A hepatobiliary system cancer that is located_in the liver. DSA01640,GSE120178,GPL16791,1000,Rheumatoid Arthritis,C0003873,Whole blood,GEO,RNA-Seq,Homo sapiens,21|126,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA01641,GSE120225,GPL21290,10,Angelman Syndrome,C0162635,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A syndrome that is characterized by delayed development, intellectual disability, severe speech impairment, and problems with movement and balance." DSA01642,GSE120225,GPL21290,658,Angelman Syndrome,C0162635,,GEO,RNA-Seq,Homo sapiens,1|1,"DO:A syndrome that is characterized by delayed development, intellectual disability, severe speech impairment, and problems with movement and balance." DSA01643,GSE120242,GPL570,0,Basal Cell Nevus Syndrome,C0004779,,GEO,Microarray,Homo sapiens,8|9,"DO:A syndrome characterized by multiple early-onset basal cell carcinoma, multiple jaw keratocysts and skeletal abnormalities." DSA01644,GSE120242,GPL570,0,Basal Cell Nevus Syndrome,C0004779,,GEO,Microarray,Homo sapiens,8|9,"DO:A syndrome characterized by multiple early-onset basal cell carcinoma, multiple jaw keratocysts and skeletal abnormalities." DSA01645,GSE120242,GPL570,0,Basal Cell Nevus Syndrome,C0004779,,GEO,Microarray,Homo sapiens,8|9,"DO:A syndrome characterized by multiple early-onset basal cell carcinoma, multiple jaw keratocysts and skeletal abnormalities." DSA01646,GSE120242,GPL570,0,Basal Cell Nevus Syndrome,C0004779,,GEO,Microarray,Homo sapiens,8|9,"DO:A syndrome characterized by multiple early-onset basal cell carcinoma, multiple jaw keratocysts and skeletal abnormalities." DSA01647,GSE120242,GPL570,0,Basal Cell Nevus Syndrome,C0004779,,GEO,Microarray,Homo sapiens,8|9,"DO:A syndrome characterized by multiple early-onset basal cell carcinoma, multiple jaw keratocysts and skeletal abnormalities." DSA01648,GSE120242,GPL570,0,Basal Cell Nevus Syndrome,C0004779,,GEO,Microarray,Homo sapiens,8|9,"DO:A syndrome characterized by multiple early-onset basal cell carcinoma, multiple jaw keratocysts and skeletal abnormalities." DSA01649,GSE120259,GPL23126,18,High-Grade Serous Ovarian Cancer,,,GEO,Microarray,Homo sapiens,5|5, DSA01650,GSE120259,GPL23126,919,High-Grade Serous Ovarian Cancer,,,GEO,Microarray,Homo sapiens,5|4, DSA01651,GSE147878,GPL10558,1000,Asthma,C0004096,Bronchus,GEO,Microarray,Homo sapiens,13|42,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01652,GSE147878,GPL10558,0,Severe Asthma,C0004096,Bronchus,GEO,Microarray,Homo sapiens,18|42,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01653,GSE120299,GPL16791,1000,Type 1 Diabetes,C0011854,Pancreatic islet,GEO,RNA-Seq,Homo sapiens,5|1,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA01654,GSE120303,GPL11154,1000,Ovarian Cancer,C1140680,,GEO,RNA-Seq,Homo sapiens,3|4,DO:A female reproductive organ cancer that is located_in the ovary. DSA01655,GSE120306,GPL20301,62,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,3|4,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01656,GSE120328,GPL18573,257,Classical Hodgkin Lymphoma,C1333064,,GEO,RNA-Seq,Homo sapiens,5|5,MONDO:Classical Hodgkin lymphoma (CHL) is a B-cell lymphoma characterized histologically by the presence of large mononuclear Hodgkin cells and multinucleated Reed-Sternberg (HRS) cells. DSA01657,GSE120340,GPL16311,0,Bipolar Disorder,C0005586,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,5|7,DO:A mood disorder that involves alternating periods of mania and depression. DSA01658,GSE120340,GPL16311,0,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,5|5,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA01659,GSE120340,GPL16311,0,Bipolar Disorder,C0005586,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,5|3,DO:A mood disorder that involves alternating periods of mania and depression. DSA01660,GSE120340,GPL16311,0,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,5|5,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA01661,GSE120341,GPL8490,0,Bipolar Disorder,C0005586,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,2|3,DO:A mood disorder that involves alternating periods of mania and depression. DSA01662,GSE120341,GPL8490,0,Bipolar Disorder,C0005586,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,2|1,DO:A mood disorder that involves alternating periods of mania and depression. DSA01663,GSE120341,GPL8490,0,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,2|3,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA01664,E-MTAB-10190,,1000,Asthma,C0004096,Blood,ArrayExpress,RNA-Seq,Homo sapiens,40|40,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01665,E-MTAB-10190,,1000,Asthma,C0004096,Blood,ArrayExpress,RNA-Seq,Homo sapiens,40|40,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01666,E-MTAB-10238,,188,Ulcer of Intestine,C0151971,Colon,ArrayExpress,RNA-Seq,Mus musculus,7|7, DSA01667,E-MTAB-10238,,1000,Ulcer of Intestine,C0151971,Colon,ArrayExpress,RNA-Seq,Mus musculus,6|6, DSA01668,E-MTAB-1030,,0,Schizophrenia,C0036341,Superior temporal gyrus,ArrayExpress,RNA-Seq,Homo sapiens,9|9,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA01669,E-MTAB-10318,,1000,Granuloma Annulare,C0085074,Skin,ArrayExpress,RNA-Seq,Homo sapiens,5|4,"MONDO:Granuloma annulare is a long-term (chronic) skin disease consisting of a rash with reddish bumps arranged in a circle or ring. The most commonly affected areas are the forearms, hands and feet. The lesions associated with granuloma annulare usually resolve without treatment. Strong steroids (applied as a cream or injection) are sometimes used to clear the rash more quickly. Most symptoms will disappear within 2 years (even without treatment), but recurrence is common. The underlying cause of granuloma annulare is unknown." DSA01670,E-MTAB-10318,,655,Leprosy,C0023343,Skin,ArrayExpress,RNA-Seq,Homo sapiens,5|4,"DO:A primary bacterial infectious disease that results_in infection located_in superficial peripheral nerves, located_in skin, located_in mucous membranes of the upper respiratory tract, located_in anterior chamber of the eyes, or located_in testes, has_material_basis_in Mycobacterium leprae, which is transmitted_by aerosol spread from infected nasal secretions to exposed nasal and oral mucosa. The infection has_symptom skin lesions, has_symptom sensory loss, has_symptom motor loss and has_symptom eye damage." DSA01671,E-MTAB-10318,,1000,Leprosy,C0023343,Skin,ArrayExpress,RNA-Seq,Homo sapiens,5|6,"DO:A primary bacterial infectious disease that results_in infection located_in superficial peripheral nerves, located_in skin, located_in mucous membranes of the upper respiratory tract, located_in anterior chamber of the eyes, or located_in testes, has_material_basis_in Mycobacterium leprae, which is transmitted_by aerosol spread from infected nasal secretions to exposed nasal and oral mucosa. The infection has_symptom skin lesions, has_symptom sensory loss, has_symptom motor loss and has_symptom eye damage." DSA01672,E-MTAB-10318,,1000,Leprosy,C0023343,Skin,ArrayExpress,RNA-Seq,Homo sapiens,5|4,"DO:A primary bacterial infectious disease that results_in infection located_in superficial peripheral nerves, located_in skin, located_in mucous membranes of the upper respiratory tract, located_in anterior chamber of the eyes, or located_in testes, has_material_basis_in Mycobacterium leprae, which is transmitted_by aerosol spread from infected nasal secretions to exposed nasal and oral mucosa. The infection has_symptom skin lesions, has_symptom sensory loss, has_symptom motor loss and has_symptom eye damage." DSA01673,GSE120464,GPL13607,0,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,5|4,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA01674,E-MTAB-10318,,1000,Leprosy,C0023343,Skin,ArrayExpress,RNA-Seq,Homo sapiens,5|8,"DO:A primary bacterial infectious disease that results_in infection located_in superficial peripheral nerves, located_in skin, located_in mucous membranes of the upper respiratory tract, located_in anterior chamber of the eyes, or located_in testes, has_material_basis_in Mycobacterium leprae, which is transmitted_by aerosol spread from infected nasal secretions to exposed nasal and oral mucosa. The infection has_symptom skin lesions, has_symptom sensory loss, has_symptom motor loss and has_symptom eye damage." DSA01675,E-MTAB-10318,,1000,Leprosy,C0023343,Skin,ArrayExpress,RNA-Seq,Homo sapiens,5|3,"DO:A primary bacterial infectious disease that results_in infection located_in superficial peripheral nerves, located_in skin, located_in mucous membranes of the upper respiratory tract, located_in anterior chamber of the eyes, or located_in testes, has_material_basis_in Mycobacterium leprae, which is transmitted_by aerosol spread from infected nasal secretions to exposed nasal and oral mucosa. The infection has_symptom skin lesions, has_symptom sensory loss, has_symptom motor loss and has_symptom eye damage." DSA01676,GSE120597,GPL11154,1000,Congenital Melanocytic Nevus,C1318558,Skin,GEO,RNA-Seq,Homo sapiens,3|27,DO:A skin disease characterized by the presence at birth of a pigmented skin lesion composed of melanocytes of more than 20 cm in projected adult diameter that has_material_basis_in somatic mutation in NRAS on chromosome 11p15.5. DSA01677,GSE120597,GPL11154,930,Congenital Melanocytic Nevus,C1318558,Skin,GEO,RNA-Seq,Homo sapiens,3|9,DO:A skin disease characterized by the presence at birth of a pigmented skin lesion composed of melanocytes of more than 20 cm in projected adult diameter that has_material_basis_in somatic mutation in NRAS on chromosome 11p15.5. DSA01678,GSE120642,GPL20301,1000,Peripheral Artery Disease,C4025272,Gastrocnemius muscle,GEO,RNA-Seq,Homo sapiens,15|20,"HPO:Narrowing of peripheral arteries with reduction of blood flow to the limbs. This feature may be quantified as an ankle-brachial index of less than 0.9, and may be manifested clinically as claudication." DSA01679,GSE120642,GPL20301,1000,Peripheral Artery Disease,C4025272,Gastrocnemius muscle,GEO,RNA-Seq,Homo sapiens,15|16,"HPO:Narrowing of peripheral arteries with reduction of blood flow to the limbs. This feature may be quantified as an ankle-brachial index of less than 0.9, and may be manifested clinically as claudication." DSA01680,GSE120652,GPL6244,419,Acute Liver Failure,C0162557,Liver,GEO,Microarray,Homo sapiens,3|3,"HPO:Hepatic failure refers to the inability of the liver to perform its normal synthetic and metabolic functions, which can result in coagulopathy and alteration in the mental status of a previously healthy individual. Hepatic failure is defined as fulminant if there is onset of encephalopathy within 4 weeks of the onset of symptoms in a patient with a previously healthy liver." DSA01681,GSE120663,GPL20795,1000,Hepatocellular Carcinoma,C0334287,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|4,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA01682,GSE120683,GPL570,3,Methylmalonic Acidemia,C0268583,Kidney,GEO,Microarray,Homo sapiens,3|3,DO:An organic acidemia that involves an accumulation of methylmalonic acid in the blood. DSA01683,GSE120691,GPL16791,742,Cervical Intraepithelial Neoplasia,C0206708,Peripheral blood,GEO,RNA-Seq,Homo sapiens,19|21,DO:An uterus carcinoma in situ that is located_in the uterine cervix. DSA01684,GSE120691,GPL16791,282,Cervical Cancer,C4048328,Peripheral blood,GEO,RNA-Seq,Homo sapiens,19|11,DO:A female reproductive organ cancer that is located_in the cervix. DSA01685,GSE120721,GPL570,1000,Atopic Dermatitis,C0011615,Dermis,GEO,Microarray,Homo sapiens,6|5,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA01686,GSE120721,GPL570,1000,Atopic Dermatitis,C0011615,Dermis,GEO,Microarray,Homo sapiens,6|5,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA01687,GSE120721,GPL570,1000,Atopic Dermatitis,C0011615,Epidermis,GEO,Microarray,Homo sapiens,10|5,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA01688,GSE120721,GPL570,1000,Atopic Dermatitis,C0011615,Epidermis,GEO,Microarray,Homo sapiens,10|5,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA01689,GSE120721,GPL570,1000,Atopic Dermatitis,C0011615,,GEO,Microarray,Homo sapiens,6|5,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA01690,GSE120721,GPL570,1000,Atopic Dermatitis,C0011615,,GEO,Microarray,Homo sapiens,6|5,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA01691,GSE120746,GPL18573,1000,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,9|9,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01692,GSE120748,GPL19057,1000,Obesity,C0028754,Epididymal white adipose tissue,GEO,RNA-Seq,Mus musculus,4|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA01693,GSE120774,GPL6244,39,Coronary Disease,C1956346,Subcutaneous fat,GEO,Microarray,Homo sapiens,9|8,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA01694,GSE120774,GPL6244,0,Coronary Disease,C1956346,,GEO,Microarray,Homo sapiens,10|9,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA01695,GSE120836,GPL20301,1000,Dilated Cardiomyopathy,C0007193,Heart,GEO,RNA-Seq,Homo sapiens,5|5,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA01696,GSE120852,GPL16791,1000,Heart Failure,C0018801,Right ventricle,GEO,RNA-Seq,Homo sapiens,5|5,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA01697,GSE120852,GPL16791,1000,Heart Failure,C0018801,Right ventricle,GEO,RNA-Seq,Homo sapiens,5|5,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA01698,GSE120852,GPL16791,748,Heart Failure,C0018801,Left ventricle,GEO,RNA-Seq,Homo sapiens,5|5,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA01699,GSE120852,GPL16791,1000,Heart Failure,C0018801,Left ventricle,GEO,RNA-Seq,Homo sapiens,5|5,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA01700,GSE120895,GPL570,1000,Heart Failure;Human Dilated Cardiomyopathy,,Heart,GEO,Microarray,Homo sapiens,8|47, DSA01701,GSE121178,GPL22120,0,Hypoxic-Ischemic Encephalopathy,C0752304,Peripheral blood,GEO,Microarray,Homo sapiens,3|3,"MONDO:A disorder caused by a lack of blood flow or gas exchange to or from the fetus in the period immediately before, during, or after the birth process." DSA01702,GSE121211,GPL17586,863,Focal Segmental Glomerulosclerosis,C0017668,Kidney tubules,GEO,Microarray,Homo sapiens,5|5,"EFO:A renal disorder characterized by sclerotic lesions in the glomeruli. Causes include drugs, viruses, and malignancies (lymphomas), or it may be idiopathic. It presents with asymptomatic proteinuria or nephritic syndrome and it may lead to renal failure." DSA01703,GSE121212,GPL16791,1000,Atopic Dermatitis,C0011615,Skin,GEO,RNA-Seq,Homo sapiens,38|53,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA01704,GSE121212,GPL16791,1000,Psoriasis,C0033860,Skin,GEO,RNA-Seq,Homo sapiens,38|55,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA01705,GSE121233,GPL17586,1000,Focal Segmental Glomerulosclerosis,C0017668,Glomerulus,GEO,Microarray,Homo sapiens,5|5,"EFO:A renal disorder characterized by sclerotic lesions in the glomeruli. Causes include drugs, viruses, and malignancies (lymphomas), or it may be idiopathic. It presents with asymptomatic proteinuria or nephritic syndrome and it may lead to renal failure." DSA01706,E-MTAB-10318,,1000,Leprosy,C0023343,Skin,ArrayExpress,RNA-Seq,Homo sapiens,5|6,"DO:A primary bacterial infectious disease that results_in infection located_in superficial peripheral nerves, located_in skin, located_in mucous membranes of the upper respiratory tract, located_in anterior chamber of the eyes, or located_in testes, has_material_basis_in Mycobacterium leprae, which is transmitted_by aerosol spread from infected nasal secretions to exposed nasal and oral mucosa. The infection has_symptom skin lesions, has_symptom sensory loss, has_symptom motor loss and has_symptom eye damage." DSA01707,E-MTAB-10321,,1000,Epithelioid Trophoblastic Tumor,C1266159,Uterus,ArrayExpress,RNA-Seq,Homo sapiens,3|3,MONDO:An epithelioid trophoblastic tumor is an extremely rare gestational trophoblastic tumor (GTT) which generally occurs several years after pregnancy. DSA01708,GSE121376,GPL21697,2,Schizophrenia,C0036341,Cortex,GEO,RNA-Seq,Homo sapiens,27|28,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA01709,GSE121444,GPL16791,3,Alzheimer's Disease,C0002395,Endothelium,GEO,RNA-Seq,Homo sapiens,2|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01710,E-MTAB-10321,,617,Placental Site Trophoblastic Tumor,C0206666,Uterus,ArrayExpress,RNA-Seq,Homo sapiens,3|2,DO:A choriocarcinoma that is characterized by low beta-hCG levels and arises from neoplastic transformation of intermediate trophoblastic cells. DSA01711,E-MTAB-10322,,72,Duchenne Muscular Dystrophy,C0013264,Gastrocnemius,ArrayExpress,RNA-Seq,Mus musculus,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA01712,GSE121487,GPL7202,20,Diabetes,C0011847,Aorta,GEO,Microarray,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA01713,GSE121487,GPL7202,40,Macroangiopathy,,Aorta,GEO,Microarray,Mus musculus,3|3, DSA01714,GSE121487,GPL7202,174,Diabetes,C0011847,Muscle,GEO,Microarray,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA01715,GSE121487,GPL7202,191,Macroangiopathy,,Muscle,GEO,Microarray,Mus musculus,3|3, DSA01716,E-MTAB-10322,,301,Duchenne Muscular Dystrophy,C0013264,Gastrocnemius,ArrayExpress,RNA-Seq,Mus musculus,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA01717,GSE121559,GPL20301,1000,Cardiomyopathy,C0878544,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA01718,GSE121620,GPL16686,0,Hemochromatosis,C0018995,Peripheral blood,GEO,Microarray,Homo sapiens,6|18,DO:A metal metabolism disorder characterized by the accumulation of iron in various organs of the body. DSA01719,GSE121636,GPL20301,1000,Renal Tumor,C0022665,Kidney,GEO,scRNA-Seq,Homo sapiens,3|3,DO:A urinary system cancer that is located_in the kidney. DSA01720,E-MTAB-10567,,1000,Trichothiodystrophy,C1955934,Skin,ArrayExpress,RNA-Seq,Homo sapiens,6|6,DO:A trichothiodystrophy characterized by skin that is extremely sensitive to ultraviolet (UV) rays from sunlight. DSA01721,GSE121699,GPL20301,1000,Congenital Heart Block,C0149530,Heart,GEO,RNA-Seq,Homo sapiens,1|1,"DO:An atrioventricular block characterized by the presence of conduction system disease of any form, which is diagnosed on or before 28 days of life." DSA01722,GSE121712,GPL20844,0,Androgen Insensitivity Syndrome,C0039585,Skin,GEO,Microarray,Homo sapiens,4|1,"DO:A disorder of sexual developement that is characterized by the inability of the cell to respond to androgens in individuals with a karyotype of 46,XY resulting in female physical traits but male genetic makeup." DSA01723,GSE121712,GPL20844,0,Androgen Insensitivity Syndrome,C0039585,Skin,GEO,Microarray,Homo sapiens,4|1,"DO:A disorder of sexual developement that is characterized by the inability of the cell to respond to androgens in individuals with a karyotype of 46,XY resulting in female physical traits but male genetic makeup." DSA01724,E-MTAB-10604,,678,Down Syndrome,C0013080,,ArrayExpress,RNA-Seq,Homo sapiens,23|17,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA01725,GSE121894,GPL25734,1000,Rheumatoid Arthritis,C0003873,Peripheral blood,GEO,Microarray,Homo sapiens,11|18,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA01726,GSE121894,GPL25734,187,Rheumatoid Arthritis,C0003873,Peripheral blood,GEO,Microarray,Homo sapiens,11|18,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA01727,GSE121946,GPL1261,0,Breast Cancer,C0678222,Lung,GEO,Microarray,Mus musculus,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA01728,GSE121946,GPL1261,137,Breast Cancer,C0678222,Lung,GEO,Microarray,Mus musculus,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA01729,GSE121946,GPL1261,1000,Breast Cancer,C0678222,Lung,GEO,Microarray,Mus musculus,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA01730,GSE121946,GPL1261,1000,Breast Cancer,C0678222,Lung,GEO,Microarray,Mus musculus,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA01731,GSE122261,GPL5175,1000,Amyotrophic Lateral Sclerosis,C0002736,Skeletal muscle,GEO,Microarray,Homo sapiens,6|6,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA01732,GSE122438,GPL15520,0,Alzheimer's Disease,C0002395,Blood,GEO,RNA-Seq,Homo sapiens,6|11,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01733,E-MTAB-10703,,1000,Acquired Immunodeficiency Syndrome,C0001175,Blood plasma,ArrayExpress,RNA-Seq,Homo sapiens,9|33,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA01734,GSE122438,GPL15520,6,Alzheimer's Disease,C0002395,Blood,GEO,RNA-Seq,Homo sapiens,2|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01735,GSE122438,GPL15520,25,Alzheimer's Disease,C0002395,Blood,GEO,RNA-Seq,Homo sapiens,1|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01736,E-MTAB-10703,,1000,Hepatitis C,C0019196,Blood plasma,ArrayExpress,RNA-Seq,Homo sapiens,59|33,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA01737,E-MTAB-10916,,502,Amyotrophic Lateral Sclerosis,C0002736,Central nervous system,ArrayExpress,RNA-Seq,Homo sapiens,6|2,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA01738,GSE122438,GPL15520,19,Alzheimer's Disease,C0002395,Blood,GEO,RNA-Seq,Homo sapiens,1|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01739,E-MTAB-10916,,1000,Amyotrophic Lateral Sclerosis,C0002736,Central nervous system,ArrayExpress,RNA-Seq,Homo sapiens,6|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA01740,GSE122459,GPL16791|GPL18573,1000,Systemic Lupus Erythematosus,C0024141,Blood,GEO,RNA-Seq,Homo sapiens,6|20,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01741,GSE122476,GPL17586,1000,Langerhans Cell Histiocytosis,C0019621,Bone,GEO,Microarray,Homo sapiens,18|39,DO:A histiocytosis that is characterized by clonal proliferation of Langerhans cells. DSA01742,GSE122552,GPL23934,9,Systemic Juvenile Idiopathic Arthritis,C1384600,,GEO,RNA-Seq,Homo sapiens,5|4,"EFO:Juvenile idiopathic arthritis (JIA), also known as juvenile rheumatoid arthritis (JRA), is the most common form of arthritis in children and adolescents. (Juvenile in this context refers to an onset before age 16, idiopathic refers to a condition with no defined cause, and arthritis is the inflammation of the synovium of a joint.) JIA is an autoimmune, non-infective, inflammatory joint disease of more than 6 weeks duration in children less than 16 years of age. The disease commonly occurs in children from the ages of 7 to 12, but it may occur in adolescents as old as 15 years of age, as well as in infants. It is a subset of arthritis seen in childhood, which may be transient and self-limited or chronic. It differs significantly from arthritis commonly seen in adults (osteoarthritis, rheumatoid arthritis), and other types of arthritis that can present in childhood which are chronic conditions (e.g. psoriatic arthritis and ankylosing spondylitis). Aetiopathology is similar to rheumatoid arthritis but with less marked cartilage erosion, and joint instability and absent rheumatoid factor. JIA affects approximately 1 in 1,000 children in any given year, with about 1 in 10,000 having a more severe form." DSA01743,GSE122552,GPL23934,2,Systemic Juvenile Idiopathic Arthritis,C1384600,,GEO,RNA-Seq,Homo sapiens,5|5,"EFO:Juvenile idiopathic arthritis (JIA), also known as juvenile rheumatoid arthritis (JRA), is the most common form of arthritis in children and adolescents. (Juvenile in this context refers to an onset before age 16, idiopathic refers to a condition with no defined cause, and arthritis is the inflammation of the synovium of a joint.) JIA is an autoimmune, non-infective, inflammatory joint disease of more than 6 weeks duration in children less than 16 years of age. The disease commonly occurs in children from the ages of 7 to 12, but it may occur in adolescents as old as 15 years of age, as well as in infants. It is a subset of arthritis seen in childhood, which may be transient and self-limited or chronic. It differs significantly from arthritis commonly seen in adults (osteoarthritis, rheumatoid arthritis), and other types of arthritis that can present in childhood which are chronic conditions (e.g. psoriatic arthritis and ankylosing spondylitis). Aetiopathology is similar to rheumatoid arthritis but with less marked cartilage erosion, and joint instability and absent rheumatoid factor. JIA affects approximately 1 in 1,000 children in any given year, with about 1 in 10,000 having a more severe form." DSA01744,GSE122592,GPL20301,1000,Acne Inversa,C0162836,Skin,GEO,RNA-Seq,Homo sapiens,4|3,"DO:A hidradenitis that is characterized by chronic inflammation of the apocrine sweat glands, has_symptom painful nodules, abscesses, sinus tract formation, scarring, erythema, pruritis, and pain, and has_material_basis_in chronic inflammation of the apocrine sweat glands leading to recurrent folliculitis and an accompanying immune response that worsens inflammation." DSA01745,GSE122649,GPL18573,720,Amyotrophic Lateral Sclerosis,C0002736,Motor cortex,GEO,RNA-Seq,Homo sapiens,12|26,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA01746,GSE122709,GPL20795,1000,Ischemic Stroke,C0948008,Blood,GEO,RNA-Seq,Homo sapiens,5|5,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA01747,GSE122709,GPL20795,1000,Ischemic Stroke,C0948008,Blood,GEO,RNA-Seq,Homo sapiens,5|5,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA01748,GSE122873,GPL18573,1000,Facioscapulohumeral Muscular Dystrophy,C0238288,Muscle,GEO,scRNA-Seq,Homo sapiens,2|2,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA01749,GSE122873,GPL18573,1000,Facioscapulohumeral Muscular Dystrophy,C0238288,Muscle,GEO,scRNA-Seq,Homo sapiens,2|2,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA01750,GSE122903,GPL20301,912,Constrictive Pericarditis,C0031048,Pericardium,GEO,RNA-Seq,Homo sapiens,3|3,"HPO:Presence of a thickened, fibrotic pericardium that forms a non-compliant shell around the heart, and resulting from chronic inflammation of the pericardium." DSA01751,GSE122917,GPL15207,0,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA01752,GSE122917,GPL15207,0,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA01753,GSE122952,GPL19057,1000,S. Pneumoniae Infected,,Breast,GEO,RNA-Seq,Mus musculus,4|4, DSA01754,E-MTAB-10916,,637,Amyotrophic Lateral Sclerosis,C0002736,Central nervous system,ArrayExpress,RNA-Seq,Homo sapiens,6|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA01755,GSE123086,GPL25864,1000,Asthma,C0004096,,GEO,Microarray,Homo sapiens,39|11,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01756,GSE123086,GPL25864,1000,Atherosclerosis,C0004153,,GEO,Microarray,Homo sapiens,39|10,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA01757,GSE123086,GPL25864,1000,Breast Cancer,C0678222,,GEO,Microarray,Homo sapiens,39|8,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA01758,GSE123086,GPL25864,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,39|8,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA01759,GSE123086,GPL25864,1000,Crohn's Disease,C0010346,,GEO,Microarray,Homo sapiens,39|11,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA01760,GSE123086,GPL25864,57,Atopic Eczema,C0013595,,GEO,Microarray,Homo sapiens,39|7,"DO:A skin disease characterized by itchy, erythematous, vesicular, weeping and crusting patches of skin." DSA01761,GSE123086,GPL25864,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,39|10,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA01762,GSE123086,GPL25864,3,Obesity,C0028754,,GEO,Microarray,Homo sapiens,39|15,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA01763,GSE123086,GPL25864,416,Psoriasis,C0033860,,GEO,Microarray,Homo sapiens,39|11,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA01764,GSE123086,GPL25864,141,Seasonal Allergic Rhinitis,C0018621,,GEO,Microarray,Homo sapiens,39|12,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA01765,GSE123086,GPL25864,19,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,39|8,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA01766,GSE123086,GPL25864,1000,Acute Tonsillitis,C0001361,,GEO,Microarray,Homo sapiens,39|6,"MONDO:An acute inflammation of the tonsils caused by viruses or bacteria. Signs and symptoms include fever, enlargement of the tonsils, difficulty swallowing, and enlargement of the regional lymph nodes." DSA01767,GSE123086,GPL25864,1000,Ulcerative Colitis,C0009324,,GEO,Microarray,Homo sapiens,39|10,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA01768,GSE123087,GPL25864,0,Breast Cancer,C0678222,,GEO,Microarray,Homo sapiens,14|24,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA01769,GSE123141,GPL16791,512,Crohn's Disease,C0010346,Intestine,GEO,RNA-Seq,Homo sapiens,9|9,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA01770,GSE123141,GPL16791,986,Ulcerative Colitis,C0009324,Intestine,GEO,RNA-Seq,Homo sapiens,9|10,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA01771,GSE123302,GPL16686,0,Autism Spectrum Disorder,C1510586,Umbilical cord blood,GEO,Microarray,Homo sapiens,91|53,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA01772,GSE123496,GPL21290,1000,Multiple Sclerosis,C0026769,Corpus callosum,GEO,RNA-Seq,Homo sapiens,5|5,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA01773,GSE123496,GPL21290,15,Multiple Sclerosis,C0026769,Frontal cortex,GEO,RNA-Seq,Homo sapiens,5|5,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA01774,GSE123496,GPL21290,74,Multiple Sclerosis,C0026769,Hippocampus,GEO,RNA-Seq,Homo sapiens,5|5,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA01775,GSE123496,GPL21290,90,Multiple Sclerosis,C0026769,Internal capsule,GEO,RNA-Seq,Homo sapiens,5|5,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA01776,GSE123496,GPL21290,10,Multiple Sclerosis,C0026769,Parietal cortex,GEO,RNA-Seq,Homo sapiens,5|5,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA01777,GSE123564,GPL18573,1000,HBS1L Mutation,,Skin,GEO,RNA-Seq,Homo sapiens,6|6, DSA01778,GSE123568,GPL15207,1000,Steroid-Induced Osteonecrosis of The Femoral Head,,,GEO,Microarray,Homo sapiens,10|30, DSA01779,GSE123658,GPL18573|GPL20301,400,Type 1 Diabetes,C0011854,Whole blood,GEO,RNA-Seq,Homo sapiens,14|32,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA01780,GSE123661,GPL17303,1000,Cirrhosis,C1623038,Liver,GEO,RNA-Seq,Homo sapiens,5|4,"MSH:Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury." DSA01781,GSE123661,GPL17303,194,Cirrhosis,C1623038,,GEO,RNA-Seq,Homo sapiens,5|4,"MSH:Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury." DSA01782,E-MTAB-10926,,1000,Severe COVID-19,D8888888,Blood,ArrayExpress,RNA-Seq,Homo sapiens,19|4,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA01783,E-MTAB-11029,,41,Parkinson's Disease,C0030567,Blood,ArrayExpress,RNA-Seq,Homo sapiens,4|5,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01784,GSE123729,GPL21970,1000,Septic Shock,C0036983,,GEO,Microarray,Homo sapiens,11|15,"DO:A commensal bacterial infectious disease that results_in infection, has_material_basis_in Streptococcus pyogenes or has_material_basis_in Staphylococcus aureus , which produce toxins that are absorbed systemically and produce the systemic manifestations. The infection has_symptom fever, has_symptom rash, has_symptom hypotension, has_symptom multiorgan failure, has_symptom desquamation, has_symptom vomiting, has_symptom diarrhea, has_symptom headache, and has_symptom nonfocal neurologic abnormalities." DSA01785,GSE123729,GPL21970,1000,Systemic Inflammatory Response Syndrome,C0242966,,GEO,Microarray,Homo sapiens,11|16,"MSH:A systemic inflammatory response to a variety of clinical insults, characterized by two or more of the following conditions: (1) fever >38 degrees C or HYPOTHERMIA <36 degrees C; (2) TACHYCARDIA >90 beat/minute; (3) tachypnea >24 breaths/minute; (4) LEUKOCYTOSIS >12,000 cells/cubic mm or 10% immature forms. While usually related to infection, SIRS can also be associated with noninfectious insults such as TRAUMA; BURNS; or PANCREATITIS. If infection is involved, a patient with SIRS is said to have SEPSIS." DSA01786,GSE123730,GPL21970,192,Septic Shock,C0036983,,GEO,Microarray,Homo sapiens,19|10,"DO:A commensal bacterial infectious disease that results_in infection, has_material_basis_in Streptococcus pyogenes or has_material_basis_in Staphylococcus aureus , which produce toxins that are absorbed systemically and produce the systemic manifestations. The infection has_symptom fever, has_symptom rash, has_symptom hypotension, has_symptom multiorgan failure, has_symptom desquamation, has_symptom vomiting, has_symptom diarrhea, has_symptom headache, and has_symptom nonfocal neurologic abnormalities." DSA01787,GSE123730,GPL21970,33,Systemic Inflammatory Response Syndrome,C0242966,,GEO,Microarray,Homo sapiens,19|16,"MSH:A systemic inflammatory response to a variety of clinical insults, characterized by two or more of the following conditions: (1) fever >38 degrees C or HYPOTHERMIA <36 degrees C; (2) TACHYCARDIA >90 beat/minute; (3) tachypnea >24 breaths/minute; (4) LEUKOCYTOSIS >12,000 cells/cubic mm or 10% immature forms. While usually related to infection, SIRS can also be associated with noninfectious insults such as TRAUMA; BURNS; or PANCREATITIS. If infection is involved, a patient with SIRS is said to have SEPSIS." DSA01788,GSE123732,GPL10558,1,Primary Myelofibrosis,C0001815,Bone marrow,GEO,Microarray,Homo sapiens,3|3,DO:A myeloid neoplasm that is located in the bone marrow which results in bone marrow being replaced by fibrous (scar) tissue. DSA01789,GSE123732,GPL10558,8,Essential Thrombocythemia,C0040028,Bone marrow,GEO,Microarray,Homo sapiens,3|5,"DO:A myeloproliferative neoplasm that is characterized by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocytes in the bone marrow, and episodes of thrombosis and/or hemorrhage and that results_in the overproduction of platelets." DSA01790,GSE12374,GPL1291,34,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,6|11,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01791,GSE123785,GPL18573,271,Generalized Pustular Psoriasis,C0343055,,GEO,RNA-Seq,Homo sapiens,11|8,"DO:A psoriasis characterized by sudden, repeated episodes of high-grade fever, generalized rash, and disseminated pustules, with hyperleukocytosis and elevated serum levels of C-reactive protein that has_material_basis_in homozygous or compound heterozygous mutation in the IL36RN gene on chromosome 2q14." DSA01792,GSE123786,GPL11154,24,Generalized Pustular Psoriasis,C0343055,Whole blood,GEO,RNA-Seq,Homo sapiens,7|9,"DO:A psoriasis characterized by sudden, repeated episodes of high-grade fever, generalized rash, and disseminated pustules, with hyperleukocytosis and elevated serum levels of C-reactive protein that has_material_basis_in homozygous or compound heterozygous mutation in the IL36RN gene on chromosome 2q14." DSA01793,GSE123932,GPL20115,3,Liver Cirrhosis,C0023890,Whole blood,GEO,Microarray,Homo sapiens,6|6,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA01794,GSE123968,GPL20301,375,Cerebral Cavernous Malformation,C2919945,,GEO,RNA-Seq,Homo sapiens,3|5,DO:A cerebral cavernous malformation that has_material_basis_in heterozygous mutation in the KRIT1 gene on chromosome 7q21. DSA01795,GSE123972,GPL20795,1000,Hepatocellular Carcinoma,C0334287,Plasma,GEO,RNA-Seq,Homo sapiens,10|30,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA01796,GSE123972,GPL20795,9,Hepatitis B,C0019163,Plasma,GEO,RNA-Seq,Homo sapiens,10|3,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus, which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice." DSA01797,GSE123972,GPL20795,150,Hepatocellular Carcinoma,C0334287,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA01798,E-MTAB-11147,,0,Epilepsy,C0014544,Cortex,ArrayExpress,RNA-Seq,Mus musculus,3|3,"DO:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions." DSA01799,GSE124030,GPL16791,444,Breast Cancer,C0678222,,GEO,RNA-Seq,Homo sapiens,1|5,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA01800,GSE124073,GPL11154,3,Systemic Sclerosis [Scleroderma],C2364016,Peripheral blood,GEO,RNA-Seq,Homo sapiens,9|9, DSA01801,GSE124073,GPL11154,64,Systemic Sclerosis [Scleroderma],C2364016,Peripheral blood,GEO,RNA-Seq,Homo sapiens,9|11, DSA01802,GSE124073,GPL11154,251,Systemic Sclerosis [Scleroderma],C2364016,Peripheral blood,GEO,RNA-Seq,Homo sapiens,9|10, DSA01803,GSE124073,GPL11154,1000,Systemic Sclerosis [Scleroderma],C2364016,Peripheral blood,GEO,RNA-Seq,Homo sapiens,9|7, DSA01804,GSE124073,GPL11154,718,Systemic Sclerosis [Scleroderma],C2364016,Peripheral blood,GEO,RNA-Seq,Homo sapiens,9|11, DSA01805,GSE124073,GPL11154,147,Systemic Sclerosis [Scleroderma],C2364016,Peripheral blood,GEO,RNA-Seq,Homo sapiens,9|7, DSA01806,GSE124226,GPL570,0,Polycystic Ovary Syndrome,C0032460,Subcutaneous adipose tissue,GEO,Microarray,Homo sapiens,4|4,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA01807,GSE124272,GPL21185,0,Intervertebral Disc Degeneration,C0158266,Peripheral blood,GEO,Microarray,Homo sapiens,8|8,DO:A bone deterioration disease that has_material_basis_in gradual dehydration and tears located_in intervertebral disc. DSA01808,GSE124281,GPL10558,1000,Primary Myelofibrosis,C0001815,Bone marrow,GEO,Microarray,Homo sapiens,8|9,DO:A myeloid neoplasm that is located in the bone marrow which results in bone marrow being replaced by fibrous (scar) tissue. DSA01809,GSE124281,GPL10558,1000,Essential Thrombocythemia,C0040028,Bone marrow,GEO,Microarray,Homo sapiens,8|5,"DO:A myeloproliferative neoplasm that is characterized by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocytes in the bone marrow, and episodes of thrombosis and/or hemorrhage and that results_in the overproduction of platelets." DSA01810,GSE124283,GPL10904,619,Gaucher Disease,C0017205,Skin,GEO,Microarray,Homo sapiens,65|6,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA01811,GSE124283,GPL10904,1000,Niemann-Pick Disease,C0028064,Skin,GEO,Microarray,Homo sapiens,65|72,DO:A sphingoliidosis characterized by the accumulation of the lipid sphingomyelin in lysosomes in cells. DSA01812,GSE124308,GPL11154,59,Autism Spectrum Disorder,C1510586,,GEO,RNA-Seq,Homo sapiens,6|8,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA01813,GSE124310,GPL16791,1000,Multiple Myeloma,C0026764,Bone marrow,GEO,scRNA-Seq,Homo sapiens,9|5,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA01814,GSE124310,GPL16791,1000,Multiple Myeloma,C0026764,Bone marrow,GEO,scRNA-Seq,Homo sapiens,9|7,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA01815,GSE124310,GPL16791,1000,Multiple Myeloma,C0026764,Bone marrow,GEO,scRNA-Seq,Homo sapiens,9|8,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA01816,GSE124310,GPL16791,1000,Multiple Myeloma,C0026764,Bone marrow,GEO,scRNA-Seq,Homo sapiens,9|3,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA01817,GSE124326,GPL16791,1000,Bipolar Disorder,C0005586,Peripheral blood,GEO,RNA-Seq,Homo sapiens,240|225,DO:A mood disorder that involves alternating periods of mania and depression. DSA01818,GSE124326,GPL16791,255,Bipolar Disorder,C0005586,Peripheral blood,GEO,RNA-Seq,Homo sapiens,240|14,DO:A mood disorder that involves alternating periods of mania and depression. DSA01819,GSE124335,GPL21290,1000,Multiple Sclerosis,C0026769,Lobe,GEO,RNA-Seq,Homo sapiens,16|16,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA01820,GSE124389,GPL20301,2,Acne,C0702166,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|11,"DO:A sebaceous gland disease characterized by areas of blackheads, whiteheads, pimples, greasy skin, and possibly scarring." DSA01821,GSE124439,GPL16791,834,Amyotrophic Lateral Sclerosis,C0002736,Frontal cortex,GEO,RNA-Seq,Homo sapiens,9|64,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA01822,GSE124439,GPL16791,51,Amyotrophic Lateral Sclerosis,C0002736,Motor cortex,GEO,RNA-Seq,Homo sapiens,8|80,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA01823,GSE124465,GPL10558,1000,Hutchinson-Gilford Progeria Syndrome,C0033300,,GEO,Microarray,Homo sapiens,9|9,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA01824,E-MTAB-11147,,1,Epilepsy,C0014544,Cortex,ArrayExpress,RNA-Seq,Mus musculus,3|3,"DO:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions." DSA01825,E-MTAB-11147,,0,Epilepsy,C0014544,Hippocampus,ArrayExpress,RNA-Seq,Mus musculus,3|3,"DO:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions." DSA01826,GSE124548,GPL20301,1000,Cystic Fibrosis,C0010674,Whole blood,GEO,RNA-Seq,Homo sapiens,20|40,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA01827,GSE124571,GPL14951,1000,Sporadic Creutzfeldt-Jakob Disease,C1852467,Frontal cortex,GEO,Microarray,Homo sapiens,10|11,"MONDO:Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease characterized by typical CJD features (rapidly progressive dementia, personality/behavioral changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia." DSA01828,GSE124664,GPL11154,217,Huntington's Disease,C0020179,,GEO,RNA-Seq,Homo sapiens,3|6,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01829,E-MTAB-11147,,1,Epilepsy,C0014544,Hippocampus,ArrayExpress,RNA-Seq,Mus musculus,3|3,"DO:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions." DSA01830,GSE124685,GPL17303,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,RNA-Seq,Homo sapiens,35|48,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA01831,GSE124688,GPL6887,0,Tuberculosis,C0041296,Whole blood,GEO,Microarray,Mus musculus,1|4,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA01832,GSE124688,GPL6887,0,Tuberculosis,C0041296,Whole blood,GEO,Microarray,Mus musculus,1|4,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA01833,GSE124688,GPL6887,1,Tuberculosis,C0041296,Whole blood,GEO,Microarray,Mus musculus,1|4,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA01834,GSE124688,GPL6887,1,Tuberculosis,C0041296,Whole blood,GEO,Microarray,Mus musculus,1|4,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA01835,GSE124688,GPL6887,0,Tuberculosis,C0041296,Whole blood,GEO,Microarray,Mus musculus,2|4,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA01836,GSE124700,GPL10558,532,Atopic Dermatitis,C0011615,Skin,GEO,Microarray,Homo sapiens,2|2,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA01837,E-MTAB-11222,,8,Cognitive Impairment,C0338656,Blood serum,ArrayExpress,RNA-Seq,Homo sapiens,3|3,"HPO:Abnormal cognition with deficits in thinking, reasoning, or remembering." DSA01838,GSE124766,GPL6480,1000,High-Grade Serous Ovarian Cancer,,Organoid,GEO,Microarray,Homo sapiens,5|12, DSA01839,E-MTAB-11222,,33,Alzheimer's Disease,C0002395,Blood serum,ArrayExpress,RNA-Seq,Homo sapiens,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01840,GSE124939,GPL20301,43,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,4|3,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01841,GSE124939,GPL20301,1000,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,2|3,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01842,GSE124939,GPL20301,38,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,4|3,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01843,GSE124939,GPL20301,55,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,4|5,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01844,GSE124939,GPL20301,34,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01845,GSE124939,GPL20301,20,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01846,GSE124939,GPL20301,1000,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,2|3,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01847,GSE125020,GPL20301,0,Autism,C1510586,,GEO,RNA-Seq,Homo sapiens,7|8,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA01848,GSE125022,GPL18573,1000,Keloid,C0022548,,GEO,RNA-Seq,Homo sapiens,2|2,"EFO:An irregularly shaped, elevated mark on the skin caused by deposits of excessive amounts of collagen during wound healing. It extends beyond the original boundaries of the wound and may enlarge progressively." DSA01849,GSE125045,GPL16570,137,Obesity,C0028754,Liver,GEO,Microarray,Mus musculus,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA01850,GSE125050,GPL16791,0,Alzheimer's Disease,C0002395,,GEO,RNA-Seq,Homo sapiens,12|7,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01851,GSE125050,GPL16791,58,Alzheimer's Disease,C0002395,Endothelium,GEO,RNA-Seq,Homo sapiens,17|10,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01852,GSE125050,GPL16791,50,Alzheimer's Disease,C0002395,Myeloid,GEO,RNA-Seq,Homo sapiens,15|10,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01853,GSE125050,GPL16791,9,Alzheimer's Disease,C0002395,,GEO,RNA-Seq,Homo sapiens,21|21,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA01854,GSE125158,GPL6480,1000,Pancreatic Cancer,C0235974,Peripheral blood,GEO,Microarray,Homo sapiens,13|17,DO:An endocrine gland cancer located_in the pancreas. DSA01855,GSE125222,GPL20301,1000,Complete Androgen Insensitivity Syndrome,C0039585,Testis,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A disorder of sexual developement that is characterized by the inability of the cell to respond to androgens in individuals with a karyotype of 46,XY resulting in female physical traits but male genetic makeup." DSA01856,GSE125239,GPL18573,4,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,4|6,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01857,GSE125239,GPL18573,398,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,4|7,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01858,GSE16728,GPL570,99,Sickle Cell Disease,C0002895,Peripheral blood,GEO,Microarray,Homo sapiens,5|5,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA01859,GSE16728,GPL570,224,Sickle Cell Disease,C0002895,Peripheral blood,GEO,Microarray,Homo sapiens,5|5,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA01860,GSE16728,GPL570,0,Sickle Cell Disease,C0002895,Peripheral blood,GEO,Microarray,Homo sapiens,5|5,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA01861,GSE16969,GPL570,0,Tuberous Sclerosis Complex,C0041341,Brain,GEO,Microarray,Homo sapiens,4|2,DO:A tuberous sclerosis that is characterized by hamartomas in multiple organ systems and has_material_basis_in heterozygous mutation in the TSC1 gene on chromosome 9q34. DSA01862,GSE16969,GPL570,1000,Tuberous Sclerosis Complex,C0041341,Brain,GEO,Microarray,Homo sapiens,4|4,DO:A tuberous sclerosis that is characterized by hamartomas in multiple organ systems and has_material_basis_in heterozygous mutation in the TSC1 gene on chromosome 9q34. DSA01863,GSE19525,GPL6481,1000,Schistosomiasis,C0036323,Spleen,GEO,Microarray,Mus musculus,2|6,"DO:A schistosomiasis that involves parasitic infection of the intestine caused by Schistosoma mansoni, Schistosoma intercalatum or Schistosomiasis japonicum. The symptoms include fever, cough, abdominal pain, diarrhea, hepatosplenomegaly, colonic polyposis with bloody diarrhea and eosinophilia." DSA01864,GSE19587,GPL571,0,Parkinson's Disease,C0030567,Brain,GEO,Microarray,Homo sapiens,5|6,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01865,GSE19587,GPL571,0,Parkinson's Disease,C0030567,Brain,GEO,Microarray,Homo sapiens,5|6,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01866,GSE20307,GPL570,723,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,36|16,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA01867,GSE20307,GPL570,0,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,20|24,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA01868,GSE20307,GPL570,170,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,36|28,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA01869,GSE20307,GPL570,0,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,20|16,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA01870,GSE20307,GPL570,1000,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,36|6,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA01871,GSE20307,GPL570,451,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,20|14,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA01872,GSE20602,GPL96,1000,Nephrosclerosis,C0027719,Glomerulus,GEO,Microarray,Homo sapiens,4|14,EFO:Hardening of the walls of the small arteries and arterioles (small arteries that convey blood from arteries to the even smaller capillaries) of the kidney. This condition is caused by hypertension (high blood pressure) DSA01873,GSE20844,GPL1261,2,Diabetes,C0011847,Glomerulus,GEO,Microarray,Mus musculus,3|4,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA01874,GSE20948,GPL570,444,Hepatitis C,C0019196,,GEO,Microarray,Homo sapiens,2|2,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA01875,GSE20948,GPL570,1000,Hepatitis C,C0019196,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA01876,GSE20948,GPL570,1000,Hepatitis C,C0019196,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA01877,GSE20948,GPL570,1000,Hepatitis C,C0019196,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA01878,GSE20948,GPL570,1000,Hepatitis C,C0019196,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA01879,GSE21369,GPL570,80,Idiopathic Interstitial Pneumonia,C2350236,Lung,GEO,Microarray,Homo sapiens,6|23,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA01880,GSE21935,GPL570,0,Schizophrenia,C0036341,Superior temporal cortex,GEO,Microarray,Homo sapiens,10|13,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA01881,GSE21935,GPL570,0,Schizophrenia,C0036341,Superior temporal cortex,GEO,Microarray,Homo sapiens,9|10,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA01882,GSE21942,GPL570,1000,Multiple Sclerosis,C0026769,,GEO,Microarray,Homo sapiens,15|14,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA01883,GSE22255,GPL570,0,Ischemic Stroke,C0948008,,GEO,Microarray,Homo sapiens,20|20,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA01884,GSE22528,GPL96,0,Allergic Asthma,C0155877,,GEO,Microarray,Homo sapiens,5|5,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01885,GSE22619,GPL570,2,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,10|10,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA01886,GSE23117,GPL570,0,Sjogren's Syndrome,C1527336,Minor salivary gland,GEO,Microarray,Homo sapiens,4|5,DO:An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. DSA01887,GSE23117,GPL570,0,Sjogren's Syndrome,C1527336,Minor salivary gland,GEO,Microarray,Homo sapiens,4|3,DO:An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. DSA01888,GSE23117,GPL570,787,Sjogren's Syndrome,C1527336,Minor salivary gland,GEO,Microarray,Homo sapiens,4|2,DO:An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. DSA01889,GSE23117,GPL570,22,Progressive Sjogren's Syndrome,C1527336,Minor salivary gland,GEO,Microarray,Homo sapiens,5|2,DO:An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. DSA01890,GSE23339,GPL6102,1000,Endometrioma,C0269102,Endometrium,GEO,Microarray,Homo sapiens,9|10,DO:A female reproductive system disease characterized by the growth of endometrial tissue that is located_in the ovary. DSA01891,GSE23832,GPL6244,0,Multiple Sclerosis,C0026769,,GEO,Microarray,Homo sapiens,4|8,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA01892,GSE23910,GPL6480,216,Down Syndrome,C0013080,Thymus,GEO,Microarray,Homo sapiens,4|4,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA01893,GSE2411,GPL339,473,Lung Injury,C0273115,Lung,GEO,Microarray,Mus musculus,6|6,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA01894,GSE2411,GPL339,1000,Lung Injury,C0273115,Lung,GEO,Microarray,Mus musculus,6|6,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA01895,GSE24206,GPL570,601,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,6|5,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA01896,GSE24206,GPL570,95,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,6|4,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA01897,GSE24206,GPL570,76,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,6|5,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA01898,GSE24206,GPL570,34,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,6|2,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA01899,GSE24206,GPL570,0,Progressive Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,5|4,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA01900,GSE24206,GPL570,1,Progressive Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,5|2,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA01901,GSE24250,GPL96,0,Huntington's Disease,C0020179,Blood,GEO,Microarray,Homo sapiens,6|8,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01902,GSE24514,GPL96,1000,Colorectal Carcinoma,C0009402,,GEO,Microarray,Homo sapiens,15|34,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA01903,GSE24807,GPL2895,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Homo sapiens,5|12,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA01904,GSE25507,GPL570,10,Autism,C1510586,Lymph node,GEO,Microarray,Homo sapiens,64|82,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA01905,GSE25518,GPL570,1000,Cryptorchidism,C0010417,Testis,GEO,Microarray,Homo sapiens,4|19,"EFO:The failure of one or both testes of a male fetus to descend from the abdomen into the scrotum during the late part of pregnancy. If not surgically corrected in early childhood, males may be at increased risk for testicular cancer later in life." DSA01906,GSE25673,GPL6244,1000,Schizophrenia,C0036341,,GEO,Microarray,Homo sapiens,12|12,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA01907,GSE26001,GPL1261,1000,Huntington's Disease,C0020179,,GEO,Microarray,Mus musculus,5|6,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01908,GSE26001,GPL1261,1000,Huntington's Disease,C0020179,,GEO,Microarray,Mus musculus,5|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01909,GSE26001,GPL1261,51,Huntington's Disease,C0020179,,GEO,Microarray,Mus musculus,5|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01910,GSE26001,GPL1261,1000,Huntington's Disease,C0020179,,GEO,Microarray,Mus musculus,5|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01911,GSE26001,GPL1261,1000,Huntington's Disease,C0020179,,GEO,Microarray,Mus musculus,5|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01912,GSE26025,GPL1261,0,Endogenous Depression,C0011573,Hippocampus,GEO,Microarray,Mus musculus,3|3,DO:A major depressive disorder characterized by near-complete absence of pleasure. DSA01913,GSE26025,GPL1261,0,Endogenous Depression,C0011573,Hippocampus,GEO,Microarray,Mus musculus,3|3,DO:A major depressive disorder characterized by near-complete absence of pleasure. DSA01914,GSE2629,GPL81,0,Muscular Dystrophy,C0026850,Muscle,GEO,Microarray,Mus musculus,3|3,"DO:A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted." DSA01915,GSE2629,GPL81,12,Muscular Dystrophy,C0026850,Muscle,GEO,Microarray,Mus musculus,3|3,"DO:A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted." DSA01916,GSE26299,GPL1261,581,Glaucoma,C0017601,,GEO,Microarray,Mus musculus,6|14,DO:An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. DSA01917,GSE26299,GPL1261,23,Glaucoma,C0017601,Retina,GEO,Microarray,Mus musculus,10|20,DO:An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. DSA01918,GSE26299,GPL1261,573,Glaucoma,C0017601,Retina,GEO,Microarray,Mus musculus,10|8,DO:An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. DSA01919,GSE26299,GPL1261,1000,Glaucoma,C0017601,Retina,GEO,Microarray,Mus musculus,10|10,DO:An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. DSA01920,GSE26299,GPL1261,13,Glaucoma,C0017601,Optic nerve head,GEO,Microarray,Mus musculus,4|7,DO:An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. DSA01921,GSE26299,GPL1261,1000,Glaucoma,C0017601,Optic nerve head,GEO,Microarray,Mus musculus,4|10,DO:An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. DSA01922,GSE26299,GPL1261,1000,Glaucoma,C0017601,Optic nerve head,GEO,Microarray,Mus musculus,4|10,DO:An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. DSA01923,GSE2657,GPL8300,0,Hodgkin Lymphoma,C0019829,,GEO,Microarray,Homo sapiens,2|2,DO:A lymphoma that is marked by the presence of a type of cell called the Reed-Sternberg cell. DSA01924,GSE2657,GPL8300,0,Sarcoidosis,C0036202,,GEO,Microarray,Homo sapiens,2|2,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA01925,GSE26725,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,Peripheral blood,GEO,Microarray,Homo sapiens,5|12,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA01926,GSE26952,GPL2700,0,Psoriasis,C0033860,Epidermis,GEO,Microarray,Homo sapiens,7|4,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA01927,GSE26952,GPL2700,2,Atopic Dermatitis,C0011615,Epidermis,GEO,Microarray,Homo sapiens,7|5,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA01928,GSE26969,GPL570,6,Intracranial Aneurysm,C0007766,Artery,GEO,Microarray,Homo sapiens,3|3,EFO:Outpouching of BASILAR ARTERY at the base of the skull. The basilar artery is the most important artery in the posterior cerebral circulation. DSA01929,GSE27011,GPL6244,211,Asthma,C0004096,,GEO,Microarray,Homo sapiens,18|19,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01930,GSE27011,GPL6244,170,Asthma,C0004096,,GEO,Microarray,Homo sapiens,18|17,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01931,GSE27011,GPL6244,701,Severe Asthma,C0004096,,GEO,Microarray,Homo sapiens,19|17,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01932,GSE27131,GPL6244,1000,Influenza,C0021400,Blood,GEO,Microarray,Homo sapiens,7|14,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA01933,GSE27200,GPL570,2,Sotos Syndrome,C4551477,Dermis,GEO,Microarray,Homo sapiens,9|9,DO:A syndrome that occurs rarely and is characterized by excessive physical growth during the first 2 to 3 years of life. DSA01934,GSE27200,GPL570,2,Sotos Syndrome,C4551477,Dermis,GEO,Microarray,Homo sapiens,9|9,DO:A syndrome that occurs rarely and is characterized by excessive physical growth during the first 2 to 3 years of life. DSA01935,GSE27276,GPL2507,1000,Glaucoma,C0017601,Trabecular meshwork,GEO,Microarray,Homo sapiens,19|17,DO:An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. DSA01936,GSE27383,GPL570,576,Schizophrenia,C0036341,,GEO,Microarray,Homo sapiens,29|21,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA01937,GSE27383,GPL570,4,Schizophrenia,C0036341,,GEO,Microarray,Homo sapiens,29|22,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA01938,GSE27628,GPL1261,709,Psoriasis,C0033860,Skin,GEO,Microarray,Mus musculus,3|3,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA01939,GSE27628,GPL1261,0,Psoriasis,C0033860,Skin,GEO,Microarray,Mus musculus,3|3,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA01940,GSE27628,GPL1261,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Mus musculus,3|3,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA01941,GSE27628,GPL1261,228,Psoriasis,C0033860,Skin,GEO,Microarray,Mus musculus,3|3,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA01942,GSE27628,GPL1261,86,Psoriasis,C0033860,Skin,GEO,Microarray,Mus musculus,2|2,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA01943,GSE28315,GPL6244,0,Epidermolysis Bullosa Simplex,C0079298,,GEO,Microarray,Homo sapiens,6|6,"DO:An epidermolysis bullosa simplex characterized by generalized non-scarring skin blistering that often occurs in clusters, progressive hyperkeratosis of the palms and soles, clumping of keratin filaments in basal epidermal cells and that has_material_basis_in mutation in either the KRT5 or KRT14 genes. This is the most severe of the epidermolysis bullosa simplex types and may result in neonatal or infant lethality in some cases." DSA01944,GSE28521,GPL6883,0,Autism,C1510586,Cerebellum,GEO,Microarray,Homo sapiens,11|10,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA01945,GSE28521,GPL6883,60,Autism,C1510586,Frontal cortex,GEO,Microarray,Homo sapiens,16|16,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA01946,GSE28521,GPL6883,0,Autism,C1510586,Temporal cortex,GEO,Microarray,Homo sapiens,13|13,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA01947,GSE28619,GPL570,1000,Alcoholic Hepatitis,C0019187,Liver,GEO,Microarray,Homo sapiens,7|15,MONDO:Acute hepatitis resulting from ingestion of alcohol. DSA01948,GSE28750,GPL570,1000,Sepsis,C0243026,Blood,GEO,Microarray,Homo sapiens,20|10,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA01949,GSE28750,GPL570,1000,Sepsis,C0243026,Blood,GEO,Microarray,Homo sapiens,20|11,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA01950,GSE29343,GPL6246,0,Neurofibromatosis Type 1,C0027831,Triceps muscle,GEO,Microarray,Mus musculus,4|4,"DO:A neurofibromatosis classically characterized by cafe-au-lait spots, Lisch nodules in the eye, and fibromatous tumors of the skin or in some cases by a high load of spinal tumors that has_material_basis_in heterozygous mutation in NF1 on 17q11.2." DSA01951,GSE29691,GPL570,1000,Global Developmental Delay,C0557874,Blood,GEO,Microarray,Homo sapiens,13|2,"HPO:A delay in the achievement of motor or mental milestones in the domains of development of a child, including motor skills, speech and language, cognitive skills, and social and emotional skills. This term should only be used to describe children younger than five years of age." DSA01952,GSE30153,GPL570,0,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,9|17,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA01953,GSE30174,GPL570,1,Prostate Cancer,C0600139,Peripheral blood,GEO,Microarray,Homo sapiens,10|10,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA01954,GSE30529,GPL571,1000,Diabetic Kidney Disease,C0011881,Kidney,GEO,Microarray,Homo sapiens,12|10,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA01955,GSE3100,GPL1261,315,Cystic Fibrosis,C0010674,Lung,GEO,Microarray,Mus musculus,6|5,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA01956,GSE3100,GPL1261,463,Cystic Fibrosis,C0010674,Lung,GEO,Microarray,Mus musculus,6|6,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA01957,GSE31106,GPL1261,456,Colorectal Adenocarcinoma,C0009402,Colorectum,GEO,Microarray,Mus musculus,3|3,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA01958,GSE31243,GPL571,0,Cerebral Palsy,C0007789,,GEO,Microarray,Homo sapiens,10|10,"DO:A spastic cerebral palsy that affects lower extremities resulting in tight leg and hip muscles. The legs cross at the knees, making it difficult to walk." DSA01959,GSE31243,GPL571,0,Cerebral Palsy,C0007789,,GEO,Microarray,Homo sapiens,10|10,"DO:A spastic cerebral palsy that affects lower extremities resulting in tight leg and hip muscles. The legs cross at the knees, making it difficult to walk." DSA01960,GSE31773,GPL570,0,Asthma,C0004096,,GEO,Microarray,Homo sapiens,8|8,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01961,GSE31773,GPL570,0,Asthma,C0004096,,GEO,Microarray,Homo sapiens,8|4,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01962,GSE31773,GPL570,1000,Asthma,C0004096,,GEO,Microarray,Homo sapiens,8|8,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01963,GSE31773,GPL570,0,Asthma,C0004096,,GEO,Microarray,Homo sapiens,8|4,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01964,GSE31773,GPL570,0,Severe Asthma,C0004096,,GEO,Microarray,Homo sapiens,4|8,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01965,GSE31773,GPL570,0,Severe Asthma,C0004096,,GEO,Microarray,Homo sapiens,4|8,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01966,GSE3184,GPL339,1000,Allergic Asthma,C0155877,Lung,GEO,Microarray,Mus musculus,10|10,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01967,GSE3184,GPL339,543,Allergic Asthma,C0155877,Lung,GEO,Microarray,Mus musculus,10|10,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA01968,GSE32323,GPL570,1000,Colorectal Carcinoma,C0009402,,GEO,Microarray,Homo sapiens,17|17,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA01969,GSE32407,GPL571,0,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,10|10,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA01970,GSE32407,GPL571,0,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,10|10,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA01971,GSE32407,GPL571,0,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,10|10,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA01972,GSE3248,GPL81,0,Huntington's Disease,C0020179,Cerebellum,GEO,Microarray,Mus musculus,3|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01973,GSE3248,GPL81,0,Huntington's Disease,C0020179,Cerebellum,GEO,Microarray,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01974,GSE3248,GPL81,12,Huntington's Disease,C0020179,Cerebellum,GEO,Microarray,Mus musculus,3|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01975,GSE3248,GPL81,0,Huntington's Disease,C0020179,Cerebellum,GEO,Microarray,Mus musculus,1|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01976,GSE3248,GPL81,0,Huntington's Disease,C0020179,Cerebellum,GEO,Microarray,Mus musculus,3|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01977,GSE3248,GPL81,1,Huntington's Disease,C0020179,Cerebellum,GEO,Microarray,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01978,GSE3248,GPL81,3,Huntington's Disease,C0020179,Cerebellum,GEO,Microarray,Mus musculus,3|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA01979,GSE3249,GPL1261,20,Leber Congenital Amaurosis,C0339527,Retina,GEO,Microarray,Mus musculus,3|3,"DO:A retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness." DSA01980,GSE3249,GPL1261,0,Leber Congenital Amaurosis,C0339527,Retina,GEO,Microarray,Mus musculus,3|3,"DO:A retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness." DSA01981,GSE3249,GPL1261,87,Leber Congenital Amaurosis,C0339527,Retina,GEO,Microarray,Mus musculus,3|3,"DO:A retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness." DSA01982,GSE32609,GPL6246,1000,Hutchinson-Gilford Progeria Syndrome,C0033300,Liver,GEO,Microarray,Mus musculus,3|3,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA01983,GSE32645,GPL4133,1,Multiple Sclerosis,C0026769,Cortex,GEO,Microarray,Homo sapiens,3|3,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA01984,GSE32645,GPL4133,0,Meningeal Tuberculosis,C0041318,Cortex,GEO,Microarray,Homo sapiens,3|3,EFO:A bacterial infection of the membranes covering the brain and the spinal cord caused by Mycobacterium tuberculosis. DSA01985,E-MTAB-11326,,600,Parkinson's Disease,C0030567,Blood,ArrayExpress,RNA-Seq,Homo sapiens,43|64,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA01986,GSE32915,GPL4133,0,Multiple Sclerosis,C0026769,Brain,GEO,Microarray,Homo sapiens,4|4,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA01987,GSE32915,GPL4133,0,Multiple Sclerosis,C0026769,Brain,GEO,Microarray,Homo sapiens,4|3,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA01988,GSE32915,GPL4133,0,Multiple Sclerosis,C0026769,Brain,GEO,Microarray,Homo sapiens,4|5,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA01989,GSE3343,GPL339,0,Amyotrophic Lateral Sclerosis,C0002736,Oculomotor nucleus,GEO,Microarray,Mus musculus,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA01990,GSE3343,GPL339,0,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,Microarray,Mus musculus,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA01991,GSE33463,GPL6947,1000,Idiopathic Pulmonary Arterial Hypertension,C3203102,,GEO,Microarray,Homo sapiens,41|30,"DO:A chronic pulmonary heart disease characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein, or pulmonary capillaries, among others, has symptoms shortness of breath, dizziness, fainting, leg swelling." DSA01992,GSE33463,GPL6947,1000,Secondary Pulmonary Arterial Hypertension,C3665995,,GEO,Microarray,Homo sapiens,41|42, DSA01993,GSE33463,GPL6947,527,Scleroderma,C0011644,,GEO,Microarray,Homo sapiens,41|19,"DO:A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies." DSA01994,GSE33463,GPL6947,1000,Interstitial Lung Disease,C0206062,,GEO,Microarray,Homo sapiens,41|8,"DO:A lung disease that is characterized by inflammation and altered lung interstitium compromising pulmonary function and often has_symptom shortness of breath, dyspnea, and/or cough." DSA01995,GSE3365,GPL96,1000,Ulcerative Colitis,C0009324,,GEO,Microarray,Homo sapiens,42|26,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA01996,GSE3365,GPL96,1000,Crohn's Disease,C0010346,,GEO,Microarray,Homo sapiens,42|59,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA01997,GSE33694,GPL6255,0,Adrenal Tumor,C0001624,Adrenal gland,GEO,Microarray,Homo sapiens,3|3,DO:An endocrine gland cancer located_in the adrenal glands which are located above the kidneys. DSA01998,GSE33694,GPL6255,9,Adrenal Tumor,C0001624,Adrenal gland,GEO,Microarray,Homo sapiens,3|3,DO:An endocrine gland cancer located_in the adrenal glands which are located above the kidneys. DSA01999,GSE34205,GPL570,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,22|28,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA02000,GSE34205,GPL570,1000,Respiratory Syncytial Virus (Rsv),C0375023,,GEO,Microarray,Homo sapiens,22|51, DSA02001,GSE34305,GPL6246,0,Fetal Alcohol Spectrum Disorder,C2985290,Brain,GEO,Microarray,Mus musculus,5|5,"MONDO:A group of disorders caused by a prenatal exposure to maternal consumption of alcohol leading to a range of behavioral, cognitive and neurological deficits in the offspring. It is characterized by physical growth problems, distinct facies, and varying psycho-neurological issues." DSA02002,GSE34308,GPL570,10,Cerebral Adrenoleukodystrophy,C4684865,,GEO,Microarray,Homo sapiens,5|5,"NCI:A subtype of adrenoleukodystrophy (ALD) occurring in approximately 40 percent of boys with ALD, primarily affecting the cerebrum, resulting in rapidly declining neurocognitive function and in most patients, premature death." DSA02003,GSE34309,GPL570,0,Cerebral Adrenoleukodystrophy,C4684865,,GEO,Microarray,Homo sapiens,3|2,"NCI:A subtype of adrenoleukodystrophy (ALD) occurring in approximately 40 percent of boys with ALD, primarily affecting the cerebrum, resulting in rapidly declining neurocognitive function and in most patients, premature death." DSA02004,GSE34309,GPL570,5,Cerebral Adrenoleukodystrophy,C4684865,,GEO,Microarray,Homo sapiens,8|5,"NCI:A subtype of adrenoleukodystrophy (ALD) occurring in approximately 40 percent of boys with ALD, primarily affecting the cerebrum, resulting in rapidly declining neurocognitive function and in most patients, premature death." DSA02005,GSE34465,GPL6244,1000,Renal Cell Carcinoma,C0007134,Peripheral blood,GEO,Microarray,Homo sapiens,9|13,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA02006,GSE34465,GPL6244,1000,Renal Cell Carcinoma,C0007134,Peripheral blood,GEO,Microarray,Homo sapiens,9|17,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA02007,GSE34469,GPL6246,0,Fetal Alcohol Spectrum Disorder,C2985290,Brain,GEO,Microarray,Mus musculus,2|2,"MONDO:A group of disorders caused by a prenatal exposure to maternal consumption of alcohol leading to a range of behavioral, cognitive and neurological deficits in the offspring. It is characterized by physical growth problems, distinct facies, and varying psycho-neurological issues." DSA02008,GSE34469,GPL6246,0,Fetal Alcohol Spectrum Disorder,C2985290,Brain,GEO,Microarray,Mus musculus,2|2,"MONDO:A group of disorders caused by a prenatal exposure to maternal consumption of alcohol leading to a range of behavioral, cognitive and neurological deficits in the offspring. It is characterized by physical growth problems, distinct facies, and varying psycho-neurological issues." DSA02009,GSE3489,GPL8300,1,HIV encephalitis,C0276548,Brain,GEO,Microarray,Homo sapiens,12|16, DSA02010,GSE35008,GPL6244,8,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,6|3,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA02011,GSE35008,GPL6244,20,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,4|5,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA02012,GSE35008,GPL6244,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,6|4,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA02013,GSE3524,GPL96,731,Oral Squamous Cell Carcinoma,C0585362,Endometrium,GEO,Microarray,Homo sapiens,4|16,"EFO:A squamous cell carcinoma arising from the oral cavity. It affects predominantly adults in their fifth and sixth decades of life and is associated with alcohol and tobacco use. Human papillomavirus is present in approximately half of the cases. It is characterized by a tendency to metastasize early to the lymph nodes. When the tumor is small, patients are often asymptomatic. Physical examination may reveal erythematous or white lesions or plaques. The majority of patients present with signs and symptoms of locally advanced disease including mucosal ulceration, pain, difficulty with speaking, chewing, and swallowing, bleeding, weight loss, and neck swelling. Patients may also present with swollen neck lymph nodes without any symptoms from the oropharyngeal tumor. The most significant prognostic factors are the size of the tumor and the lymph nodes status." DSA02014,GSE3554,GPL1261,0,Glaucoma,C0017601,Retina,GEO,Microarray,Mus musculus,3|3,DO:An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. DSA02015,GSE3583,GPL1261,1000,Huntington's Disease,C0020179,,GEO,Microarray,Mus musculus,3|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA02016,GSE3583,GPL1261,1000,Huntington's Disease,C0020179,,GEO,Microarray,Mus musculus,3|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA02017,GSE36297,GPL571,0,Type 2 Diabetes,C0011860,Vastus lateralis,GEO,Microarray,Homo sapiens,10|6,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA02018,GSE36398,GPL6244,0,Facioscapulohumeral Muscular Dystrophy,C0238288,Deltoid,GEO,Microarray,Homo sapiens,12|13,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA02019,GSE36398,GPL6244,0,Facioscapulohumeral Muscular Dystrophy,C0238288,Biceps,GEO,Microarray,Homo sapiens,12|13,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA02020,GSE36474,GPL570,221,Multiple Myeloma,C0026764,Bone marrow,GEO,Microarray,Homo sapiens,3|4,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA02021,GSE36791,GPL10558,1000,Aneurysm,C0002940,Blood,GEO,Microarray,Homo sapiens,18|43,"DO:A cardiovascular system disease that primarily affects the blood vessels which includes the arteries, veins and capillaries that carry blood to and from the heart." DSA02022,GSE36807,GPL570,367,Crohn's Disease,C0010346,Intestine,GEO,Microarray,Homo sapiens,7|13,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02023,GSE36807,GPL570,1000,Ulcerative Colitis,C0009324,Intestine,GEO,Microarray,Homo sapiens,7|15,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02024,GSE36980,GPL6244,1,Alzheimer's Disease,C0002395,Frontal cortex,GEO,Microarray,Homo sapiens,18|15,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA02025,GSE36980,GPL6244,343,Alzheimer's Disease,C0002395,Temporal cortex,GEO,Microarray,Homo sapiens,19|10,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA02026,GSE36980,GPL6244,619,Alzheimer's Disease,C0002395,Hippocampus,GEO,Microarray,Homo sapiens,10|8,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA02027,GSE37283,GPL13158,15,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,5|4,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02028,GSE37283,GPL13158,1000,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,5|11,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02029,GSE37815,GPL6102,1000,Bladder Cancer,C0699885,,GEO,Microarray,Homo sapiens,6|18,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02030,GSE38010,GPL570,1000,Multiple Sclerosis,C0026769,Brain,GEO,Microarray,Homo sapiens,2|2,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA02031,GSE38010,GPL570,1000,Multiple Sclerosis,C0026769,Brain,GEO,Microarray,Homo sapiens,2|2,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA02032,GSE38424,GPL10558,1000,Renal Cell Carcinoma,C0007134,,GEO,Microarray,Homo sapiens,4|4,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA02033,GSE38680,GPL570,1000,Pompe Disease,C0017921,Biceps,GEO,Microarray,Homo sapiens,10|9,DO:A glycogen storage disease that has_material_basis_in deficiency of the lysosomal acid alpha-glucosidase enzyme resulting in damage to muscle and nerve cells due to an accumulation of glycogen in the lysosome. DSA02034,GSE38713,GPL570,1000,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,13|8,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02035,GSE38713,GPL570,1000,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,13|15,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02036,GSE38713,GPL570,0,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,13|7,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02037,GSE38955,GPL6244,31,Myelodysplastic Syndrome,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,6|4,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA02038,GSE39159,GPL6246,642,Down Syndrome,C0013080,Skeletal muscle,GEO,Microarray,Mus musculus,4|4,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA02039,GSE39621,GPL1261,167,Niemann-Pick Disease Type C,C0220756,Brain,GEO,Microarray,Mus musculus,5|11,DO:A Niemann-Pick disease that has_material_basis_in an autosomal recessive mutation of NPC1 on chromosome 18q11.2. DSA02040,GSE40012,GPL6947,1000,Bacterial Pneumonia,C0004626,Blood,GEO,Microarray,Homo sapiens,36|61,DO:A pneumonia involving inflammation of the lungs caused by bacteria. DSA02041,GSE40012,GPL6947,1000,Influenza And Pneumonia,C0155870,Blood,GEO,Microarray,Homo sapiens,36|39, DSA02042,GSE40012,GPL6947,1000,Bacterial pneumonia;influenza A pneumonia,,Blood,GEO,Microarray,Homo sapiens,36|14, DSA02043,GSE40012,GPL6947,1000,Systemic Inflammatory Response Syndrome,C0242966,Blood,GEO,Microarray,Homo sapiens,36|40,"MSH:A systemic inflammatory response to a variety of clinical insults, characterized by two or more of the following conditions: (1) fever >38 degrees C or HYPOTHERMIA <36 degrees C; (2) TACHYCARDIA >90 beat/minute; (3) tachypnea >24 breaths/minute; (4) LEUKOCYTOSIS >12,000 cells/cubic mm or 10% immature forms. While usually related to infection, SIRS can also be associated with noninfectious insults such as TRAUMA; BURNS; or PANCREATITIS. If infection is involved, a patient with SIRS is said to have SEPSIS." DSA02044,GSE4036,GPL570,0,Schizophrenia,C0036341,Brain,GEO,Microarray,Homo sapiens,14|14,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA02045,GSE41044,GPL6246,1000,Methylmalonic Acidemia,C0268583,Kidney,GEO,Microarray,Mus musculus,4|4,DO:An organic acidemia that involves an accumulation of methylmalonic acid in the blood. DSA02046,GSE4107,GPL570,1000,Colorectal Carcinoma,C0009402,Mucosa,GEO,Microarray,Homo sapiens,10|12,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA02047,GSE41649,GPL96,0,Allergic Asthma,C0155877,Bronchus,GEO,Microarray,Homo sapiens,4|4,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02048,GSE4172,GPL570,51,Inflammatory Myopathy,C0027121,Right ventricle,GEO,Microarray,Homo sapiens,4|8,DO:A myopathy characterized by muscle inflammation. DSA02049,GSE4183,GPL570,1000,Colon Adenoma,C4551463,Colon,GEO,Microarray,Homo sapiens,8|14,"MONDO:An adenoma that arises from the colon. The group of colonic adenomas includes tubular, villous, and tubulovillous adenomas, traditional serrated adenomas, sessile serrated adenomas/polyps, and familial adenomatous polyposis." DSA02050,GSE4183,GPL570,1000,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,8|15,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA02051,GSE4183,GPL570,833,Inflammatory Bowel Disease,C0021390,Colon,GEO,Microarray,Homo sapiens,8|15,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA02052,GSE4250,GPL570,0,Hereditary Gingival Fibromatosis,C0399440,Gingiva,GEO,Microarray,Homo sapiens,2|2,"DO:A gingival overgrowth characterized by benign, slowly progressive, nonhemorrhagic, fibrous enlargement of the oral masticatory mucosa." DSA02053,GSE42806,GPL570,1000,Tibial Muscular Dystrophy,C1450052,,GEO,Microarray,Homo sapiens,5|7,DO:A distal muscular dystrophy characterized by autosomal dominant inheritance of late-onset muscular dystrophy beginning in the anterior comparment of the legs that has_material_basis_in heterozygous mutation in the TTN gene on chromosome 2q31. DSA02054,GSE42825,GPL10558,1000,Sarcoidosis,C0036202,Blood,GEO,Microarray,Homo sapiens,23|11,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA02055,GSE42825,GPL10558,1000,Tuberculosis,C0041296,Blood,GEO,Microarray,Homo sapiens,23|8,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA02056,GSE42955,GPL6244,21,Dilated Cardiomyopathy,C0007193,Heart,GEO,Microarray,Homo sapiens,5|12,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA02057,GSE42955,GPL6244,23,Ischemic Cardiomyopathy,C0349782,Heart,GEO,Microarray,Homo sapiens,5|12,EFO:Ischemic cardiomyopathy is a cardiomyopathy in which a weakness in the muscle of the heart due to inadequate oxygen delivery to the myocardium with coronary artery disease being the most common cause. DSA02058,GSE42956,GPL10558,698,Down Syndrome,C0013080,,GEO,Microarray,Homo sapiens,15|6,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA02059,GSE42956,GPL10558,1000,Down Syndrome,C0013080,,GEO,Microarray,Homo sapiens,15|12,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA02060,GSE4302,GPL570,318,Asthma,C0004096,,GEO,Microarray,Homo sapiens,28|42,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02061,GSE4316,GPL570,0,Primary Open Angle Glaucoma,C0339573,Trabecular meshwork,GEO,Microarray,Homo sapiens,3|2,"DO:An open-angle glaucoma that is characterized by the absence of any apparent obstruction of aqueous outflow through the trabecular meshwork with gonioscopy, but often with elevated intraocular pressure." DSA02062,GSE43553,GPL571,1000,Cryopyrin-Associated Periodic Syndromes,C2316212,Peripheral blood,GEO,Microarray,Homo sapiens,20|23,"MONDO:Cryopyrin associated periodic syndrome (CAPS) defines a group of autoinflammatory diseases, characterized by recurrent episodes of systemic inflammatory attacks in the absence of infection or autoimmune disease. CAPS comprises 3 disorders on a continuum of severity: severe CINCA syndrome, intermediate Muckle-Wells syndrome (MWS) and milder familial cold urticaria (FCAS)." DSA02063,GSE44723,GPL570,1,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,Microarray,Homo sapiens,4|6,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA02064,GSE44723,GPL570,0,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,Microarray,Homo sapiens,4|4,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA02065,GSE44971,GPL570,1000,Pilocytic Astrocytoma,C0334583,Cerebellum,GEO,Microarray,Homo sapiens,9|35,DO:A childhood low-grade glioma that is characterized by cells that look like fibers when viewed under a microscope and is located_in the brain. DSA02066,GSE4612,GPL339,597,Portal inflammation,,Liver,GEO,Microarray,Mus musculus,3|3, DSA02067,GSE4619,GPL570,23,Myelodysplastic Syndrome,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,11|18,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA02068,GSE4619,GPL570,1000,Myelodysplastic Syndrome,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,11|19,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA02069,GSE4619,GPL570,46,Myelodysplastic Syndrome,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,11|9,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA02070,GSE4619,GPL570,259,Myelodysplastic Syndrome,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,11|9,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA02071,GSE46449,GPL570,1000,Bipolar Disorder,C0005586,Blood,GEO,Microarray,Homo sapiens,39|6,DO:A mood disorder that involves alternating periods of mania and depression. DSA02072,GSE46449,GPL570,1000,Bipolar Disorder,C0005586,Blood,GEO,Microarray,Homo sapiens,38|43,DO:A mood disorder that involves alternating periods of mania and depression. DSA02073,GSE4678,GPL339,23,Familial Hypertrophic Cardiomyopathy,C0949658,Myocardium,GEO,Microarray,Mus musculus,3|4,DO:A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYH7 gene on chromosome 14q12. DSA02074,GSE4678,GPL339,6,Familial Hypertrophic Cardiomyopathy,C0949658,Myocardium,GEO,Microarray,Mus musculus,3|3,DO:A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYH7 gene on chromosome 14q12. DSA02075,GSE47199,GPL6244,0,Bk Viral Infection,C1096691,,GEO,Microarray,Homo sapiens,14|19,"NCI:An infection caused by the BK virus. It usually causes an asymptomatic infection, except in immunocompromised individuals where it may cause nephropathy or hemorrhagic cystitis." DSA02076,GSE47199,GPL6244,0,Bk Viral Infection,C1096691,,GEO,Microarray,Homo sapiens,14|7,"NCI:An infection caused by the BK virus. It usually causes an asymptomatic infection, except in immunocompromised individuals where it may cause nephropathy or hemorrhagic cystitis." DSA02077,GSE47199,GPL6244,1000,Bk Virus Nephropathy,C1697878,,GEO,Microarray,Homo sapiens,11|3,DO:A viral infectious disease has_material_basis_in BK polyomavirus. DSA02078,GSE47472,GPL10558,1000,Abdominal Aortic Aneurysm,C0162871,Aorta,GEO,Microarray,Homo sapiens,8|14,DO:An aortic aneurysm that is located_in the abdominal aorta. DSA02079,GSE47552,GPL6244,1000,Multiple Myeloma,C0026764,Bone marrow,GEO,Microarray,Homo sapiens,5|41,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA02080,GSE47552,GPL6244,1000,Monoclonal Gammopathy of Undetermined Significance,C0026470,Bone marrow,GEO,Microarray,Homo sapiens,5|20,DO:A blood protein disease that is characterized by the presence of an abnormal protein called monoclonal protein in the blood. DSA02081,GSE47552,GPL6244,1000,Smoldering Multiple Myeloma,C1531608,Bone marrow,GEO,Microarray,Homo sapiens,5|33,EFO:A plasma cell myeloma lacking clinical manifestations and organ impairment. DSA02082,GSE48000,GPL10558,1000,Recurrent Thromboembolism,C4025286,Blood,GEO,Microarray,Homo sapiens,25|40,"HPO:Repeated episodes of obstruction of blood flow due to an embolus, i.e., blood clot that has traveled from its point of origin within the blood stream." DSA02083,GSE48000,GPL10558,1000,Recurrent Thromboembolism,C4025286,Blood,GEO,Microarray,Homo sapiens,25|33,"HPO:Repeated episodes of obstruction of blood flow due to an embolus, i.e., blood clot that has traveled from its point of origin within the blood stream." DSA02084,GSE48000,GPL10558,183,Recurrent Thromboembolism,C4025286,Blood,GEO,Microarray,Homo sapiens,25|35,"HPO:Repeated episodes of obstruction of blood flow due to an embolus, i.e., blood clot that has traveled from its point of origin within the blood stream." DSA02085,GSE48060,GPL570,45,Myocardial Infarction,C0027051,Peripheral blood,GEO,Microarray,Homo sapiens,21|31,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA02086,GSE48080,GPL4133,9,Sepsis,C0243026,,GEO,Microarray,Homo sapiens,3|5,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA02087,GSE48080,GPL4133,1,Sepsis,C0243026,,GEO,Microarray,Homo sapiens,3|5,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA02088,GSE48080,GPL4133,15,Sepsis,C0243026,,GEO,Microarray,Homo sapiens,3|5,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA02089,GSE48080,GPL4133,3,Sepsis,C0243026,,GEO,Microarray,Homo sapiens,3|5,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA02090,GSE48280,GPL6244,311,Dermatomyositis,C0011633,Skeletal muscle,GEO,Microarray,Homo sapiens,5|5,DO:A myositis that results_in inflammation located_in muscle or located_in skin where a skin rash is often seen prior to the onset of muscle weakness. The disease may result from either a viral infection or an autoimmune reaction. DSA02091,GSE48280,GPL6244,0,Polymyositis,C0085655,Skeletal muscle,GEO,Microarray,Homo sapiens,5|5,EFO:Polymyositis (PM)(\ inflammation of many muscles\ ) is a type of chronic inflammation of the muscles (inflammatory myopathy) related to dermatomyositis and inclusion body myositis. DSA02092,GSE48280,GPL6244,126,Inclusion Body Myositis,C0238190,Skeletal muscle,GEO,Microarray,Homo sapiens,5|4,"DO:A myositis that is characterized by late onset of skeletal muscle inflammation, weakness, and atrophy with cytoplasmic granules and vacuoles in the muscle." DSA02093,GSE48301,GPL6244,0,Endometrium In Polycystic Ovary Syndrome,,Endometrium,GEO,Microarray,Homo sapiens,4|3, DSA02094,GSE48301,GPL6244,21,Endometrium In Polycystic Ovary Syndrome,,Endometrium,GEO,Microarray,Homo sapiens,3|4, DSA02095,GSE48301,GPL6244,0,Endometrium In Polycystic Ovary Syndrome,,Endometrium,GEO,Microarray,Homo sapiens,4|3, DSA02096,GSE48301,GPL6244,9,Endometrium In Polycystic Ovary Syndrome,,Endometrium,GEO,Microarray,Homo sapiens,4|4, DSA02097,GSE48574,GPL570,333,Iscu Myopathy,,Vastus lateralis,GEO,Microarray,Homo sapiens,5|3, DSA02098,GSE48634,GPL10558,0,Crohn's Disease,C0010346,Rectum,GEO,Microarray,Homo sapiens,26|13,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02099,GSE48634,GPL10558,0,Crohn's Disease,C0010346,Descending colon,GEO,Microarray,Homo sapiens,17|9,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02100,GSE48634,GPL10558,0,Crohn's Disease,C0010346,Ascending colon,GEO,Microarray,Homo sapiens,13|7,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02101,GSE48634,GPL10558,0,Crohn's Disease,C0010346,Terminal ileum,GEO,Microarray,Homo sapiens,13|5,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02102,GSE48634,GPL10558,70,Ulcerative Colitis,C0009324,Rectum,GEO,Microarray,Homo sapiens,26|20,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02103,GSE48634,GPL10558,1,Ulcerative Colitis,C0009324,Descending colon,GEO,Microarray,Homo sapiens,17|20,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02104,GSE48634,GPL10558,0,Ulcerative Colitis,C0009324,Ascending colon,GEO,Microarray,Homo sapiens,13|16,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02105,GSE48634,GPL10558,0,Ulcerative Colitis,C0009324,Terminal ileum,GEO,Microarray,Homo sapiens,13|12,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02106,GSE49036,GPL570,0,Lewy Body Disease,C0752347,Substantia nigra,GEO,Microarray,Homo sapiens,8|5,"DO:A dementia that is characterized by the development of abnormal proteinaceous (alpha-synuclein) cytoplasmic inclusions, called Lewy bodies, throughout the brain that results in progressive decline in mental abilities." DSA02107,GSE49036,GPL570,0,Parkinson's Disease,C0030567,Substantia nigra,GEO,Microarray,Homo sapiens,8|7,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA02108,GSE49036,GPL570,1000,Parkinson's Disease,C0030567,Substantia nigra,GEO,Microarray,Homo sapiens,8|8,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA02109,GSE49515,GPL570,1000,Gastric Cancer,C0699791,,GEO,Microarray,Homo sapiens,10|3,DO:A gastrointestinal system cancer that is located_in the stomach. DSA02110,GSE49515,GPL570,1000,Hepatocellular Carcinoma,C0334287,,GEO,Microarray,Homo sapiens,10|10,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA02111,E-MTAB-11636,,209,Type 2 Diabetes Mellitus,C0011847,Small intestine,ArrayExpress,RNA-Seq,Mus musculus,8|7,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA02112,GSE50628,GPL570,1,Seizure,C0036572,Blood,GEO,Microarray,Homo sapiens,5|5,HPO:A seizure is an intermittent abnormality of nervous system physiology characterised by a transient occurrence of signs and/or symptoms due to abnormal excessive or synchronous neuronal activity in the brain. DSA02113,GSE50628,GPL570,0,Seizure,C0036572,Blood,GEO,Microarray,Homo sapiens,3|3,HPO:A seizure is an intermittent abnormality of nervous system physiology characterised by a transient occurrence of signs and/or symptoms due to abnormal excessive or synchronous neuronal activity in the brain. DSA02114,GSE50628,GPL570,0,Seizure,C0036572,Blood,GEO,Microarray,Homo sapiens,5|5,HPO:A seizure is an intermittent abnormality of nervous system physiology characterised by a transient occurrence of signs and/or symptoms due to abnormal excessive or synchronous neuronal activity in the brain. DSA02115,GSE50628,GPL570,0,Seizure,C0036572,Blood,GEO,Microarray,Homo sapiens,3|3,HPO:A seizure is an intermittent abnormality of nervous system physiology characterised by a transient occurrence of signs and/or symptoms due to abnormal excessive or synchronous neuronal activity in the brain. DSA02116,GSE50635,GPL6244,112,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,8|8,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02117,GSE50635,GPL6244,0,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,8|8,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02118,GSE50635,GPL6244,113,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,8|9,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02119,GSE50635,GPL6244,0,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,8|8,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02120,GSE50772,GPL570,1000,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,20|61,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02121,GSE51392,GPL13158,0,Allergic Asthma,C0155877,Bronchial epithelium,GEO,Microarray,Homo sapiens,6|6,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02122,GSE51392,GPL13158,0,Allergic Asthma,C0155877,Bronchial epithelium,GEO,Microarray,Homo sapiens,6|6,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02123,GSE51392,GPL13158,0,Allergic Asthma,C0155877,Nasal epithelium,GEO,Microarray,Homo sapiens,6|6,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02124,GSE51392,GPL13158,0,Allergic Asthma,C0155877,Nasal epithelium,GEO,Microarray,Homo sapiens,6|6,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02125,GSE51392,GPL13158,0,Allergic Rhinitis,C2607914,Bronchial epithelium,GEO,Microarray,Homo sapiens,6|5,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA02126,GSE51392,GPL13158,0,Allergic Rhinitis,C2607914,Bronchial epithelium,GEO,Microarray,Homo sapiens,6|5,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA02127,GSE51392,GPL13158,0,Allergic Rhinitis,C2607914,Nasal epithelium,GEO,Microarray,Homo sapiens,6|5,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA02128,GSE51392,GPL13158,0,Allergic Rhinitis,C2607914,Nasal epithelium,GEO,Microarray,Homo sapiens,6|5,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA02129,GSE51808,GPL13158,1000,Dengue Disease,C0011311,Blood,GEO,Microarray,Homo sapiens,9|18,"DO:A viral infectious disease that results in infection, has_material_basis_in Dengue virus" DSA02130,GSE51808,GPL13158,1000,Dengue Disease,C0011311,Blood,GEO,Microarray,Homo sapiens,9|10,"DO:A viral infectious disease that results in infection, has_material_basis_in Dengue virus" DSA02131,GSE51808,GPL13158,5,Dengue Disease,C0011311,Blood,GEO,Microarray,Homo sapiens,9|19,"DO:A viral infectious disease that results in infection, has_material_basis_in Dengue virus" DSA02132,GSE51931,GPL6246,0,Cach Syndrome,C1858991,Abdominal adipose tissue,GEO,Microarray,Mus musculus,3|3,"DO:A leukodystrophy characterized by variable neurologic features resulting from deficiency in astrocyte maturation, including progressive cerebellar ataxia, spasticity, and cognitive impairment associated with white matter lesions on brain imaging with onset from early infancy to adulthood." DSA02133,GSE51931,GPL6246,270,Cach Syndrome,C1858991,Muscle,GEO,Microarray,Mus musculus,3|3,"DO:A leukodystrophy characterized by variable neurologic features resulting from deficiency in astrocyte maturation, including progressive cerebellar ataxia, spasticity, and cognitive impairment associated with white matter lesions on brain imaging with onset from early infancy to adulthood." DSA02134,GSE51931,GPL6246,503,Cach Syndrome,C1858991,Liver,GEO,Microarray,Mus musculus,3|3,"DO:A leukodystrophy characterized by variable neurologic features resulting from deficiency in astrocyte maturation, including progressive cerebellar ataxia, spasticity, and cognitive impairment associated with white matter lesions on brain imaging with onset from early infancy to adulthood." DSA02135,GSE5281,GPL570,1000,Alzheimer's Disease,C0002395,Entorhinal cortex,GEO,Microarray,Homo sapiens,13|10,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA02136,GSE5281,GPL570,1000,Alzheimer's Disease,C0002395,Hippocampus,GEO,Microarray,Homo sapiens,13|10,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA02137,GSE5281,GPL570,1000,Alzheimer's Disease,C0002395,Brain,GEO,Microarray,Homo sapiens,12|16,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA02138,GSE5281,GPL570,1000,Alzheimer's Disease,C0002395,Posterior cingulate,GEO,Microarray,Homo sapiens,13|9,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA02139,GSE5281,GPL570,1000,Alzheimer's Disease,C0002395,Superior frontal gyrus,GEO,Microarray,Homo sapiens,11|23,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA02140,GSE5281,GPL570,30,Alzheimer's Disease,C0002395,Primary visual cortex,GEO,Microarray,Homo sapiens,12|19,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA02141,GSE53431,GPL10558,1000,Psoriasis,C0033860,Epidermis,GEO,Microarray,Homo sapiens,12|12,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA02142,GSE53441,GPL570,652,Sickle Cell Disease,C0002895,,GEO,Microarray,Homo sapiens,10|24,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA02143,GSE5348,GPL339,59,Wilson Disease,C0019202,Liver,GEO,Microarray,Mus musculus,3|3,"DO:A metal metabolism disease that is characterized by excess copper stored in various body tissues, particularly the liver, brain, and corneas of the eyes." DSA02144,GSE5370,GPL96,1000,Dermatomyositis,C0011633,Skeletal muscle,GEO,Microarray,Homo sapiens,4|5,DO:A myositis that results_in inflammation located_in muscle or located_in skin where a skin rash is often seen prior to the onset of muscle weakness. The disease may result from either a viral infection or an autoimmune reaction. DSA02145,GSE5389,GPL96,19,Bipolar Disorder,C0005586,Brain,GEO,Microarray,Homo sapiens,11|10,DO:A mood disorder that involves alternating periods of mania and depression. DSA02146,GSE5390,GPL96,1000,Down Syndrome,C0013080,Brain,GEO,Microarray,Homo sapiens,8|7,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA02147,GSE5406,GPL96,1000,Heart Failure,C0018801,Heart,GEO,Microarray,Homo sapiens,16|86,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA02148,GSE5406,GPL96,1000,Heart Failure,C0018801,Heart,GEO,Microarray,Homo sapiens,16|108,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA02149,GSE54992,GPL570,1000,Tuberculosis,C0041296,,GEO,Microarray,Homo sapiens,6|9,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA02150,GSE55447,GPL10558,0,Systemic Lupus Erythematosus,C0024141,Peripheral blood,GEO,Microarray,Homo sapiens,5|21,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02151,GSE55447,GPL10558,3,Systemic Lupus Erythematosus,C0024141,Peripheral blood,GEO,Microarray,Homo sapiens,5|21,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02152,GSE55447,GPL10558,2,Systemic Lupus Erythematosus,C0024141,Peripheral blood,GEO,Microarray,Homo sapiens,5|21,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02153,GSE55447,GPL10558,1,Systemic Lupus Erythematosus,C0024141,Peripheral blood,GEO,Microarray,Homo sapiens,5|21,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02154,GSE55447,GPL10558,0,Systemic Lupus Erythematosus,C0024141,Peripheral blood,GEO,Microarray,Homo sapiens,5|21,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02155,GSE55447,GPL10558,0,Systemic Lupus Erythematosus,C0024141,Peripheral blood,GEO,Microarray,Homo sapiens,5|21,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02156,GSE5550,GPL201,1000,Chronic Myelogenous Leukemia,C0023473,Bone marrow,GEO,Microarray,Homo sapiens,8|9,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA02157,GSE5563,GPL570,1000,Vulvar Intraepithelial Neoplasia,C0346210,Vulva,GEO,Microarray,Homo sapiens,9|9,"EFO:Intraepithelial neoplasia of the vulvar squamous epithelium. There is no evidence of invasion. This category includes vulvar high grade squamous intraepithelial lesion and vulvar intraepithelial neoplasia, differentiated type." DSA02158,GSE57178,GPL6244,1000,Chronic Idiopathic Urticaria,C0578870,Skin,GEO,Microarray,Homo sapiens,6|6,HPO:Urticaria characterized by spontaneously recurring hives for 6 weeks or longer. DSA02159,GSE57178,GPL6244,1000,Chronic Idiopathic Urticaria,C0578870,Skin,GEO,Microarray,Homo sapiens,6|6,HPO:Urticaria characterized by spontaneously recurring hives for 6 weeks or longer. DSA02160,GSE5786,GPL1261,5,Huntington's Disease,C0020179,Striatum,GEO,Microarray,Mus musculus,3|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA02161,GSE58208,GPL570,1000,Hepatocellular Carcinoma,C0334287,,GEO,Microarray,Homo sapiens,5|10,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA02162,GSE58208,GPL570,1000,Hepatitis B,C0019163,,GEO,Microarray,Homo sapiens,5|12,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus, which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice." DSA02163,GSE58435,GPL570,0,Turner Syndrome,C0041408,Embryo,GEO,Microarray,Homo sapiens,5|5,DO:A disorder of sexual development that is characterized by a progressive loss of germ cells on the developing gonads of an embryo. DSA02164,GSE59312,GPL570,1000,Hepatitis C,C0019196,Blood,GEO,Microarray,Homo sapiens,20|59,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA02165,GSE6011,GPL96,1000,Duchenne Muscular Dystrophy,C0013264,Quadriceps,GEO,Microarray,Homo sapiens,14|23,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02166,GSE6012,GPL96,923,Atopic Eczema,C0013595,Skin,GEO,Microarray,Homo sapiens,10|10,"DO:A skin disease characterized by itchy, erythematous, vesicular, weeping and crusting patches of skin." DSA02167,GSE6078,GPL1261,0,Intestinal Polyposis,C1257915,,GEO,Microarray,Mus musculus,2|3,HPO:The presence of multiple polyps in the intestine. DSA02168,GSE6088,GPL570,0,Familial Hypercholesterolemia,C0020445,,GEO,Microarray,Homo sapiens,13|7,DO:A familial hyperlipidemia characterized by very high levels of low-density lipoprotein (LDL) and early cardiovascular disease. DSA02169,GSE6088,GPL570,0,Familial Hypercholesterolemia,C0020445,,GEO,Microarray,Homo sapiens,13|3,DO:A familial hyperlipidemia characterized by very high levels of low-density lipoprotein (LDL) and early cardiovascular disease. DSA02170,GSE61635,GPL570,1000,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,30|99,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02171,GSE61853,GPL10558,1,Myelodysplastic Syndrome,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,7|3,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA02172,GSE61853,GPL10558,0,Myelodysplastic Syndrome,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,7|4,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA02173,E-MTAB-11910,,1000,Prostate Cancer,C0600139,Prostate gland,ArrayExpress,RNA-Seq,Homo sapiens,20|20,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02174,GSE62632,GPL6244,35,Autism Spectrum Disorder,C0004352,,GEO,Microarray,Homo sapiens,9|3,"DO:An autism spectrum disorder that is characterized by symptoms across all three symptom domains (communication, social, restricted repetitive interests and behaviors), delayed language development, and symptom onset prior to age 3 years." DSA02175,GSE62632,GPL6244,988,Autism Spectrum Disorder,C0004352,,GEO,Microarray,Homo sapiens,3|3,"DO:An autism spectrum disorder that is characterized by symptoms across all three symptom domains (communication, social, restricted repetitive interests and behaviors), delayed language development, and symptom onset prior to age 3 years." DSA02176,GSE66360,GPL570,1000,Myocardial Infarction,C0027051,,GEO,Microarray,Homo sapiens,50|49,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA02177,GSE66494,GPL6480,1000,Chronic Kidney Disease,C1561643,Kidney,GEO,Microarray,Homo sapiens,8|53,DO:A kidney failure that is characterized by the gradual loss of kidney function. DSA02178,GSE6678,GPL1261,1000,Infantile Krabbe Disease,C0751273,Breast,GEO,Microarray,Mus musculus,9|9,"MSH:An autosomal recessive metabolic disorder caused by a deficiency of GALACTOSYLCERAMIDASE leading to intralysosomal accumulation of galactolipids such as GALACTOSYLCERAMIDES and PSYCHOSINE. It is characterized by demyelination associated with large multinucleated globoid cells, predominantly involving the white matter of the central nervous system. The loss of MYELIN disrupts normal conduction of nerve impulses." DSA02179,GSE66795,GPL10558,445,Primary Sjogren Syndrome,C0151449,Blood,GEO,Microarray,Homo sapiens,29|21,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA02180,GSE66795,GPL10558,751,Primary Sjogren Syndrome,C0151449,Blood,GEO,Microarray,Homo sapiens,29|74,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA02181,GSE66795,GPL10558,540,Primary Sjogren Syndrome,C0151449,Blood,GEO,Microarray,Homo sapiens,29|36,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA02182,GSE6691,GPL96,449,Chronic Lymphocytic Leukemia,C0023434,Bone marrow,GEO,Microarray,Homo sapiens,8|11,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA02183,GSE6691,GPL96,1000,Multiple Myeloma,C0026764,Bone marrow,GEO,Microarray,Homo sapiens,5|12,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA02184,GSE6691,GPL96,198,Waldenstrom Macroglobulinemia,C0024419,Bone marrow,GEO,Microarray,Homo sapiens,8|10,DO:A B-cell lymphocytic neoplasm characterized by an uncontrolled increase of B-cells. DSA02185,GSE6691,GPL96,1000,Waldenstrom Macroglobulinemia,C0024419,Bone marrow,GEO,Microarray,Homo sapiens,5|10,DO:A B-cell lymphocytic neoplasm characterized by an uncontrolled increase of B-cells. DSA02186,GSE6731,GPL8300,226,Crohn's Disease,C0010346,Colon,GEO,Microarray,Homo sapiens,4|7,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02187,GSE6731,GPL8300,1000,Crohn's Disease,C0010346,Colon,GEO,Microarray,Homo sapiens,4|12,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02188,GSE6731,GPL8300,760,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,4|5,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02189,GSE6731,GPL8300,1000,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,4|4,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02190,GSE67492,GPL6244,348,Pulmonary Arterial Hypertension,C2973725,Heart right ventricular wall,GEO,Microarray,Homo sapiens,2|2,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA02191,GSE67492,GPL6244,0,Idiopathic Dilated Cardiomyopathy,C1449563,Heart right ventricular wall,GEO,Microarray,Homo sapiens,2|2,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LMNA gene on chromosome 1q21. DSA02192,GSE67596,GPL570,233,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,13|14,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA02193,GSE67596,GPL570,12,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,13|8,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA02194,GSE67596,GPL570,597,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,15|14,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA02195,GSE67596,GPL570,1000,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,15|8,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA02196,GSE6798,GPL570,10,Polycystic Ovary Syndrome,C0032460,Vastus lateralis,GEO,Microarray,Homo sapiens,13|16,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA02197,GSE6872,GPL570,1000,Teratozoospermia,C0403824,,GEO,Microarray,Homo sapiens,13|8,EFO:presence of structurally anomalous spermatozoa in the semen; malformations include the physical bending of the sperm to produce kinks or bends DSA02198,GSE69252,GPL6244,2,Cutaneous Leishmaniasis,C0023283,,GEO,Microarray,Homo sapiens,4|2,"DO:A leishmaniasis that involves skin infection caused by Leishmania species, resulting in one or more cutaneous lesions." DSA02199,GSE69252,GPL6244,0,Cutaneous Leishmaniasis,C0023283,,GEO,Microarray,Homo sapiens,4|3,"DO:A leishmaniasis that involves skin infection caused by Leishmania species, resulting in one or more cutaneous lesions." DSA02200,GSE69252,GPL6244,0,Cutaneous Leishmaniasis,C0023283,,GEO,Microarray,Homo sapiens,4|2,"DO:A leishmaniasis that involves skin infection caused by Leishmania species, resulting in one or more cutaneous lesions." DSA02201,GSE69252,GPL6244,0,Cutaneous Leishmaniasis,C0023283,,GEO,Microarray,Homo sapiens,4|3,"DO:A leishmaniasis that involves skin infection caused by Leishmania species, resulting in one or more cutaneous lesions." DSA02202,GSE69601,GPL6244,0,Idiopathic Pulmonary Hypertension,C0152171,,GEO,Microarray,Homo sapiens,3|3,"DO:A chronic pulmonary heart disease characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein, or pulmonary capillaries, among others, has symptoms shortness of breath, dizziness, fainting, leg swelling." DSA02203,GSE70683,GPL6244,0,Arterial Tortuosity Syndrome,C1859726,Skin,GEO,Microarray,Homo sapiens,3|3,DO:A connective tissue disease that is characterized by elongation and generalized tortuosity of the major arteries including the aorta. DSA02204,GSE7476,GPL570,1000,Bladder Cancer,C0699885,Bladder,GEO,Microarray,Homo sapiens,3|3,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02205,GSE7476,GPL570,1000,Bladder Cancer,C0699885,Bladder,GEO,Microarray,Homo sapiens,3|3,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02206,GSE7476,GPL570,1000,Bladder Cancer,C0699885,Bladder,GEO,Microarray,Homo sapiens,3|3,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02207,GSE7486,GPL570,6,Northern Epilepsy Syndrome,C1864923,,GEO,Microarray,Homo sapiens,12|8,"DO:A neuronal ceroid lipofuscinosis that is characterized by onset at 5 to 10 years of age of epilepsy followed by progressive mental retardation and a mixed combination of 'granular,' 'curvilinear,' and 'fingerprint' profile lipopigment patterns and has_material_basis_in a Finnish founder mutation in the CLN8 gene on chromosome 8p23." DSA02208,GSE77087,GPL10558,1000,Respiratory Syncytial Virus Infectious Disease,C0035235,Blood,GEO,Microarray,Homo sapiens,23|61,"DO:A viral infectious disease that results_in infection located_in upper respiratory tract or located_in lower respiratory tract, has_material_basis_in Human respiratory syncytial virus, which is transmitted_by droplet spread of nasal secretions from an infected person while coughing or sneezing, or transmitted_by contaminated fomites. The infection has_symptom runny nose, has_symptom fever, has_symptom cough, has_symptom wheezing, and has_symptom respiratory distress." DSA02209,GSE77087,GPL10558,1000,Respiratory Syncytial Virus Infectious Disease,C0035235,Blood,GEO,Microarray,Homo sapiens,23|20,"DO:A viral infectious disease that results_in infection located_in upper respiratory tract or located_in lower respiratory tract, has_material_basis_in Human respiratory syncytial virus, which is transmitted_by droplet spread of nasal secretions from an infected person while coughing or sneezing, or transmitted_by contaminated fomites. The infection has_symptom runny nose, has_symptom fever, has_symptom cough, has_symptom wheezing, and has_symptom respiratory distress." DSA02210,GSE78851,GPL6244,1000,Adenomyosis,C0341858,Endometrium,GEO,Microarray,Homo sapiens,4|2,"DO:A uterine disease that is characterized by the presence of endometrial tissue grows outside of the endometrium, such as into the myometrium." DSA02211,GSE8835,GPL96,1,Chronic Lymphocytic Leukemia,C0023434,Peripheral blood,GEO,Microarray,Homo sapiens,12|22,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA02212,GSE8835,GPL96,1000,Chronic Lymphocytic Leukemia,C0023434,Peripheral blood,GEO,Microarray,Homo sapiens,12|20,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA02213,GSE9128,GPL96,0,Ischemic Cardiomyopathy,C0349782,,GEO,Microarray,Homo sapiens,3|4,EFO:Ischemic cardiomyopathy is a cardiomyopathy in which a weakness in the muscle of the heart due to inadequate oxygen delivery to the myocardium with coronary artery disease being the most common cause. DSA02214,GSE9128,GPL96,0,Non ischemic cardiomyopathy,,,GEO,Microarray,Homo sapiens,3|4, DSA02215,GSE9348,GPL570,1000,Colorectal Carcinoma,C0009402,,GEO,Microarray,Homo sapiens,12|70,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA02216,GSE9579,GPL571,137,Acute Appendicitis,C0003615,Appendix,GEO,Microarray,Homo sapiens,4|9,"DO:A gastrointestinal system infectious disease that involves inflammation and infection of the appendix caused by the blockage of the lumen with a small, hard piece of stool, a foreign body or worms. Mucus backs up in the appendiceal lumen, causing bacteria that live inside the appendix to multiply. The infection has_symptom pain, in the upper abdomen initially and later in the lower abdomen, has_symptom nausea, has_symptom vomiting and has_symptom fever." DSA02217,GSE9692,GPL570,1000,Septic Shock,C0036983,Blood,GEO,Microarray,Homo sapiens,15|30,"DO:A commensal bacterial infectious disease that results_in infection, has_material_basis_in Streptococcus pyogenes or has_material_basis_in Staphylococcus aureus , which produce toxins that are absorbed systemically and produce the systemic manifestations. The infection has_symptom fever, has_symptom rash, has_symptom hypotension, has_symptom multiorgan failure, has_symptom desquamation, has_symptom vomiting, has_symptom diarrhea, has_symptom headache, and has_symptom nonfocal neurologic abnormalities." DSA02218,GSE15629,GPL6244,90,Intracranial Aneurysm,C0007766,Vessel wall,GEO,Microarray,Homo sapiens,5|8,EFO:Outpouching of BASILAR ARTERY at the base of the skull. The basilar artery is the most important artery in the posterior cerebral circulation. DSA02219,GSE15629,GPL6244,607,Intracranial Aneurysm,C0007766,Vessel wall,GEO,Microarray,Homo sapiens,5|6,EFO:Outpouching of BASILAR ARTERY at the base of the skull. The basilar artery is the most important artery in the posterior cerebral circulation. DSA02220,GSE20916,GPL570,1000,Adenocarcinoma,C0001418,Colon,GEO,Microarray,Homo sapiens,34|36,"DO:A carcinoma that has_material_basis_in abnormally proliferating cells, derives_from epithelial cells, which originate in glandular tissue." DSA02221,GSE20916,GPL570,1000,Adenoma,C0001430,Colon,GEO,Microarray,Homo sapiens,34|45,DO:A pancreatic cystadenoma that is characterized by innumerable small cysts lined by bland clear cells. DSA02222,GSE20916,GPL570,1000,Colon Tumor,C0009375,Colon,GEO,Microarray,Homo sapiens,34|30,DO:A colorectal cancer that is located_in the colon. DSA02223,GSE2459,GPL81,8,Transverse Aortic Constriction,,Heart left ventricle,GEO,Microarray,Mus musculus,9|6, DSA02224,GSE27448,GPL2895,1,Bladder Cancer,C0699885,Bladder,GEO,Microarray,Homo sapiens,5|10,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02225,GSE3203,GPL1261,1000,Influenza,C0021400,Lymph node,GEO,Microarray,Mus musculus,4|4,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA02226,GSE34874,GPL6246,160,Colitis,C0009319,Colon,GEO,Microarray,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA02227,GSE34874,GPL6246,137,Colitis,C0009319,Colon,GEO,Microarray,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA02228,GSE4120,GPL339,0,Right Ventricular Dysfunction,C0242707,Right ventricle,GEO,Microarray,Mus musculus,5|5,"MSH:A condition in which the RIGHT VENTRICLE of the heart was functionally impaired. This condition usually leads to HEART FAILURE or MYOCARDIAL INFARCTION, and other cardiovascular complications. Diagnosis is made by measuring the diminished ejection fraction and a depressed level of motility of the right ventricular wall." DSA02229,GSE42589,GPL6244,1000,Cleft Lip/Palate,C0158646,Dental pulp,GEO,Microarray,Homo sapiens,6|7,"HPO:The presence of a cleft in the oral cavity, the two main types of which are cleft lip and cleft palate. In cleft lip, there is the congenital failure of the maxillary and median nasal processes to fuse, forming a groove or fissure in the lip. In cleft palate, there is a congenital failure of the palate to fuse properly, forming a grooved depression or fissure in the roof of the mouth. Clefts of the lip and palate can occur individually or together. It is preferable to code each defect separately." DSA02230,GSE4587,GPL570,49,Melanoma,C0025202,Skin,GEO,Microarray,Homo sapiens,2|2,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA02231,GSE4587,GPL570,336,Melanoma,C0025202,Skin,GEO,Microarray,Homo sapiens,2|2,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA02232,GSE4587,GPL570,7,Melanoma,C0025202,Skin,GEO,Microarray,Homo sapiens,2|2,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA02233,GSE4587,GPL570,52,Melanoma,C0025202,Skin,GEO,Microarray,Homo sapiens,2|3,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA02234,GSE48027,GPL6246,85,Tuberculosis,C0041296,Lung,GEO,Microarray,Mus musculus,4|6,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA02235,GSE48027,GPL6246,1000,Tuberculosis,C0041296,Lung,GEO,Microarray,Mus musculus,4|2,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA02236,GSE48438,GPL6246,1,Chronic Myelogenous Leukemia,C0023473,,GEO,Microarray,Mus musculus,5|5,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA02237,GSE53147,GPL6887,154,Vitiligo,C0042900,Skin,GEO,Microarray,Mus musculus,3|3,DO:An autoimmune disease that causes depigmentation of patches of skin resulting from loss of function or death of melanoctyes. DSA02238,GSE61412,GPL6246,1000,Pancreatic Ductal Adenocarcinoma,C1335302,,GEO,Microarray,Mus musculus,3|3,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA02239,GSE63032,GPL6246,1000,Colon Tumor,C0009375,Heart,GEO,Microarray,Mus musculus,3|3,DO:A colorectal cancer that is located_in the colon. DSA02240,GSE63032,GPL6246,936,Colon Tumor,C0009375,Gastrocnemius muscle,GEO,Microarray,Mus musculus,3|3,DO:A colorectal cancer that is located_in the colon. DSA02241,GSE64756,GPL1261,1000,Bladder Urothelial Carcinoma,C0699885,Bladder,GEO,Microarray,Mus musculus,2|2,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02242,GSE64756,GPL1261,1000,Bladder Urothelial Carcinoma,C0699885,Bladder,GEO,Microarray,Mus musculus,2|2,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02243,GSE8000,GPL1261,512,Cardiomyopathy,C0878544,Heart,GEO,Microarray,Mus musculus,8|6,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA02244,GSE8000,GPL1261,63,Cardiomyopathy,C0878544,Heart,GEO,Microarray,Mus musculus,8|7,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA02245,GSE466,GPL81,1000,Duchenne Muscular Dystrophy,C0013264,Skeletal muscle,GEO,Microarray,Mus musculus,5|5,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02246,GSE642,GPL81,796,Diabetes,C0011847,Kidney,GEO,Microarray,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA02247,GSE642,GPL81,77,Diabetes,C0011847,Kidney,GEO,Microarray,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA02248,GSE43696,GPL6480,34,Asthma,C0004096,,GEO,Microarray,Homo sapiens,20|50,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02249,GSE43696,GPL6480,873,Asthma,C0004096,,GEO,Microarray,Homo sapiens,20|38,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02250,GSE12679,GPL570,2,Schizophrenia,C0036341,,GEO,Microarray,Homo sapiens,5|11,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA02251,GSE12679,GPL570,0,Schizophrenia,C0036341,,GEO,Microarray,Homo sapiens,6|5,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA02252,GSE12679,GPL570,0,Bipolar Disorder,C0005586,,GEO,Microarray,Homo sapiens,6|5,DO:A mood disorder that involves alternating periods of mania and depression. DSA02253,E-MTAB-11919,,39,Systemic Lupus Erythematosus,C0024141,Blood,ArrayExpress,RNA-Seq,Homo sapiens,5|5,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02254,GSE11393,GPL571,0,Familial Combined Hyperlipidemia,C0020474,Blood,GEO,Microarray,Homo sapiens,3|3,HPO:Hyperapobetalipoproteinemia is defined as the combination of a normal low density lipoprotein (LDL) cholesterol in the face of an increased LDL apolipoprotein B (apoB) protein. DSA02255,GSE12452,GPL570,1000,Nasopharyngeal Carcinoma,C2931822,Nasopharynx,GEO,Microarray,Homo sapiens,10|31,"DO:A pharynx cancer that is located in the nasopharynx, the uppermost region of the pharynx or throat, where the nasal passages and auditory tubes join the remainder of the upper respiratory tract." DSA02256,GSE2725,GPL96,10,Uterine Fibroid,C0042133,Myometrium,GEO,Microarray,Homo sapiens,3|7,DO:An uterine benign neoplasm derived from the smooth muscle layer of the uterus. DSA02257,GSE3167,GPL96,1000,Bladder Cancer,C0699885,Bladder,GEO,Microarray,Homo sapiens,9|41,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02258,GSE765,GPL81,10,Cystic Fibrosis,C0010674,Small intestine,GEO,Microarray,Mus musculus,3|3,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA02259,GSE10953,GPL339,0,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,Microarray,Mus musculus,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA02260,GSE10953,GPL339,0,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,Microarray,Mus musculus,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA02261,GSE10953,GPL339,0,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,Microarray,Mus musculus,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA02262,GSE1010,GPL96,0,Familial Combined Hyperlipidemia,C0020474,,GEO,Microarray,Homo sapiens,12|12,HPO:Hyperapobetalipoproteinemia is defined as the combination of a normal low density lipoprotein (LDL) cholesterol in the face of an increased LDL apolipoprotein B (apoB) protein. DSA02263,GSE3868,GPL96,43,Prostate Tumor,C0600139,Prostate,GEO,Microarray,Homo sapiens,7|22,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02264,GSE1551,GPL96,1000,Dermatomyositis,C0011633,Muscle,GEO,Microarray,Homo sapiens,10|13,DO:A myositis that results_in inflammation located_in muscle or located_in skin where a skin rash is often seen prior to the onset of muscle weakness. The disease may result from either a viral infection or an autoimmune reaction. DSA02265,GSE2503,GPL96,14,Actinic Keratosis,C0022602,Skin,GEO,Microarray,Homo sapiens,6|4,"EFO:An actinic keratosis (ak-TIN-ik ker-uh-TOE-sis) is a rough, scaly patch on your skin that develops from years of exposure to the sun. It's most commonly found on your face, lips, ears, back of your hands, forearms, scalp or neck. Also known as solar keratosis, an actinic keratosis enlarges slowly and usually causes no signs or symptoms other than a patch or small spot on your skin. These lesions take years to develop, usually first appearing in older adults. A small percentage of actinic keratosis lesions can eventually become skin cancer. You can reduce your risk of actinic keratosis by minimizing your sun exposure and protecting your skin from ultraviolet (UV) rays." DSA02266,GSE2503,GPL96,224,Squamous Cell Carcinoma,C0007137,Skin,GEO,Microarray,Homo sapiens,6|5,DO:A carcinoma that derives_from squamous epithelial cells. DSA02267,GSE1988,GPL339,1,Cardiac Dysfunction,C0747102,Heart,GEO,Microarray,Mus musculus,4|3,EFO:The inability of the ovaries to function. DSA02268,GSE13355,GPL570,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,64|58,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA02269,GSE13355,GPL570,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,58|58,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA02270,GSE3189,GPL96,1000,Melanoma,C0025202,Skin,GEO,Microarray,Homo sapiens,7|45,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA02271,GSE3889,GPL1261,1000,Hypercholesterolemia,C0020443,Liver,GEO,Microarray,Mus musculus,5|5,HPO:An increased concentration of cholesterol in the blood. DSA02272,GSE703,GPL80,97,Pulmonary Arterial Hypertension,C2973725,,GEO,Microarray,Homo sapiens,6|14,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA02273,GSE2127,GPL339,4,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Mus musculus,3|3,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA02274,GSE2127,GPL339,10,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Mus musculus,3|3,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA02275,GSE6054,GPL570,32,Familial Hypercholesterolemia,C0020445,,GEO,Microarray,Homo sapiens,13|6,DO:A familial hyperlipidemia characterized by very high levels of low-density lipoprotein (LDL) and early cardiovascular disease. DSA02276,GSE6054,GPL570,11,Familial Hypercholesterolemia,C0020445,,GEO,Microarray,Homo sapiens,13|4,DO:A familial hyperlipidemia characterized by very high levels of low-density lipoprotein (LDL) and early cardiovascular disease. DSA02277,GSE15573,GPL6102,839,Rheumatoid Arthritis,C0003873,Blood,GEO,Microarray,Homo sapiens,15|18,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA02278,GSE16715,GPL570,964,Williams-Beuren Syndrome,C0175702,Skin,GEO,Microarray,Homo sapiens,9|8,"DO:A syndrome that is characterized by mild to moderate intellectual disability, a broad forehead, a short nose with a broad tip, full cheeks, and a wide mouth with full lips and difficulty with visual-spatial tasks and has_material_basis_in hemizygous deletion of 1.5 to 1.8 Mb on chromosome 7q11.23." DSA02279,GSE4390,GPL81,1,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,Microarray,Mus musculus,2|2,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA02280,GSE867,GPL81,7,Autoimmune Hepatitis,C4721555,Liver,GEO,Microarray,Mus musculus,4|4,DO:An autoimmune disease of gastrointestinal tract that results_in inflammation located_in liver caused by the body's immune system attacking the liver cells. DSA02281,GSE1472,GPL32,1000,Duchenne Muscular Dystrophy,C0013264,Muscle,GEO,Microarray,Mus musculus,5|5,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02282,GSE1472,GPL32,699,Duchenne Muscular Dystrophy,C0013264,Extraocular muscle,GEO,Microarray,Mus musculus,5|5,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02283,GSE5788,GPL96,916,T-Cell Prolymphocytic Leukemia,C2363142,Peripheral blood,GEO,Microarray,Homo sapiens,8|6,EFO:A slow-growing type of leukemia (blood cancer) in which too many lymphocytes are found in the bone marrow and/or blood. The T-cell is specified as the defective cell line. DSA02284,E-MTAB-11919,,6,Systemic Lupus Erythematosus,C0024141,Blood,ArrayExpress,RNA-Seq,Homo sapiens,5|5,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02285,E-MTAB-1197,,1000,Poikiloderma With Neutropenia,C1858723,,ArrayExpress,RNA-Seq,Homo sapiens,1|1,"DO:A skin disease characterized by poikiloderma, hyperkeratotic nails, generalized hyperkeratosis on palms and soles, neutropenia, short stature, and recurrent pulmonary infections and has_material_basis_in mutation in the C16ORF57 gene on chromosome 16q13." DSA02286,GSE53659,GPL1261,1000,Pancreatic Tumor,C0030297,,GEO,Microarray,Mus musculus,5|6,DO:An endocrine gland cancer located_in the pancreas. DSA02287,GSE10325,GPL96,0,Systemic Lupus Erythematosus,C0024141,Peripheral blood,GEO,Microarray,Homo sapiens,9|14,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02288,GSE10325,GPL96,1,Systemic Lupus Erythematosus,C0024141,Peripheral blood,GEO,Microarray,Homo sapiens,9|14,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02289,GSE10325,GPL96,0,Systemic Lupus Erythematosus,C0024141,Peripheral blood,GEO,Microarray,Homo sapiens,10|11,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02290,E-MTAB-1197,,1000,Poikiloderma With Neutropenia,C1858723,,ArrayExpress,RNA-Seq,Homo sapiens,1|1,"DO:A skin disease characterized by poikiloderma, hyperkeratotic nails, generalized hyperkeratosis on palms and soles, neutropenia, short stature, and recurrent pulmonary infections and has_material_basis_in mutation in the C16ORF57 gene on chromosome 16q13." DSA02291,GSE18670,GPL570,1000,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,Microarray,Homo sapiens,6|6,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA02292,GSE18670,GPL570,1000,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,Microarray,Homo sapiens,6|6,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA02293,GSE18670,GPL570,19,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,Microarray,Homo sapiens,6|6,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA02294,GSE9452,GPL570,1000,Ulcerative Colitis,C0009324,Descending colon,GEO,Microarray,Homo sapiens,3|8,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02295,GSE9452,GPL570,10,Ulcerative Colitis,C0009324,Descending colon,GEO,Microarray,Homo sapiens,3|9,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02296,GSE9452,GPL570,0,Ulcerative Colitis,C0009324,Sigmoideum,GEO,Microarray,Homo sapiens,2|3,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02297,GSE1481,GPL96,0,Lethal Congenital Contracture Syndrome,C1854664,Spinal cord,GEO,Microarray,Homo sapiens,2|3,DO:A lethal congenital contracture syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the mRNA export mediator GLE1 on chromosome 9q34. DSA02298,GSE14905,GPL570,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,21|33,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA02299,GSE14905,GPL570,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,28|33,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA02300,GSE16464,GPL570,0,Osteoarthritis,C0157946,,GEO,Microarray,Homo sapiens,3|3,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA02301,GSE16464,GPL570,0,Osteoarthritis,C0157946,,GEO,Microarray,Homo sapiens,3|3,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA02302,GSE18965,GPL96,1000,Atopic Asthma,C0004096,,GEO,Microarray,Homo sapiens,7|9,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02303,GSE11886,GPL570,0,Ankylosing Spondylitis,C0038013,Peripheral blood,GEO,Microarray,Homo sapiens,9|7,"DO:A bone inflammation disease that results_in inflammation in the joints of the spine and pelvis. The disease has_symptom pain, has_symptom stiffness in the spine, has_symptom stiffness in the neck, has_symptom stiffness in the hips, has_symptom stiffness in the jaw and has_symptom stiffness in the rib cage." DSA02304,GSE11886,GPL570,0,Ankylosing Spondylitis,C0038013,Peripheral blood,GEO,Microarray,Homo sapiens,9|8,"DO:A bone inflammation disease that results_in inflammation in the joints of the spine and pelvis. The disease has_symptom pain, has_symptom stiffness in the spine, has_symptom stiffness in the neck, has_symptom stiffness in the hips, has_symptom stiffness in the jaw and has_symptom stiffness in the rib cage." DSA02305,GSE2899,GPL81,0,Type 2 Diabetes,C0011860,Adipose tissue,GEO,Microarray,Mus musculus,2|2,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA02306,GSE2899,GPL81,0,Type 2 Diabetes,C0011860,Liver,GEO,Microarray,Mus musculus,2|2,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA02307,GSE2899,GPL81,0,Type 2 Diabetes,C0011860,Soleus,GEO,Microarray,Mus musculus,2|2,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA02308,GSE2899,GPL81,0,Type 2 Diabetes,C0011860,Pancreatic islet,GEO,Microarray,Mus musculus,2|2,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA02309,GSE3744,GPL570,1000,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,7|40,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02310,GSE3384,GPL81,2,Nemaline Myopathy,C0206157,Diaphragm muscle,GEO,Microarray,Mus musculus,4|4,"DO:A congenital muscular dystrophy characterized by muscle weakness, cognitive impairment and brain abnormalities and has_material_basis_in mutation to the POMT1 gene that encodes O-mannosyltransferase." DSA02311,GSE3384,GPL81,0,Nemaline Myopathy,C0206157,Muscle,GEO,Microarray,Mus musculus,3|3,"DO:A congenital muscular dystrophy characterized by muscle weakness, cognitive impairment and brain abnormalities and has_material_basis_in mutation to the POMT1 gene that encodes O-mannosyltransferase." DSA02312,GSE3384,GPL81,0,Nemaline Myopathy,C0206157,Gastrocnemius muscle,GEO,Microarray,Mus musculus,4|4,"DO:A congenital muscular dystrophy characterized by muscle weakness, cognitive impairment and brain abnormalities and has_material_basis_in mutation to the POMT1 gene that encodes O-mannosyltransferase." DSA02313,GSE3384,GPL81,0,Nemaline Myopathy,C0206157,Plantaris muscle,GEO,Microarray,Mus musculus,3|3,"DO:A congenital muscular dystrophy characterized by muscle weakness, cognitive impairment and brain abnormalities and has_material_basis_in mutation to the POMT1 gene that encodes O-mannosyltransferase." DSA02314,GSE3384,GPL81,2,Nemaline Myopathy,C0206157,Tibialis anterior,GEO,Microarray,Mus musculus,4|4,"DO:A congenital muscular dystrophy characterized by muscle weakness, cognitive impairment and brain abnormalities and has_material_basis_in mutation to the POMT1 gene that encodes O-mannosyltransferase." DSA02315,GSE35182,GPL6246,1000,Myocarditis,C0027059,Heart,GEO,Microarray,Mus musculus,6|6,DO:An extrinsic cardiomyopathy that is characterized as an inflammation of the heart muscle. DSA02316,GSE35182,GPL6246,8,Myocarditis,C0027059,Heart,GEO,Microarray,Mus musculus,6|6,DO:An extrinsic cardiomyopathy that is characterized as an inflammation of the heart muscle. DSA02317,GSE2254,GPL81,0,Type 1 Diabetes,C0011854,Pancreatic islet,GEO,Microarray,Mus musculus,8|4,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA02318,GSE2254,GPL81,0,Type 1 Diabetes,C0011854,Pancreatic islet,GEO,Microarray,Mus musculus,8|3,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA02319,GSE2254,GPL81,1,Type 1 Diabetes,C0011854,Pancreatic islet,GEO,Microarray,Mus musculus,8|3,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA02320,GSE2866,GPL81,0,Succinic Semialdehyde Dehydrogenase Deficiency,C0268631,Brain,GEO,Microarray,Mus musculus,7|7,DO:A gamma-amino butyric acid metabolism disorder that is characterized by a deficiency of succinic semialdehyde dehydrogenase resulting in elevated levels of gamma-hydroxybutyric acid. DSA02321,GSE2866,GPL81,0,Succinic Semialdehyde Dehydrogenase Deficiency,C0268631,Brain,GEO,Microarray,Mus musculus,3|3,DO:A gamma-amino butyric acid metabolism disorder that is characterized by a deficiency of succinic semialdehyde dehydrogenase resulting in elevated levels of gamma-hydroxybutyric acid. DSA02322,GSE2866,GPL81,1,Succinic Semialdehyde Dehydrogenase Deficiency,C0268631,Brain,GEO,Microarray,Mus musculus,3|3,DO:A gamma-amino butyric acid metabolism disorder that is characterized by a deficiency of succinic semialdehyde dehydrogenase resulting in elevated levels of gamma-hydroxybutyric acid. DSA02323,GSE2685,GPL80,1000,Gastric Cancer,C0699791,,GEO,Microarray,Homo sapiens,8|22,DO:A gastrointestinal system cancer that is located_in the stomach. DSA02324,GSE2549,GPL96,1000,Malignant Pleural Mesothelioma,C0812413,,GEO,Microarray,Homo sapiens,5|40,DO:A pleural cancer that has_material_basis_in mesothelium cells. DSA02325,GSE422,GPL81,427,Adenomatous Polyposis Coli,C0032580,,GEO,Microarray,Mus musculus,6|5,DO:An intestinal disease that has_material_basis_in mutations in the APC gene and involves formation of numerous polyps in the epithelium of the large intestine which are initially benign and later transform into colon cancer. DSA02326,GSE422,GPL81,539,Adenomatous Polyposis Coli,C0032580,,GEO,Microarray,Mus musculus,6|5,DO:An intestinal disease that has_material_basis_in mutations in the APC gene and involves formation of numerous polyps in the epithelium of the large intestine which are initially benign and later transform into colon cancer. DSA02327,GSE1919,GPL91,160,Osteoarthritis,C0157946,Synovium,GEO,Microarray,Homo sapiens,5|5,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA02328,GSE1919,GPL91,450,Rheumatoid Arthritis,C0003873,Synovium,GEO,Microarray,Homo sapiens,5|5,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA02329,GSE2191,GPL8300,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,Microarray,Homo sapiens,4|54,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA02330,E-MTAB-12014,,1000,Breast Cancer,C0678222,Breast,ArrayExpress,RNA-Seq,Homo sapiens,10|10,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02331,GSE10064,GPL2895,0,Multiple Sclerosis,C0026769,,GEO,Microarray,Homo sapiens,4|6,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA02332,GSE21521,GPL570,0,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,29|25,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA02333,GSE21521,GPL570,41,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,29|28,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA02334,GSE21521,GPL570,1,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,29|30,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA02335,GSE21521,GPL570,1000,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,29|18,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA02336,GSE21521,GPL570,349,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,29|15,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA02337,GSE6364,GPL570,1,Endometriosis,C0014175,Uterus,GEO,Microarray,Homo sapiens,5|6,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA02338,GSE6364,GPL570,28,Endometriosis,C0014175,Uterus,GEO,Microarray,Homo sapiens,3|6,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA02339,GSE6364,GPL570,1,Endometriosis,C0014175,Uterus,GEO,Microarray,Homo sapiens,8|9,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA02340,GSE6955,GPL8300,0,Rett Syndrome,C0035372,Superior frontal gyrus,GEO,Microarray,Homo sapiens,3|3,"DO:A pervasive developmental disease that is characterized by normal early growth and development followed by a slowing of development, loss of purposeful use of the hands, distinctive hand movements, slowed brain and head growth, problems with walking, seizures, and intellectual disability." DSA02341,GSE34619,GPL6244,1000,Barrett's Esophagus,C0004763,Esophagus,GEO,Microarray,Homo sapiens,8|10,DO:An esophageal disease characterized by a change of normal esophageal squamous epithelium to a columnar and intestinal-type epithelium. DSA02342,GSE19650,GPL570,1000,Pancreatic Intraductal Papillary-Mucinous Adenoma,C1518868,Pancreas,GEO,Microarray,Homo sapiens,7|6,"MONDO:A non-invasive pancreatic intraductal papillary mucinous neoplasm characterized by the presence of neoplastic epithelial cells that form a single layer and are well polarized. The neoplastic cells exhibit small and uniform nuclei, mild pleomorphism, and rare mitotic figures." DSA02343,GSE19650,GPL570,1000,Intraductal Papillary Adenocarcinoma,C0334372,Pancreas,GEO,Microarray,Homo sapiens,7|6,NCI:Breast ductal carcinoma in situ characterized by the presence of filiform arborizing fibrovascular cores lined by neoplastic ductal epithelium. (WHO 2019) DSA02344,GSE19650,GPL570,1000,Pancreatic Intraductal Papillary-Mucinous Neoplasm,C4511687,Pancreas,GEO,Microarray,Homo sapiens,7|3,DO:A pancreatic cancer that is characterized as a slow-growing epithelial neoplasm with ductal differentiation that arises from the exocrine pancreas and grows mostly within the pancreatic ducts. DSA02345,GSE4757,GPL570,0,Alzheimer's Disease,C0002395,Brain,GEO,Microarray,Homo sapiens,10|10,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA02346,GSE19429,GPL570,1000,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,17|183,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA02347,GSE935,GPL8300,0,X-Linked Chronic Granulomatous Disease,C1844376,,GEO,Microarray,Homo sapiens,4|5,DO:A chronic granulomatous disease characterized by X-linked inheritance that has_material_basis_in mutation in the CYBB gene on chromosome Xp21.1-p11.4. DSA02348,GSE935,GPL8300,0,X-Linked Chronic Granulomatous Disease,C1844376,,GEO,Microarray,Homo sapiens,4|4,DO:A chronic granulomatous disease characterized by X-linked inheritance that has_material_basis_in mutation in the CYBB gene on chromosome Xp21.1-p11.4. DSA02349,GSE935,GPL8300,0,X-Linked Chronic Granulomatous Disease,C1844376,,GEO,Microarray,Homo sapiens,4|4,DO:A chronic granulomatous disease characterized by X-linked inheritance that has_material_basis_in mutation in the CYBB gene on chromosome Xp21.1-p11.4. DSA02350,GSE935,GPL8300,0,X-Linked Chronic Granulomatous Disease,C1844376,,GEO,Microarray,Homo sapiens,4|5,DO:A chronic granulomatous disease characterized by X-linked inheritance that has_material_basis_in mutation in the CYBB gene on chromosome Xp21.1-p11.4. DSA02351,GSE935,GPL8300,0,X-Linked Chronic Granulomatous Disease,C1844376,,GEO,Microarray,Homo sapiens,4|5,DO:A chronic granulomatous disease characterized by X-linked inheritance that has_material_basis_in mutation in the CYBB gene on chromosome Xp21.1-p11.4. DSA02352,GSE935,GPL8300,0,X-Linked Chronic Granulomatous Disease,C1844376,,GEO,Microarray,Homo sapiens,4|6,DO:A chronic granulomatous disease characterized by X-linked inheritance that has_material_basis_in mutation in the CYBB gene on chromosome Xp21.1-p11.4. DSA02353,GSE935,GPL8300,0,X-Linked Chronic Granulomatous Disease,C1844376,,GEO,Microarray,Homo sapiens,4|6,DO:A chronic granulomatous disease characterized by X-linked inheritance that has_material_basis_in mutation in the CYBB gene on chromosome Xp21.1-p11.4. DSA02354,GSE12610,GPL1261,0,Diabetes,C0011847,Retina,GEO,Microarray,Mus musculus,2|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA02355,GSE3004,GPL8300,2,Allergic Asthma,C0155877,Bronchial epithelium,GEO,Microarray,Homo sapiens,5|5,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02356,GSE5388,GPL96,0,Bipolar Disorder,C0005586,Brain,GEO,Microarray,Homo sapiens,31|30,DO:A mood disorder that involves alternating periods of mania and depression. DSA02357,GSE1611,GPL81,0,Down Syndrome,C0013080,Cerebellum,GEO,Microarray,Mus musculus,2|2,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA02358,GSE1611,GPL81,0,Down Syndrome,C0013080,Cerebellum,GEO,Microarray,Mus musculus,2|2,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA02359,GSE1611,GPL81,0,Down Syndrome,C0013080,Cerebellum,GEO,Microarray,Mus musculus,2|2,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA02360,GSE1462,GPL96,0,Mitochondrial Encephalomyopathies,C0162666,Skeletal muscle,GEO,Microarray,Homo sapiens,3|4,"MONDO:A heterogenous group of disorders characterized by alterations of mitochondrial metabolism that result in muscle and nervous system dysfunction. These are often multisystemic and vary considerably in age at onset (usually in the first or second decade of life), distribution of affected muscles, severity, and course. (From Adams et al., Principles of Neurology, 6th ed, pp984-5)" DSA02361,GSE1462,GPL96,2,Mitochondrial Encephalomyopathies,C0162666,Skeletal muscle,GEO,Microarray,Homo sapiens,3|4,"MONDO:A heterogenous group of disorders characterized by alterations of mitochondrial metabolism that result in muscle and nervous system dysfunction. These are often multisystemic and vary considerably in age at onset (usually in the first or second decade of life), distribution of affected muscles, severity, and course. (From Adams et al., Principles of Neurology, 6th ed, pp984-5)" DSA02362,GSE1462,GPL96,0,Mitochondrial Encephalomyopathies,C0162666,Skeletal muscle,GEO,Microarray,Homo sapiens,3|4,"MONDO:A heterogenous group of disorders characterized by alterations of mitochondrial metabolism that result in muscle and nervous system dysfunction. These are often multisystemic and vary considerably in age at onset (usually in the first or second decade of life), distribution of affected muscles, severity, and course. (From Adams et al., Principles of Neurology, 6th ed, pp984-5)" DSA02363,GSE13083,GPL96,1000,Barrett's Esophagus,C0004763,Esophagus,GEO,Microarray,Homo sapiens,7|7,DO:An esophageal disease characterized by a change of normal esophageal squamous epithelium to a columnar and intestinal-type epithelium. DSA02364,GSE9877,GPL96,1000,Sickle Cell Disease,C0002895,,GEO,Microarray,Homo sapiens,27|9,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA02365,GSE9877,GPL96,1000,Sickle Cell Disease,C0002895,,GEO,Microarray,Homo sapiens,27|11,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA02366,GSE48964,GPL6244,2,Obesity,C0028754,Subcutaneous white adipose tissue,GEO,Microarray,Homo sapiens,3|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA02367,GSE4697,GPL2995,1,Obesity,C0028754,Hypothalamus,GEO,Microarray,Mus musculus,4|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA02368,GSE1987,GPL91,592,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Homo sapiens,9|7,DO:A respiratory system cancer that is located_in the lung. DSA02369,GSE1987,GPL91,659,Lung Squamous Cell Carcinoma,C0149782,Lung,GEO,Microarray,Homo sapiens,9|17,DO:A non-small cell lung carcinoma that has_material_basis_in the squamous cell. DSA02370,GSE1402,GPL8300,1000,Juvenile Spondyloarthropathy,C0409676,,GEO,Microarray,Homo sapiens,11|5,"MONDO:A group of chronic, inflammatory childhood diseases characterized by arthritis and enthesitis. This disorder can affect the axial skeleton in late childhood or young adulthood." DSA02371,GSE1402,GPL8300,4,Juvenile Spondyloarthropathy,C0409676,,GEO,Microarray,Homo sapiens,11|6,"MONDO:A group of chronic, inflammatory childhood diseases characterized by arthritis and enthesitis. This disorder can affect the axial skeleton in late childhood or young adulthood." DSA02372,GSE1402,GPL8300,0,Juvenile Rheumatoid Arthritis,C3714757,,GEO,Microarray,Homo sapiens,11|5,"EFO:Juvenile idiopathic arthritis (JIA), also known as juvenile rheumatoid arthritis (JRA), is the most common form of arthritis in children and adolescents. (Juvenile in this context refers to an onset before age 16, idiopathic refers to a condition with no defined cause, and arthritis is the inflammation of the synovium of a joint.) JIA is an autoimmune, non-infective, inflammatory joint disease of more than 6 weeks duration in children less than 16 years of age. The disease commonly occurs in children from the ages of 7 to 12, but it may occur in adolescents as old as 15 years of age, as well as in infants. It is a subset of arthritis seen in childhood, which may be transient and self-limited or chronic. It differs significantly from arthritis commonly seen in adults (osteoarthritis, rheumatoid arthritis), and other types of arthritis that can present in childhood which are chronic conditions (e.g. psoriatic arthritis and ankylosing spondylitis). Aetiopathology is similar to rheumatoid arthritis but with less marked cartilage erosion, and joint instability and absent rheumatoid factor. JIA affects approximately 1 in 1,000 children in any given year, with about 1 in 10,000 having a more severe form." DSA02373,GSE1402,GPL8300,1000,Juvenile Rheumatoid Arthritis,C3714757,,GEO,Microarray,Homo sapiens,11|5,"EFO:Juvenile idiopathic arthritis (JIA), also known as juvenile rheumatoid arthritis (JRA), is the most common form of arthritis in children and adolescents. (Juvenile in this context refers to an onset before age 16, idiopathic refers to a condition with no defined cause, and arthritis is the inflammation of the synovium of a joint.) JIA is an autoimmune, non-infective, inflammatory joint disease of more than 6 weeks duration in children less than 16 years of age. The disease commonly occurs in children from the ages of 7 to 12, but it may occur in adolescents as old as 15 years of age, as well as in infants. It is a subset of arthritis seen in childhood, which may be transient and self-limited or chronic. It differs significantly from arthritis commonly seen in adults (osteoarthritis, rheumatoid arthritis), and other types of arthritis that can present in childhood which are chronic conditions (e.g. psoriatic arthritis and ankylosing spondylitis). Aetiopathology is similar to rheumatoid arthritis but with less marked cartilage erosion, and joint instability and absent rheumatoid factor. JIA affects approximately 1 in 1,000 children in any given year, with about 1 in 10,000 having a more severe form." DSA02374,GSE1402,GPL8300,1000,Juvenile Rheumatoid Arthritis,C3714757,,GEO,Microarray,Homo sapiens,11|15,"EFO:Juvenile idiopathic arthritis (JIA), also known as juvenile rheumatoid arthritis (JRA), is the most common form of arthritis in children and adolescents. (Juvenile in this context refers to an onset before age 16, idiopathic refers to a condition with no defined cause, and arthritis is the inflammation of the synovium of a joint.) JIA is an autoimmune, non-infective, inflammatory joint disease of more than 6 weeks duration in children less than 16 years of age. The disease commonly occurs in children from the ages of 7 to 12, but it may occur in adolescents as old as 15 years of age, as well as in infants. It is a subset of arthritis seen in childhood, which may be transient and self-limited or chronic. It differs significantly from arthritis commonly seen in adults (osteoarthritis, rheumatoid arthritis), and other types of arthritis that can present in childhood which are chronic conditions (e.g. psoriatic arthritis and ankylosing spondylitis). Aetiopathology is similar to rheumatoid arthritis but with less marked cartilage erosion, and joint instability and absent rheumatoid factor. JIA affects approximately 1 in 1,000 children in any given year, with about 1 in 10,000 having a more severe form." DSA02375,GSE1402,GPL8300,1000,Juvenile Rheumatoid Arthritis,C3714757,,GEO,Microarray,Homo sapiens,11|10,"EFO:Juvenile idiopathic arthritis (JIA), also known as juvenile rheumatoid arthritis (JRA), is the most common form of arthritis in children and adolescents. (Juvenile in this context refers to an onset before age 16, idiopathic refers to a condition with no defined cause, and arthritis is the inflammation of the synovium of a joint.) JIA is an autoimmune, non-infective, inflammatory joint disease of more than 6 weeks duration in children less than 16 years of age. The disease commonly occurs in children from the ages of 7 to 12, but it may occur in adolescents as old as 15 years of age, as well as in infants. It is a subset of arthritis seen in childhood, which may be transient and self-limited or chronic. It differs significantly from arthritis commonly seen in adults (osteoarthritis, rheumatoid arthritis), and other types of arthritis that can present in childhood which are chronic conditions (e.g. psoriatic arthritis and ankylosing spondylitis). Aetiopathology is similar to rheumatoid arthritis but with less marked cartilage erosion, and joint instability and absent rheumatoid factor. JIA affects approximately 1 in 1,000 children in any given year, with about 1 in 10,000 having a more severe form." DSA02376,GSE5500,GPL1261,94,Heart Failure,C0018801,,GEO,Microarray,Mus musculus,4|6,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA02377,GSE5500,GPL1261,148,Heart Failure,C0018801,,GEO,Microarray,Mus musculus,5|6,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA02378,GSE11343,GPL1261,0,Diabetes,C0011847,Sciatic nerve,GEO,Microarray,Mus musculus,4|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA02379,GSE11343,GPL1261,0,Diabetes,C0011847,Sciatic nerve,GEO,Microarray,Mus musculus,5|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA02380,GSE50892,GPL6244,1000,Liver Cirrhosis,C0023890,Kidney,GEO,Microarray,Homo sapiens,9|8,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA02381,GSE1009,GPL8300,72,Diabetic Kidney Disease,C0011881,Kidney,GEO,Microarray,Homo sapiens,3|3,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA02382,GSE7305,GPL570,1000,Endometriosis,C0014175,Endometrium,GEO,Microarray,Homo sapiens,10|10,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA02383,GSE12654,GPL8300,0,Schizophrenia,C0036341,Prefrontal cortex,GEO,Microarray,Homo sapiens,15|13,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA02384,GSE12654,GPL8300,0,Bipolar Disorder,C0005586,Prefrontal cortex,GEO,Microarray,Homo sapiens,15|11,DO:A mood disorder that involves alternating periods of mania and depression. DSA02385,GSE12654,GPL8300,0,Mental Depression,C0011570,Prefrontal cortex,GEO,Microarray,Homo sapiens,15|11,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA02386,GSE2724,GPL96,443,Uterine Fibroid,C0042133,Myometrium,GEO,Microarray,Homo sapiens,11|7,DO:An uterine benign neoplasm derived from the smooth muscle layer of the uterus. DSA02387,GSE10500,GPL8300,1000,Rheumatoid Arthritis,C0003873,Synovial fluid,GEO,Microarray,Homo sapiens,3|5,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA02388,GSE1025,GPL81,0,Duchenne Muscular Dystrophy,C0013264,Hindlimb muscle,GEO,Microarray,Mus musculus,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02389,GSE1025,GPL81,0,Duchenne Muscular Dystrophy,C0013264,Hindlimb muscle,GEO,Microarray,Mus musculus,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02390,GSE1025,GPL81,70,Duchenne Muscular Dystrophy,C0013264,Hindlimb muscle,GEO,Microarray,Mus musculus,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02391,GSE1025,GPL81,22,Duchenne Muscular Dystrophy,C0013264,Hindlimb muscle,GEO,Microarray,Mus musculus,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02392,GSE1025,GPL81,400,Duchenne Muscular Dystrophy,C0013264,Hindlimb muscle,GEO,Microarray,Mus musculus,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02393,GSE1025,GPL81,20,Duchenne Muscular Dystrophy,C0013264,Hindlimb muscle,GEO,Microarray,Mus musculus,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02394,GSE7753,GPL570,1000,Systemic Juvenile Idiopathic Arthritis,C1384600,,GEO,Microarray,Homo sapiens,30|17,"EFO:Juvenile idiopathic arthritis (JIA), also known as juvenile rheumatoid arthritis (JRA), is the most common form of arthritis in children and adolescents. (Juvenile in this context refers to an onset before age 16, idiopathic refers to a condition with no defined cause, and arthritis is the inflammation of the synovium of a joint.) JIA is an autoimmune, non-infective, inflammatory joint disease of more than 6 weeks duration in children less than 16 years of age. The disease commonly occurs in children from the ages of 7 to 12, but it may occur in adolescents as old as 15 years of age, as well as in infants. It is a subset of arthritis seen in childhood, which may be transient and self-limited or chronic. It differs significantly from arthritis commonly seen in adults (osteoarthritis, rheumatoid arthritis), and other types of arthritis that can present in childhood which are chronic conditions (e.g. psoriatic arthritis and ankylosing spondylitis). Aetiopathology is similar to rheumatoid arthritis but with less marked cartilage erosion, and joint instability and absent rheumatoid factor. JIA affects approximately 1 in 1,000 children in any given year, with about 1 in 10,000 having a more severe form." DSA02395,GSE1629,GPL96,1000,Caries,C0011334,Dental pulp,GEO,Microarray,Homo sapiens,2|2,"DO:A teeth hard tissue disease that is characterized by damage to a tooth that can happen when decay-causing bacteria in your mouth make acids that attack the tooth鈥檚 surface, or enamel." DSA02396,GSE8607,GPL8300,1000,Testicular Seminoma,C0036631,Testis,GEO,Microarray,Homo sapiens,3|22,DO:A germinoma that has_material_basis_in cells that make sperm and eggs. DSA02397,GSE8607,GPL8300,1000,Testicular Seminoma,C0036631,Testis,GEO,Microarray,Homo sapiens,3|14,DO:A germinoma that has_material_basis_in cells that make sperm and eggs. DSA02398,GSE8607,GPL8300,1000,Testicular Seminoma,C0036631,Testis,GEO,Microarray,Homo sapiens,3|4,DO:A germinoma that has_material_basis_in cells that make sperm and eggs. DSA02399,GSE3467,GPL570,1000,Papillary Thyroid Carcinoma,C0238463,Thyroid,GEO,Microarray,Homo sapiens,9|9,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA02400,GSE3621,GPL1261,1,Huntington's Disease,C0020179,Brain,GEO,Microarray,Mus musculus,3|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA02401,GSE3621,GPL1261,0,Huntington's Disease,C0020179,Brain,GEO,Microarray,Mus musculus,3|2,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA02402,GSE3621,GPL1261,20,Huntington's Disease,C0020179,Brain,GEO,Microarray,Mus musculus,3|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA02403,GSE7621,GPL570,0,Parkinson's Disease,C0030567,Substantia nigra,GEO,Microarray,Homo sapiens,9|16,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA02404,E-MTAB-12184,,1000,Osteoarthritis,C0157946,Knee,ArrayExpress,RNA-Seq,Homo sapiens,6|6,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA02405,GSE52471,GPL571,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,13|18,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA02406,GSE52471,GPL571,1000,Discoid Lupus Rash,C0024138,Skin,GEO,Microarray,Homo sapiens,13|7,"DO:An autoimmune disease that is characterized by a constellation of findings that include elevated antibodies to nuclear antigens, antiphospholipids, low complement levels, ulcers, non-scarring alopecia, renal or neurologic damage, and low white blood cell and platelet counts, has_symptom rashes, fatigue, arthritis, hair loss, seizures, and symptoms related to affected organs." DSA02407,GSE833,GPL80,15,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,Microarray,Homo sapiens,4|5,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA02408,GSE833,GPL80,105,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,Microarray,Homo sapiens,4|2,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA02409,GSE55945,GPL570,1000,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,8|13,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02410,GSE15568,GPL96,18,Cystic Fibrosis,C0010674,Rectal mucosa,GEO,Microarray,Homo sapiens,13|16,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA02411,GSE39791,GPL10558,1000,Hepatocellular Carcinoma,C0334287,,GEO,Microarray,Homo sapiens,72|72,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA02412,GSE1739,GPL201,134,Severe Acute Respiratory Syndrome,C1175175,Blood,GEO,Microarray,Homo sapiens,4|10,"DO:A Coronavirus infection that results_in infection located_in respiratory tract, has_material_basis_in SARS coronavirus (SARS-CoV), which is transmitted_by droplet spread of respiratory secretions, transmitted_by ingestion of contaminated food, or transmitted_by fomites. The infection has_symptom fever, has_symptom headache, has_symptom body aches, has_symptom dry cough, and has_symptom hypoxia." DSA02413,GSE1420,GPL96,260,Barrett's Esophagus,C0004763,Esophageal epithelium,GEO,Microarray,Homo sapiens,8|8,DO:An esophageal disease characterized by a change of normal esophageal squamous epithelium to a columnar and intestinal-type epithelium. DSA02414,GSE1420,GPL96,1000,Esophageal Adenocarcinoma,C0279628,Esophageal epithelium,GEO,Microarray,Homo sapiens,8|8,DO:An esophageal carcinoma that derives_from epithelial cells of glandular origin. DSA02415,GSE6614,GPL81,0,Seizure,C0036572,Brain,GEO,Microarray,Mus musculus,6|3,HPO:A seizure is an intermittent abnormality of nervous system physiology characterised by a transient occurrence of signs and/or symptoms due to abnormal excessive or synchronous neuronal activity in the brain. DSA02416,GSE6614,GPL81,3,Seizure,C0036572,Brain,GEO,Microarray,Mus musculus,5|5,HPO:A seizure is an intermittent abnormality of nervous system physiology characterised by a transient occurrence of signs and/or symptoms due to abnormal excessive or synchronous neuronal activity in the brain. DSA02417,GSE6614,GPL81,1,Seizure,C0036572,Brain,GEO,Microarray,Mus musculus,5|4,HPO:A seizure is an intermittent abnormality of nervous system physiology characterised by a transient occurrence of signs and/or symptoms due to abnormal excessive or synchronous neuronal activity in the brain. DSA02418,GSE769,GPL81,0,Cystic Fibrosis,C0010674,Pancreas,GEO,Microarray,Mus musculus,3|3,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA02419,GSE47516,GPL1261,6,Progressive Myoclonus Epilepsy,C0751778,Cerebellum,GEO,Microarray,Mus musculus,4|4,DO:An autosomal dominant cerebellar ataxia that has_material_basis_in expansion of CAG triplet repeats (glutamine) encoding a polyglutamine tract in the atrophin-1 protein. DSA02420,GSE47516,GPL1261,53,Progressive Myoclonus Epilepsy,C0751778,Cerebellum,GEO,Microarray,Mus musculus,3|3,DO:An autosomal dominant cerebellar ataxia that has_material_basis_in expansion of CAG triplet repeats (glutamine) encoding a polyglutamine tract in the atrophin-1 protein. DSA02421,GSE47516,GPL1261,1000,Progressive Myoclonus Epilepsy,C0751778,Cerebellum,GEO,Microarray,Mus musculus,4|3,DO:An autosomal dominant cerebellar ataxia that has_material_basis_in expansion of CAG triplet repeats (glutamine) encoding a polyglutamine tract in the atrophin-1 protein. DSA02422,GSE15090,GPL570,0,Facioscapulohumeral Muscular Dystrophy,C0238288,Biceps,GEO,Microarray,Homo sapiens,5|5,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA02423,GSE15090,GPL570,0,Facioscapulohumeral Muscular Dystrophy,C0238288,Biceps,GEO,Microarray,Homo sapiens,5|5,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA02424,GSE36820,GPL570,1000,Salivary Gland Adenoid Cystic Carcinoma,C0279751,Nasal cavity,GEO,Microarray,Homo sapiens,3|11,"MONDO:An adenoid cystic carcinoma arising from the salivary gland. It is characterized by the presence of epithelial and myoepithelial cells forming tubular, cribriform, and solid patterns. It usually presents as a slow growing mass. Patients may experience pain because of the tumor propensity for perineural invasion. The tumor may follow an aggressive clinical course with recurrences and mestastases to distant sites including lungs, bones, brain, and liver." DSA02425,GSE8762,GPL570,0,Huntington's Disease,C0020179,Blood,GEO,Microarray,Homo sapiens,10|12,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA02426,GSE574,GPL91,0,Idiopathic Thrombocytopenic Purpura,C0920163,,GEO,Microarray,Homo sapiens,2|2,HPO:The presence of thrombocytopenia in combination with detection of antiplatelet antibodies. DSA02427,GSE574,GPL91,0,Idiopathic Thrombocytopenic Purpura,C0920163,,GEO,Microarray,Homo sapiens,2|2,HPO:The presence of thrombocytopenia in combination with detection of antiplatelet antibodies. DSA02428,GSE6475,GPL571,475,Acne,C0702166,Skin,GEO,Microarray,Homo sapiens,6|6,"DO:A sebaceous gland disease characterized by areas of blackheads, whiteheads, pimples, greasy skin, and possibly scarring." DSA02429,GSE6475,GPL571,940,Acne,C0702166,Skin,GEO,Microarray,Homo sapiens,6|6,"DO:A sebaceous gland disease characterized by areas of blackheads, whiteheads, pimples, greasy skin, and possibly scarring." DSA02430,GSE6631,GPL8300,1000,Head And Neck Squamous Cell Carcinoma,C1168401,Mucosa,GEO,Microarray,Homo sapiens,22|22,"DO:A head and neck carcinoma that has_material_basis_in squamous cells that line the moist, mucosal surfaces inside the head and neck." DSA02431,GSE6575,GPL570,0,Autism Spectrum Disorder,C1510586,Whole blood,GEO,Microarray,Homo sapiens,12|17,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA02432,GSE6575,GPL570,0,Autism Spectrum Disorder,C1510586,Whole blood,GEO,Microarray,Homo sapiens,12|18,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA02433,GSE6575,GPL570,0,Intellectual Disability,C3714756,Whole blood,GEO,Microarray,Homo sapiens,12|9,"DO:A specific developmental disorder that involves significant limitations both in mental functioning and in adaptive behavior such as communicating, taking care of him or herself, and social skills." DSA02434,GSE2276,GPL81,45,Allergic Asthma,C0155877,Lung,GEO,Microarray,Mus musculus,3|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02435,GSE61304,GPL570,1000,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,4|56,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02436,GSE3252,GPL339,1,Congenital Merosin-Deficient Muscular Dystrophy 1A,C1263858,Muscle,GEO,Microarray,Mus musculus,4|4,DO:A congenital muscular dystrophy characterized by autosomal recessive inheritance of muscle weakness that is apparent at birth or in the first 6 months of life and frequent development of periventricular white matter abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the LAMA2 gene on chromosome 6q22. DSA02437,GSE1724,GPL8300,0,Idiopathic Fibrosing Alveolitis,C1800706,Lung,GEO,Microarray,Homo sapiens,3|3,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA02438,GSE1724,GPL8300,0,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,3|3,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA02439,GSE1724,GPL8300,0,Idiopathic Fibrosing Alveolitis,C1800706,Lung,GEO,Microarray,Homo sapiens,3|3,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA02440,GSE1724,GPL8300,0,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,3|3,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA02441,GSE4479,GPL1261,122,Sepsis,C0243026,,GEO,Microarray,Mus musculus,5|5,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA02442,GSE9038,GPL1261,19,Huntington's Disease,C0020179,Cerebellum,GEO,Microarray,Mus musculus,6|6,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA02443,GSE9038,GPL1261,165,Huntington's Disease,C0020179,Striatum,GEO,Microarray,Mus musculus,6|6,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA02444,GSE1751,GPL96,2,Huntington's Disease,C0020179,Blood,GEO,Microarray,Homo sapiens,14|5,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA02445,GSE1751,GPL96,1000,Huntington's Disease,C0020179,Blood,GEO,Microarray,Homo sapiens,14|12,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA02446,GSE1947,GPL81,11,Peripheral Neuropathy,C0031117,Sciatic nerve,GEO,Microarray,Mus musculus,3|3,DO:A nervous system disease that affects the peripheral nervous system. DSA02447,GSE1947,GPL81,0,Peripheral Neuropathy,C0031117,Sciatic nerve,GEO,Microarray,Mus musculus,3|3,DO:A nervous system disease that affects the peripheral nervous system. DSA02448,GSE1947,GPL81,73,Peripheral Neuropathy,C0031117,Sciatic nerve,GEO,Microarray,Mus musculus,3|2,DO:A nervous system disease that affects the peripheral nervous system. DSA02449,GSE1947,GPL81,117,Peripheral Neuropathy,C0031117,Sciatic nerve,GEO,Microarray,Mus musculus,3|2,DO:A nervous system disease that affects the peripheral nervous system. DSA02450,GSE16032,GPL570,786,Severe Asthma,C0004096,,GEO,Microarray,Homo sapiens,5|5,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02451,GSE510,GPL207,2,Peritonitis;Sepsis,,Spleen,GEO,Microarray,Mus musculus,3|3, DSA02452,GSE15824,GPL570,1000,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,5|12,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA02453,GSE15824,GPL570,1000,Astrocytoma,C0004114,Brain,GEO,Microarray,Homo sapiens,5|8,"DO:A malignant glioma that is has_material_basis_in astrocyte cells, a type of star-shaped glial cell, located in the brain and spinal cord." DSA02454,GSE15824,GPL570,696,Oligodendroglioma,C0028945,Brain,GEO,Microarray,Homo sapiens,5|7,"EFO:A well-differentiated (WHO grade II), diffusely infiltrating neuroglial tumor, typically located in the cerebral hemispheres. It is composed predominantly of cells which morphologically resemble oligodendroglia. The neoplastic cells have rounded homogeneous nuclei and, on paraffin sections, a swollen, clear cytoplasm ('honeycomb' appearance). (Adapted from WHO)" DSA02455,GSE15824,GPL570,38,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,5|3,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA02456,GSE17612,GPL570,0,Schizophrenia,C0036341,Brain,GEO,Microarray,Homo sapiens,23|28,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA02457,GSE32924,GPL570,1000,Atopic Dermatitis,C0011615,Skin,GEO,Microarray,Homo sapiens,8|13,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA02458,GSE32924,GPL570,0,Atopic Dermatitis,C0011615,Skin,GEO,Microarray,Homo sapiens,12|13,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA02459,GSE36314,GPL8300,75,Prolactinoma,C0033375,Placenta,GEO,Microarray,Homo sapiens,3|4,"EFO:Prolactinoma is a usually benign neoplasm of the pituitary gland that results in hyperprolactinemia. The most common clinical manifestations are amenorrhea and infertility in women; and impotence, decreased libido and infertility in men." DSA02460,GSE19314,GPL570,1000,Sarcoidosis,C0036202,Lung,GEO,Microarray,Homo sapiens,20|38,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA02461,GSE19314,GPL570,495,Hypersensitivity Pneumonitis,C0002390,Lung,GEO,Microarray,Homo sapiens,20|6,"DO:An interstitial lung disease involving inflammation of alveoli and smallest airways (bronchioles) of the lung caused by an allergic reaction to inhaled organic dusts containing microorganisms or proteins, and chemicals. Symptoms include chills, cough, fever, malaise, shortness of breath, loss of appetite and weight loss." DSA02462,GSE3325,GPL570,1000,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,6|7,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02463,GSE3325,GPL570,1000,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,6|6,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02464,GSE3325,GPL570,1000,Metastatic Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,7|6,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02465,E-MTAB-12205,,1000,Oral Squamous Cell Carcinoma,C0585362,Oral mucosa,ArrayExpress,RNA-Seq,Homo sapiens,7|9,"EFO:A squamous cell carcinoma arising from the oral cavity. It affects predominantly adults in their fifth and sixth decades of life and is associated with alcohol and tobacco use. Human papillomavirus is present in approximately half of the cases. It is characterized by a tendency to metastasize early to the lymph nodes. When the tumor is small, patients are often asymptomatic. Physical examination may reveal erythematous or white lesions or plaques. The majority of patients present with signs and symptoms of locally advanced disease including mucosal ulceration, pain, difficulty with speaking, chewing, and swallowing, bleeding, weight loss, and neck swelling. Patients may also present with swollen neck lymph nodes without any symptoms from the oropharyngeal tumor. The most significant prognostic factors are the size of the tumor and the lymph nodes status." DSA02466,E-MTAB-12205,,1000,Oral Mucosa Leukoplakia,C0023532,Oral mucosa,ArrayExpress,RNA-Seq,Homo sapiens,7|4,DO:A skin disease characterized by a defect in the normal process of keratinization of the mucosa. DSA02467,GSE7177,GPL570,27,Myotonic Dystrophy Type 1,C0027126,,GEO,Microarray,Homo sapiens,3|3,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA02468,GSE7177,GPL570,26,Myotonic Dystrophy Type 1,C0027126,,GEO,Microarray,Homo sapiens,3|3,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA02469,GSE7178,GPL570,31,Myotonic Dystrophy Type 1,C0027126,,GEO,Microarray,Homo sapiens,3|3,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA02470,GSE7178,GPL570,14,Myotonic Dystrophy Type 1,C0027126,,GEO,Microarray,Homo sapiens,3|3,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA02471,GSE7179,GPL570,248,Myotonic Dystrophy Type 1,C0027126,,GEO,Microarray,Homo sapiens,3|3,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA02472,GSE7179,GPL570,106,Myotonic Dystrophy Type 1,C0027126,,GEO,Microarray,Homo sapiens,3|3,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA02473,GSE3064,GPL201,0,X-Linked Dystonia Disorders Parkinsonism,C1839130,Caudate nucleus,GEO,Microarray,Homo sapiens,2|2,DO:A focal dystonia that is characterized by parkinsonism that is frequently accompanied by focal dystonia and progresses to generalized dystonia that has_material_basis_in X-linked recessive inheritance of SVA retrotransposon insertion in the intron of the TATA-box binding protein associated factor 1 gene (TAF1) on chromosome Xq13.1. DSA02474,GSE26910,GPL570,431,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,6|6,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02475,GSE26910,GPL570,120,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,6|6,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02476,GSE21422,GPL570,1000,Invasive Ductal Breast Carcinoma,C1134719,Breast,GEO,Microarray,Homo sapiens,5|5,DO:A breast ductal carcinoma that is characterized by infiltration into the fibrous or fatty tissue of the breast outside of the duct where it originated. DSA02477,GSE21422,GPL570,1000,Ductal Carcinoma In Situ,C0007124,Breast,GEO,Microarray,Homo sapiens,5|9,"EFO:A malignant tumor arising from epithelial cells. Carcinomas that arise from glandular epithelium are called adenocarcinomas, those that arise from squamous epithelium are called squamous cell carcinomas, and those that arise from transitional epithelium are called transitional cell carcinomas. Morphologically, the malignant epithelial cells may display abnormal mitotic figures, anaplasia, and necrosis. Carcinomas are graded by the degree of cellular differentiation as well, moderately, or poorly differentiated. Carcinomas invade the surrounding tissues and tend to metastasize to other anatomic sites. Lung carcinoma, skin carcinoma, breast carcinoma, colon carcinoma, and prostate carcinoma are the most frequently seen carcinomas." DSA02478,GSE5581,GPL339,1,Retinoschisis,C0152439,Retina,GEO,Microarray,Mus musculus,3|3,HPO:Splitting of the neuroretinal layers of the retina. DSA02479,GSE3585,GPL96,112,Dilated Cardiomyopathy,C0007193,Heart,GEO,Microarray,Homo sapiens,5|7,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA02480,GSE2501,GPL81,213,Thymic Carcinoma,C0205969,,GEO,Microarray,Mus musculus,4|6,"DO:A thymus cancer that derives_from epithelial cells. The tumor cells in a thymic carcinoma look very different from the normal cells of the thymus, grow more quickly, and have usually spread to other parts of the body when the cancer is found." DSA02481,GSE57957,GPL10558,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,39|39,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA02482,GSE33319,GPL6885,1000,Cystic Fibrosis,C0010674,Liver,GEO,Microarray,Mus musculus,4|4,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA02483,GSE2528,GPL81,1000,Breast Cancer,C0678222,Mammary gland,GEO,Microarray,Mus musculus,3|7,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02484,GSE2528,GPL81,0,Breast Cancer,C0678222,Mammary gland,GEO,Microarray,Mus musculus,3|4,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02485,GSE18064,GPL1261,43,Rift Valley Fever,C0035613,,GEO,Microarray,Mus musculus,3|3,"DO:A viral infectious disease that results_in infection, has_material_basis_in Rift Valley fever virus, which is transmitted_by Aedes mosquitoes. The virus affects domestic animals (cattle, buffalo, sheep, goats, and camels) and humans. The infection has_symptom jaundice, has_symptom vomiting blood, has_symptom passing blood in the feces, has_symptom ecchymoses (caused by bleeding in the skin), has_symptom bleeding from the nose or gums, has_symptom menorrhagia and has_symptom bleeding from venepuncture sites." DSA02486,GSE18064,GPL1261,303,Rift Valley Fever,C0035613,,GEO,Microarray,Mus musculus,3|3,"DO:A viral infectious disease that results_in infection, has_material_basis_in Rift Valley fever virus, which is transmitted_by Aedes mosquitoes. The virus affects domestic animals (cattle, buffalo, sheep, goats, and camels) and humans. The infection has_symptom jaundice, has_symptom vomiting blood, has_symptom passing blood in the feces, has_symptom ecchymoses (caused by bleeding in the skin), has_symptom bleeding from the nose or gums, has_symptom menorrhagia and has_symptom bleeding from venepuncture sites." DSA02487,GSE16461,GPL570,0,Multiple Sclerosis,C0026769,,GEO,Microarray,Homo sapiens,4|4,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA02488,GSE16461,GPL570,0,Multiple Sclerosis,C0026769,,GEO,Microarray,Homo sapiens,4|4,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA02489,GSE4616,GPL81,1,Diabetes,C0011847,Myocardium,GEO,Microarray,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA02490,GSE4616,GPL81,0,Diabetes,C0011847,Myocardium,GEO,Microarray,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA02491,GSE43292,GPL6244,1000,Atherosclerosis,C0004153,Heart,GEO,Microarray,Homo sapiens,32|32,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA02492,GSE1008,GPL81,0,Duchenne Muscular Dystrophy,C0013264,Extraocular muscle,GEO,Microarray,Mus musculus,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02493,GSE1008,GPL81,0,Duchenne Muscular Dystrophy,C0013264,Extraocular muscle,GEO,Microarray,Mus musculus,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02494,GSE1008,GPL81,0,Duchenne Muscular Dystrophy,C0013264,Extraocular muscle,GEO,Microarray,Mus musculus,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02495,GSE1008,GPL81,0,Duchenne Muscular Dystrophy,C0013264,Extraocular muscle,GEO,Microarray,Mus musculus,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02496,GSE1674,GPL81,8,Hypertension,C0020538,Adrenal gland,GEO,Microarray,Mus musculus,3|3,DO:An artery disease characterized by chronic elevated blood pressure in the arteries. DSA02497,GSE2172,GPL81,0,Inflammatory Bowel Disease,C0021390,Colon,GEO,Microarray,Mus musculus,2|2,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA02498,GSE9750,GPL96,1000,Cervical Cancer,C4048328,,GEO,Microarray,Homo sapiens,24|28,DO:A female reproductive organ cancer that is located_in the cervix. DSA02499,GSE9750,GPL96,1000,Cervical Cancer,C4048328,,GEO,Microarray,Homo sapiens,24|9,DO:A female reproductive organ cancer that is located_in the cervix. DSA02500,GSE14277,GPL1261,1000,Lung Cancer,C0684249,Lung,GEO,Microarray,Mus musculus,5|5,DO:A respiratory system cancer that is located_in the lung. DSA02501,GSE593,GPL96,203,Uterine Leiomyoma,C0042133,Myometrium,GEO,Microarray,Homo sapiens,5|5,DO:An uterine benign neoplasm derived from the smooth muscle layer of the uterus. DSA02502,GSE16515,GPL570,1000,Pancreatic Cancer,C0235974,Pancreas,GEO,Microarray,Homo sapiens,16|36,DO:An endocrine gland cancer located_in the pancreas. DSA02503,GSE14335,GPL571,61,Diamond-Blackfan Anemia,C1260899,,GEO,Microarray,Homo sapiens,6|4,DO:A congenital hypoplastic anemia that is characterized by anemia (low red blood cell counts) with decreased erythroid progenitors in the bone marrow and has_material_basis_insufficient levels of red blood cells due to bone marrow dysfunction. DSA02504,GSE26051,GPL570,54,Tendinopathy,C1568272,Biceps,GEO,Microarray,Homo sapiens,23|23,"MONDO:Inflammation of a tendon, usually resulting from an overuse injury. It is characterized by swelling of the tendon, tenderness around the inflamed tendon, and pain while moving the affected area of the body." DSA02505,GSE10162,GPL1261,151,Dent Disease,C0878681,Kidney,GEO,Microarray,Mus musculus,3|3,"DO:A renal tubular transport disease that is characterized by tubular proteinuria, hypercalciuria, calcium nephrolithiasis, nephrocalcinosis and chronic kidney failure and has_material_basis_in X-linked recessive inheritance of mutations in the CLCN5 gene or OCRL1 gene." DSA02506,GSE7036,GPL570,0,Bipolar Disorder,C0005586,,GEO,Microarray,Homo sapiens,3|3,DO:A mood disorder that involves alternating periods of mania and depression. DSA02507,GSE3410,GPL96,100,Idiopathic Myelofibrosis,C0001815,Bone marrow,GEO,Microarray,Homo sapiens,3|3,DO:A myeloid neoplasm that is located in the bone marrow which results in bone marrow being replaced by fibrous (scar) tissue. DSA02508,E-MTAB-12205,,1000,Oral Mucosa Leukoplakia,C0023532,Oral mucosa,ArrayExpress,RNA-Seq,Homo sapiens,7|8,DO:A skin disease characterized by a defect in the normal process of keratinization of the mucosa. DSA02509,GSE34526,GPL570,1,Polycystic Ovary Syndrome,C0032460,,GEO,Microarray,Homo sapiens,3|7,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA02510,GSE2507,GPL81,1000,Muscular Dystrophy,C0026850,Left ventricle,GEO,Microarray,Mus musculus,5|5,"DO:A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted." DSA02511,GSE2507,GPL81,353,Muscular Dystrophy,C0026850,Quadriceps,GEO,Microarray,Mus musculus,5|5,"DO:A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted." DSA02512,GSE420,GPL8300,0,Atherosclerosis,C0004153,Artery,GEO,Microarray,Homo sapiens,4|4,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA02513,GSE474,GPL96,0,Obesity,C0028754,Skeletal muscle,GEO,Microarray,Homo sapiens,8|16,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA02514,GSE8157,GPL570,1000,Polycystic Ovary Syndrome,C0032460,Vastus lateralis,GEO,Microarray,Homo sapiens,13|10,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA02515,GSE8514,GPL570,174,Aldosterone-Producing Adenoma,C0206667,Adrenal gland,GEO,Microarray,Homo sapiens,5|10,DO:An endocrine organ benign neoplasm that is a benign tumor of the glandular type (adenoma) in the adrenal gland. DSA02516,GSE15471,GPL570,1000,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,Microarray,Homo sapiens,39|39,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA02517,GSE20347,GPL571,1000,Esophagus Squamous Cell Carcinoma,C0279626,,GEO,Microarray,Homo sapiens,17|17,DO:An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus. DSA02518,GSE12649,GPL96,0,Bipolar Disorder,C0005586,Prefrontal cortex,GEO,Microarray,Homo sapiens,34|33,DO:A mood disorder that involves alternating periods of mania and depression. DSA02519,GSE12649,GPL96,0,Schizophrenia,C0036341,Prefrontal cortex,GEO,Microarray,Homo sapiens,34|35,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA02520,GSE55389,GPL6246,1,Diabetes,C0011847,Neural retina,GEO,Microarray,Mus musculus,4|4,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA02521,GSE1363,GPL81,0,Primary Pulmonary Hypoplasia,C0456891,Lung,GEO,Microarray,Mus musculus,8|8,"MONDO:Primary pulmonary hypoplasia is a rare, isolated, genetic developmental defect during embryogenesis characterized by congential malformation of pulmonary parenchyma with absence of other anomalies. Neonatally patients present with decreased breath sounds, small lung volume and severe respiratory distress that is not responsive to aggressive treatment (including surfactant instillation/ mechanical respiratory support). It is usually not compatible with life." DSA02522,GSE1026,GPL81,0,Duchenne Muscular Dystrophy,C0013264,Diaphragm muscle,GEO,Microarray,Mus musculus,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02523,GSE1026,GPL81,0,Duchenne Muscular Dystrophy,C0013264,Diaphragm muscle,GEO,Microarray,Mus musculus,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02524,GSE1026,GPL81,20,Duchenne Muscular Dystrophy,C0013264,Diaphragm muscle,GEO,Microarray,Mus musculus,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02525,GSE1026,GPL81,88,Duchenne Muscular Dystrophy,C0013264,Diaphragm muscle,GEO,Microarray,Mus musculus,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02526,GSE1026,GPL81,241,Duchenne Muscular Dystrophy,C0013264,Diaphragm muscle,GEO,Microarray,Mus musculus,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02527,GSE1026,GPL81,76,Duchenne Muscular Dystrophy,C0013264,Diaphragm muscle,GEO,Microarray,Mus musculus,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02528,GSE3678,GPL570,1000,Papillary Thyroid Cancer,C0238463,Thyroid,GEO,Microarray,Homo sapiens,7|7,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA02529,GSE6764,GPL570,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,10|7,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA02530,GSE6764,GPL570,1000,Liver Cirrhosis,C0023890,Liver,GEO,Microarray,Homo sapiens,10|10,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA02531,GSE6764,GPL570,687,Liver Cirrhosis,C0023890,Liver,GEO,Microarray,Homo sapiens,10|3,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA02532,GSE6764,GPL570,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,10|10,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA02533,GSE6764,GPL570,346,Liver Dysplasia,,Liver,GEO,Microarray,Homo sapiens,10|7, DSA02534,GSE6764,GPL570,829,Liver Dysplasia,,Liver,GEO,Microarray,Homo sapiens,10|10, DSA02535,GSE6764,GPL570,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,10|10,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA02536,GSE6764,GPL570,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,10|8,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA02537,GSE6764,GPL570,0,Progressive Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,10|7,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA02538,GSE6764,GPL570,1000,Progressive Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,8|10,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA02539,GSE6764,GPL570,0,High Grade Liver Dysplasia,,Liver,GEO,Microarray,Homo sapiens,10|7, DSA02540,GSE4692,GPL2995,1000,Obesity,C0028754,Adipose tissue,GEO,Microarray,Mus musculus,3|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA02541,GSE11524,GPL570,635,Sickle Cell Disease,C0002895,Peripheral blood,GEO,Microarray,Homo sapiens,12|18,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA02542,GSE16538,GPL570,517,Pulmonary Sarcoidosis,C0036205,Lung,GEO,Microarray,Homo sapiens,6|6,"DO:A sarcoidosis that is characterized by noncaseating granulomatous infiltration of the lungs and supporting lymph nodes, bilateral hilar adenopathy, and pulmonary issues, has_symptom shortness of breath, fatigue, wheezing, and chronic cough, and develops_from a type IV hypersensitivity reaction." DSA02543,GSE16524,GPL570,7,Setleis Syndrome,,,GEO,Microarray,Homo sapiens,4|4, DSA02544,GSE1122,GPL80,15,Emphysema,C0034067,Lung,GEO,Microarray,Homo sapiens,5|5,DO:A chronic obstructive pulmonary disease that is characterized by permanent enlargement of air spaces distal to the terminal bronchioles and the destruction of the alveolar walls. DSA02545,GSE1122,GPL80,1,Emphysema,C0034067,Lung,GEO,Microarray,Homo sapiens,5|5,DO:A chronic obstructive pulmonary disease that is characterized by permanent enlargement of air spaces distal to the terminal bronchioles and the destruction of the alveolar walls. DSA02546,GSE35561,GPL6244,0,Down Syndrome,C0013080,,GEO,Microarray,Homo sapiens,3|3,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA02547,GSE20910,GPL570,22,Down Syndrome,C0013080,Bone marrow,GEO,Microarray,Homo sapiens,26|23,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA02548,GSE3075,GPL339,1,Spinal Muscular Atrophy With Respiratory Distress Type 1,C1858517,Lumbar spinal cord,GEO,Microarray,Mus musculus,3|3,DO:A spinal muscular atrophy characterized by autosomal recessive inheritance of severe respiratory distress resulting from diaphragmatic paralysis that predominantly involves the upper limbs and distal muscles that has_material_basis_in homozygous or compound heterozygous mutation in the IGHMBP2 gene on chromosome 11q13. DSA02549,GSE5090,GPL96,0,Polycystic Ovary Syndrome,C0032460,Omental adipose tissue,GEO,Microarray,Homo sapiens,7|8,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA02550,GSE23343,GPL570,0,Type 2 Diabetes,C0011860,Liver,GEO,Microarray,Homo sapiens,7|10,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA02551,GSE13887,GPL570,0,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,9|10,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02552,GSE12643,GPL8300,0,Type 2 Diabetes,C0011860,Myotube,GEO,Microarray,Homo sapiens,10|10,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA02553,GSE10921,GPL4191,0,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,Microarray,Homo sapiens,3|4,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA02554,GSE1650,GPL96,1,Chronic Obstructive Pulmonary Disease,C0024117,Lung,GEO,Microarray,Homo sapiens,12|18,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA02555,GSE6399,GPL1261,4,Cardiomyopathy,C0878544,Heart,GEO,Microarray,Mus musculus,8|6,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA02556,GSE842,GPL81,200,Multiple Sclerosis,C0026769,Spinal cord,GEO,Microarray,Mus musculus,3|6,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA02557,GSE3112,GPL96,764,Polymyositis,C0085655,Skeletal muscle,GEO,Microarray,Homo sapiens,11|6,EFO:Polymyositis (PM)(\ inflammation of many muscles\ ) is a type of chronic inflammation of the muscles (inflammatory myopathy) related to dermatomyositis and inclusion body myositis. DSA02558,GSE3112,GPL96,1000,Inclusion Body Myositis,C0238190,Skeletal muscle,GEO,Microarray,Homo sapiens,11|23,"DO:A myositis that is characterized by late onset of skeletal muscle inflammation, weakness, and atrophy with cytoplasmic granules and vacuoles in the muscle." DSA02559,GSE6710,GPL96,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,13|13,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA02560,GSE5764,GPL570,1,Invasive Lobular Carcinoma,C0279565,Breast,GEO,Microarray,Homo sapiens,10|5,"EFO:An infiltrating lobular adenocarcinoma of the breast. The malignant cells lack cohesion and are arranged individually or in a linear manner (Indian files), or as narrow trabeculae within the stroma. The malignant cells are usually smaller than those of ductal carcinoma, are less pleomorphic, and have fewer mitotic figures." DSA02561,GSE5764,GPL570,2,Invasive Ductal Carcinoma,C1134719,Breast,GEO,Microarray,Homo sapiens,10|5,DO:A breast ductal carcinoma that is characterized by infiltration into the fibrous or fatty tissue of the breast outside of the duct where it originated. DSA02562,GSE3676,GPL81,0,Azoospermia,C0004509,Testis,GEO,Microarray,Mus musculus,2|2,DO:A male infertility disease characterized by the absence of any measurable level of sperm in semen. DSA02563,GSE10631,GPL96,1000,Large Granular Lymphocytic Leukemia,C1955861,,GEO,Microarray,Homo sapiens,14|30,MONDO:T-cell large granular lymphocyte leukemia (T-cell LGL leukemia) is a lymphoproliferative malignancy that arises from the mature T-cell (CD3+) lineage. DSA02564,GSE1719,GPL8300,767,Macular Degeneration,C0024437,,GEO,Microarray,Homo sapiens,18|18,DO:A retinitis pigmentosa that has_material_basis_in mutation in the FSCN2 gene on chromosome 17q25. DSA02565,GSE860,GPL91,0,Post-Traumatic Stress Disorder,C0038436,,GEO,Microarray,Homo sapiens,16|17,DO:An anxiety disorder which results from a traumatic experience that results in psychological trauma. DSA02566,GSE10971,GPL570,1000,Serous Cystadenocarcinoma,C0206701,Fallopian tube,GEO,Microarray,Homo sapiens,24|13,DO:A cystadenocarcinoma that derives_from epithelial cells originating in glandular tissue forming serous lesions. DSA02567,GSE6980,GPL1261,1000,Multiple Myeloma,C0026764,Spleen,GEO,Microarray,Mus musculus,5|6,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA02568,GSE54958,GPL6244,1000,Papillary Thyroid Carcinoma,C0238463,Thyroid,GEO,Microarray,Homo sapiens,6|11,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA02569,GSE54958,GPL6244,1000,Papillary Thyroid Carcinoma,C0238463,Thyroid,GEO,Microarray,Homo sapiens,6|14,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA02570,GSE2006,GPL96,148,Idiopathic Hemorrhagic Thrombocythemia,C0040028,,GEO,Microarray,Homo sapiens,5|6,"DO:A myeloproliferative neoplasm that is characterized by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocytes in the bone marrow, and episodes of thrombosis and/or hemorrhage and that results_in the overproduction of platelets." DSA02571,GSE4290,GPL570,1000,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,23|77,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA02572,GSE4290,GPL570,1000,Oligodendroglioma,C0028945,Brain,GEO,Microarray,Homo sapiens,23|50,"EFO:A well-differentiated (WHO grade II), diffusely infiltrating neuroglial tumor, typically located in the cerebral hemispheres. It is composed predominantly of cells which morphologically resemble oligodendroglia. The neoplastic cells have rounded homogeneous nuclei and, on paraffin sections, a swollen, clear cytoplasm ('honeycomb' appearance). (Adapted from WHO)" DSA02573,GSE4290,GPL570,1000,Astrocytoma,C0004114,Brain,GEO,Microarray,Homo sapiens,23|26,"DO:A malignant glioma that is has_material_basis_in astrocyte cells, a type of star-shaped glial cell, located in the brain and spinal cord." DSA02574,GSE2236,GPL1261,0,Congestive Heart Failure,C0018802,Heart,GEO,Microarray,Mus musculus,2|2,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA02575,GSE6613,GPL96,0,Parkinson's Disease,C0030567,Blood,GEO,Microarray,Homo sapiens,22|50,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA02576,GSE1623,GPL81,844,Type 1 Diabetes,C0011854,Pancreas,GEO,Microarray,Mus musculus,2|2,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA02577,GSE1621,GPL81,1,Transverse Aortic Constriction,,Heart,GEO,Microarray,Mus musculus,4|5, DSA02578,GSE1621,GPL81,60,Transverse Aortic Constriction,,Heart,GEO,Microarray,Mus musculus,4|4, DSA02579,GSE1621,GPL81,0,Transverse Aortic Constriction,,Heart,GEO,Microarray,Mus musculus,4|5, DSA02580,GSE63941,GPL570,1000,Esophageal Squamous Cell Carcinoma,C0279626,,GEO,Microarray,Homo sapiens,3|9,DO:An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus. DSA02581,GSE45164,GPL571,380,Skin Squamous Cell Carcinoma,C0553723,Skin,GEO,Microarray,Homo sapiens,3|10,DO:A skin carcinoma that has_material_basis_in squamous cells. DSA02582,GSE60502,GPL96,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,18|18,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA02583,GSE65144,GPL570,1000,Anaplastic Thyroid Carcinoma,C0238461,Thyroid,GEO,Microarray,Homo sapiens,13|12,DO:A thyroid gland carcinoma that is composed of undifferentiated cells. DSA02584,GSE56088,GPL10558,2,Thalassaemia,C0039730,Peripheral blood,GEO,Microarray,Homo sapiens,6|6,DO:A hemolytic anemia characterized by decreased synthesis of one or more hemoglobin polypeptide chains. DSA02585,GSE56088,GPL10558,1000,Thalassaemia,C0039730,Peripheral blood,GEO,Microarray,Homo sapiens,6|6,DO:A hemolytic anemia characterized by decreased synthesis of one or more hemoglobin polypeptide chains. DSA02586,E-MTAB-12205,,881,Oral Mucosa Leukoplakia,C0023532,Oral mucosa,ArrayExpress,RNA-Seq,Homo sapiens,7|4,DO:A skin disease characterized by a defect in the normal process of keratinization of the mucosa. DSA02587,E-MTAB-12205,,1000,Oral Squamous Cell Carcinoma,C0585362,Oral mucosa,ArrayExpress,RNA-Seq,Homo sapiens,7|5,"EFO:A squamous cell carcinoma arising from the oral cavity. It affects predominantly adults in their fifth and sixth decades of life and is associated with alcohol and tobacco use. Human papillomavirus is present in approximately half of the cases. It is characterized by a tendency to metastasize early to the lymph nodes. When the tumor is small, patients are often asymptomatic. Physical examination may reveal erythematous or white lesions or plaques. The majority of patients present with signs and symptoms of locally advanced disease including mucosal ulceration, pain, difficulty with speaking, chewing, and swallowing, bleeding, weight loss, and neck swelling. Patients may also present with swollen neck lymph nodes without any symptoms from the oropharyngeal tumor. The most significant prognostic factors are the size of the tumor and the lymph nodes status." DSA02588,E-MTAB-12252,,82,Type 1 Diabetes,C0011854,Lumbar spinal cord,ArrayExpress,RNA-Seq,Homo sapiens,5|5,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA02589,GSE63901,GPL10558,0,Early Pregnancy Loss,C3830362,Endometrium,GEO,Microarray,Homo sapiens,26|20,MSH:A loss of PREGNANCY from natural causes before the 20th week of pregnancy. (2017/18 ICD-10-CM) DSA02590,GSE63901,GPL10558,21,Early Pregnancy Loss,C3830362,Endometrium,GEO,Microarray,Homo sapiens,26|18,MSH:A loss of PREGNANCY from natural causes before the 20th week of pregnancy. (2017/18 ICD-10-CM) DSA02591,GSE53552,GPL570,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,24|25,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA02592,GSE7803,GPL96,1000,Microinvasive Squamous Cell Carcinoma,C0334252,Cervix,GEO,Microarray,Homo sapiens,10|21,NCI:A squamous cell carcinoma with minimal stromal invasion. DSA02593,GSE7803,GPL96,1000,Squamous Intraepithelial Lesion,C0333873,Cervix,GEO,Microarray,Homo sapiens,10|7,"MSH:A cytological test finding often from PAP SMEARS that shows abnormal lesions of SQUAMOUS EPITHELIAL CELLS of the CERVIX. It is a diagnostic criterion used in the Bethesda System for UTERINE CERVICAL NEOPLASMS and represents the PAP TEST result that is abnormal. Although squamous intraepithelial lesions test result does not mean UTERINE CERVICAL NEOPLASMS it requires follow-ups (e.g., HPV DNA TESTS; and COLPOSCOPY)." DSA02594,GSE13849,GPL570,584,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,59|61,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA02595,GSE67940,GPL6480,219,Asthma,C0004096,Bronchus,GEO,Microarray,Homo sapiens,31|29,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02596,GSE67940,GPL6480,15,Asthma,C0004096,Bronchus,GEO,Microarray,Homo sapiens,44|29,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02597,GSE6956,GPL571,1000,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,20|69,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02598,GSE62430,GPL10558,0,Thalassaemia,C0039730,Peripheral blood,GEO,Microarray,Homo sapiens,6|6,DO:A hemolytic anemia characterized by decreased synthesis of one or more hemoglobin polypeptide chains. DSA02599,GSE62430,GPL10558,16,Thalassaemia,C0039730,Peripheral blood,GEO,Microarray,Homo sapiens,6|6,DO:A hemolytic anemia characterized by decreased synthesis of one or more hemoglobin polypeptide chains. DSA02600,GSE19419,GPL6244,0,Dyt1 Dystonia Disorders,,Blood,GEO,Microarray,Homo sapiens,15|22, DSA02601,GSE19419,GPL6244,0,Dyt1 Dystonia Disorders,,Blood,GEO,Microarray,Homo sapiens,15|23, DSA02602,GSE18842,GPL570,1000,Lung Cancer,C0684249,Lung,GEO,Microarray,Homo sapiens,45|46,DO:A respiratory system cancer that is located_in the lung. DSA02603,GSE63142,GPL6480,828,Asthma,C0004096,Bronchus,GEO,Microarray,Homo sapiens,27|72,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02604,GSE63142,GPL6480,1000,Asthma,C0004096,Bronchus,GEO,Microarray,Homo sapiens,27|56,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02605,GSE33113,GPL570,1000,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,6|90,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA02606,GSE18781,GPL570,0,Spondyloarthropathy,C0949690,Peripheral blood,GEO,Microarray,Homo sapiens,25|18,"EFO:Heterogeneous group of arthritic diseases sharing clinical and radiologic features. They are associated with the HLA-B27 ANTIGEN and some with a triggering infection. Most involve the axial joints in the SPINE, particularly the SACROILIAC JOINT, but can also involve asymmetric peripheral joints. Subsets include ANKYLOSING SPONDYLITIS; REACTIVE ARTHRITIS; PSORIATIC ARTHRITIS; and others." DSA02607,GSE18781,GPL570,1000,Sarcoidosis,C0036202,Peripheral blood,GEO,Microarray,Homo sapiens,25|12,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA02608,GSE9844,GPL570,1000,Tongue Squamous Cell Carcinoma,C0349566,,GEO,Microarray,Homo sapiens,12|26,DO:A head and neck squamous cell carcinoma that is located_in the tongue. DSA02609,GSE9960,GPL570,0,Sepsis,C0243026,,GEO,Microarray,Homo sapiens,16|17,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA02610,GSE9960,GPL570,0,Sepsis,C0243026,,GEO,Microarray,Homo sapiens,16|17,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA02611,GSE9960,GPL570,0,Sepsis,C0243026,,GEO,Microarray,Homo sapiens,16|10,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA02612,GSE9960,GPL570,0,Sepsis,C0243026,,GEO,Microarray,Homo sapiens,16|9,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA02613,GSE14245,GPL570,0,Pancreatic Cancer,C0235974,Saliva,GEO,Microarray,Homo sapiens,12|12,DO:An endocrine gland cancer located_in the pancreas. DSA02614,GSE1297,GPL96,0,Alzheimer's Disease,C0002395,Hippocampus,GEO,Microarray,Homo sapiens,9|7,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA02615,GSE1297,GPL96,0,Alzheimer's Disease,C0002395,Hippocampus,GEO,Microarray,Homo sapiens,9|8,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA02616,GSE1297,GPL96,0,Alzheimer's Disease,C0002395,Hippocampus,GEO,Microarray,Homo sapiens,9|7,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA02617,GSE16020,GPL570,167,Autosomal Dominant Macrothrombocytopenia,C4304021,,GEO,Microarray,Homo sapiens,7|3,"DO:A blood platelet disease characterized by autosomal dominant inheritance with macrothrombocytopenia, platelet anisocytosis, prolonged bleeding time but only mildly increased bleeding tendency that has_material_basis_in heterozygous mutation in the ITGA2B gene on chromosome 17q21.31 or the ITGB3 gene on chromosome 17q21.32." DSA02618,GSE16020,GPL570,44,Autosomal Dominant Macrothrombocytopenia,C4304021,,GEO,Microarray,Homo sapiens,5|5,"DO:A blood platelet disease characterized by autosomal dominant inheritance with macrothrombocytopenia, platelet anisocytosis, prolonged bleeding time but only mildly increased bleeding tendency that has_material_basis_in heterozygous mutation in the ITGA2B gene on chromosome 17q21.31 or the ITGB3 gene on chromosome 17q21.32." DSA02619,E-MTAB-12271,,506,Impulse Control Disorder,C0021122,Heart,ArrayExpress,RNA-Seq,Mus musculus,3|3,DO:A disease of mental health that involves a failure to resist an impulsive act or behaviour that may be harmful to self or others. DSA02620,GSE179128,GPL16791,1000,Pediatric Crohn's Disease,C2931133,Colon,GEO,RNA-Seq,Homo sapiens,6|5, DSA02621,GSE179128,GPL16791,1000,Pediatric Ulcerative Colitis,C2931173,Colon,GEO,RNA-Seq,Homo sapiens,6|7, DSA02622,GSE166353,GPL21103,62,Acute Hepatitis,C0267797,Liver,GEO,RNA-Seq,Mus musculus,12|12,"HPO:Acute hepatic injury resulting from inflammation typically accompanied by increased serum alanine transaminase activity. Etiologies include viral hepatitis, drugs, toxins, and autoimmune disorders." DSA02623,GSE166353,GPL21103,1000,Acute Hepatitis,C0267797,Liver,GEO,RNA-Seq,Mus musculus,8|8,"HPO:Acute hepatic injury resulting from inflammation typically accompanied by increased serum alanine transaminase activity. Etiologies include viral hepatitis, drugs, toxins, and autoimmune disorders." DSA02624,GSE178309,GPL16791,734,Acute Myeloid Leukemia,C0023467,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA02625,GSE17054,GPL570,587,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,4|9,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA02626,GSE171654,GPL23159,2,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,3|8,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA02627,GSE175701,GPL16791,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,Blood,GEO,RNA-Seq,Homo sapiens,5|8,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA02628,E-MTAB-12271,,398,Rheumatic Disease,C0035435,Heart,ArrayExpress,RNA-Seq,Mus musculus,3|3,"MONDO:Inflammatory and degenerative diseases of connective tissue structures, such as arthritis." DSA02629,GSE175384,GPL18573,1000,AL Amyloidosis,C0268381,,GEO,RNA-Seq,Homo sapiens,40|32,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA02630,E-MTAB-12309,,50,Ulcerative Colitis,C0009324,,ArrayExpress,RNA-Seq,Homo sapiens,3|3,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02631,GSE167308,GPL20301,1000,Alcoholic Cirrhosis,C0023891,Liver,GEO,RNA-Seq,Homo sapiens,5|14,MONDO:A disorder of the liver characterized by the presence of fibrotic scar tissue instead of healthy liver tissue. This condition is attributed to excessive consumption of alcoholic beverages. DSA02632,E-MTAB-12309,,130,Ulcerative Colitis,C0009324,,ArrayExpress,RNA-Seq,Homo sapiens,3|2,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02633,GSE167225,GPL13607,0,Allergic Rhinitis,C2607914,Sputum,GEO,Microarray,Homo sapiens,5|4,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA02634,GSE167225,GPL13607,3,Allergic Rhinitis,C2607914,Sputum,GEO,Microarray,Homo sapiens,4|4,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA02635,GSE165870,GPL24676,129,Aplastic Anemia,C0002874,Bone marrow,GEO,RNA-Seq,Homo sapiens,2|6,"DO:An anemia that is characterized by a deficiency of red blood cells, white blood cells and platelets produced by bone marrow." DSA02636,E-MTAB-12618,,1000,Severe Acute Respiratory Syndrome,C1175175,Lung,ArrayExpress,RNA-Seq,Mus musculus,3|3,"DO:A Coronavirus infection that results_in infection located_in respiratory tract, has_material_basis_in SARS coronavirus (SARS-CoV), which is transmitted_by droplet spread of respiratory secretions, transmitted_by ingestion of contaminated food, or transmitted_by fomites. The infection has_symptom fever, has_symptom headache, has_symptom body aches, has_symptom dry cough, and has_symptom hypoxia." DSA02637,E-MTAB-12618,,1000,Severe Acute Respiratory Syndrome,C1175175,Lung,ArrayExpress,RNA-Seq,Mus musculus,3|3,"DO:A Coronavirus infection that results_in infection located_in respiratory tract, has_material_basis_in SARS coronavirus (SARS-CoV), which is transmitted_by droplet spread of respiratory secretions, transmitted_by ingestion of contaminated food, or transmitted_by fomites. The infection has_symptom fever, has_symptom headache, has_symptom body aches, has_symptom dry cough, and has_symptom hypoxia." DSA02638,GSE175541,GPL24676,1000,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,1|4,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02639,GSE175541,GPL24676,1000,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,1|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02640,GSE175541,GPL24676,1000,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,3|4,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02641,GSE175541,GPL24676,1000,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,3|4,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02642,GSE179156,GPL570,1000,Asthma,C0004096,Large airway epithelium,GEO,Microarray,Homo sapiens,29|38,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02643,GSE165813,GPL31954,1000,Astroblastoma,C0334587,Brain,GEO,Microarray,Homo sapiens,22|26,"DO:A malignant astrocytoma that is characterized by tumor cells with characteristics suggestive of an astrocytic origin (positive for GFAP), arranged perivascularly." DSA02644,GSE175776,GPL18573,1000,Ataxia Telangiectasia,C0004135,Cerebellum,GEO,RNA-Seq,Homo sapiens,6|6,"DO:An autosomal recessive cerebellar ataxia that is characterized by cerebellar ataxia, telangiectases, immune defects, and a predisposition to malignancy and that has_material_basis_in homozygous or compound heterozygous mutation in the ATM gene on chromosome 11q22." DSA02645,GSE178205,GPL24676,287,Autism Spectrum Disorder,C1510586,Brain,GEO,RNA-Seq,Homo sapiens,9|11,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA02646,GSE165322,GPL16791,1000,Autosomal Dominant Retinitis Pigmentosa,,Skin,GEO,RNA-Seq,Homo sapiens,3|3, DSA02647,E-MTAB-12631,,1000,Cornelia De Lange Syndrome,C0270972,Blood,ArrayExpress,RNA-Seq,Homo sapiens,6|3,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA02648,GSE165254,GPL21697,737,Behcet's Disease,C0004943,Blood,GEO,RNA-Seq,Homo sapiens,11|14,"DO:A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis." DSA02649,GSE171213,GPL24676,359,Brain Tumor,C0006118,Peripheral blood,GEO,RNA-Seq,Homo sapiens,7|3,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA02650,GSE171213,GPL24676,1000,Brain Tumor,C0006118,Peripheral blood,GEO,RNA-Seq,Homo sapiens,7|3,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA02651,GSE166044,GPL18573,1000,Breast Cancer,C0678222,Breast,GEO,RNA-Seq,Homo sapiens,15|15,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02652,GSE165934,GPL23126,1000,Bronchial Asthma,C0004096,,GEO,Microarray,Homo sapiens,9|10,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA02653,GSE175570,GPL23479,1000,Cancer,C0006625,Muscle,GEO,RNA-Seq,Mus musculus,3|3,"HPO:Severe weight loss, wasting of muscle, loss of appetite, and general debility related to a chronic disease." DSA02654,GSE176260,GPL24676,1000,Candidemia,C0877445,Whole blood,GEO,RNA-Seq,Homo sapiens,15|11,MONDO:A fungal infection by any of the Candida species in a sterile body compartment. DSA02655,GSE176261,GPL24676,1000,Candidemia,C0877445,Whole blood,GEO,RNA-Seq,Homo sapiens,15|19,MONDO:A fungal infection by any of the Candida species in a sterile body compartment. DSA02656,GSE164883,GPL10558,1000,Coeliac Disease,C0007570,Gut,GEO,Microarray,Homo sapiens,22|26,"DO:An autoimmune disease of gastrointestinal tract that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite." DSA02657,GSE168527,GPL20301,1000,Coeliac Disease,C0007570,,GEO,RNA-Seq,Homo sapiens,5|1,"DO:An autoimmune disease of gastrointestinal tract that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite." DSA02658,GSE168527,GPL20301,1000,Coeliac Disease,C0007570,,GEO,RNA-Seq,Homo sapiens,5|1,"DO:An autoimmune disease of gastrointestinal tract that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite." DSA02659,E-MTAB-12631,,1000,Cornelia De Lange Syndrome,C0270972,Blood,ArrayExpress,RNA-Seq,Homo sapiens,6|3,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA02660,GSE165512,GPL16791,1000,Crohn's Disease,C0010346,Colon,GEO,RNA-Seq,Homo sapiens,40|84,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02661,GSE175564,GPL21626,1000,Chronic Lymphocytic Leukemia,C0023434,Spleen,GEO,RNA-Seq,Mus musculus,3|3,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA02662,GSE179121,GPL21626,1000,Chronic Lymphocytic Leukemia,C0023434,Spleen,GEO,RNA-Seq,Mus musculus,3|3,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA02663,GSE179121,GPL21626,562,Chronic Lymphocytic Leukemia,C0023434,Spleen,GEO,RNA-Seq,Mus musculus,3|3,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA02664,E-MTAB-12631,,1000,Cornelia De Lange Syndrome,C0270972,Blood,ArrayExpress,RNA-Seq,Homo sapiens,6|3,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA02665,GSE175541,GPL24676,1000,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,RNA-Seq,Homo sapiens,1|1,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA02666,GSE175541,GPL24676,1000,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,RNA-Seq,Homo sapiens,1|3,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA02667,GSE175541,GPL24676,350,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,RNA-Seq,Homo sapiens,3|4,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA02668,GSE175541,GPL24676,51,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,RNA-Seq,Homo sapiens,3|4,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA02669,E-MTAB-12631,,1000,Cornelia De Lange Syndrome,C0270972,Blood,ArrayExpress,RNA-Seq,Homo sapiens,6|3,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA02670,GSE168199,GPL13112,0,Chronic Obstructive Pulmonary Disease,C0024117,Cortex,GEO,RNA-Seq,Mus musculus,6|4,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA02671,GSE172049,GPL570,1,Cortical Hyperostosis With Syndactyly,C0265301,Whole blood,GEO,Microarray,Homo sapiens,4|5,"DO:A hyperostosis characterized by excessive bone formation most prominent in the skull, mandible, clavicle, ribs and diaphyses of long bones; bone formation occurs throughout life." DSA02672,GSE168845,GPL21185,1000,Clear Cell Renal Cell Carcinoma,C0007134,Kidney,GEO,Microarray,Homo sapiens,4|4,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA02673,E-MTAB-12791,,1000,Bacterial Infection,C0004623,Blood,ArrayExpress,RNA-Seq,Homo sapiens,18|3,"DO:A disease by infectious agent that results_in infection, has_material_basis_in Bacteria." DSA02674,GSE176095,GPL21103,1000,"Arthritis, Collagen-Induced",C0971858,Joint,GEO,RNA-Seq,Mus musculus,5|5,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA02675,GSE176095,GPL21103,1000,"Arthritis, Collagen-Induced",C0971858,Joint,GEO,RNA-Seq,Mus musculus,5|5,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA02676,GSE176095,GPL21103,1000,"Arthritis, Collagen-Induced",C0971858,Joint,GEO,RNA-Seq,Mus musculus,5|5,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA02677,GSE176095,GPL21103,1000,"Arthritis, Collagen-Induced",C0971858,Joint,GEO,RNA-Seq,Mus musculus,5|5,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA02678,GSE176095,GPL21103,1000,"Arthritis, Collagen-Induced",C0971858,Joint,GEO,RNA-Seq,Mus musculus,5|5,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA02679,GSE176095,GPL21103,1000,"Arthritis, Collagen-Induced",C0971858,Joint,GEO,RNA-Seq,Mus musculus,5|5,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA02680,GSE176095,GPL21103,1000,"Arthritis, Collagen-Induced",C0971858,Liver,GEO,RNA-Seq,Mus musculus,5|5,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA02681,GSE176095,GPL21103,1000,"Arthritis, Collagen-Induced",C0971858,Liver,GEO,RNA-Seq,Mus musculus,5|5,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA02682,GSE176095,GPL21103,1000,"Arthritis, Collagen-Induced",C0971858,Liver,GEO,RNA-Seq,Mus musculus,5|5,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA02683,GSE176095,GPL21103,1000,"Arthritis, Collagen-Induced",C0971858,Liver,GEO,RNA-Seq,Mus musculus,5|5,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA02684,GSE176095,GPL21103,1000,"Arthritis, Collagen-Induced",C0971858,Liver,GEO,RNA-Seq,Mus musculus,5|5,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA02685,GSE176095,GPL21103,1000,"Arthritis, Collagen-Induced",C0971858,Liver,GEO,RNA-Seq,Mus musculus,5|5,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA02686,GSE176095,GPL21103,167,"Arthritis, Collagen-Induced",C0971858,Muscle,GEO,RNA-Seq,Mus musculus,5|5,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA02687,GSE176095,GPL21103,1000,"Arthritis, Collagen-Induced",C0971858,Muscle,GEO,RNA-Seq,Mus musculus,5|5,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA02688,GSE176095,GPL21103,112,"Arthritis, Collagen-Induced",C0971858,Muscle,GEO,RNA-Seq,Mus musculus,5|5,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA02689,GSE176095,GPL21103,777,"Arthritis, Collagen-Induced",C0971858,Muscle,GEO,RNA-Seq,Mus musculus,4|5,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA02690,GSE176095,GPL21103,663,"Arthritis, Collagen-Induced",C0971858,Muscle,GEO,RNA-Seq,Mus musculus,5|5,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA02691,GSE176095,GPL21103,257,"Arthritis, Collagen-Induced",C0971858,Muscle,GEO,RNA-Seq,Mus musculus,5|5,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA02692,GSE44076,GPL13667,1000,Colon Tumor,C0009375,Colon,GEO,Microarray,Homo sapiens,50|98,DO:A colorectal cancer that is located_in the colon. DSA02693,GSE169005,GPL19057,1000,Colon Tumor,C0009375,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:A colorectal cancer that is located_in the colon. DSA02694,GSE174302,GPL20795,1000,Colorectal Carcinoma,C0009402,Plasma,GEO,RNA-Seq,Homo sapiens,46|52,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA02695,GSE17269,GPL570,0,Common Variable Immunodeficiency,C0009447,Peripheral blood,GEO,Microarray,Homo sapiens,4|3,DO:An agammaglobulinemia that is characterized by low Ig levels with phenotypically normal B cells that can proliferate but do not develop into Ig-producing cells and that esults in insufficient production of antibodies needed to respond to exposure of pathogens. DSA02696,GSE166780,GPL20795,178,Coronary Artery Disease,C1956346,,GEO,RNA-Seq,Homo sapiens,8|8,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA02697,GSE166780,GPL20795,1000,Coronary Artery Disease,C1956346,,GEO,RNA-Seq,Homo sapiens,8|8,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA02698,GSE165080,GPL24676,130,COVID-19,D8888888,Peripheral blood,GEO,RNA-Seq,Homo sapiens,11|22,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02699,GSE165461,GPL18573,190,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,8|39,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02700,GSE165461,GPL18573,110,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,8|25,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02701,GSE165532,GPL20301|GPL28038,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,8|7,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02702,GSE166253,GPL20795,1000,COVID-19,D8888888,Blood,GEO,RNA-Seq,Homo sapiens,10|6,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02703,GSE166253,GPL20795,1000,COVID-19,D8888888,Blood,GEO,RNA-Seq,Homo sapiens,10|10,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02704,GSE166530,GPL24676,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,5|33,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02705,GSE166992,GPL18573,1000,COVID-19,D8888888,,GEO,scRNA-Seq,Homo sapiens,3|6,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02706,E-MTAB-12791,,1000,COVID-19,D8888888,Blood,ArrayExpress,RNA-Seq,Homo sapiens,18|69,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02707,GSE168998,GPL15520,34,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,2|4,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02708,E-MTAB-12791,,1000,Viral Infection,C0042769,Blood,ArrayExpress,RNA-Seq,Homo sapiens,18|5,"DO:A disease by infectious agent that results in infection, has_material_basis_in Viruses." DSA02709,GSE171130,GPL11154|GPL30209,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02710,GSE171130,GPL11154|GPL30209,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02711,GSE171130,GPL11154|GPL30209,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02712,GSE171130,GPL11154|GPL30209,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02713,GSE171381,GPL24676,1000,COVID-19,D8888888,Decidua,GEO,scRNA-Seq,Homo sapiens,2|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02714,GSE171381,GPL24676,1000,COVID-19,D8888888,Placental villi,GEO,scRNA-Seq,Homo sapiens,3|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02715,E-MTAB-13019,,12,Lymphedema,C0024236,Arm,ArrayExpress,RNA-Seq,Homo sapiens,4|4,HPO:Localized fluid retention and tissue swelling caused by a compromised lymphatic system. DSA02716,E-MTAB-1961,,1000,Breast Adenocarcinoma,C0858252,,ArrayExpress,RNA-Seq,Homo sapiens,2|2,DO:A breast carcinoma that originates in the milk ducts and/or lobules (glandular tissue) of the breast. DSA02717,GSE171995,GPL16791,0,COVID-19,D8888888,Placental villi,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02718,E-MTAB-3664,,2,Spinal Muscular Atrophy,C0026847,Brain,ArrayExpress,RNA-Seq,Homo sapiens,8|8,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA02719,E-MTAB-3664,,71,Spinal Muscular Atrophy,C0026847,Liver,ArrayExpress,RNA-Seq,Homo sapiens,8|8,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA02720,GSE174668,GPL26167,4,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02721,GSE174668,GPL26167,3,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02722,GSE174668,GPL26167,3,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02723,GSE174668,GPL26167,7,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02724,GSE174668,GPL26167,15,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02725,GSE174668,GPL26167,28,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02726,GSE174668,GPL26167,0,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02727,GSE174668,GPL26167,2,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02728,GSE174843,GPL30173|GPL30181,459,COVID-19,D8888888,Retina,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02729,GSE174843,GPL30173|GPL30181,49,COVID-19,D8888888,Retina,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02730,E-MTAB-3664,,15,Spinal Muscular Atrophy,C0026847,Muscle,ArrayExpress,RNA-Seq,Homo sapiens,8|8,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA02731,E-MTAB-3664,,3,Spinal Muscular Atrophy,C0026847,Spinal cord,ArrayExpress,RNA-Seq,Homo sapiens,8|8,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA02732,E-MTAB-4054,,1000,Barrett's Esophagus,C0004763,Esophagus,ArrayExpress,RNA-Seq,Homo sapiens,18|19,DO:An esophageal disease characterized by a change of normal esophageal squamous epithelium to a columnar and intestinal-type epithelium. DSA02733,E-MTAB-4054,,1000,Barrett's Esophagus,C0004763,Esophagus,ArrayExpress,RNA-Seq,Homo sapiens,18|8,DO:An esophageal disease characterized by a change of normal esophageal squamous epithelium to a columnar and intestinal-type epithelium. DSA02734,E-MTAB-4054,,1000,Esophageal Adenocarcinoma,C0279628,Esophagus,ArrayExpress,RNA-Seq,Homo sapiens,18|17,DO:An esophageal carcinoma that derives_from epithelial cells of glandular origin. DSA02735,GSE176480,GPL24676,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,10|8,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02736,GSE178824,GPL18573,640,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,4|4,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02737,GSE178824,GPL18573,477,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,4|4,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02738,GSE178824,GPL18573,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,4|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02739,GSE177477,GPL23159,1000,COVID-19,D8888888,Blood,GEO,Microarray,Homo sapiens,18|11,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02740,GSE177477,GPL23159,1000,COVID-19,D8888888,Blood,GEO,Microarray,Homo sapiens,18|18,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA02741,GSE166429,GPL16791,1000,C4 Deficiency,C3899844,Skin,GEO,RNA-Seq,Homo sapiens,5|5,"NCI:Lack of production of functional C4 protein, due to a genetic defect requiring homozygous loss of both the C4A and C4B genetic paralogs. Approximately 75% of patients with a C4 deficiency will develop a severe systemic lupus erythematosus at an early age. Patients also present with frequent sinopulmonary infections often with Streptococcus pneumoniae." DSA02742,GSE166925,GPL20301,1000,Crohn's Disease,C0010346,Intestine,GEO,RNA-Seq,Homo sapiens,42|34,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02743,GSE173294,GPL16791,1000,Crohn's Disease,C0010346,Small intestine,GEO,RNA-Seq,Homo sapiens,1|1,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02744,GSE173294,GPL16791,1000,Crohn's Disease,C0010346,Small intestine,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02745,GSE173294,GPL16791,1000,Crohn's Disease,C0010346,Small intestine,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02746,GSE173294,GPL16791,1000,Crohn's Disease,C0010346,Small intestine,GEO,RNA-Seq,Homo sapiens,1|1,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02747,GSE173294,GPL16791,1000,Crohn's Disease,C0010346,Small intestine,GEO,RNA-Seq,Homo sapiens,2|2,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02748,GSE173294,GPL16791,1000,Crohn's Disease,C0010346,Small intestine,GEO,RNA-Seq,Homo sapiens,2|2,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02749,GSE174792,GPL16791,248,Crohn's Disease,C0010346,Small intestine,GEO,RNA-Seq,Homo sapiens,5|3,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02750,GSE174792,GPL16791,315,Crohn's Disease,C0010346,Small intestine,GEO,RNA-Seq,Homo sapiens,3|5,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02751,GSE174792,GPL16791,122,Crohn's Disease,C0010346,Small intestine,GEO,RNA-Seq,Homo sapiens,5|3,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02752,GSE174792,GPL16791,1000,Crohn's Disease,C0010346,Small intestine,GEO,RNA-Seq,Homo sapiens,3|5,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02753,GSE17732,GPL571,1000,Cryopyrin-Associated Periodic Syndromes,C2316212,Whole blood,GEO,Microarray,Homo sapiens,6|3,"MONDO:Cryopyrin associated periodic syndrome (CAPS) defines a group of autoinflammatory diseases, characterized by recurrent episodes of systemic inflammatory attacks in the absence of infection or autoimmune disease. CAPS comprises 3 disorders on a continuum of severity: severe CINCA syndrome, intermediate Muckle-Wells syndrome (MWS) and milder familial cold urticaria (FCAS)." DSA02754,GSE176528,GPL24247,36,Cyfip2 Deficiency,,Retina,GEO,RNA-Seq,Mus musculus,3|3, DSA02755,E-MTAB-4586,,311,Parkinson's Disease,C0030567,,ArrayExpress,RNA-Seq,Homo sapiens,16|8,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA02756,GSE176205,GPL20301,1000,Degenerative Intervertebral Discs,C2717759,Nucleus pulposus,GEO,RNA-Seq,Homo sapiens,3|5,"MSH:Degenerative changes in the INTERVERTEBRAL DISC due to aging or structural damage, especially to the vertebral end-plates." DSA02757,E-MTAB-4586,,337,Parkinson's Disease,C0030567,,ArrayExpress,RNA-Seq,Homo sapiens,16|4,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA02758,E-MTAB-4586,,169,Parkinson's Disease,C0030567,,ArrayExpress,RNA-Seq,Homo sapiens,16|4,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA02759,E-MTAB-4902,,1000,Visceral Leishmaniasis,C0023290,Whole blood,ArrayExpress,RNA-Seq,Homo sapiens,5|3,"DO:A leishmaniasis that is the most severe form of the disease caused by protozoan parasites of the Leishmania genus, resulting in the infection of the internal organs such as liver, spleen and bone marrow. The symptoms include fever, weight loss, and an enlarged spleen and liver." DSA02760,E-MTAB-5449,,56,Heart Failure,C0018801,Left ventricle,ArrayExpress,RNA-Seq,Mus musculus,3|3,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA02761,E-MTAB-5464,,532,Crohn's Disease,C0010346,Ascending colon,ArrayExpress,RNA-Seq,Homo sapiens,5|3,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02762,E-MTAB-5464,,1000,Crohn's Disease,C0010346,Sigmoid colon,ArrayExpress,RNA-Seq,Homo sapiens,10|4,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02763,E-MTAB-5464,,1000,Crohn's Disease,C0010346,Terminal ileum,ArrayExpress,RNA-Seq,Homo sapiens,10|7,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02764,E-MTAB-5464,,124,Ulcerative Colitis,C0009324,Ascending colon,ArrayExpress,RNA-Seq,Homo sapiens,5|2,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02765,E-MTAB-5464,,1000,Ulcerative Colitis,C0009324,Sigmoid colon,ArrayExpress,RNA-Seq,Homo sapiens,10|4,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02766,E-MTAB-5464,,1,Ulcerative Colitis,C0009324,Terminal ileum,ArrayExpress,RNA-Seq,Homo sapiens,10|10,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02767,GSE169494,GPL24676,1000,Developmental Dysplasia of The Hip,C1306065,Hip joint capsule,GEO,RNA-Seq,Homo sapiens,6|6,EFO:A spectrum of hip abnormalities commonly presenting in infancy involving the relationship between the femoral head and the acetabulum and that includes subluxation or dislocation at rest or upon provocation. DSA02768,E-MTAB-5464,,131,Crohn's Disease,C0010346,Ascending colon,ArrayExpress,RNA-Seq,Homo sapiens,5|2,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02769,E-MTAB-5464,,1000,Crohn's Disease,C0010346,Sigmoid colon,ArrayExpress,RNA-Seq,Homo sapiens,10|6,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02770,E-MTAB-5464,,1000,Crohn's Disease,C0010346,Terminal ileum,ArrayExpress,RNA-Seq,Homo sapiens,10|3,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02771,E-MTAB-5464,,1000,Ulcerative Colitis,C0009324,Ascending colon,ArrayExpress,RNA-Seq,Homo sapiens,5|3,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02772,E-MTAB-5464,,1000,Ulcerative Colitis,C0009324,Sigmoid colon,ArrayExpress,RNA-Seq,Homo sapiens,10|7,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02773,E-MTAB-5464,,1000,Ulcerative Colitis,C0009324,Terminal ileum,ArrayExpress,RNA-Seq,Homo sapiens,10|1,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02774,E-MTAB-5616,,46,Juvenile Dermatomyositis,C0263666,Blood,ArrayExpress,RNA-Seq,Homo sapiens,4|18,EFO:Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness. DSA02775,E-MTAB-5668,,1000,Alzheimer's Disease,C0002395,Hippocampus,ArrayExpress,RNA-Seq,Mus musculus,20|18,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA02776,E-MTAB-5668,,1000,Alzheimer's Disease,C0002395,Hippocampus,ArrayExpress,RNA-Seq,Mus musculus,20|20,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA02777,GSE175759,GPL16791,615,Diabetic Kidney Disease,C0011881,Tubulointerstitium,GEO,RNA-Seq,Homo sapiens,22|3,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA02778,GSE178299,GPL20844,0,Diffuse Cutaneous Systemic Sclerosis,C1258104,,GEO,Microarray,Homo sapiens,5|5,"EFO:A variant of systemic scleroderma characterized by sclerosis of the skin, Raynaud phenomenon, and organ involvement, including pulmonary fibrosis, renal disease, and gastrointestinal tract involvement." DSA02779,GSE178299,GPL20844,0,Diffuse Cutaneous Systemic Sclerosis,C1258104,,GEO,Microarray,Homo sapiens,5|5,"EFO:A variant of systemic scleroderma characterized by sclerosis of the skin, Raynaud phenomenon, and organ involvement, including pulmonary fibrosis, renal disease, and gastrointestinal tract involvement." DSA02780,GSE165303,GPL18573|GPL20795,1000,Dilated Cardiomyopathy,C0007193,Heart,GEO,RNA-Seq,Homo sapiens,51|50,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA02781,GSE167021,GPL18573,51,Down Syndrome,C0013080,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA02782,GSE167021,GPL18573,79,Down Syndrome,C0013080,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA02783,E-MTAB-567,,1000,Prostate Carcinoma,C0600139,Prostate gland,ArrayExpress,RNA-Seq,Homo sapiens,13|14,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02784,E-MTAB-5678,,1000,Actinic Keratosis,C0022602,Skin,ArrayExpress,RNA-Seq,Homo sapiens,4|13,"EFO:An actinic keratosis (ak-TIN-ik ker-uh-TOE-sis) is a rough, scaly patch on your skin that develops from years of exposure to the sun. It's most commonly found on your face, lips, ears, back of your hands, forearms, scalp or neck. Also known as solar keratosis, an actinic keratosis enlarges slowly and usually causes no signs or symptoms other than a patch or small spot on your skin. These lesions take years to develop, usually first appearing in older adults. A small percentage of actinic keratosis lesions can eventually become skin cancer. You can reduce your risk of actinic keratosis by minimizing your sun exposure and protecting your skin from ultraviolet (UV) rays." DSA02785,GSE173252,GPL20301,1000,Dupuytren's Disease,C4082974,Dermis,GEO,scRNA-Seq,Homo sapiens,3|3,EFO:A fibromatosis of the palmar fascia characterized by thickening and contracture of the fibrous bands on the palmar surfaces of the hand and fingers. It arises most commonly in men between the ages of 30 and 50. DSA02786,GSE168278,GPL24247,1000,Dyslipidemia,C0242339,Adipose tissue,GEO,scRNA-Seq,Mus musculus,1|1,HPO:Any deviation from the normal concentration of a lipid in the blood circulation. DSA02787,GSE174302,GPL20795,1000,Esophageal Cancer,C0152018,Plasma,GEO,RNA-Seq,Homo sapiens,46|31,DO:A esophageal cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA02788,E-MTAB-5678,,1000,Sebaceous of Jadassohn Nevus,C4552097,Skin,ArrayExpress,RNA-Seq,Homo sapiens,4|7,"DO:A syndrome characterized by sebaceous nevi typically on the face and associated with variable ipsilateral abnormalities of the central nervous system, ocular anomalies, and skeletal defects that has_material_basis_in somatic mosaic mutations in NRAS, HRAS, or KRAS on chromosomes 1p13.2, 11p15.5, or 12p12.1, respectively." DSA02789,GSE17732,GPL571,72,Familial Mediterranean Fever,C0031069,Whole blood,GEO,Microarray,Homo sapiens,6|2,"DO:A peroxisomal disease that is characterized by cortical atrophy, microcephaly, dysmorphic facies, muscular hypotonia and intellectual disability and has_material_basis_in mutation in the MVK gene that results in deficiency of mevalonate kinase and impaired cholesterol. biosynthesis." DSA02790,E-MTAB-5678,,1000,Squamous Cell Carcinoma,C0007137,Skin,ArrayExpress,RNA-Seq,Homo sapiens,4|5,DO:A carcinoma that derives_from squamous epithelial cells. DSA02791,E-MTAB-5783,,1000,Crohn's Disease,C0010346,Small intestine,ArrayExpress,RNA-Seq,Homo sapiens,32|36,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02792,GSE174605,GPL29761,0,Focal Cortical Dysplasia,C2938983,Organoid,GEO,Microarray,Homo sapiens,4|4,"HPO:A type of malformation of cortical development that primarily affects areas of neocortex. It can be identified on conventional magnetic resonance imaging as focal cortical thickening, abnormal gyration, and blurring between gray and white matter, often associated with clusters of heterotopic neurons." DSA02793,GSE175759,GPL16791,1000,Focal Segmental Glomerulosclerosis,C0017668,Tubulointerstitium,GEO,RNA-Seq,Homo sapiens,22|3,"EFO:A renal disorder characterized by sclerotic lesions in the glomeruli. Causes include drugs, viruses, and malignancies (lymphomas), or it may be idiopathic. It presents with asymptomatic proteinuria or nephritic syndrome and it may lead to renal failure." DSA02794,GSE171830,GPL10558,1000,Fuchs Endothelial Corneal Dystrophy,C0016781,,GEO,Microarray,Homo sapiens,6|6,"DO:A corneal dystrophy that is characterized by corneal edema, iris atrophy, and secondary angle-closure glaucoma caused by an inflammatory or infectious insult that causes the endothelium to fail to pump aqueous humor from the cornea, leading to fluid accumulation, microcystic edema, and angle-closure glaucoma." DSA02795,GSE168439,GPL21163,1000,Gastroenteritis,C0017160,,GEO,Microarray,Mus musculus,4|4,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA02796,GSE166201,GPL24676,1000,Gata2 Deficiency,C3280030,,GEO,RNA-Seq,Homo sapiens,2|1,"MONDO:A disorder arising from deficiency in the GATA2 with a wide spectrum of phenotypes. Autosomal dominant mutations of GATA2 cause a haploinsufficiency, which, in consequence, cause individuals to develop hematological, immunological, lymphatic, or other presentations. These often progress to severe organ (e.g. lung) failure, opportunistic infections, myelodysplastic syndrome, and/or acute myeloid leukemia. The most common clinical denominator is the propensity for myeloid neoplasia (myelodysplastic syndrome" DSA02797,GSE166201,GPL24676,1000,Gata2 Deficiency,C3280030,,GEO,RNA-Seq,Homo sapiens,2|1,"MONDO:A disorder arising from deficiency in the GATA2 with a wide spectrum of phenotypes. Autosomal dominant mutations of GATA2 cause a haploinsufficiency, which, in consequence, cause individuals to develop hematological, immunological, lymphatic, or other presentations. These often progress to severe organ (e.g. lung) failure, opportunistic infections, myelodysplastic syndrome, and/or acute myeloid leukemia. The most common clinical denominator is the propensity for myeloid neoplasia (myelodysplastic syndrome" DSA02798,E-MTAB-6018,,17,Autism Spectrum Disorder,C1510586,Skin,ArrayExpress,RNA-Seq,Homo sapiens,5|8,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA02799,GSE173078,GPL20301,40,Gingivitis,C0017574,Gingiva,GEO,RNA-Seq,Homo sapiens,12|12,HPO:Inflammation of the gingiva. DSA02800,GSE167363,GPL24676,1000,Gram-Negative Sepsis,C0036685,Blood,GEO,RNA-Seq,Homo sapiens,2|4, DSA02801,GSE167363,GPL24676,601,Gram-Negative Sepsis,C0036685,Blood,GEO,RNA-Seq,Homo sapiens,2|6, DSA02802,GSE168409,GPL21290,4,Gulf War Illness,,,GEO,RNA-Seq,Homo sapiens,19|20, DSA02803,GSE168409,GPL21290,0,Gulf War Illness,,,GEO,RNA-Seq,Homo sapiens,20|18, DSA02804,GSE168409,GPL21290,1,Gulf War Illness,,,GEO,RNA-Seq,Homo sapiens,20|20, DSA02805,GSE175764,GPL18573,187,Heart Failure,C0018801,Heart,GEO,RNA-Seq,Homo sapiens,5|5,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA02806,E-MTAB-6018,,35,Autism Spectrum Disorder,C1510586,Skin,ArrayExpress,RNA-Seq,Homo sapiens,5|8,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA02807,E-MTAB-6018,,0,Autism Spectrum Disorder,C1510586,Skin,ArrayExpress,RNA-Seq,Homo sapiens,5|8,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA02808,E-MTAB-6018,,322,Autism Spectrum Disorder,C1510586,Skin,ArrayExpress,RNA-Seq,Homo sapiens,5|8,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA02809,E-MTAB-6018,,0,Autism Spectrum Disorder,C1510586,Skin,ArrayExpress,RNA-Seq,Homo sapiens,5|8,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA02810,E-MTAB-6018,,32,Autism Spectrum Disorder,C1510586,Skin,ArrayExpress,RNA-Seq,Homo sapiens,5|8,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA02811,GSE166695,GPL19057,1000,Huntington's Disease,C0020179,,GEO,RNA-Seq,Mus musculus,2|2,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA02812,GSE170997,GPL17021,69,Huntington's Disease,C0020179,Brain,GEO,RNA-Seq,Mus musculus,31|24,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA02813,GSE1767,GPL1449,1000,Huntington's Disease,C0020179,Whole blood,GEO,Microarray,Homo sapiens,19|12,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA02814,GSE178101,GPL24676,1000,Hydrosalpinx (Disease),C0221376,Fallopian tube,GEO,RNA-Seq,Homo sapiens,4|1,NCI:Fluid accumulation and dilatation of the fallopian tube due to tubal blockage. DSA02815,GSE165879,GPL19057|GPL21103,1000,Hyperhomocysteinemia,C0598608,,GEO,RNA-Seq,Mus musculus,4|4,DO:An amino acid metabolic disorder that involves an abnormally large level of homocysteine in the blood. DSA02816,E-MTAB-6018,,317,Autism Spectrum Disorder,C1510586,Skin,ArrayExpress,RNA-Seq,Homo sapiens,5|8,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA02817,GSE176153,GPL17303,1,Hypothyroidism,C0020676,Whole blood,GEO,RNA-Seq,Homo sapiens,4|4,DO:A thyroid gland disease which involves an underproduction of thyroid hormone. DSA02818,GSE171398,GPL16791,46,Idiopathic Intracranial Hypertension,C0033845,Adipose tissue,GEO,RNA-Seq,Homo sapiens,7|13,"MONDO:Idiopathic intracranial hypertension is a neurological disorder characterized by isolated increased intracranial pressure manifesting with recurrent and persistent headaches, nausea, vomiting, progressive and transient obstruction of the visual field, papilledema. Visual loss can be irreversible." DSA02819,E-MTAB-6018,,21,Autism Spectrum Disorder,C1510586,Skin,ArrayExpress,RNA-Seq,Homo sapiens,5|8,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA02820,E-MTAB-6018,,14,Autism Spectrum Disorder,C1510586,Skin,ArrayExpress,RNA-Seq,Homo sapiens,5|8,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA02821,GSE166059,GPL20301,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,RNA-Seq,Homo sapiens,4|10,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA02822,GSE166059,GPL20301,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,RNA-Seq,Homo sapiens,4|8,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA02823,GSE166059,GPL20301,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,RNA-Seq,Homo sapiens,5|10,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA02824,GSE176001,GPL24676,1000,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,RNA-Seq,Homo sapiens,1|2,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA02825,GSE176001,GPL24676,1000,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,RNA-Seq,Homo sapiens,1|2,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA02826,GSE176001,GPL24676,1000,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,RNA-Seq,Homo sapiens,1|2,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA02827,GSE176001,GPL24676,1000,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,RNA-Seq,Homo sapiens,2|2,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA02828,GSE176001,GPL24676,1000,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,RNA-Seq,Homo sapiens,2|2,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA02829,GSE176001,GPL24676,1000,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,RNA-Seq,Homo sapiens,2|2,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA02830,E-MTAB-6293,,1000,Spinocerebellar Ataxia Type 2,C0752121,Cerebellum,ArrayExpress,RNA-Seq,Mus musculus,32|32,"DO:An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene." DSA02831,E-MTAB-6413,,271,Hyperlactatemia,C0795692,Blood,ArrayExpress,RNA-Seq,Homo sapiens,7|13,MSH:Increase in blood LACTATE concentration often associated with SEPTIC SHOCK; LUNG INJURY; SEPSIS; and DRUG TOXICITY. When hyperlactatemia is associated with low body pH (acidosis) it is LACTIC ACIDOSIS. DSA02832,GSE171314,GPL20795,1000,IgA Nephropathy,C0017661,Kidney,GEO,RNA-Seq,Homo sapiens,1|4,DO:A glomerulonephritis characterized by build up of IgA antibody in the glomerulus. DSA02833,GSE175759,GPL16791,1000,IgA Nephropathy,C0017661,Tubulointerstitium,GEO,RNA-Seq,Homo sapiens,22|46,DO:A glomerulonephritis characterized by build up of IgA antibody in the glomerulus. DSA02834,E-MTAB-6413,,0,Cerebral Malaria,C0024534,Blood,ArrayExpress,RNA-Seq,Homo sapiens,8|13,"DO:A malaria that involves neurologic damage resulting from blockage of the blood vessels, caused due to the infection of the red blood cells by Plasmodium species." DSA02835,E-MTAB-6490,,1000,Retinitis Pigmentosa,C0035334,,ArrayExpress,RNA-Seq,Homo sapiens,7|8,DO:A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss. DSA02836,GSE166522,GPL24247,346,Osteomyelitis,C0029443,Bone,GEO,RNA-Seq,Mus musculus,3|3,DO:A bone inflammation disease that has_material_basis_in infection located_in bone or located_in bone marrow. DSA02837,GSE166522,GPL24247,1000,Osteomyelitis,C0029443,Bone,GEO,RNA-Seq,Mus musculus,3|3,DO:A bone inflammation disease that has_material_basis_in infection located_in bone or located_in bone marrow. DSA02838,GSE179128,GPL16791,187,Crohn's Disease,C0010346,Colon,GEO,RNA-Seq,Homo sapiens,6|5,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA02839,GSE179128,GPL16791,2,Ulcerative Colitis,C0009324,Colon,GEO,RNA-Seq,Homo sapiens,6|6,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02840,E-MTAB-6490,,447,Retinitis Pigmentosa,C0035334,,ArrayExpress,RNA-Seq,Homo sapiens,7|8,DO:A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss. DSA02841,GSE165399,GPL20795,1000,Intraductal Papillary Neoplasm,C1879344,,GEO,RNA-Seq,Homo sapiens,1|1,DO:A biliary tract benign neoplasm characterized by multiple papillary tumors in the intrahepatic and/or extrahepatic biliary tree. DSA02842,GSE171443,GPL13112,1000,Intrahepatic Cholangiocarcinoma,C0345905,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:A cholangiocarcinoma that arises from the intrahepatic bile duct epithelium in any site of the intrahepatic biliary tree. DSA02843,GSE171443,GPL13112,1000,Intrahepatic Cholangiocarcinoma,C0345905,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:A cholangiocarcinoma that arises from the intrahepatic bile duct epithelium in any site of the intrahepatic biliary tree. DSA02844,GSE171443,GPL13112,1000,Intrahepatic Cholangiocarcinoma,C0345905,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:A cholangiocarcinoma that arises from the intrahepatic bile duct epithelium in any site of the intrahepatic biliary tree. DSA02845,GSE171443,GPL13112,1000,Intrahepatic Cholangiocarcinoma,C0345905,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:A cholangiocarcinoma that arises from the intrahepatic bile duct epithelium in any site of the intrahepatic biliary tree. DSA02846,GSE174825,GPL18573,1000,Invasive Aspergillosis,C0238013,Blood,GEO,RNA-Seq,Homo sapiens,27|38,"MONDO:An aspergillosis that is a serious fungal infection of the lung with pneumonia caused by Aspergillus, which spreads to other parts of the body through bloodstream in patients with acute leukemia and recipients of tissue transplants. Clinical symptoms include pulmonary nodules and hemorrhage." DSA02847,GSE169500,GPL17301,1000,IPF Alveolar Septae,,Lung,GEO,RNA-Seq,Homo sapiens,10|10, DSA02848,GSE169500,GPL17301,1000,IPF Fibrobalst Foci,,Lung,GEO,RNA-Seq,Homo sapiens,10|10, DSA02849,GSE166869,GPL24676,4,Irritable Bowel Syndrome,C0022104,Duodenum,GEO,RNA-Seq,Homo sapiens,3|10,"DO:An intestinal disease that is characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause." DSA02850,GSE166869,GPL24676,70,Irritable Bowel Syndrome,C0022104,Jejunum,GEO,RNA-Seq,Homo sapiens,12|7,"DO:An intestinal disease that is characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause." DSA02851,GSE166869,GPL24676,2,Irritable Bowel Syndrome,C0022104,Duodenum,GEO,RNA-Seq,Homo sapiens,3|9,"DO:An intestinal disease that is characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause." DSA02852,GSE166869,GPL24676,61,Irritable Bowel Syndrome,C0022104,Jejunum,GEO,RNA-Seq,Homo sapiens,12|9,"DO:An intestinal disease that is characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause." DSA02853,E-MTAB-7145,,558,Systemic Lupus Erythematosus,C0024141,Blood,ArrayExpress,RNA-Seq,Homo sapiens,2|2,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA02854,E-MTAB-7146,,1000,Multiple Myeloma,C0026764,Blood,ArrayExpress,RNA-Seq,Homo sapiens,1|1,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA02855,GSE16499,GPL5175,954,Chronic Heart Failure,C0018801,Left ventricle,GEO,Microarray,Homo sapiens,15|15,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA02856,E-MTAB-727,,1000,Cardiac Hypertrophy,C1383860,Heart,ArrayExpress,RNA-Seq,Mus musculus,3|3,"EFO:an increase in size of the cardiac tissue, not due to increased cell number" DSA02857,GSE165385,GPL16791,420,Ketosis-Prone Diabetes (Mellitus),C3837958,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA02858,GSE165385,GPL16791,1000,Ketosis-Prone Diabetes (Mellitus),C3837958,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA02859,GSE165385,GPL16791,1000,Ketosis-Prone Diabetes (Mellitus),C3837958,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA02860,GSE168813,GPL17303,7,Late-Onset Form of Familial Alzheimer Disease,C0002395,Blood,GEO,RNA-Seq,Homo sapiens,10|5,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA02861,GSE166050,GPL21103,1000,Leptospirosis,C0023364,,GEO,RNA-Seq,Mus musculus,3|3,"DO:A primary bacterial infectious disease that involves systemic infection, has_material_basis_in Leptospira, which is transmitted by contact with water, food, or soil containing urine from the infected animals. The infection has symptom jaundice, has symptom chills, has symptom fever, has symptom muscle pain, and has symptom hepatomegaly." DSA02862,GSE166050,GPL21103,1000,Leptospirosis,C0023364,,GEO,RNA-Seq,Mus musculus,3|3,"DO:A primary bacterial infectious disease that involves systemic infection, has_material_basis_in Leptospira, which is transmitted by contact with water, food, or soil containing urine from the infected animals. The infection has symptom jaundice, has symptom chills, has symptom fever, has symptom muscle pain, and has symptom hepatomegaly." DSA02863,GSE166050,GPL21103,1000,Leptospirosis,C0023364,,GEO,RNA-Seq,Mus musculus,3|3,"DO:A primary bacterial infectious disease that involves systemic infection, has_material_basis_in Leptospira, which is transmitted by contact with water, food, or soil containing urine from the infected animals. The infection has symptom jaundice, has symptom chills, has symptom fever, has symptom muscle pain, and has symptom hepatomegaly." DSA02864,GSE166050,GPL21103,1000,Leptospirosis,C0023364,,GEO,RNA-Seq,Mus musculus,3|3,"DO:A primary bacterial infectious disease that involves systemic infection, has_material_basis_in Leptospira, which is transmitted by contact with water, food, or soil containing urine from the infected animals. The infection has symptom jaundice, has symptom chills, has symptom fever, has symptom muscle pain, and has symptom hepatomegaly." DSA02865,E-MTAB-727,,768,Cardiac Hypertrophy,C1383860,Heart,ArrayExpress,RNA-Seq,Mus musculus,3|3,"EFO:an increase in size of the cardiac tissue, not due to increased cell number" DSA02866,E-MTAB-7287,,1000,Duchenne Muscular Dystrophy,C0013264,Skeletal muscle,ArrayExpress,RNA-Seq,Mus musculus,4|4,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02867,GSE174302,GPL20795,1000,Liver Cancer,C2239176,Plasma,GEO,RNA-Seq,Homo sapiens,46|27,DO:A hepatobiliary system cancer that is located_in the liver. DSA02868,GSE171248,GPL16791,1000,Liver Cirrhosis,C0023890,Liver,GEO,RNA-Seq,Homo sapiens,8|8,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA02869,GSE166752,GPL19057,714,Fibrosis; Liver,C0239946,Liver,GEO,RNA-Seq,Mus musculus,6|6,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA02870,GSE166752,GPL19057,22,Fibrosis; Liver,C0239946,Liver,GEO,RNA-Seq,Mus musculus,6|6,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA02871,GSE173961,GPL24247,1000,Fibrosis; Liver,C0239946,,GEO,RNA-Seq,Mus musculus,3|3,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA02872,E-MTAB-7315,,1000,Colitis,C0009319,Colon,ArrayExpress,RNA-Seq,Mus musculus,12|16,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA02873,GSE171294,GPL24676,41,Fibrosis; Liver,C0239946,Liver,GEO,RNA-Seq,Homo sapiens,4|4,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA02874,E-MTAB-7340,,885,Klinefelter Syndrome,C0022735,Skin,ArrayExpress,RNA-Seq,Homo sapiens,9|6,DO:A chromosomal duplication syndrome that is characterized by infertility and that has_material_basis_in an extra X chromosome in cells in men. DSA02875,GSE166861,GPL18573,1000,Localized Scleroderma,C0036420,Skin,GEO,RNA-Seq,Homo sapiens,6|16,"DO:A rheumatic disease that involves the abnormal growth of connective tissue, which supports the skin and internal organs." DSA02876,GSE166863,GPL18573,12,Localized Scleroderma,C0036420,Skin,GEO,RNA-Seq,Homo sapiens,6|4,"DO:A rheumatic disease that involves the abnormal growth of connective tissue, which supports the skin and internal organs." DSA02877,GSE166863,GPL18573,167,Localized Scleroderma,C0036420,Skin,GEO,RNA-Seq,Homo sapiens,6|9,"DO:A rheumatic disease that involves the abnormal growth of connective tissue, which supports the skin and internal organs." DSA02878,GSE174302,GPL20795,1000,Lung Cancer,C0684249,Plasma,GEO,RNA-Seq,Homo sapiens,46|35,DO:A respiratory system cancer that is located_in the lung. DSA02879,GSE175759,GPL16791,1000,Lupus Nephritis,C0024143,Tubulointerstitium,GEO,RNA-Seq,Homo sapiens,22|3,DO:A glomerulonephritis that is characterized by inflammation of the kidneys resulting from systemic lupus erythematosus. DSA02880,GSE169024,GPL17021,1000,Mammary Tumor,C1512981,Blood,GEO,RNA-Seq,Mus musculus,3|3,NCI:Production of a new growth or growths in the mammary gland. DSA02881,GSE169024,GPL17021,1000,Mammary Tumor,C1512981,Lung,GEO,RNA-Seq,Mus musculus,3|3,NCI:Production of a new growth or growths in the mammary gland. DSA02882,GSE169024,GPL17021,496,Mammary Tumor,C1512981,Lymph node,GEO,RNA-Seq,Mus musculus,3|3,NCI:Production of a new growth or growths in the mammary gland. DSA02883,GSE169024,GPL17021,319,Mammary Tumor,C1512981,Spleen,GEO,RNA-Seq,Mus musculus,3|4,NCI:Production of a new growth or growths in the mammary gland. DSA02884,GSE179036,GPL19057|GPL21493,1000,Mammary Tumor,C1512981,Mammary gland,GEO,RNA-Seq,Mus musculus,4|3,NCI:Production of a new growth or growths in the mammary gland. DSA02885,GSE179036,GPL19057|GPL21493,1000,Mammary Tumor,C1512981,Mammary gland,GEO,RNA-Seq,Mus musculus,4|3,NCI:Production of a new growth or growths in the mammary gland. DSA02886,GSE175759,GPL16791,1000,Membranous Nephropathy,C0017665,Tubulointerstitium,GEO,RNA-Seq,Homo sapiens,22|4,"EFO:A type of glomerulonephritis that is characterized by the accumulation of immune deposits ( COMPLEMENT MEMBRANE ATTACK COMPLEX) on the outer aspect of the GLOMERULAR BASEMENT MEMBRANE. It progresses from subepithelial dense deposits, to basement membrane reaction and eventual thickening of the basement membrane." DSA02887,GSE175759,GPL16791,1000,Minimal Change Disease,C0027721,Tubulointerstitium,GEO,RNA-Seq,Homo sapiens,22|9,"DO:A nephrosis characterized by marked increase in glomerular protein permeability resulting in marked elevation of urine protein levels, hypoalbuminemia, hyperlipidemia, and hypercoagulability." DSA02888,GSE175384,GPL18573,1000,Monoclonal Gammopathy of Undetermined Significance,C0026470,,GEO,RNA-Seq,Homo sapiens,40|6,DO:A blood protein disease that is characterized by the presence of an abnormal protein called monoclonal protein in the blood. DSA02889,E-MTAB-7596,,1000,African Trypanosomiasis,C0041228,Adipose tissue,ArrayExpress,RNA-Seq,Mus musculus,3|2,"DO:A trypanosomiasis that results from infection by Trypanosoma brucei and gambiense, which is transmitted by the bite of an infected tsetse fly (Glossina spp). The symptoms include fever, headache, joint pain, itching, confusion, sensory disturbances, poor coordination and sleep disturbances." DSA02890,E-MTAB-7698,,1000,Duchenne Muscular Dystrophy,C0013264,Tibialis anterior,ArrayExpress,RNA-Seq,Mus musculus,4|4,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02891,GSE175384,GPL18573,1000,Multiple Myeloma,C0026764,,GEO,RNA-Seq,Homo sapiens,40|31,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA02892,E-MTAB-7698,,1000,Duchenne Muscular Dystrophy,C0013264,Tibialis anterior,ArrayExpress,RNA-Seq,Mus musculus,4|4,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA02893,GSE168527,GPL20301,151,Multiple Sclerosis,C0026769,,GEO,RNA-Seq,Homo sapiens,5|3,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA02894,GSE168527,GPL20301,685,Multiple Sclerosis,C0026769,,GEO,RNA-Seq,Homo sapiens,5|5,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA02895,GSE17048,GPL6947,0,Multiple Sclerosis,C0026769,Whole blood,GEO,Microarray,Homo sapiens,45|43,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA02896,GSE17048,GPL6947,2,Multiple Sclerosis,C0026769,Whole blood,GEO,Microarray,Homo sapiens,45|36,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA02897,GSE17048,GPL6947,0,Multiple Sclerosis,C0026769,Whole blood,GEO,Microarray,Homo sapiens,45|20,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA02898,GSE173789,GPL20795,1000,Multiple Sclerosis,C0026769,Peripheral blood,GEO,RNA-Seq,Homo sapiens,14|23,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA02899,GSE17393,GPL571,0,Multiple Sclerosis,C0026769,,GEO,Microarray,Homo sapiens,7|8,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA02900,E-MTAB-7714,,1000,Spinocerebellar Ataxia Type 1,C0752120,Cerebellum,ArrayExpress,RNA-Seq,Homo sapiens,1|1,"DO:An autosomal dominant cerebellar ataxia that is characterized by ataxia, dysarthria, dysphagia, dystonia and peripheral neuropathy that begins in early adulthood, has_material_basis_in the expanded (CAG)n trinucleotide repeat of ataxin-1 gene on chromosome 6p22." DSA02901,E-MTAB-7770,,1000,Hereditary Spastic Paraplegia 3A,C2931355,Skin,ArrayExpress,RNA-Seq,Homo sapiens,10|8,DO:A hereditary spastic paraplegia that is characterized by lower limb weakness and spasticity that is generally non-progressive or extremely slow and has_material_basis_in mutation in the ATL1 gene on chromosome 14q22. DSA02902,E-MTAB-7770,,1000,Hereditary Spastic Paraplegia 3A,C2931355,Skin,ArrayExpress,RNA-Seq,Homo sapiens,6|8,DO:A hereditary spastic paraplegia that is characterized by lower limb weakness and spasticity that is generally non-progressive or extremely slow and has_material_basis_in mutation in the ATL1 gene on chromosome 14q22. DSA02903,GSE166489,GPL24676,221,Neonatal-Onset Multisystem Inflammatory Disease,C0409818,,GEO,RNA-Seq,Homo sapiens,6|4,"DO:An autoimmune disease characterized by neonatal onset of cutaneous symptoms, chronic meningitis, and joint manifestations with recurrent fever and inflammation that has_material_basis_in heterozygous mutation in the NLRP3 gene on chromosome 1q." DSA02904,E-MTAB-7830,,1,Tuberculosis,C0041296,Blood,ArrayExpress,RNA-Seq,Homo sapiens,50|43,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA02905,GSE178388,GPL24676,121,Neonatal-Onset Multisystem Inflammatory Disease,C0409818,Blood,GEO,RNA-Seq,Homo sapiens,9|3,"DO:An autoimmune disease characterized by neonatal onset of cutaneous symptoms, chronic meningitis, and joint manifestations with recurrent fever and inflammation that has_material_basis_in heterozygous mutation in the NLRP3 gene on chromosome 1q." DSA02906,GSE173205,GPL24676,1000,Mycosis Fungoides,C0026948,Skin,GEO,scRNA-Seq,Homo sapiens,4|2,"MONDO:Classical mycosis fungoides is the most common type of mycosis fungoides (MF), a form of cutaneous T-cell lymphoma, and is characterized by slow progression from patches to more infiltrated plaques and eventually to tumors." DSA02907,GSE173205,GPL24676,1000,Mycosis Fungoides,C0026948,Skin,GEO,scRNA-Seq,Homo sapiens,4|3,"MONDO:Classical mycosis fungoides is the most common type of mycosis fungoides (MF), a form of cutaneous T-cell lymphoma, and is characterized by slow progression from patches to more infiltrated plaques and eventually to tumors." DSA02908,GSE173205,GPL24676,1000,Mycosis Fungoides,C0026948,Skin,GEO,scRNA-Seq,Homo sapiens,4|3,"MONDO:Classical mycosis fungoides is the most common type of mycosis fungoides (MF), a form of cutaneous T-cell lymphoma, and is characterized by slow progression from patches to more infiltrated plaques and eventually to tumors." DSA02909,GSE173205,GPL24676,1000,Mycosis Fungoides,C0026948,Skin,GEO,scRNA-Seq,Homo sapiens,4|6,"MONDO:Classical mycosis fungoides is the most common type of mycosis fungoides (MF), a form of cutaneous T-cell lymphoma, and is characterized by slow progression from patches to more infiltrated plaques and eventually to tumors." DSA02910,GSE173205,GPL24676,1000,Mycosis Fungoides,C0026948,Skin,GEO,scRNA-Seq,Homo sapiens,4|4,"MONDO:Classical mycosis fungoides is the most common type of mycosis fungoides (MF), a form of cutaneous T-cell lymphoma, and is characterized by slow progression from patches to more infiltrated plaques and eventually to tumors." DSA02911,GSE173205,GPL24676,1000,Mycosis Fungoides,C0026948,Skin,GEO,scRNA-Seq,Homo sapiens,4|3,"MONDO:Classical mycosis fungoides is the most common type of mycosis fungoides (MF), a form of cutaneous T-cell lymphoma, and is characterized by slow progression from patches to more infiltrated plaques and eventually to tumors." DSA02912,GSE166798,GPL20795,8,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA02913,E-MTAB-7830,,1000,Tuberculosis,C0041296,Blood,ArrayExpress,RNA-Seq,Homo sapiens,50|65,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA02914,E-MTAB-7860,,1000,Ulcerative Colitis,C0009324,Colon,ArrayExpress,RNA-Seq,Homo sapiens,8|8,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02915,E-MTAB-7860,,1000,Ulcerative Colitis,C0009324,Crypt of colon,ArrayExpress,RNA-Seq,Homo sapiens,8|8,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02916,E-MTAB-7860,,1000,Ulcerative Colitis,C0009324,Crypt of colon,ArrayExpress,RNA-Seq,Homo sapiens,32|32,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02917,GSE168622,GPL23227,1000,Neuropathy In Association With Hereditary Ataxia,C0451669,,GEO,RNA-Seq,Homo sapiens,2|3,DO:A nervous system disease characterized by autosomal recessive inheritance of spinocerebellar ataxia and peripheral neuropathy that has_material_basis_in homozygosity for a mutation in the TDP1 gene on chromosome 14q32.11. DSA02918,GSE165660,GPL17021|GPL18694,27,Neurodevelopmental Disorder,C1535926,Cortex,GEO,RNA-Seq,Mus musculus,3|3,"MSH:These are a group of conditions with onset in the developmental period. The disorders typically manifest early in development, often before the child enters grade school, and are characterized by developmental deficits that produce impairments of personal, social, academic, or occupational functioning. (From DSM-5)." DSA02919,GSE165660,GPL17021|GPL18694,5,Neurodevelopmental Disorder,C1535926,Cortex,GEO,RNA-Seq,Mus musculus,3|6,"MSH:These are a group of conditions with onset in the developmental period. The disorders typically manifest early in development, often before the child enters grade school, and are characterized by developmental deficits that produce impairments of personal, social, academic, or occupational functioning. (From DSM-5)." DSA02920,GSE165660,GPL17021|GPL18694,12,Neurodevelopmental Disorder,C1535926,Cortex,GEO,RNA-Seq,Mus musculus,3|6,"MSH:These are a group of conditions with onset in the developmental period. The disorders typically manifest early in development, often before the child enters grade school, and are characterized by developmental deficits that produce impairments of personal, social, academic, or occupational functioning. (From DSM-5)." DSA02921,E-MTAB-7860,,1000,Ulcerative Colitis,C0009324,Colon,ArrayExpress,RNA-Seq,Homo sapiens,8|8,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02922,GSE173735,GPL18573|GPL19057|GPL24247,24,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Homo sapiens,4|4,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA02923,GSE173670,GPL20301,91,Non-Sjogren's sicca,,Peripheral blood,GEO,RNA-Seq,Homo sapiens,11|8, DSA02924,GSE166047,GPL18573,26,Obesity,C0028754,Adipose tissue,GEO,RNA-Seq,Homo sapiens,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA02925,GSE166047,GPL18573,778,Obesity,C0028754,Adipose tissue,GEO,RNA-Seq,Homo sapiens,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA02926,GSE171710,GPL19057,8,Obesity,C0028754,Heart,GEO,RNA-Seq,Mus musculus,4|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA02927,GSE171710,GPL19057,82,Obesity,C0028754,Heart,GEO,RNA-Seq,Mus musculus,4|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA02928,GSE171710,GPL19057,1,Obesity,C0028754,Heart,GEO,RNA-Seq,Mus musculus,4|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA02929,GSE171710,GPL19057,165,Obesity,C0028754,Heart,GEO,RNA-Seq,Mus musculus,4|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA02930,GSE171710,GPL19057,95,Obesity,C0028754,Heart,GEO,RNA-Seq,Mus musculus,4|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA02931,GSE171710,GPL19057,7,Obesity,C0028754,Heart,GEO,RNA-Seq,Mus musculus,4|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA02932,GSE173186,GPL24247,1000,Memory Dysfunction,C3887551,Olfactory epithelium,GEO,RNA-Seq,Mus musculus,3|3,"DO:A cognitive disorder where the memory is disturbed or lost and involves the loss of memories previously established, loss of the ability to create new memories, or loss of the ability to learn new information." DSA02933,GSE173186,GPL24247,1000,Memory Dysfunction,C3887551,Olfactory epithelium,GEO,RNA-Seq,Mus musculus,3|3,"DO:A cognitive disorder where the memory is disturbed or lost and involves the loss of memories previously established, loss of the ability to create new memories, or loss of the ability to learn new information." DSA02934,GSE173186,GPL24247,1000,Memory Dysfunction,C3887551,Olfactory epithelium,GEO,RNA-Seq,Mus musculus,3|3,"DO:A cognitive disorder where the memory is disturbed or lost and involves the loss of memories previously established, loss of the ability to create new memories, or loss of the ability to learn new information." DSA02935,GSE173186,GPL24247,1000,Memory Dysfunction,C3887551,Olfactory epithelium,GEO,RNA-Seq,Mus musculus,3|3,"DO:A cognitive disorder where the memory is disturbed or lost and involves the loss of memories previously established, loss of the ability to create new memories, or loss of the ability to learn new information." DSA02936,GSE174409,GPL18573,1000,Opioid Use Disorder; Severe,C4237239,Brain,GEO,RNA-Seq,Homo sapiens,20|20, DSA02937,GSE174409,GPL18573,1000,Opioid Use Disorder; Severe,C4237239,Brain,GEO,RNA-Seq,Homo sapiens,20|20, DSA02938,E-MTAB-7860,,1000,Ulcerative Colitis,C0009324,Crypt of colon,ArrayExpress,RNA-Seq,Homo sapiens,8|8,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02939,E-MTAB-7860,,30,Ulcerative Colitis,C0009324,Crypt of colon,ArrayExpress,RNA-Seq,Homo sapiens,32|32,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA02940,GSE169077,GPL96,24,Osteoarthritis,C0157946,,GEO,Microarray,Homo sapiens,5|6,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA02941,GSE166029,GPL28460,1000,Ovarian Cancer,C1140680,,GEO,Microarray,Homo sapiens,3|3,DO:A female reproductive organ cancer that is located_in the ovary. DSA02942,GSE166029,GPL28460,1000,Ovarian Cancer,C1140680,,GEO,Microarray,Homo sapiens,3|3,DO:A female reproductive organ cancer that is located_in the ovary. DSA02943,E-MTAB-7876,,4,Amyotrophic Lateral Sclerosis,C0002736,Callosal sulcus,ArrayExpress,RNA-Seq,Homo sapiens,14|14,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA02944,GSE165082,GPL11154,0,Parkinson's Disease,C0030567,Whole blood,GEO,RNA-Seq,Homo sapiens,14|12,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA02945,E-MTAB-7876,,789,Amyotrophic Lateral Sclerosis,C0002736,Corticospinal tract,ArrayExpress,RNA-Seq,Homo sapiens,16|13,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA02946,E-MTAB-7907,,198,Fungal Keratitis,C1262117,Cornea,ArrayExpress,RNA-Seq,Homo sapiens,1|1,"DO:A corneal ulcer that is characterized by ulceration of the cornea secondary to fungal infection and is caused by minor trauma and subsequent infection by mycotic organisms, such as candida, apergillus, fusarium, and rhizopus." DSA02947,E-MTAB-7907,,179,Fungal Keratitis,C1262117,Cornea,ArrayExpress,RNA-Seq,Homo sapiens,1|1,"DO:A corneal ulcer that is characterized by ulceration of the cornea secondary to fungal infection and is caused by minor trauma and subsequent infection by mycotic organisms, such as candida, apergillus, fusarium, and rhizopus." DSA02948,E-MTAB-7962,,1000,Restrictive Respiratory Disease,C1609528,Nasal cavity,ArrayExpress,RNA-Seq,Homo sapiens,6|8, DSA02949,E-MTAB-7965,,518,Restrictive Respiratory Disease,C1609528,Sputum,ArrayExpress,RNA-Seq,Homo sapiens,2|10, DSA02950,GSE169755,GPL20301,625,Parkinson's Disease,C0030567,Brain,GEO,RNA-Seq,Homo sapiens,6|6,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA02951,GSE172409,GPL24676,1000,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,3|8,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA02952,GSE172409,GPL24676,1000,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,2|5,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA02953,GSE165316,GPL24676,1,Peanut Allergy,C0559470,,GEO,RNA-Seq,Homo sapiens,5|2,DO:A legume allergy that is an allergy or hypersensitivity to dietary substances from peanuts causing an overreaction of the immune system which in a small percentage of people may lead to severe physical symptoms. DSA02954,GSE165316,GPL24676,2,Food Allergy,C0016470,,GEO,RNA-Seq,Homo sapiens,5|4,"DO:A hypersensitivity reaction type I disease that is an abnormal response to a food, triggered by the body's immune system." DSA02955,GSE173078,GPL20301,189,Periodontitis,C0031099,Gingiva,GEO,RNA-Seq,Homo sapiens,12|12,"EFO:Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology)" DSA02956,GSE174609,GPL20795,1000,Periodontitis,C0031099,,GEO,scRNA-Seq,Homo sapiens,4|4,"EFO:Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology)" DSA02957,E-MTAB-7965,,1000,Restrictive Respiratory Disease,C1609528,Blood,ArrayExpress,RNA-Seq,Homo sapiens,8|10, DSA02958,GSE17732,GPL571,0,Pfapa Syndrome,C4082167,Whole blood,GEO,Microarray,Homo sapiens,6|6,"MONDO:An auto inflammatory syndrome characterized by recurrent febrile episodes associated with aphthous stomatitis, pharyngitis and cervical adenitis." DSA02959,GSE17732,GPL571,1000,Pfapa Syndrome,C4082167,Whole blood,GEO,Microarray,Homo sapiens,6|6,"MONDO:An auto inflammatory syndrome characterized by recurrent febrile episodes associated with aphthous stomatitis, pharyngitis and cervical adenitis." DSA02960,GSE174060,GPL17586,1000,Polycythemia Vera,C0032463,Peripheral blood,GEO,Microarray,Homo sapiens,6|3,"DO:A myeloproliferative neoplasm characterized by erythroid hyperplasia, myeloid leukocytosis, thrombocytosis, and splenomegaly." DSA02961,GSE171248,GPL16791,460,Porto-sinusoidal vascular disease,,Liver,GEO,RNA-Seq,Homo sapiens,8|8, DSA02962,GSE174060,GPL17586,215,Post–Polycythemia Vera Myelofibrosis,,Peripheral blood,GEO,Microarray,Homo sapiens,6|1, DSA02963,GSE168759,GPL24676,6,Post-Infection Irritable Bowel Syndrome,,Colon,GEO,RNA-Seq,Homo sapiens,5|5, DSA02964,GSE174412,GPL21273,8,Neurocognitive Disorders,C4041080,Prefrontal cortex,GEO,RNA-Seq,Mus musculus,3|3,"DO:A disease of mental health that affects cognitive functions including memory processing, perception and problem solving." DSA02965,GSE171031,GPL27566,109,Post-Traumatic Osteoarthritis Nos,C2894027,Knee joint,GEO,Microarray,Mus musculus,12|12, DSA02966,E-MTAB-8162,,1000,Tuberculosis,C0041296,Blood,ArrayExpress,RNA-Seq,Homo sapiens,2|8,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA02967,GSE174060,GPL17586,1000,Primary Myelofibrosis,C0001815,Peripheral blood,GEO,Microarray,Homo sapiens,6|3,DO:A myeloid neoplasm that is located in the bone marrow which results in bone marrow being replaced by fibrous (scar) tissue. DSA02968,GSE164885,GPL24676,437,Primary Sjogren Syndrome,C0151449,Peripheral blood,GEO,RNA-Seq,Homo sapiens,4|4,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA02969,GSE173670,GPL20301,1000,Primary Sjogren Syndrome,C0151449,Peripheral blood,GEO,RNA-Seq,Homo sapiens,11|12,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA02970,GSE173635,GPL20301,16,Primary Sjogren Syndrome,C0151449,Peripheral blood,GEO,RNA-Seq,Homo sapiens,5|7,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA02971,GSE173635,GPL20301,65,Primary Sjogren Syndrome,C0151449,Peripheral blood,GEO,RNA-Seq,Homo sapiens,7|7,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA02972,GSE173635,GPL20301,11,Primary Sjogren Syndrome,C0151449,Peripheral blood,GEO,RNA-Seq,Homo sapiens,7|7,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA02973,GSE164967,GPL17021,89,Prostatic Intraepithelial Neoplasia,C0282612,Prostate,GEO,RNA-Seq,Mus musculus,3|3,"EFO:A neoplastic proliferation of the epithelial cells that line the acini and the ducts of the prostate gland. The neoplastic epithelial cells are confined within the acini and the ducts and they do not invade the surrounding prostatic stroma. Morphologically, it is classified as low or high grade." DSA02974,GSE164967,GPL17021,1000,Prostatic Intraepithelial Neoplasia,C0282612,Prostate,GEO,RNA-Seq,Mus musculus,3|2,"EFO:A neoplastic proliferation of the epithelial cells that line the acini and the ducts of the prostate gland. The neoplastic epithelial cells are confined within the acini and the ducts and they do not invade the surrounding prostatic stroma. Morphologically, it is classified as low or high grade." DSA02975,GSE17078,GPL96,1000,Protein C Deficiency,C0398625,,GEO,Microarray,Homo sapiens,27|3,DO:A thrombophilia that is characterized by increased risk of developing abnormal blood clots. DSA02976,GSE166388,GPL570,833,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,4|4,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA02977,GSE173706,GPL24676,1000,Psoriasis,C0033860,Skin,GEO,RNA-Seq,Homo sapiens,8|13,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA02978,GSE173706,GPL24676,1000,Psoriasis,C0033860,Skin,GEO,RNA-Seq,Homo sapiens,11|13,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA02979,GSE173387,GPL20795,1000,Psoriasis Vulgaris,C0263361,Peripheral blood,GEO,RNA-Seq,Homo sapiens,2|2, DSA02980,E-MTAB-8162,,156,Tuberculosis,C0041296,Blood,ArrayExpress,RNA-Seq,Homo sapiens,2|9,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA02981,E-MTAB-8162,,8,Tuberculosis,C0041296,Blood,ArrayExpress,RNA-Seq,Homo sapiens,2|8,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA02982,E-MTAB-8162,,1000,Tuberculosis,C0041296,Blood,ArrayExpress,RNA-Seq,Homo sapiens,2|9,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA02983,E-MTAB-8290,,1000,Tuberculosis,C0041296,Blood,ArrayExpress,RNA-Seq,Homo sapiens,127|54,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA02984,E-MTAB-8448,,1000,Colorectal Carcinoma,C0009402,Colon,ArrayExpress,RNA-Seq,Homo sapiens,58|66,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA02985,E-MTAB-8448,,1000,Colorectal Carcinoma,C0009402,Colon,ArrayExpress,RNA-Seq,Homo sapiens,58|82,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA02986,E-MTAB-8448,,1000,Colorectal Carcinoma,C0009402,Colon,ArrayExpress,RNA-Seq,Homo sapiens,58|90,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA02987,E-MTAB-8455,,44,7Q11.23 Microduplication Syndrome,,Skin,ArrayExpress,RNA-Seq,Homo sapiens,11|3, DSA02988,E-MTAB-8455,,200,7Q11.23 Microduplication Syndrome,,Skin,ArrayExpress,RNA-Seq,Homo sapiens,11|6, DSA02989,GSE165004,GPL16699,1000,Pregnancy Loss,C0000786,Endometrium,GEO,Microarray,Homo sapiens,24|24,"HPO:A pregnancy that ends at a stage in which the fetus is incapable of surviving on its own, defined as the spontaneous loss of a fetus before the 22th week of pregnancy." DSA02990,GSE172009,GPL20301|GPL24676,191,Relapsing-Remitting Multiple Sclerosis,C0751967,Blood,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A multiple sclerosis that is characterized by relapse (attacks of symptom flare-ups) followed by remission (periods of recovery). Symptoms may vary from mild to severe, and relapses and remissions may last for days or months. More than 80 percent of people who have MS begin with relapsing-remitting cycles." DSA02991,GSE171431,GPL20258,67,Reproductive And Metabolic Disorders,,Ovary,GEO,Microarray,Mus musculus,3|3, DSA02992,GSE171431,GPL20258,263,Reproductive And Metabolic Disorders,,Adipose tissue,GEO,Microarray,Mus musculus,3|3, DSA02993,GSE165322,GPL16791,1000,Retinal Pigment Epithelium,,,GEO,RNA-Seq,Homo sapiens,3|3, DSA02994,GSE169082,GPL20795,1000,Rheumatoid Arthritis,C0003873,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|4,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA02995,GSE167186,GPL20301|GPL24676,0,Sarcopenia,C0872084,Skeletal muscle,GEO,RNA-Seq,Homo sapiens,16|12,EFO:Progressive decline in muscle mass due to aging which results in decreased functional capacity of muscles. DSA02996,E-MTAB-8455,,45,Williams Syndrome,C0175702,Skin,ArrayExpress,RNA-Seq,Homo sapiens,11|4,"DO:A syndrome that is characterized by mild to moderate intellectual disability, a broad forehead, a short nose with a broad tip, full cheeks, and a wide mouth with full lips and difficulty with visual-spatial tasks and has_material_basis_in hemizygous deletion of 1.5 to 1.8 Mb on chromosome 7q11.23." DSA02997,GSE165604,GPL16791,44,Schizophrenia,C0036341,,GEO,RNA-Seq,Homo sapiens,18|19,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA02998,GSE166059,GPL20301,1000,Scleroderma-Associated Interstitial Lung Disease,C0339904,Lung,GEO,RNA-Seq,Homo sapiens,4|3,HPO:It is a bilateral reticular pattern of linear or lineonodular densities that are most pronounced in basilar portions of the lungs on standard chest x-ray. It is the third minor criterion for scleroderma diagnosis. DSA02999,GSE166059,GPL20301,650,Scleroderma-Associated Interstitial Lung Disease,C0339904,Lung,GEO,RNA-Seq,Homo sapiens,4|2,HPO:It is a bilateral reticular pattern of linear or lineonodular densities that are most pronounced in basilar portions of the lungs on standard chest x-ray. It is the third minor criterion for scleroderma diagnosis. DSA03000,GSE166059,GPL20301,1000,Scleroderma-Associated Interstitial Lung Disease,C0339904,Lung,GEO,RNA-Seq,Homo sapiens,5|3,HPO:It is a bilateral reticular pattern of linear or lineonodular densities that are most pronounced in basilar portions of the lungs on standard chest x-ray. It is the third minor criterion for scleroderma diagnosis. DSA03001,E-MTAB-8455,,559,Williams Syndrome,C0175702,Skin,ArrayExpress,RNA-Seq,Homo sapiens,11|4,"DO:A syndrome that is characterized by mild to moderate intellectual disability, a broad forehead, a short nose with a broad tip, full cheeks, and a wide mouth with full lips and difficulty with visual-spatial tasks and has_material_basis_in hemizygous deletion of 1.5 to 1.8 Mb on chromosome 7q11.23." DSA03002,GSE168796,GPL24247,149,Sepsis,C0243026,Lung,GEO,RNA-Seq,Mus musculus,6|6,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA03003,GSE175453,GPL18573|GPL24676,1000,Sepsis,C0243026,,GEO,scRNA-Seq,Homo sapiens,5|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA03004,GSE165518,GPL20795,1000,Severe Fever With Thrombocytopenia Syndrome,,,GEO,RNA-Seq,Homo sapiens,6|23, DSA03005,GSE165518,GPL20795,1000,Severe Fever With Thrombocytopenia Syndrome,,,GEO,RNA-Seq,Homo sapiens,6|3, DSA03006,E-MTAB-8455,,62,Williams Syndrome,C0175702,Skin,ArrayExpress,RNA-Seq,Homo sapiens,11|4,"DO:A syndrome that is characterized by mild to moderate intellectual disability, a broad forehead, a short nose with a broad tip, full cheeks, and a wide mouth with full lips and difficulty with visual-spatial tasks and has_material_basis_in hemizygous deletion of 1.5 to 1.8 Mb on chromosome 7q11.23." DSA03007,GSE175499,GPL24676,1000,Severe Fever With Thrombocytopenia Syndrome,,,GEO,scRNA-Seq,Homo sapiens,4|8, DSA03008,E-MTAB-8919,,1000,Kallmann Syndrome,C0162809,Blood plasma,ArrayExpress,RNA-Seq,Homo sapiens,2|1,"DO:A syndrome characterized by the classical triad of optic nerve hypoplasia, pituitary gland hypoplasia and midline brain defects that has_material_basis_in mutation in the HESX1 gene on chromosome 3p14." DSA03009,E-MTAB-9045,,1000,Cornelia De Lange Syndrome,C0270972,Prefrontal cortex,ArrayExpress,RNA-Seq,Homo sapiens,12|8,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA03010,GSE168534,GPL21290,1000,Sickle Cell Disease,C0002895,Peripheral blood,GEO,RNA-Seq,Homo sapiens,6|13,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA03011,E-MTAB-9053,,1000,Peripartum Cardiomyopathy,C0877208,Skin,ArrayExpress,RNA-Seq,Homo sapiens,17|25,DO:A dilated cardiomyopathy that is characterized by a weakness of the heart muscle that begins sometime during the final month of pregnancy through about five months after delivery. DSA03012,GSE176510,GPL28577,49,Sjogren's Syndrome,C1527336,Conjunctiva,GEO,Microarray,Homo sapiens,19|7,DO:An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. DSA03013,GSE169573,GPL29913,0,Skin Inflammation,C3875321,Skin,GEO,Microarray,Homo sapiens,10|5,"HPO:The presence of inflammation of the skin. That is, an abnormality of the skin resulting from the local accumulation of fluid, plasma proteins, and leukocytes." DSA03014,GSE169573,GPL29913,0,Skin Inflammation,C3875321,Skin,GEO,Microarray,Homo sapiens,10|5,"HPO:The presence of inflammation of the skin. That is, an abnormality of the skin resulting from the local accumulation of fluid, plasma proteins, and leukocytes." DSA03015,GSE174056,GPL20301,4,Spinal Muscular Atrophy,C0026847,Whole blood,GEO,RNA-Seq,Homo sapiens,5|5,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA03016,GSE178367,GPL17021,925,Spinocerebellar Ataxia Type 3,C0024408,Cerebellum,GEO,RNA-Seq,Mus musculus,3|3,DO:An autosomal dominant cerebellar ataxia that is characterized by slow degeneration of the hindbrain and has_material_basis_in expansion of CAG triplet repeats (glutamine) in the ATXN3 gene. DSA03017,GSE166761,GPL20301,1000,STK4 Deficiency,,,GEO,RNA-Seq,Homo sapiens,6|2, DSA03018,GSE166761,GPL20301,1000,STK4 Deficiency,,,GEO,RNA-Seq,Homo sapiens,6|2, DSA03019,GSE166761,GPL20301,1000,STK4 Deficiency,,,GEO,RNA-Seq,Homo sapiens,6|2, DSA03020,GSE174302,GPL20795,1000,Stomach Cancer,C0699791,Plasma,GEO,RNA-Seq,Homo sapiens,46|37,DO:A gastrointestinal system cancer that is located_in the stomach. DSA03021,GSE167108,GPL16417,453,Systemic Lupus Erythematosus,C0024141,Peritoneal cavity,GEO,RNA-Seq,Mus musculus,3|3,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03022,GSE168527,GPL20301,339,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,5|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03023,GSE168527,GPL20301,1000,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,5|3,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03024,GSE169080,GPL20795,1000,Systemic Lupus Erythematosus,C0024141,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03025,GSE175839,GPL11154,208,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03026,GSE175913,GPL16791,508,Systemic Lupus Erythematosus,C0024141,Whole blood,GEO,RNA-Seq,Homo sapiens,5|8,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03027,GSE175913,GPL16791,84,Systemic Lupus Erythematosus,C0024141,Whole blood,GEO,RNA-Seq,Homo sapiens,5|8,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03028,GSE175913,GPL16791,154,Systemic Lupus Erythematosus,C0024141,Whole blood,GEO,RNA-Seq,Homo sapiens,5|8,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03029,GSE177029,GPL24676,981,Systemic Lupus Erythematosus,C0024141,Placenta,GEO,RNA-Seq,Homo sapiens,8|8,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03030,GSE179153,GPL10558,0,Systemic Sclerosis [Scleroderma],C2364016,,GEO,Microarray,Homo sapiens,28|46, DSA03031,GSE169686,GPL21273,74,Tauopathy,C0949664,Hippocampus,GEO,RNA-Seq,Mus musculus,18|19,DO:A neurodegenerative disease that has_material_basis_in the pathological aggregation of tau protein in so-called neurofibrillary tangles (NFT) in the human brain. DSA03032,GSE169686,GPL21273,1,Tauopathy,C0949664,Hippocampus,GEO,RNA-Seq,Mus musculus,15|14,DO:A neurodegenerative disease that has_material_basis_in the pathological aggregation of tau protein in so-called neurofibrillary tangles (NFT) in the human brain. DSA03033,E-MTAB-9053,,724,Peripartum Cardiomyopathy,C0877208,Skin,ArrayExpress,RNA-Seq,Homo sapiens,16|24,DO:A dilated cardiomyopathy that is characterized by a weakness of the heart muscle that begins sometime during the final month of pregnancy through about five months after delivery. DSA03034,E-MTAB-9281,,1000,Cervical Adenocarcinoma,C0279672,Uterine cervix,ArrayExpress,RNA-Seq,Homo sapiens,5|24,DO:A cervix carcinoma that derives_from epithelial cells of glandular origin. DSA03035,GSE175898,GPL24676,535,Timothy Syndrome,C1832916,Cortical spheroidscortical spheroid,GEO,RNA-Seq,Homo sapiens,21|14,"DO:A syndrome that is characterized by cardiac, hand/foot, facial, and neurodevelopmental features. The two forms are type 1 (classic) and type 2, a rare form that has_material_basis_in mutations in a transcript variant of CACNA1C on chromosome 12p13.33." DSA03036,GSE175898,GPL24676,352,Timothy Syndrome,C1832916,Cortical spheroid,GEO,RNA-Seq,Homo sapiens,32|27,"DO:A syndrome that is characterized by cardiac, hand/foot, facial, and neurodevelopmental features. The two forms are type 1 (classic) and type 2, a rare form that has_material_basis_in mutations in a transcript variant of CACNA1C on chromosome 12p13.33." DSA03037,GSE17732,GPL571,0,Tnf Receptor-Associated Periodic Fever Syndrome (Traps),C1275126,Whole blood,GEO,Microarray,Homo sapiens,6|1,"DO:A primary immunodeficiency disease characterized by recurrent fever, abdominal pain, localized tender skin lesions, arthralgia and myalgia associated with skin, joint, ocular and serosal inflammation that has_material_basis_in heterozygous mutation in the TNFRSF1A gene on chromosome 12p13." DSA03038,GSE167459,GPL24247,322,Brain Damage,C0006109,Forebrain,GEO,RNA-Seq,Mus musculus,5|4,MONDO:Chronic form of encephalitis. DSA03039,GSE167459,GPL24247,2,Brain Damage,C0006109,Forebrain,GEO,RNA-Seq,Mus musculus,6|5,MONDO:Chronic form of encephalitis. DSA03040,GSE17635,GPL2700,498,Type 1 Diabetes,C0011854,Peripheral blood,GEO,Microarray,Homo sapiens,11|11,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA03041,GSE172391,GPL21493,482,Low-Grade Glioma,C1997217,Brain,GEO,RNA-Seq,Mus musculus,2|4,"MONDO:A grade I or grade II glioma arising from the central nervous system. This category includes pilocytic astrocytoma, diffuse astrocytoma, subependymal giant cell astrocytoma, ependymoma, oligodendroglioma, oligoastrocytoma, and angiocentric glioma." DSA03042,GSE165512,GPL16791,1000,Ulcerative Colitis,C0009324,Colon,GEO,RNA-Seq,Homo sapiens,40|40,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA03043,GSE13796,GPL1261,1000,Acute Myeloid Leukemia,C0023467,Bone marrow,GEO,Microarray,Mus musculus,4|9,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03044,GSE13796,GPL1261,1000,Acute Myeloid Leukemia,C0023467,Bone marrow,GEO,Microarray,Mus musculus,4|8,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03045,GSE13796,GPL1261,1000,Acute Myeloid Leukemia,C0023467,Bone marrow,GEO,Microarray,Mus musculus,4|4,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03046,GSE164918,GPL24676,1000,Ulcerative Colitis,C0009324,Sigmoid colon mucosa,GEO,RNA-Seq,Homo sapiens,4|1,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA03047,GSE164918,GPL24676,1000,Ulcerative Colitis,C0009324,Sigmoid colon mucosa,GEO,RNA-Seq,Homo sapiens,6|1,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA03048,GSE164918,GPL24676,1000,Ulcerative Colitis,C0009324,Sigmoid colon mucosa,GEO,RNA-Seq,Homo sapiens,6|1,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA03049,GSE178753,GPL30304,41,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,5|5,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA03050,GSE178753,GPL30304,0,Ulcerative Colitis,C0009324,Colon mucosa,GEO,Microarray,Homo sapiens,5|5,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA03051,GSE165004,GPL16699,1000,Unexplained Infertility,C0021361,Endometrium,GEO,Microarray,Homo sapiens,24|24,EFO:Diminished or absent ability of a female to achieve conception. DSA03052,GSE169718,GPL24247,1000,Villous Atrophy,C0554101,Intestine,GEO,RNA-Seq,Mus musculus,2|2,HPO:The enteric villi are atrophic or absent. DSA03053,GSE13796,GPL1261,1000,Acute Myeloid Leukemia,C0023467,Bone marrow,GEO,Microarray,Mus musculus,4|7,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03054,GSE166663,GPL27644,723,Vogt-Koyanagi-Harada Disease,C0042170,Blood,GEO,RNA-Seq,Homo sapiens,7|14,"DO:An autoimmune disease that is caused by T helper cell mediated autoimmune attack of melanocytes resulting in inflammation of the inside of the eye, whitening of hair, skin pigment loss, and meningitis." DSA03055,GSE137342,GPL10558,1000,Sepsis,C0243026,Whole blood,GEO,Microarray,Homo sapiens,12|14,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA03056,GSE137342,GPL10558,1000,Sepsis,C0243026,Whole blood,GEO,Microarray,Homo sapiens,12|15,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA03057,GSE137342,GPL10558,1000,Sepsis,C0243026,Whole blood,GEO,Microarray,Homo sapiens,12|6,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA03058,GSE137342,GPL10558,1000,Sepsis,C0243026,Whole blood,GEO,Microarray,Homo sapiens,12|7,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA03059,GSE137345,GPL24557,0,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,Microarray,Mus musculus,3|3,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA03060,GSE137345,GPL24557,0,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,Microarray,Mus musculus,3|3,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA03061,GSE137354,GPL17586,0,Polycystic Ovary Syndrome,C0032460,Endometrium,GEO,Microarray,Homo sapiens,3|3,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA03062,GSE137369,GPL6244,2,Monoclonal Gammopathy of Undetermined Significance,C0026470,Bone marrow,GEO,Microarray,Homo sapiens,8|10,DO:A blood protein disease that is characterized by the presence of an abnormal protein called monoclonal protein in the blood. DSA03063,GSE137369,GPL6244,52,Smoldering Myeloma,C1531608,Bone marrow,GEO,Microarray,Homo sapiens,8|10,EFO:A plasma cell myeloma lacking clinical manifestations and organ impairment. DSA03064,GSE137369,GPL6244,6,Multiple Myeloma,C0026764,Bone marrow,GEO,Microarray,Homo sapiens,8|24,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA03065,GSE137380,GPL20301,39,Autoimmune Lymphoproliferative Syndrome,C1328840,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A hypersensitivity reaction type IV disease that is an inherited disorder in which the body cannot properly regulate the number of immune system cells (lymphocytes). It is characterized by the production of an abnormally large number of lymphocytes. Accumulation of excess lymphocytes results in enlargement of the lymph nodes, the liver, and the spleen." DSA03066,GSE16390,GPL1261,1000,Chronic Atrophic Gastritis,C0017154,,GEO,Microarray,Mus musculus,12|12,"HPO:Atrophic gastritis (AG) is a histopathological entity that is characterized by chronic inflammation of the gastric mucosa with loss of gastric glandular cells and replacement by intestinal-type epithelium, pyloric-type glands, and fibrous tissue." DSA03067,GSE137419,GPL6244,2,Monoclonal Gammopathy of Undetermined Significance,C0026470,,GEO,Microarray,Homo sapiens,8|10,DO:A blood protein disease that is characterized by the presence of an abnormal protein called monoclonal protein in the blood. DSA03068,GSE137419,GPL6244,6,Multiple Myeloma,C0026764,,GEO,Microarray,Homo sapiens,8|24,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA03069,GSE137419,GPL6244,52,Smoldering Myeloma,C1531608,,GEO,Microarray,Homo sapiens,8|10,EFO:A plasma cell myeloma lacking clinical manifestations and organ impairment. DSA03070,GSE137429,GPL18573,1000,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,scRNA-Seq,Homo sapiens,2|2,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA03071,GSE16390,GPL1261,1000,Gastric Adenocarcinoma,C0278701,,GEO,Microarray,Mus musculus,12|6,DO:A stomach carcinoma that derives_from epithelial cells of glandular origin. DSA03072,GSE16677,GPL570,372,Down Syndrome,C0013080,,GEO,Microarray,Homo sapiens,5|6,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA03073,GSE137482,GPL19057,1000,Ischemic Stroke,C0948008,Brain,GEO,RNA-Seq,Mus musculus,6|6,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA03074,GSE137482,GPL19057,1000,Ischemic Stroke,C0948008,Brain,GEO,RNA-Seq,Mus musculus,6|6,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA03075,GSE137496,GPL20301,986,Severe Congenital Neutropenia,C1853118,Bone marrow,GEO,scRNA-Seq,Homo sapiens,1|1,DO:A neutropenia characterized by a maturation arrest of granulopoiesis at the level or promyelocytes and early onset of severe bacterial infections. DSA03076,GSE137505,GPL13112,54,Nijmegen Breakage Syndrome,C0398791,Liver,GEO,RNA-Seq,Mus musculus,3|3,"DO:A syndrome characterized by chromosomal instability, microcephaly, growth retardation, immunodeficiency, cellular hypersensitivity to X-rays, and predisposition to cancer that has_material_basis_in homozygous or compound heterozygous mutation in NBN on chromosome 8q21.3." DSA03077,GSE137557,GPL17692,1000,Chronic Obstructive Pulmonary Disease,C0024117,Lung,GEO,Microarray,Homo sapiens,8|8,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA03078,GSE137557,GPL17692,1000,Chronic Obstructive Pulmonary Disease,C0024117,Lung,GEO,Microarray,Homo sapiens,6|6,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA03079,GSE137581,GPL21163,1000,Atherosclerosis,C0004153,Ascending aorta,GEO,Microarray,Mus musculus,3|3,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA03080,GSE137595,GPL24242,1,Stroke,C0948008,Brain,GEO,Microarray,Mus musculus,4|8,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA03081,GSE137596,GPL21697,1000,Cerebral Cavernous Malformation,C2919945,Brain,GEO,RNA-Seq,Homo sapiens,4|10,DO:A cerebral cavernous malformation that has_material_basis_in heterozygous mutation in the KRIT1 gene on chromosome 7q21. DSA03082,GSE13760,GPL571,0,Type 2 Diabetes,C0011860,Artery,GEO,Microarray,Homo sapiens,5|9,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA03083,GSE137610,GPL19096,1000,Liver Tumor,C0345904,Liver,GEO,Microarray,Mus musculus,4|4,DO:A hepatobiliary system cancer that is located_in the liver. DSA03084,GSE137619,GPL21290,28,Multiple Sclerosis,C0026769,Choroid plexus,GEO,RNA-Seq,Homo sapiens,6|5,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA03085,GSE137631,GPL18573,371,Obesity,C0028754,Vastus lateralis,GEO,RNA-Seq,Homo sapiens,6|6,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA03086,GSE137633,GPL17021,1000,Tumors of The Central Nervous System,C0085136,Brain,GEO,RNA-Seq,Mus musculus,3|3,DO:A nervous system cancer that is located_in the central nervous system. DSA03087,GSE137633,GPL17021,1000,Tumors of The Central Nervous System,C0085136,Brain,GEO,RNA-Seq,Mus musculus,3|4,DO:A nervous system cancer that is located_in the central nervous system. DSA03088,GSE137633,GPL17021,1000,Central Nervous System Tumor,C0206743,Brain,GEO,RNA-Seq,Mus musculus,3|3,"DO:A brain cancer that is usually located in the brain, but can occur anywhere in the central nervous system." DSA03089,GSE137633,GPL17021,1000,Extracranial Solid Tumor,C4726566,Brain,GEO,RNA-Seq,Mus musculus,3|4,NCI:A solid neoplasm involving any anatomic site other than the brain. DSA03090,GSE137635,GPL11180,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Mus musculus,2|2,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA03091,GSE137681,GPL17021,1000,Marfan Syndrome,C0024796,Mitral valve,GEO,RNA-Seq,Mus musculus,1|1,"DO:A connective tissue disease that is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens." DSA03092,GSE137684,GPL17077,0,Polycystic Ovary Syndrome,C0032460,Ovary,GEO,Microarray,Homo sapiens,4|4,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA03093,GSE137762,GPL21103,1000,Brain Metastatic,C0220650,Brain,GEO,RNA-Seq,Mus musculus,4|4,NCI:A malignant neoplasm that has spread to the brain from another anatomic site or system. The majority are carcinomas (usually lung or breast carcinomas). DSA03094,GSE137762,GPL21103,3,Brain Metastatic,C0220650,Brain,GEO,RNA-Seq,Mus musculus,5|5,NCI:A malignant neoplasm that has spread to the brain from another anatomic site or system. The majority are carcinomas (usually lung or breast carcinomas). DSA03095,GSE137762,GPL21103,2,Brain Metastatic,C0220650,Brain,GEO,RNA-Seq,Mus musculus,5|5,NCI:A malignant neoplasm that has spread to the brain from another anatomic site or system. The majority are carcinomas (usually lung or breast carcinomas). DSA03096,GSE137762,GPL21103,5,Brain Metastatic,C0220650,Brain,GEO,RNA-Seq,Mus musculus,4|5,NCI:A malignant neoplasm that has spread to the brain from another anatomic site or system. The majority are carcinomas (usually lung or breast carcinomas). DSA03097,GSE137762,GPL21103,0,Brain Metastatic,C0220650,Brain,GEO,RNA-Seq,Mus musculus,4|5,NCI:A malignant neoplasm that has spread to the brain from another anatomic site or system. The majority are carcinomas (usually lung or breast carcinomas). DSA03098,GSE137842,GPL570,0,Bone Metastases,C0153690,,GEO,Microarray,Homo sapiens,1|3,EFO:Transfer of a neoplasm from its primary site to bones. DSA03099,GSE137842,GPL570,0,Metastatic Cancer To The Breast,C0346993,,GEO,Microarray,Homo sapiens,3|3,"NCI:The spread of a malignant neoplasm to the breast. This may be from a primary breast malignant neoplasm on the opposite side, or from a malignant neoplasm at a distant site." DSA03100,GSE16679,GPL1261,6,Leukemia,C0023418,,GEO,Microarray,Mus musculus,4|4,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA03101,GSE17538,GPL1261,1000,Metastatic Colon Carcinoma,C4744565,Colon,GEO,Microarray,Mus musculus,3|3,NCI:A carcinoma that arises from the colon and has metastasized to another anatomic site. DSA03102,GSE18033,GPL1261,10,Chronic Obstructive Pulmonary Disease,C0024117,Gastrocnemius muscle,GEO,Microarray,Mus musculus,6|50,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA03103,GSE137910,GPL11154,372,X-Linked Juvenile Retinoschisis 1,C0271091,Retina,GEO,RNA-Seq,Homo sapiens,4|4,DO:A retinoschisis characterized by schisis (splitting) of the neural retina leading to reduced visual acuity in males due that has_material_basis_in the RS1 gene on chromosome Xp22. DSA03104,GSE137939,GPL15433,128,Down Syndrome,C0013080,Hippocampus,GEO,RNA-Seq,Homo sapiens,5|4,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA03105,GSE137960,GPL17791,1000,Pancreatic Ductal Adenocarcinoma,C1335302,Abdominal muscle,GEO,Microarray,Mus musculus,3|3,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA03106,GSE137960,GPL17791,2,Pancreatic Ductal Adenocarcinoma,C1335302,Diaphragm,GEO,Microarray,Mus musculus,3|3,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA03107,GSE137960,GPL17791,1000,Pancreatic Ductal Adenocarcinoma,C1335302,Tibialis anterior,GEO,Microarray,Mus musculus,3|3,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA03108,GSE137979,GPL17791,1000,Pancreatic Ductal Adenocarcinoma,C1335302,Tibialis anterior,GEO,Microarray,Mus musculus,12|17,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA03109,GSE137979,GPL17791,1000,Pancreatic Ductal Adenocarcinoma,C1335302,Diaphragm,GEO,Microarray,Mus musculus,12|17,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA03110,GSE137985,GPL17791,208,Pancreatic Ductal Adenocarcinoma,C1335302,Diaphragm,GEO,Microarray,Mus musculus,15|20,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA03111,GSE137985,GPL17791,295,Pancreatic Ductal Adenocarcinoma,C1335302,Tibialis anterior,GEO,Microarray,Mus musculus,15|20,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA03112,GSE137996,GPL21185,1000,Keratopathy,C0235270,Conjunctiva,GEO,Microarray,Homo sapiens,20|20,MONDO:Any disorder of the cornea. DSA03113,GSE18216,GPL1261,1000,Breast Cancer,C0678222,Breast,GEO,Microarray,Mus musculus,3|9,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03114,GSE138053,GPL20301,1000,Spinal And Bulbar Muscular Atrophy,C1839259,Motor cortex,GEO,RNA-Seq,Homo sapiens,2|1,DO:A spinal muscular dystrophy that has_material_basis_in an X-linked recessive expansion of CAG triplet repeats (glutamine) in exon 1 of AR gene encoding the androgen receptor. DSA03115,GSE138053,GPL20301,1000,Spinal And Bulbar Muscular Atrophy,C1839259,Lumbar spinal cord,GEO,RNA-Seq,Homo sapiens,1|1,DO:A spinal muscular dystrophy that has_material_basis_in an X-linked recessive expansion of CAG triplet repeats (glutamine) in exon 1 of AR gene encoding the androgen receptor. DSA03116,GSE138053,GPL20301,1000,Spinal And Bulbar Muscular Atrophy,C1839259,Brain,GEO,RNA-Seq,Homo sapiens,2|1,DO:A spinal muscular dystrophy that has_material_basis_in an X-linked recessive expansion of CAG triplet repeats (glutamine) in exon 1 of AR gene encoding the androgen receptor. DSA03117,GSE138053,GPL20301,0,Spinal And Bulbar Muscular Atrophy,C1839259,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A spinal muscular dystrophy that has_material_basis_in an X-linked recessive expansion of CAG triplet repeats (glutamine) in exon 1 of AR gene encoding the androgen receptor. DSA03118,GSE138053,GPL20301,0,Spinal And Bulbar Muscular Atrophy,C1839259,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A spinal muscular dystrophy that has_material_basis_in an X-linked recessive expansion of CAG triplet repeats (glutamine) in exon 1 of AR gene encoding the androgen receptor. DSA03119,GSE138076,GPL9052,87,Common Variable Immunodeficiency,C0009447,,GEO,RNA-Seq,Homo sapiens,3|3,DO:An agammaglobulinemia that is characterized by low Ig levels with phenotypically normal B cells that can proliferate but do not develop into Ig-producing cells and that esults in insufficient production of antibodies needed to respond to exposure of pathogens. DSA03120,GSE138080,GPL4133,1000,Cervical Cancer,C4048328,,GEO,Microarray,Homo sapiens,10|15,DO:A female reproductive organ cancer that is located_in the cervix. DSA03121,GSE138080,GPL4133,1000,Cervical Cancer,C4048328,,GEO,Microarray,Homo sapiens,10|10,DO:A female reproductive organ cancer that is located_in the cervix. DSA03122,GSE138082,GPL16791,0,Schizophrenia,C0036341,Hippocampus,GEO,RNA-Seq,Homo sapiens,13|13,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA03123,GSE138082,GPL16791,1,Schizophrenia,C0036341,Hippocampus,GEO,RNA-Seq,Homo sapiens,13|13,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA03124,GSE138082,GPL16791,1,Schizophrenia,C0036341,Hippocampus,GEO,RNA-Seq,Homo sapiens,13|13,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA03125,GSE138118,GPL17692,1000,Urothelial Carcinoma of The Urinary Bladder,C0279680,Blood,GEO,Microarray,Homo sapiens,29|36,DO:A bladder carcinoma that has_material_basis_in transitional cells located_in the lining of the bladder. DSA03126,GSE138118,GPL17692,11,Urothelial Carcinoma of The Urinary Bladder,C0279680,Blood,GEO,Microarray,Homo sapiens,29|10,DO:A bladder carcinoma that has_material_basis_in transitional cells located_in the lining of the bladder. DSA03127,GSE138142,GPL24247,57,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,RNA-Seq,Mus musculus,4|4,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA03128,GSE138167,GPL16791,66,Cystic Fibrosis,C0010674,Bronchus,GEO,RNA-Seq,Homo sapiens,5|7,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA03129,GSE138167,GPL16791,28,Cystic Fibrosis,C0010674,Bronchus,GEO,RNA-Seq,Homo sapiens,5|7,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA03130,GSE138260,GPL27556,1000,Alzheimer's Disease,C0002395,Brain,GEO,Microarray,Homo sapiens,19|17,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03131,GSE138312,GPL21290,5,Non-Alcoholic Fatty Liver Disease,C0400966,,GEO,RNA-Seq,Homo sapiens,16|21,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA03132,GSE138312,GPL21290,1000,Non-Alcoholic Fatty Liver Disease,C0400966,,GEO,RNA-Seq,Homo sapiens,16|21,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA03133,GSE138437,GPL24676,1000,Pancreatic Cancer,C0235974,Pancreas,GEO,RNA-Seq,Homo sapiens,3|2,DO:An endocrine gland cancer located_in the pancreas. DSA03134,GSE138437,GPL24676,1000,Pancreatic Cancer,C0235974,Pancreas,GEO,RNA-Seq,Homo sapiens,3|3,DO:An endocrine gland cancer located_in the pancreas. DSA03135,GSE138437,GPL24676,1000,Pancreatic Cancer,C0235974,Pancreas,GEO,RNA-Seq,Homo sapiens,3|3,DO:An endocrine gland cancer located_in the pancreas. DSA03136,GSE138437,GPL24676,1000,Pancreatic Cancer,C0235974,Pancreas,GEO,RNA-Seq,Homo sapiens,3|3,DO:An endocrine gland cancer located_in the pancreas. DSA03137,GSE138437,GPL24676,1000,Pancreatic Cancer,C0235974,Pancreas,GEO,RNA-Seq,Homo sapiens,3|3,DO:An endocrine gland cancer located_in the pancreas. DSA03138,GSE138437,GPL24676,1000,Pancreatic Cancer,C0235974,Pancreas,GEO,RNA-Seq,Homo sapiens,3|3,DO:An endocrine gland cancer located_in the pancreas. DSA03139,GSE138437,GPL24676,1000,Pancreatic Cancer,C0235974,Pancreas,GEO,RNA-Seq,Homo sapiens,3|2,DO:An endocrine gland cancer located_in the pancreas. DSA03140,GSE138437,GPL24676,1000,Pancreatic Cancer,C0235974,Pancreas,GEO,RNA-Seq,Homo sapiens,3|2,DO:An endocrine gland cancer located_in the pancreas. DSA03141,GSE138575,GPL11154,192,Polycystic Ovary Syndrome,C0032460,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA03142,GSE138580,GPL27583,1000,Tuberculosis,C0041296,Bone marrow,GEO,RNA-Seq,Mus musculus,2|3,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA03143,GSE138580,GPL27583,1000,Tuberculosis,C0041296,Bone marrow,GEO,RNA-Seq,Mus musculus,2|3,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA03144,GSE138614,GPL21697,1000,Multiple Sclerosis,C0026769,Brain,GEO,RNA-Seq,Homo sapiens,25|73,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA03145,GSE138669,GPL18573,1000,Systemic Sclerosis [Scleroderma],C2364016,Skin,GEO,scRNA-Seq,Homo sapiens,10|12, DSA03146,GSE18216,GPL1261,1000,Breast Cancer,C0678222,Breast,GEO,Microarray,Mus musculus,3|5,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03147,GSE138695,GPL18573,1000,Alzheimer's Disease,C0002395,Brain,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03148,GSE138702,GPL21290,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,RNA-Seq,Homo sapiens,10|9,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03149,GSE138784,GPL18573,1000,Severe Combined Immunodeficiency,C0085110,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A severe combined immunodeficiency that is characterized by deficiency of MHC class II molecules that causes lack of immune protection against bacteria, viruses, and fungi and thus causes early death in childhood, and has_material_basis_in autosomal recessive inheritance of mutation in the CIITA, RFX5, RFXANK, and RFXAP genes." DSA03150,GSE138784,GPL18573,1000,Severe Combined Immunodeficiency,C0085110,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A severe combined immunodeficiency that is characterized by deficiency of MHC class II molecules that causes lack of immune protection against bacteria, viruses, and fungi and thus causes early death in childhood, and has_material_basis_in autosomal recessive inheritance of mutation in the CIITA, RFX5, RFXANK, and RFXAP genes." DSA03151,GSE21444,GPL1261,1000,Invasive Breast Carcinoma,C0853879,Breast,GEO,Microarray,Mus musculus,5|5,"EFO:A carcinoma that infiltrates the breast parenchyma. The vast majority are adenocarcinomas arising from the terminal ductal lobular unit (TDLU). Often, the invasive adenocarcinoma co-exists with ductal or lobular carcinoma in situ. It is the most common carcinoma affecting women." DSA03152,GSE138852,GPL18573,1000,Alzheimer's Disease,C0002395,Entorhinal cortex,GEO,scRNA-Seq,Homo sapiens,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03153,GSE138861,GPL23159,44,Myeloid Leukemia Associated With Down Syndrome,C2825149,,GEO,Microarray,Homo sapiens,5|8,"NCI:Acute myeloid leukemia or myelodysplastic syndrome occurring in children with Down syndrome. The acute myeloid leukemia is usually an acute megakaryoblastic leukemia, and is associated with GATA1 gene mutation." DSA03154,GSE138861,GPL23159,0,Acute Megakaryoblastic Leukemia,C0023462,Mesenchyme,GEO,Microarray,Homo sapiens,5|5,DO:An acute myeloid leukemia that derives from blood-forming tissue in which megakaryocytes proliferate in the bone marrow and circulate in the blood in large numbers. DSA03155,GSE138883,GPL16686,13,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03156,GSE138883,GPL16686,8,Chronic Myeloid Leukemia,C0023473,,GEO,Microarray,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA03157,GSE138883,GPL16686,21,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03158,GSE138883,GPL16686,116,Chronic Myeloid Leukemia,C0023473,,GEO,Microarray,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA03159,GSE139038,GPL27630,184,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,6|41,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03160,GSE21444,GPL1261,330,Ductal Carcinoma In Situ,C0007124,Breast,GEO,Microarray,Mus musculus,5|5,"EFO:A malignant tumor arising from epithelial cells. Carcinomas that arise from glandular epithelium are called adenocarcinomas, those that arise from squamous epithelium are called squamous cell carcinomas, and those that arise from transitional epithelium are called transitional cell carcinomas. Morphologically, the malignant epithelial cells may display abnormal mitotic figures, anaplasia, and necrosis. Carcinomas are graded by the degree of cellular differentiation as well, moderately, or poorly differentiated. Carcinomas invade the surrounding tissues and tend to metastasize to other anatomic sites. Lung carcinoma, skin carcinoma, breast carcinoma, colon carcinoma, and prostate carcinoma are the most frequently seen carcinomas." DSA03161,GSE139173,GPL21103,751,Acute Pancreatitis,C0001339,Pancreas,GEO,RNA-Seq,Mus musculus,3|3,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA03162,GSE139188,GPL21290,14,Autosomal Dominant Hyper-Ige Syndrome,C2936739,Umbilical cord,GEO,RNA-Seq,Homo sapiens,3|3,DO:A hyper IgE syndrome that has_material_basis_in heterozygous mutation in the STAT3 gene on chromosome 17q21. DSA03163,GSE139202,GPL11154,68,Autosomal Dominant Hyper-Ige Syndrome,C2936739,Skin,GEO,RNA-Seq,Homo sapiens,3|3,DO:A hyper IgE syndrome that has_material_basis_in heterozygous mutation in the STAT3 gene on chromosome 17q21. DSA03164,GSE139222,GPL570,0,Orofacial Cleft,C1861537,,GEO,Microarray,Homo sapiens,5|5,DO:An orofacial cleft characterized by autosomal dominant inheritance that has_material_basis_in variation in chromosome region 6p24.3. DSA03165,GSE139247,GPL15207,0,Atopic Dermatitis,C0011615,Peripheral blood,GEO,Microarray,Homo sapiens,3|3,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA03166,GSE139324,GPL18573,1000,Head And Neck Squamous Cell Carcinoma,C1168401,Peripheral blood,GEO,scRNA-Seq,Homo sapiens,6|26,"DO:A head and neck carcinoma that has_material_basis_in squamous cells that line the moist, mucosal surfaces inside the head and neck." DSA03167,GSE139350,GPL20795,693,Systemic Lupus Erythematosus,C0024141,Blood,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03168,GSE139358,GPL21290,25,Systemic Lupus Erythematosus,C0024141,Blood,GEO,RNA-Seq,Homo sapiens,7|9,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03169,GSE21444,GPL1261,93,Ductal Carcinoma In Situ,C0007124,Breast,GEO,Microarray,Mus musculus,5|5,"EFO:A malignant tumor arising from epithelial cells. Carcinomas that arise from glandular epithelium are called adenocarcinomas, those that arise from squamous epithelium are called squamous cell carcinomas, and those that arise from transitional epithelium are called transitional cell carcinomas. Morphologically, the malignant epithelial cells may display abnormal mitotic figures, anaplasia, and necrosis. Carcinomas are graded by the degree of cellular differentiation as well, moderately, or poorly differentiated. Carcinomas invade the surrounding tissues and tend to metastasize to other anatomic sites. Lung carcinoma, skin carcinoma, breast carcinoma, colon carcinoma, and prostate carcinoma are the most frequently seen carcinomas." DSA03170,GSE21444,GPL1261,490,Ductal Carcinoma In Situ,C0007124,Breast,GEO,Microarray,Mus musculus,5|5,"EFO:A malignant tumor arising from epithelial cells. Carcinomas that arise from glandular epithelium are called adenocarcinomas, those that arise from squamous epithelium are called squamous cell carcinomas, and those that arise from transitional epithelium are called transitional cell carcinomas. Morphologically, the malignant epithelial cells may display abnormal mitotic figures, anaplasia, and necrosis. Carcinomas are graded by the degree of cellular differentiation as well, moderately, or poorly differentiated. Carcinomas invade the surrounding tissues and tend to metastasize to other anatomic sites. Lung carcinoma, skin carcinoma, breast carcinoma, colon carcinoma, and prostate carcinoma are the most frequently seen carcinomas." DSA03171,GSE21444,GPL1261,360,Ductal Carcinoma In Situ,C0007124,Breast,GEO,Microarray,Mus musculus,5|5,"EFO:A malignant tumor arising from epithelial cells. Carcinomas that arise from glandular epithelium are called adenocarcinomas, those that arise from squamous epithelium are called squamous cell carcinomas, and those that arise from transitional epithelium are called transitional cell carcinomas. Morphologically, the malignant epithelial cells may display abnormal mitotic figures, anaplasia, and necrosis. Carcinomas are graded by the degree of cellular differentiation as well, moderately, or poorly differentiated. Carcinomas invade the surrounding tissues and tend to metastasize to other anatomic sites. Lung carcinoma, skin carcinoma, breast carcinoma, colon carcinoma, and prostate carcinoma are the most frequently seen carcinomas." DSA03172,GSE139384,GPL10558,0,Alzheimer's Disease,C0002395,Brain,GEO,Microarray,Homo sapiens,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03173,GSE139384,GPL10558,0,Alzheimer's Disease,C0002395,Brain,GEO,Microarray,Homo sapiens,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03174,GSE139400,GPL570,0,Obesity,C0028754,Rectus femoris,GEO,Microarray,Homo sapiens,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA03175,GSE21444,GPL1261,1000,Ductal Carcinoma In Situ,C0007124,Breast,GEO,Microarray,Mus musculus,5|5,"EFO:A malignant tumor arising from epithelial cells. Carcinomas that arise from glandular epithelium are called adenocarcinomas, those that arise from squamous epithelium are called squamous cell carcinomas, and those that arise from transitional epithelium are called transitional cell carcinomas. Morphologically, the malignant epithelial cells may display abnormal mitotic figures, anaplasia, and necrosis. Carcinomas are graded by the degree of cellular differentiation as well, moderately, or poorly differentiated. Carcinomas invade the surrounding tissues and tend to metastasize to other anatomic sites. Lung carcinoma, skin carcinoma, breast carcinoma, colon carcinoma, and prostate carcinoma are the most frequently seen carcinomas." DSA03176,GSE22778,GPL1261,1,Myeloid Leukemia,C0023470,,GEO,Microarray,Mus musculus,3|2,DO:A myelodysplastic myeloproliferative neoplasm characterized by the principal involvement of the neutrophil series with leukocytosis and multilineage dysplasia. The neoplastic cells do not have a Philadelphia chromosome or the BCR/ABL fusion gene. DSA03177,GSE139534,GPL16791,1000,Lymphangioleiomyomatosis,C0751674,Lung,GEO,scRNA-Seq,Homo sapiens,2|2,"DO:A lung disease that is characterized by progressive cystic destruction of the lung and lymphatic abnormalities, frequently associated with renal angiomyolipomas." DSA03178,GSE139602,GPL13667,1000,Chronic Liver Disease,C0341439,Liver,GEO,Microarray,Homo sapiens,6|5,"NCI:Hepatic necrosis, inflammation, or scarring due to any cause that persists for more than 6 months. Manifestations may include signs and symptoms of cholestasis, portal hypertension, and/or abnormal liver function tests." DSA03179,GSE139602,GPL13667,1000,Cirrhosis,C1623038,Liver,GEO,Microarray,Homo sapiens,6|8,"MSH:Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury." DSA03180,GSE139602,GPL13667,1000,Cirrhosis,C1623038,Liver,GEO,Microarray,Homo sapiens,6|12,"MSH:Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury." DSA03181,GSE139602,GPL13667,1000,Acute-On-Chronic Liver Failure,C3850141,Liver,GEO,Microarray,Homo sapiens,6|8,"EFO:Acute-on-chronic liver failure (ACLF) is an extreme condition during the natural history of chronic HBV infection, with a relatively high short-term mortality." DSA03182,GSE139613,GPL16791,1000,T-Cell Acute Lymphoblastic Leukemia,C1961099,,GEO,RNA-Seq,Homo sapiens,3|5,DO:An acute lymphoblastic leukemia that is characterized by too many T-cell lymphoblasts found in the bone marrow and blood. DSA03183,GSE139614,GPL16791,604,T-Cell Acute Lymphoblastic Leukemia,C1961099,,GEO,RNA-Seq,Homo sapiens,10|4,DO:An acute lymphoblastic leukemia that is characterized by too many T-cell lymphoblasts found in the bone marrow and blood. DSA03184,GSE24637,GPL1261,0,Type 2 Diabetes,C0011860,Liver,GEO,Microarray,Mus musculus,8|8,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA03185,GSE24637,GPL1261,0,Type 2 Diabetes,C0011860,Pancreas,GEO,Microarray,Mus musculus,8|8,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA03186,GSE139671,GPL18573,1000,Waldenstrom Macroglobulinemia,C0024419,Bone marrow,GEO,RNA-Seq,Homo sapiens,3|4,DO:A B-cell lymphocytic neoplasm characterized by an uncontrolled increase of B-cells. DSA03187,GSE139671,GPL18573,1000,Waldenstrom Macroglobulinemia,C0024419,Bone marrow,GEO,RNA-Seq,Homo sapiens,3|4,DO:A B-cell lymphocytic neoplasm characterized by an uncontrolled increase of B-cells. DSA03188,GSE139825,GPL10558,1000,Pulmonary Tuberculosis,C0041327,Bronchus,GEO,Microarray,Homo sapiens,5|9,"DO:A tuberculosis that is a contagious disease located_in lungs. The infection has_symptom fever, has_symptom cough, has_symptom difficulty in breathing, has_symptom inflammatory infiltrations, has_symptom formation of tubercles, has_symptom caseation, has_symptom pleural effusion, and has_symptom fibrosis." DSA03189,GSE13985,GPL570,0,Familial Hypercholesterolemia,C0020445,Blood,GEO,Microarray,Homo sapiens,5|5,DO:A familial hyperlipidemia characterized by very high levels of low-density lipoprotein (LDL) and early cardiovascular disease. DSA03190,GSE139871,GPL10558,530,Tuberculosis,C0041296,Peripheral blood,GEO,Microarray,Homo sapiens,14|10,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA03191,GSE139900,GPL20301,714,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA03192,GSE139900,GPL20301,263,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA03193,GSE139900,GPL20301,596,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA03194,GSE139900,GPL20301,287,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA03195,GSE139913,GPL18460,1000,Sepsis,C0243026,,GEO,RNA-Seq,Homo sapiens,5|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA03196,GSE140015,GPL20301,40,Spinal And Bulbar Muscular Atrophy,C1839259,,GEO,RNA-Seq,Homo sapiens,4|4,DO:A spinal muscular dystrophy that has_material_basis_in an X-linked recessive expansion of CAG triplet repeats (glutamine) in exon 1 of AR gene encoding the androgen receptor. DSA03197,GSE140089,GPL24676,474,Parkinson's Disease,C0030567,Vastus lateralis,GEO,RNA-Seq,Homo sapiens,12|17,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03198,GSE140089,GPL24676,60,Parkinson's Disease,C0030567,Vastus lateralis,GEO,RNA-Seq,Homo sapiens,12|16,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03199,GSE140101,GPL16791,1000,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA03200,GSE140126,GPL11154,125,Cushing Syndrome,C0010481,Visceral adipose tissue,GEO,RNA-Seq,Homo sapiens,12|6,DO:An adrenal gland hyperfunction disease that results in the overproduction of aldosterone by the adrenal glands. DSA03201,GSE140153,GPL19057,1000,Lung Tumor,C0242379,Lung,GEO,RNA-Seq,Mus musculus,1|4,DO:A lung cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells and is located_in the lungs and has_symptom cough and has_symptom chest discomfort or pain and has_symptom weight loss and has_symptom hemoptysis. DSA03202,GSE24637,GPL1261,1,Type 2 Diabetes,C0011860,Muscle,GEO,Microarray,Mus musculus,8|8,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA03203,GSE24637,GPL1261,0,Type 2 Diabetes,C0011860,Adipose tissue,GEO,Microarray,Mus musculus,8|8,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA03204,GSE140225,GPL18573,2,Diffuse Large B-Cell Lymphoma,C0079744,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|3,DO:A B-cell lymphoma that is a cancer of B cells presenting as an aggressive tumour which can arise in virtually any part of the body. DSA03205,GSE140231,GPL20301,1000,Parkinson's Disease,C0030567,Substantia nigra,GEO,scRNA-Seq,Homo sapiens,5|7,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03206,GSE140261,GPL16791,1000,Facioscapulohumeral Dystrophy,C0238288,Muscle,GEO,RNA-Seq,Homo sapiens,8|27,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA03207,GSE140275,GPL16791,1000,Stroke,C0948008,Blood,GEO,RNA-Seq,Homo sapiens,3|3,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA03208,GSE140286,GPL17021,20,Alzheimer's Disease,C0002395,Cortex,GEO,RNA-Seq,Mus musculus,2|2,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03209,GSE140286,GPL17021,709,Alzheimer's Disease,C0002395,Cortex,GEO,RNA-Seq,Mus musculus,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03210,GSE140286,GPL17021,1000,Alzheimer's Disease,C0002395,Cortex,GEO,RNA-Seq,Mus musculus,2|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03211,GSE140380,GPL21290,1000,Alzheimer's Disease,C0002395,Skin,GEO,RNA-Seq,Homo sapiens,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03212,GSE140385,GPL16791,188,Chronic Myeloid Leukemia,C0023473,Blood,GEO,RNA-Seq,Homo sapiens,4|3,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA03213,GSE140627,GPL16791,1000,Type 1 Diabetes,C0011854,Kidney,GEO,RNA-Seq,Homo sapiens,2|4,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA03214,GSE140627,GPL16791,318,Type 1 Diabetes,C0011854,Kidney,GEO,RNA-Seq,Homo sapiens,2|4,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA03215,GSE140627,GPL16791,0,Type 1 Diabetes,C0011854,Kidney,GEO,RNA-Seq,Homo sapiens,4|4,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA03216,GSE140713,GPL6480,1000,Acquired Immunodeficiency Syndrome,C0001175,Peripheral blood,GEO,Microarray,Homo sapiens,7|50,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA03217,GSE140844,GPL11154,93,Aplastic Anemia,C0002874,,GEO,RNA-Seq,Homo sapiens,8|12,"DO:An anemia that is characterized by a deficiency of red blood cells, white blood cells and platelets produced by bone marrow." DSA03218,GSE140898,GPL16791,166,Hutchinson-Gilford Progeria Syndrome,C0033300,Smooth muscle,GEO,RNA-Seq,Homo sapiens,3|8,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA03219,GSE140902,GPL11154,1000,Urothelial Carcinoma,C2145472,Bladder,GEO,RNA-Seq,Homo sapiens,3|3,"EFO:A malignant neoplasm derived from the transitional epithelium of the urinary tract (urinary bladder, ureter, urethra, or renal pelvis). It is frequently papillary." DSA03220,GSE140902,GPL11154,1000,Urothelial Carcinoma,C2145472,Bladder,GEO,RNA-Seq,Homo sapiens,3|3,"EFO:A malignant neoplasm derived from the transitional epithelium of the urinary tract (urinary bladder, ureter, urethra, or renal pelvis). It is frequently papillary." DSA03221,GSE140963,GPL17021,1000,Prostate Tumor,C0600139,Prostate,GEO,RNA-Seq,Mus musculus,2|2,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03222,GSE140963,GPL17021,1000,Prostate Tumor,C0600139,Prostate,GEO,RNA-Seq,Mus musculus,2|2,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03223,GSE27716,GPL570,0,Invasive Lung Mucinous Adenocarcinoma,C4522160,Lung,GEO,Microarray,Homo sapiens,17|23,"NCI:An invasive adenocarcinoma that arises from the lung. It is characterized by the presence of tall columnar cells and mucin production. This category refers to cases formerly classified as mucinous bronchioloalveolar carcinoma, excluding cases that meet the criteria for adenocarcinoma in situ or mucinous minimally invasive adenocarcinoma." DSA03224,GSE31317,GPL1261,1000,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Mus musculus,8|3,DO:A respiratory system cancer that is located_in the lung. DSA03225,GSE31317,GPL1261,1000,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Mus musculus,8|3,DO:A respiratory system cancer that is located_in the lung. DSA03226,GSE141174,GPL6104,700,Colorectal Carcinoma,C0009402,Colorectum,GEO,Microarray,Homo sapiens,3|3,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA03227,GSE141192,GPL21103,1000,Tuberculosis,C0041296,Blood,GEO,RNA-Seq,Mus musculus,5|4,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA03228,GSE141205,GPL21103,1000,Tuberculosis,C0041296,Lung,GEO,RNA-Seq,Mus musculus,5|4,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA03229,GSE141432,GPL18573,1000,Obesity,C0028754,White adipose tissue,GEO,RNA-Seq,Homo sapiens,9|8,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA03230,GSE141432,GPL18573,1000,Obesity,C0028754,White adipose tissue,GEO,RNA-Seq,Homo sapiens,9|8,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA03231,GSE141439,GPL11154|GPL20301,1000,Malignant Peripheral Nerve Sheath Tumor,C0751690,,GEO,RNA-Seq,Homo sapiens,7|8,EFO:A tumor of the peripheral nervous system composed of neoplastic Schwann cells. The vast majority of schwannomas follow a benign clinical course. Only rare cases associated with a malignant clinical course have been reported. DSA03232,GSE141446,GPL18573,722,Diarrhea,C0011991,Cervix,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A gastrointestinal system disease described as the condition of having frequent loose or liquid bowel movements. Acute diarrhea is a common cause of death in developing countries and the second most common cause of infant deaths worldwide. The loss of fluids through diarrhea can cause severe dehydration which is one cause of death in diarrhea sufferers. Along with water, sufferers also lose dangerous amounts of important salts, electrolytes, and other nutrients. There are at least four types of diarrhea: secretory diarrhea, osmotic diarrhea, motility-related diarrhea, and inflammatory diarrhea." DSA03233,GSE141446,GPL18573,1000,Diarrhea,C0011991,Cervix,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A gastrointestinal system disease described as the condition of having frequent loose or liquid bowel movements. Acute diarrhea is a common cause of death in developing countries and the second most common cause of infant deaths worldwide. The loss of fluids through diarrhea can cause severe dehydration which is one cause of death in diarrhea sufferers. Along with water, sufferers also lose dangerous amounts of important salts, electrolytes, and other nutrients. There are at least four types of diarrhea: secretory diarrhea, osmotic diarrhea, motility-related diarrhea, and inflammatory diarrhea." DSA03234,GSE141446,GPL18573,1000,Diarrhea,C0011991,Cervix,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A gastrointestinal system disease described as the condition of having frequent loose or liquid bowel movements. Acute diarrhea is a common cause of death in developing countries and the second most common cause of infant deaths worldwide. The loss of fluids through diarrhea can cause severe dehydration which is one cause of death in diarrhea sufferers. Along with water, sufferers also lose dangerous amounts of important salts, electrolytes, and other nutrients. There are at least four types of diarrhea: secretory diarrhea, osmotic diarrhea, motility-related diarrhea, and inflammatory diarrhea." DSA03235,GSE141446,GPL18573,1000,Diarrhea,C0011991,Cervix,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A gastrointestinal system disease described as the condition of having frequent loose or liquid bowel movements. Acute diarrhea is a common cause of death in developing countries and the second most common cause of infant deaths worldwide. The loss of fluids through diarrhea can cause severe dehydration which is one cause of death in diarrhea sufferers. Along with water, sufferers also lose dangerous amounts of important salts, electrolytes, and other nutrients. There are at least four types of diarrhea: secretory diarrhea, osmotic diarrhea, motility-related diarrhea, and inflammatory diarrhea." DSA03236,GSE141512,GPL17586,236,Myocardial Infarction,C0027051,Blood,GEO,Microarray,Homo sapiens,6|6,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA03237,GSE141531,GPL24676,864,Retinitis Pigmentosa,C0035334,Retina,GEO,RNA-Seq,Homo sapiens,5|5,DO:A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss. DSA03238,GSE141578,GPL24676|GPL28038,1000,Parkinson's Disease,C0030567,Cerebrospinal fluid,GEO,scRNA-Seq,Homo sapiens,11|8,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03239,GSE141578,GPL24676|GPL28038,1000,Dementia With Lewy Bodies,C0752347,Cerebrospinal fluid,GEO,scRNA-Seq,Homo sapiens,11|2,"DO:A dementia that is characterized by the development of abnormal proteinaceous (alpha-synuclein) cytoplasmic inclusions, called Lewy bodies, throughout the brain that results in progressive decline in mental abilities." DSA03240,GSE29377,GPL6104,1000,Melanoma,C0025202,,GEO,Microarray,Homo sapiens,8|82,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA03241,GSE29378,GPL6947,39,Alzheimer's Disease,C0002395,Hippocampus,GEO,Microarray,Homo sapiens,16|16,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03242,GSE29378,GPL6947,8,Alzheimer's Disease,C0002395,Hippocampus,GEO,Microarray,Homo sapiens,16|15,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03243,GSE29417,GPL6246,158,Bipolar Disorder,C0005586,Hippocampus,GEO,Microarray,Mus musculus,6|6,DO:A mood disorder that involves alternating periods of mania and depression. DSA03244,GSE29429,GPL10558,1000,Acquired Immunodeficiency Syndrome,C0001175,Blood,GEO,Microarray,Homo sapiens,17|30,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA03245,GSE29429,GPL6947,1000,Acquired Immunodeficiency Syndrome,C0001175,Blood,GEO,Microarray,Homo sapiens,27|67,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA03246,GSE29429,GPL6947,1000,Acquired Immunodeficiency Syndrome,C0001175,Blood,GEO,Microarray,Homo sapiens,11|80,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA03247,GSE29507,GPL4133,1000,Tuberculous Meningitis,C0041318,Frontal cortex,GEO,Microarray,Homo sapiens,4|5,EFO:A bacterial infection of the membranes covering the brain and the spinal cord caused by Mycobacterium tuberculosis. DSA03248,GSE29570,GPL6244,1000,Cervical Cancer,C4048328,Exocervix,GEO,Microarray,Homo sapiens,17|45,DO:A female reproductive organ cancer that is located_in the cervix. DSA03249,GSE29674,GPL1261,0,Multiple Endocrine Neoplasia Syndrome,C0027662,Pancreatic islet,GEO,Microarray,Mus musculus,5|5,"MONDO:Multiple endocrine neoplasia (MEN) is a group of rare inherited cancer syndromes characterized by the development of two or more endocrine gland tumors, sometimes with tumor development in other tissues or organs." DSA03250,GSE29681,GPL1261,1000,Huntington's Disease,C0020179,Striatum,GEO,Microarray,Mus musculus,10|8,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA03251,GSE29681,GPL1261,1000,Huntington's Disease,C0020179,Striatum,GEO,Microarray,Mus musculus,7|7,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA03252,GSE29746,GPL4133,0,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,11|9,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA03253,GSE29746,GPL4133,46,Osteoarthritis,C0157946,,GEO,Microarray,Homo sapiens,11|11,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA03254,GSE29807,GPL570,0,Very Low Birth Weight,C0282666,Umbilical cord blood,GEO,Microarray,Homo sapiens,4|8,"EFO:An infant whose weight at birth is less than 1500 grams (3.3 lbs), regardless of gestational age." DSA03255,GSE29819,GPL570,556,Cardiomyopathy,C0878544,Left ventricle,GEO,Microarray,Homo sapiens,6|6,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA03256,GSE29819,GPL570,26,Cardiomyopathy,C0878544,Right ventricle,GEO,Microarray,Homo sapiens,6|6,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA03257,GSE29819,GPL570,454,Dilated Cardiomyopathy,C0007193,Left ventricle,GEO,Microarray,Homo sapiens,6|7,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA03258,GSE29819,GPL570,929,Dilated Cardiomyopathy,C0007193,Right ventricle,GEO,Microarray,Homo sapiens,6|7,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA03259,GSE29918,GPL5175,1000,Global Developmental Delay,C0557874,,GEO,Microarray,Homo sapiens,6|4,"HPO:A delay in the achievement of motor or mental milestones in the domains of development of a child, including motor skills, speech and language, cognitive skills, and social and emotional skills. This term should only be used to describe children younger than five years of age." DSA03260,GSE29918,GPL5175,1000,Global Developmental Delay,C0557874,,GEO,Microarray,Homo sapiens,6|4,"HPO:A delay in the achievement of motor or mental milestones in the domains of development of a child, including motor skills, speech and language, cognitive skills, and social and emotional skills. This term should only be used to describe children younger than five years of age." DSA03261,GSE29927,GPL11095,233,Lung Squamous Cell Carcinoma,C0149782,Lung,GEO,Microarray,Homo sapiens,10|10,DO:A non-small cell lung carcinoma that has_material_basis_in the squamous cell. DSA03262,GSE29938,GPL11095,3,Cutaneous Lupus Erythematosus,C0024137,Dermis,GEO,Microarray,Homo sapiens,4|4,DO:A lupus erythematosus that causes skin lesions on parts of the body that are exposed to sunlight. DSA03263,GSE29938,GPL11095,20,Cutaneous Lupus Erythematosus,C0024137,Dermis,GEO,Microarray,Homo sapiens,4|4,DO:A lupus erythematosus that causes skin lesions on parts of the body that are exposed to sunlight. DSA03264,GSE29938,GPL11095,0,Cutaneous Lupus Erythematosus,C0024137,Dermis,GEO,Microarray,Homo sapiens,4|4,DO:A lupus erythematosus that causes skin lesions on parts of the body that are exposed to sunlight. DSA03265,GSE29938,GPL11095,1,Cutaneous Lupus Erythematosus,C0024137,Dermis,GEO,Microarray,Homo sapiens,3|4,DO:A lupus erythematosus that causes skin lesions on parts of the body that are exposed to sunlight. DSA03266,GSE29938,GPL11095,3,Cutaneous Lupus Erythematosus,C0024137,Dermis,GEO,Microarray,Homo sapiens,4|4,DO:A lupus erythematosus that causes skin lesions on parts of the body that are exposed to sunlight. DSA03267,GSE29938,GPL11095,0,Cutaneous Lupus Erythematosus,C0024137,Dermis,GEO,Microarray,Homo sapiens,4|4,DO:A lupus erythematosus that causes skin lesions on parts of the body that are exposed to sunlight. DSA03268,GSE29977,GPL570,0,Polycythemia Due To High Altitude,C0865276,Peripheral blood,GEO,Microarray,Homo sapiens,5|5,DO:A primary polycythemia that has_material_basis_in homozygous or compound heterozygous mutation in the VHL gene (608537) on chromosome 3p25. DSA03269,GSE29988,GPL6887,816,Renal Cysts,C3887499,Kidney,GEO,Microarray,Mus musculus,4|4,"EFO:Abnormal fluid filled sac within the kidney, either acquired or congenital." DSA03270,GSE29988,GPL6887,1000,Renal Cysts,C3887499,Kidney,GEO,Microarray,Mus musculus,4|4,"EFO:Abnormal fluid filled sac within the kidney, either acquired or congenital." DSA03271,GSE30063,GPL570,165,Chronic Obstructive Pulmonary Disease,C0024117,Small airway,GEO,Microarray,Homo sapiens,34|1,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA03272,GSE30118,GPL9365,0,Lung Squamous Cell Carcinoma,C0149782,Lung,GEO,Microarray,Homo sapiens,2|5,DO:A non-small cell lung carcinoma that has_material_basis_in the squamous cell. DSA03273,GSE30129,GPL6246,1,Autoimmune Polyendocrinopathy Syndrome,C0085409,,GEO,Microarray,Mus musculus,3|3,"DO:An autoimmune disease that is characterized by onset in infancy of refractory diarrhea, endocrinopathies, type 1 diabetes mellitus, and dermatitis that has_material_basis_in X-linked recessive mutation in the forkhead box P3 (FOXP3) gene on chromosome Xp11." DSA03274,GSE30129,GPL6246,0,Autoimmune Polyendocrinopathy Syndrome,C0085409,,GEO,Microarray,Mus musculus,3|3,"DO:An autoimmune disease that is characterized by onset in infancy of refractory diarrhea, endocrinopathies, type 1 diabetes mellitus, and dermatitis that has_material_basis_in X-linked recessive mutation in the forkhead box P3 (FOXP3) gene on chromosome Xp11." DSA03275,GSE30134,GPL3985,1,Chronic Pancreatitis,C0149521,Pancreas,GEO,Microarray,Homo sapiens,9|8,"EFO:INFLAMMATION of the PANCREAS that is characterized by recurring or persistent ABDOMINAL PAIN with or without STEATORRHEA or DIABETES MELLITUS. It is characterized by the irregular destruction of the pancreatic parenchyma which may be focal, segmental, or diffuse." DSA03276,GSE30134,GPL3985,0,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,Microarray,Homo sapiens,9|15,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA03277,GSE30134,GPL3985,152,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,Microarray,Homo sapiens,9|6,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA03278,GSE30134,GPL3985,265,Metastatic Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,Microarray,Homo sapiens,15|6,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA03279,GSE30195,GPL570,50,Myelodysplastic Syndrome,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,4|9,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA03280,GSE30195,GPL570,244,Myelodysplastic Syndrome,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,4|6,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA03281,GSE30201,GPL570,1000,Myelodysplastic Syndrome,C3463824,,GEO,Microarray,Homo sapiens,11|8,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA03282,GSE30208,GPL6102,359,Type 1 Diabetes,C0011854,Peripheral blood,GEO,Microarray,Homo sapiens,26|37,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA03283,GSE30209,GPL6102,24,Type 1 Diabetes,C0011854,Peripheral blood,GEO,Microarray,Homo sapiens,29|29,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA03284,GSE30369,GPL6104,1000,Kufs Disease,C0027877,Peripheral blood,GEO,Microarray,Homo sapiens,4|4,"DO:A neuronal ceroid lipofuscinosis that is characterized by autosomal dominant inhetitance, onset of symptoms (psychiatric manifestations, seizures, cerebellar ataxia, and cognitive decline) in adulthood and has_material_basis_in heterozygous mutation in the DNAJC5 gene (611203) on chromosome 20q13." DSA03285,GSE30528,GPL571,1000,Diabetic Kidney Disease,C0011881,Glomerulus,GEO,Microarray,Homo sapiens,13|9,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA03286,GSE39388,GPL570,1000,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,3|6,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03287,GSE39355,GPL1261,0,Prostate Cancer,C0600139,,GEO,Microarray,Mus musculus,3|4,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03288,GSE30661,GPL6885,540,Respiratory Distress Syndrome,C0852283,Lung,GEO,Microarray,Mus musculus,2|2,"EFO:A respiratory failure that is characterized by deficiency of the surfactant coating the inner surface of the lungs, by failure of the lungs to expand and contract properly during breathing with resulting collapse, and by the accumulation of a protein-containing film lining the alveoli and their ducts." DSA03289,GSE3067,GPL1261,0,Resistance To Thyroid Hormone,C4722330,Heart,GEO,Microarray,Mus musculus,7|7,DO:A congenital hypothyroidism that has_material_basis_in heterozygous mutation in the PAX8 gene on chromosome 2q13. DSA03290,GSE3067,GPL1261,0,Resistance To Thyroid Hormone,C4722330,Heart,GEO,Microarray,Mus musculus,7|7,DO:A congenital hypothyroidism that has_material_basis_in heterozygous mutation in the PAX8 gene on chromosome 2q13. DSA03291,GSE30688,GPL1261,0,Cutaneous Melanoma,C0151779,Lymph node,GEO,Microarray,Mus musculus,3|3,DO:A skin cancer that has_material_basis_in melanocytes. DSA03292,GSE30688,GPL1261,1000,Cutaneous Melanoma,C0151779,Lymph node,GEO,Microarray,Mus musculus,3|3,DO:A skin cancer that has_material_basis_in melanocytes. DSA03293,GSE30784,GPL570,1000,Oral Squamous Cell Carcinoma,C0585362,Oral cavity,GEO,Microarray,Homo sapiens,45|167,"EFO:A squamous cell carcinoma arising from the oral cavity. It affects predominantly adults in their fifth and sixth decades of life and is associated with alcohol and tobacco use. Human papillomavirus is present in approximately half of the cases. It is characterized by a tendency to metastasize early to the lymph nodes. When the tumor is small, patients are often asymptomatic. Physical examination may reveal erythematous or white lesions or plaques. The majority of patients present with signs and symptoms of locally advanced disease including mucosal ulceration, pain, difficulty with speaking, chewing, and swallowing, bleeding, weight loss, and neck swelling. Patients may also present with swollen neck lymph nodes without any symptoms from the oropharyngeal tumor. The most significant prognostic factors are the size of the tumor and the lymph nodes status." DSA03294,GSE30784,GPL570,1000,Oral Squamous Cell Carcinoma,C0585362,Oral cavity,GEO,Microarray,Homo sapiens,45|17,"EFO:A squamous cell carcinoma arising from the oral cavity. It affects predominantly adults in their fifth and sixth decades of life and is associated with alcohol and tobacco use. Human papillomavirus is present in approximately half of the cases. It is characterized by a tendency to metastasize early to the lymph nodes. When the tumor is small, patients are often asymptomatic. Physical examination may reveal erythematous or white lesions or plaques. The majority of patients present with signs and symptoms of locally advanced disease including mucosal ulceration, pain, difficulty with speaking, chewing, and swallowing, bleeding, weight loss, and neck swelling. Patients may also present with swollen neck lymph nodes without any symptoms from the oropharyngeal tumor. The most significant prognostic factors are the size of the tumor and the lymph nodes status." DSA03295,GSE30806,GPL570,2,Inclusion Body Myopathy; Sporadic,C0751713,Vastus lateralis,GEO,Microarray,Homo sapiens,3|7,"DO:A myositis that is characterized by late onset of skeletal muscle inflammation, weakness, and atrophy with cytoplasmic granules and vacuoles in the muscle." DSA03296,GSE30807,GPL570,0,Osteosarcoma,C0029463,,GEO,Microarray,Homo sapiens,1|2,DO:A bone sarcoma that is located_in bone that has_material_basis_in cells of mesenchymal origin. DSA03297,GSE30885,GPL8321,86,Breast Cancer,C0678222,Liver,GEO,Microarray,Mus musculus,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03298,GSE30885,GPL8321,6,Breast Cancer,C0678222,Lung,GEO,Microarray,Mus musculus,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03299,GSE30933,GPL6255,1000,Friedreich Ataxia,C0016719,Peripheral blood,GEO,Microarray,Homo sapiens,40|34,"HPO:Unilateral overgrowth of facial tissues, including muscles, bones and skin." DSA03300,GSE30933,GPL6255,1000,Friedreich Ataxia,C0016719,Peripheral blood,GEO,Microarray,Homo sapiens,40|34,"HPO:Unilateral overgrowth of facial tissues, including muscles, bones and skin." DSA03301,GSE30960,GPL7202,341,Dystonia Disorders Disorders,C0393593,Dorsal root ganglion,GEO,Microarray,Mus musculus,3|3,DO:A dystonia that affects most or all of the body. DSA03302,GSE30980,GPL1261,0,Cleft Palate,C0008925,Mandibular arche,GEO,Microarray,Mus musculus,3|3,"DO:A cleft palate seen as an isolated malformation, distinct from cleft lip with or without cleft palate." DSA03303,GSE31013,GPL1261,1000,Lung Cancer,C0684249,Lung,GEO,Microarray,Mus musculus,6|6,DO:A respiratory system cancer that is located_in the lung. DSA03304,GSE31014,GPL96,0,Guillain-Barre Syndrome,C0018378,Blood,GEO,Microarray,Homo sapiens,7|7,DO:An autoimmune disease of peripheral nervous system that causes body's immune system to attack part of the peripheral nervous system. DSA03305,GSE31023,GPL13497,23,Metastatic Colorectal Cancer,C4721579,Peripheral blood,GEO,Microarray,Homo sapiens,3|6, DSA03306,GSE31056,GPL10526,1000,Oral Squamous Cell Carcinoma,C0585362,Tongue,GEO,Microarray,Homo sapiens,24|23,"EFO:A squamous cell carcinoma arising from the oral cavity. It affects predominantly adults in their fifth and sixth decades of life and is associated with alcohol and tobacco use. Human papillomavirus is present in approximately half of the cases. It is characterized by a tendency to metastasize early to the lymph nodes. When the tumor is small, patients are often asymptomatic. Physical examination may reveal erythematous or white lesions or plaques. The majority of patients present with signs and symptoms of locally advanced disease including mucosal ulceration, pain, difficulty with speaking, chewing, and swallowing, bleeding, weight loss, and neck swelling. Patients may also present with swollen neck lymph nodes without any symptoms from the oropharyngeal tumor. The most significant prognostic factors are the size of the tumor and the lymph nodes status." DSA03307,GSE31095,GPL4133,315,Glioma,C0017638,Brain,GEO,Microarray,Homo sapiens,12|8,DO:A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine. DSA03308,GSE31139,GPL11417,278,Metastatic Melanoma,C0025202,,GEO,Microarray,Homo sapiens,11|26,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA03309,GSE31328,GPL7202,537,Congenital Lipoid Adrenal Hyperplasia,C0342474,Kidney,GEO,Microarray,Mus musculus,7|4,DO:A steroid inherited metabolic disorder that is characterized by adrenal insufficiency and variable degrees of hyper or hypo androgeny manifestations resulting from steroidogenic enzyme deficiency. DSA03310,GSE31356,GPL96,0,Dupuytren's Disease,C4082974,,GEO,Microarray,Homo sapiens,3|3,EFO:A fibromatosis of the palmar fascia characterized by thickening and contracture of the fibrous bands on the palmar surfaces of the hand and fingers. It arises most commonly in men between the ages of 30 and 50. DSA03311,GSE31372,GPL1261,0,Alzheimer's Disease,C0002395,Forebrain,GEO,Microarray,Mus musculus,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03312,GSE31372,GPL1261,0,Alzheimer's Disease,C0002395,Forebrain,GEO,Microarray,Mus musculus,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03313,GSE31372,GPL1261,22,Alzheimer's Disease,C0002395,Forebrain,GEO,Microarray,Mus musculus,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03314,GSE31409,GPL6246,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Mus musculus,8|21,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA03315,GSE31460,GPL6883,146,5Q-Syndrome,C0740302,Peripheral blood,GEO,Microarray,Homo sapiens,6|6,"DO:A chromosomal deletion syndrome characterized by severe macrocytic anemia erythroid hypoplasia in the bone marrow, hypolobated micromegakaryocytes and that has_material_basis_in somatic deletion of 1 allele of the RPS14, MIR145, MIR146A and/or DDX41 genes on chromosome 5q." DSA03316,GSE31624,GPL1261,14,Alzheimer's Disease,C0002395,Hippocampus,GEO,Microarray,Mus musculus,11|11,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03317,GSE31682,GPL2986,1000,Epithelial Ovarian Cancer,C0677886,Blood,GEO,Microarray,Homo sapiens,20|48,DO:A female reproductive organ cancer that is located_in the ovary. DSA03318,GSE31757,GPL5188,0,Sickle Cell Disease,C0002895,Blood,GEO,Microarray,Homo sapiens,4|6,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA03319,GSE31821,GPL570,0,Atrial Fibrillation,C0004238,Auricle,GEO,Microarray,Homo sapiens,2|4,"DO:A heart conduction disease that is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular and has symptoms palpitations, weakness, fatigue, lightheadedness, dizziness, confusion, shortness of breath and chest pain." DSA03320,GSE3185,GPL8300,129,High Grade Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,9|6,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA03321,GSE31879,GPL570,1000,Melanoma,C0025202,,GEO,Microarray,Homo sapiens,4|10,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA03322,GSE31934,GPL11097,115,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,3|3,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA03323,GSE31989,GPL11098,3,Diabetes,C0011847,Liver,GEO,Microarray,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA03324,GSE31990,GPL11098,93,Retinitis Pigmentosa,C0035334,Retina,GEO,Microarray,Mus musculus,3|3,DO:A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss. DSA03325,GSE31990,GPL11098,32,Retinitis Pigmentosa,C0035334,Retina,GEO,Microarray,Mus musculus,3|3,DO:A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss. DSA03326,GSE31990,GPL11098,0,Retinitis Pigmentosa,C0035334,Retina,GEO,Microarray,Mus musculus,3|3,DO:A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss. DSA03327,GSE31990,GPL11098,25,Retinitis Pigmentosa,C0035334,Retina,GEO,Microarray,Mus musculus,3|3,DO:A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss. DSA03328,GSE32007,GPL6887,0,Cerebral Malaria,C0024534,Brain,GEO,Microarray,Mus musculus,3|3,"DO:A malaria that involves neurologic damage resulting from blockage of the blood vessels, caused due to the infection of the red blood cells by Plasmodium species." DSA03329,GSE32007,GPL6887,1000,Cerebral Malaria,C0024534,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A malaria that involves neurologic damage resulting from blockage of the blood vessels, caused due to the infection of the red blood cells by Plasmodium species." DSA03330,GSE32057,GPL570,34,Shwachman-Diamond Syndrome,C0272170,Bone marrow,GEO,Microarray,Homo sapiens,7|9,"DO:A syndrome characterized by exocrine pancreatic insufficiency, bone marrow failure and skeletal abnormalities." DSA03331,GSE32078,GPL1261,0,Diabetes;Heart Malformation,,Heart,GEO,Microarray,Mus musculus,3|3, DSA03332,GSE32078,GPL1261,0,Diabetes;Heart Malformation,,Heart,GEO,Microarray,Mus musculus,3|3, DSA03333,GSE32175,GPL570,1000,Lung Cancer,C0684249,Saliva,GEO,Microarray,Homo sapiens,10|10,DO:A respiratory system cancer that is located_in the lung. DSA03334,GSE3218,GPL96,1000,Germ Cell Tumor,C0205851,,GEO,Microarray,Homo sapiens,6|15,DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from germ cells. DSA03335,GSE3218,GPL96,1000,Germ Cell Tumor,C0205851,,GEO,Microarray,Homo sapiens,6|12,DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from germ cells. DSA03336,GSE3218,GPL96,1000,Germ Cell Tumor,C0205851,,GEO,Microarray,Homo sapiens,6|15,DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from germ cells. DSA03337,GSE3218,GPL96,1000,Germ Cell Tumor,C0205851,,GEO,Microarray,Homo sapiens,6|10,DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from germ cells. DSA03338,GSE3218,GPL96,1000,Germ Cell Tumor,C0205851,,GEO,Microarray,Homo sapiens,6|44,DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from germ cells. DSA03339,GSE3218,GPL97,1000,Germ Cell Tumor,C0205851,,GEO,Microarray,Homo sapiens,6|15,DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from germ cells. DSA03340,GSE3218,GPL97,1000,Germ Cell Tumor,C0205851,,GEO,Microarray,Homo sapiens,6|12,DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from germ cells. DSA03341,GSE3218,GPL97,1000,Germ Cell Tumor,C0205851,,GEO,Microarray,Homo sapiens,6|15,DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from germ cells. DSA03342,GSE3218,GPL97,1000,Germ Cell Tumor,C0205851,,GEO,Microarray,Homo sapiens,6|10,DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from germ cells. DSA03343,GSE3218,GPL97,1000,Germ Cell Tumor,C0205851,,GEO,Microarray,Homo sapiens,6|44,DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from germ cells. DSA03344,GSE32192,GPL9250,394,Huntington's Disease,C0020179,Striatum,GEO,RNA-Seq,Mus musculus,1|1,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA03345,GSE32192,GPL9250,299,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,1|1,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA03346,GSE32280,GPL570,0,Major Depressive Disorder,C1269683,Peripheral blood,GEO,Microarray,Homo sapiens,8|8,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA03347,GSE32280,GPL570,0,Subsyndromal Symptomatic Depression,,Peripheral blood,GEO,Microarray,Homo sapiens,8|8, DSA03348,GSE32317,GPL570,9,Progressive Osteoarthritis,C0157946,Synovium,GEO,Microarray,Homo sapiens,10|9,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA03349,GSE32453,GPL6104,0,Hypertrophic Obstructive Cardiomyopathy,C4551472,Cardiac septum,GEO,Microarray,Homo sapiens,5|8,DO:An intrinsic cardiomyopathy that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause. DSA03350,GSE32472,GPL6244,1000,Bronchopulmonary Dysplasia,C0006287,Blood,GEO,Microarray,Homo sapiens,35|34,"MONDO:Bronchopulmonary dysplasia is a chronic respiratory disease that results from complications related to lung injury during the treatment of infant acute respiratory distress syndrome in low-birth-weight premature infants or from abnormal lung development in older infants. Clinical signs are tachypnea, tachycardia and signs of respiratory distress such as intercostal recession, grunting and nasal flaring." DSA03351,GSE32472,GPL6244,1,Bronchopulmonary Dysplasia,C0006287,Blood,GEO,Microarray,Homo sapiens,39|34,"MONDO:Bronchopulmonary dysplasia is a chronic respiratory disease that results from complications related to lung injury during the treatment of infant acute respiratory distress syndrome in low-birth-weight premature infants or from abnormal lung development in older infants. Clinical signs are tachypnea, tachycardia and signs of respiratory distress such as intercostal recession, grunting and nasal flaring." DSA03352,GSE32472,GPL6244,1000,Bronchopulmonary Dysplasia,C0006287,Blood,GEO,Microarray,Homo sapiens,38|38,"MONDO:Bronchopulmonary dysplasia is a chronic respiratory disease that results from complications related to lung injury during the treatment of infant acute respiratory distress syndrome in low-birth-weight premature infants or from abnormal lung development in older infants. Clinical signs are tachypnea, tachycardia and signs of respiratory distress such as intercostal recession, grunting and nasal flaring." DSA03353,GSE32472,GPL6244,1000,Bronchopulmonary Dysplasia,C0006287,Blood,GEO,Microarray,Homo sapiens,35|13,"MONDO:Bronchopulmonary dysplasia is a chronic respiratory disease that results from complications related to lung injury during the treatment of infant acute respiratory distress syndrome in low-birth-weight premature infants or from abnormal lung development in older infants. Clinical signs are tachypnea, tachycardia and signs of respiratory distress such as intercostal recession, grunting and nasal flaring." DSA03354,GSE32472,GPL6244,279,Bronchopulmonary Dysplasia,C0006287,Blood,GEO,Microarray,Homo sapiens,39|11,"MONDO:Bronchopulmonary dysplasia is a chronic respiratory disease that results from complications related to lung injury during the treatment of infant acute respiratory distress syndrome in low-birth-weight premature infants or from abnormal lung development in older infants. Clinical signs are tachypnea, tachycardia and signs of respiratory distress such as intercostal recession, grunting and nasal flaring." DSA03355,GSE32472,GPL6244,1000,Bronchopulmonary Dysplasia,C0006287,Blood,GEO,Microarray,Homo sapiens,38|10,"MONDO:Bronchopulmonary dysplasia is a chronic respiratory disease that results from complications related to lung injury during the treatment of infant acute respiratory distress syndrome in low-birth-weight premature infants or from abnormal lung development in older infants. Clinical signs are tachypnea, tachycardia and signs of respiratory distress such as intercostal recession, grunting and nasal flaring." DSA03356,GSE32472,GPL6244,1000,Bronchopulmonary Dysplasia,C0006287,Blood,GEO,Microarray,Homo sapiens,35|15,"MONDO:Bronchopulmonary dysplasia is a chronic respiratory disease that results from complications related to lung injury during the treatment of infant acute respiratory distress syndrome in low-birth-weight premature infants or from abnormal lung development in older infants. Clinical signs are tachypnea, tachycardia and signs of respiratory distress such as intercostal recession, grunting and nasal flaring." DSA03357,GSE32472,GPL6244,1000,Bronchopulmonary Dysplasia,C0006287,Blood,GEO,Microarray,Homo sapiens,39|13,"MONDO:Bronchopulmonary dysplasia is a chronic respiratory disease that results from complications related to lung injury during the treatment of infant acute respiratory distress syndrome in low-birth-weight premature infants or from abnormal lung development in older infants. Clinical signs are tachypnea, tachycardia and signs of respiratory distress such as intercostal recession, grunting and nasal flaring." DSA03358,GSE32472,GPL6244,1000,Bronchopulmonary Dysplasia,C0006287,Blood,GEO,Microarray,Homo sapiens,38|14,"MONDO:Bronchopulmonary dysplasia is a chronic respiratory disease that results from complications related to lung injury during the treatment of infant acute respiratory distress syndrome in low-birth-weight premature infants or from abnormal lung development in older infants. Clinical signs are tachypnea, tachycardia and signs of respiratory distress such as intercostal recession, grunting and nasal flaring." DSA03359,GSE32537,GPL6244,1000,Idiopathic Interstitial Pneumonia,C2350236,Lung,GEO,Microarray,Homo sapiens,50|167,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA03360,GSE32575,GPL6102,1000,Obesity,C0028754,,GEO,Microarray,Homo sapiens,12|18,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA03361,GSE32586,GPL6885,1,Autosomal Dominant Polycystic Kidney Disease,C0085413,Kidney,GEO,Microarray,Mus musculus,27|29,DO:A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3. DSA03362,GSE32586,GPL8540,0,Autosomal Dominant Polycystic Kidney Disease,C0085413,Kidney,GEO,Microarray,Mus musculus,7|7,DO:A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3. DSA03363,GSE32591,GPL14663,1000,Lupus Nephritis,C0024143,Tubulointerstitium,GEO,Microarray,Homo sapiens,15|32,DO:A glomerulonephritis that is characterized by inflammation of the kidneys resulting from systemic lupus erythematosus. DSA03364,GSE32591,GPL14663,1000,Lupus Nephritis,C0024143,Glomerulus,GEO,Microarray,Homo sapiens,14|32,DO:A glomerulonephritis that is characterized by inflammation of the kidneys resulting from systemic lupus erythematosus. DSA03365,GSE32600,GPL6096,9,H1N1 Influenza,C2076600,Lung,GEO,Microarray,Mus musculus,3|3,"EFO:An influenza that results_in infection located_in respiratory tract of pigs and humans, has_material_basis_in Influenza C virus, or has_material_basis_in Influenza A virus subtypes (H1N1, H1N2, H3N1, H3N2, and H2N3), which are transmitted_by direct contact with infected pigs. The infection in humans has_symptom fever, has_symptom lethargy, has_symptom lack of appetite, has_symptom coughing, has_symptom runny nose, has_symptom sore throat, has_symptom nausea, has_symptom vomiting, and has_symptom diarrhea." DSA03366,GSE32697,GPL6246,81,Colitis,C0009319,Colon,GEO,Microarray,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA03367,GSE3280,GPL570,0,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,Microarray,Homo sapiens,1|3,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03368,GSE32887,GPL570,1000,Cutaneous Sarcoidosis,C0036203,Skin,GEO,Microarray,Homo sapiens,16|15,MONDO:Formation of non-necrotizing granulomas in the skin. It may be a manifestation of systemic sarcoidosis or may also arise in isolation. DSA03369,GSE32988,GPL6480,1000,Multiple Sclerosis,C0026769,Peripheral blood,GEO,Microarray,Homo sapiens,8|16,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA03370,GSE32988,GPL6480,1000,Multiple Sclerosis,C0026769,Peripheral blood,GEO,Microarray,Homo sapiens,8|8,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA03371,GSE32988,GPL6480,553,Multiple Sclerosis,C0026769,Peripheral blood,GEO,Microarray,Homo sapiens,8|8,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA03372,GSE32988,GPL6480,1000,Multiple Sclerosis,C0026769,Peripheral blood,GEO,Microarray,Homo sapiens,8|8,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA03373,GSE3307,GPL96,1000,Amyotrophic Lateral Sclerosis,C0002736,Skeletal muscle,GEO,Microarray,Homo sapiens,16|9,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA03374,GSE3307,GPL96,1000,Acute Quadriplegic Myopathy,,Skeletal muscle,GEO,Microarray,Homo sapiens,16|5, DSA03375,GSE3307,GPL96,821,Becker Muscular Dystrophy,C0917713,Skeletal muscle,GEO,Microarray,Homo sapiens,16|5,"DO:A muscular dystrophy that involves slowly worsening muscle weakness of the legs and pelvis, and has_material_basis_in X-linked recessive inheritance of mutation in the dystrophin gene on chromosome Xp21." DSA03376,GSE3307,GPL96,1000,Duchenne Muscular Dystrophy,C0013264,Skeletal muscle,GEO,Microarray,Homo sapiens,16|10,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA03377,GSE3307,GPL96,1000,Facioscapulohumeral Muscular Dystrophy,C0238288,Skeletal muscle,GEO,Microarray,Homo sapiens,16|14,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA03378,GSE3307,GPL96,1000,Juvenile Dermatomyositis,C0263666,Skeletal muscle,GEO,Microarray,Homo sapiens,16|21,EFO:Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness. DSA03379,GSE3307,GPL96,6,Facioscapulohumeral Muscular Dystrophy,C0238288,Skeletal muscle,GEO,Microarray,Homo sapiens,16|2,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA03380,GSE3307,GPL96,617,Emery-Dreifuss Muscular Dystrophy,C0410189,Skeletal muscle,GEO,Microarray,Homo sapiens,16|4,DO:A muscular dystrophy that chiefly affects muscles used for movement (skeletal) and heart (cardiac) muscle. DSA03381,GSE3307,GPL96,6,Emery-Dreifuss Muscular Dystrophy,C0410189,Skeletal muscle,GEO,Microarray,Homo sapiens,16|4,DO:A muscular dystrophy that chiefly affects muscles used for movement (skeletal) and heart (cardiac) muscle. DSA03382,GSE3307,GPL96,1000,Hereditary Spastic Paraplegia,C0037773,Skeletal muscle,GEO,Microarray,Homo sapiens,16|4,"DO:A hereditary spastic paraplegia that is characterized by spasticity of the leg muscles, progressive muscle weakness, paraplegia, muscle wasting in the hands and feet (distal amyotrophy), small stature, developmental delay, learning disorders, speech difficulties (dysarthria), and mood swings, and has_material_basis_in a mutation of the SPG20 gene." DSA03383,GSE3307,GPL96,1000,Limb-Girdle Muscular Dystrophy Type 2A,C1869123,Skeletal muscle,GEO,Microarray,Homo sapiens,16|10,DO:An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding the proteolytic enzyme calpain-3 (CAPN3) on chromosome 15q15. DSA03384,GSE3307,GPL96,1000,Limb-Girdle Muscular Dystrophy Type 2B,C1850889,Skeletal muscle,GEO,Microarray,Homo sapiens,16|5,DO:An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding the skeletal muscle protein dysferlin (DYSF) on chromosome 2p13. DSA03385,GSE3307,GPL96,1000,Limb-Girdle Muscular Dystrophy Type 2A,C1869123,Skeletal muscle,GEO,Microarray,Homo sapiens,16|7,DO:An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding the proteolytic enzyme calpain-3 (CAPN3) on chromosome 15q15. DSA03386,GSE3307,GPL97,884,Amyotrophic Lateral Sclerosis,C0002736,Skeletal muscle,GEO,Microarray,Homo sapiens,17|9,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA03387,GSE3307,GPL97,51,Becker Muscular Dystrophy,C0917713,Skeletal muscle,GEO,Microarray,Homo sapiens,17|5,"DO:A muscular dystrophy that involves slowly worsening muscle weakness of the legs and pelvis, and has_material_basis_in X-linked recessive inheritance of mutation in the dystrophin gene on chromosome Xp21." DSA03388,GSE3307,GPL97,1000,Duchenne Muscular Dystrophy,C0013264,Skeletal muscle,GEO,Microarray,Homo sapiens,17|10,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA03389,GSE3307,GPL97,88,Emery-Dreifuss Muscular Dystrophy,C0410189,Skeletal muscle,GEO,Microarray,Homo sapiens,17|5,DO:A muscular dystrophy that chiefly affects muscles used for movement (skeletal) and heart (cardiac) muscle. DSA03390,GSE3307,GPL97,4,Emery-Dreifuss Muscular Dystrophy,C0410189,Skeletal muscle,GEO,Microarray,Homo sapiens,17|3,DO:A muscular dystrophy that chiefly affects muscles used for movement (skeletal) and heart (cardiac) muscle. DSA03391,GSE3307,GPL97,476,Facioscapulohumeral Muscular Dystrophy,C0238288,Skeletal muscle,GEO,Microarray,Homo sapiens,17|14,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA03392,GSE3307,GPL97,1000,Juvenile Dermatomyositis,C0263666,Skeletal muscle,GEO,Microarray,Homo sapiens,17|21,EFO:Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness. DSA03393,GSE3307,GPL97,277,Limb-Girdle Muscular Dystrophy Type 2A,C1869123,Skeletal muscle,GEO,Microarray,Homo sapiens,17|10,DO:An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding the proteolytic enzyme calpain-3 (CAPN3) on chromosome 15q15. DSA03394,GSE3307,GPL97,99,Limb-Girdle Muscular Dystrophy Type 2B,C1850889,Skeletal muscle,GEO,Microarray,Homo sapiens,17|5,DO:An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding the skeletal muscle protein dysferlin (DYSF) on chromosome 2p13. DSA03395,GSE3307,GPL97,105,Limb-Girdle Muscular Dystrophy Type 2A,C1869123,Skeletal muscle,GEO,Microarray,Homo sapiens,17|7,DO:An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding the proteolytic enzyme calpain-3 (CAPN3) on chromosome 15q15. DSA03396,GSE3307,GPL97,400,Acute Quadriplegic Myopathy,,Skeletal muscle,GEO,Microarray,Homo sapiens,17|3, DSA03397,GSE3307,GPL97,249,Hereditary Spastic Paraplegia,C0037773,Skeletal muscle,GEO,Microarray,Homo sapiens,17|4,"DO:A hereditary spastic paraplegia that is characterized by spasticity of the leg muscles, progressive muscle weakness, paraplegia, muscle wasting in the hands and feet (distal amyotrophy), small stature, developmental delay, learning disorders, speech difficulties (dysarthria), and mood swings, and has_material_basis_in a mutation of the SPG20 gene." DSA03398,GSE33075,GPL570,31,Chronic Myeloid Leukemia,C0023473,Bone marrow,GEO,Microarray,Homo sapiens,9|10,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA03399,GSE33111,GPL6884,0,Anencephaly;Spina Bifida,,Skin,GEO,Microarray,Homo sapiens,4|3, DSA03400,GSE33111,GPL6884,0,Spina Bifida,C0080178,Skin,GEO,Microarray,Homo sapiens,4|2,"DO:A spina bifida characterized by protrusion of the spinal cord through an opening, covered by meningeal membranes." DSA03401,GSE33126,GPL6947,1000,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,9|9,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA03402,GSE33205,GPL5175,1000,Head And Neck Squamous Cell Carcinoma,C1168401,,GEO,Microarray,Homo sapiens,25|44,"DO:A head and neck carcinoma that has_material_basis_in squamous cells that line the moist, mucosal surfaces inside the head and neck." DSA03403,GSE33223,GPL570,43,Acute Myeloid Leukemia With Multilineage Dysplasia,C1292773,,GEO,Microarray,Homo sapiens,10|9,MONDO:An acute myeloid leukemia arising de novo and not as a result of treatment. It is characterized by the presence of myelodysplastic features in at least 50% of the cells of at least two hematopoietic cell lines. Patients often present with severe cytopenia. DSA03404,GSE33223,GPL570,393,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,Microarray,Homo sapiens,10|11,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03405,GSE33328,GPL9115,1000,Glioblastoma Multiforme,C1621958,Brain,GEO,RNA-Seq,Homo sapiens,1|1,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA03406,GSE33440,GPL6947,41,Diabetes,C0011847,,GEO,Microarray,Homo sapiens,6|16,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA03407,GSE33457,GPL6193,0,Rett Syndrome,C0035372,Amygdala,GEO,Microarray,Mus musculus,4|4,"DO:A pervasive developmental disease that is characterized by normal early growth and development followed by a slowing of development, loss of purposeful use of the hands, distinctive hand movements, slowed brain and head growth, problems with walking, seizures, and intellectual disability." DSA03408,GSE33457,GPL6193,0,Mecp2 Duplication Or Triplication Syndrome,,Amygdala,GEO,Microarray,Mus musculus,5|5, DSA03409,GSE33566,GPL6480,1000,Idiopathic Pulmonary Fibrosis,C1800706,Peripheral blood,GEO,Microarray,Homo sapiens,30|93,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA03410,GSE33615,GPL4133,1000,T-Cell Leukemia,C0023492,,GEO,Microarray,Homo sapiens,21|26,"EFO:A malignant disease of the T-lymphocytes in the bone marrow, thymus, and/or blood." DSA03411,GSE33615,GPL4133,1000,T-Cell Leukemia,C0023492,,GEO,Microarray,Homo sapiens,21|20,"EFO:A malignant disease of the T-lymphocytes in the bone marrow, thymus, and/or blood." DSA03412,GSE33630,GPL570,1000,Anaplastic Thyroid Carcinoma,C0238461,Thyroid,GEO,Microarray,Homo sapiens,45|11,DO:A thyroid gland carcinoma that is composed of undifferentiated cells. DSA03413,GSE33630,GPL570,1000,Papillary Thyroid Carcinoma,C0238463,Thyroid,GEO,Microarray,Homo sapiens,45|49,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA03414,GSE40715,GPL1261,1000,Mammary Carcinoma,C0678222,Mammary gland,GEO,Microarray,Mus musculus,3|5,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03415,GSE40715,GPL1261,1000,Mammary Carcinoma,C0678222,Mammary gland,GEO,Microarray,Mus musculus,3|5,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03416,GSE40715,GPL1261,1000,Mammary Carcinoma,C0678222,Mammary gland,GEO,Microarray,Mus musculus,3|5,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03417,GSE33769,GPL570,1000,Coenzyme Q10 Deficiency,C1843920,,GEO,Microarray,Homo sapiens,3|3,"MONDO:A genetically heterogeneous condition, typically inherited in an autosomal recessive fashion, characterized by coenzyme Q10 deficiency." DSA03418,GSE33769,GPL570,713,Coenzyme Q10 Deficiency,C1843920,,GEO,Microarray,Homo sapiens,3|6,"MONDO:A genetically heterogeneous condition, typically inherited in an autosomal recessive fashion, characterized by coenzyme Q10 deficiency." DSA03419,GSE33769,GPL570,1000,Coenzyme Q10 Deficiency,C1843920,,GEO,Microarray,Homo sapiens,3|3,"MONDO:A genetically heterogeneous condition, typically inherited in an autosomal recessive fashion, characterized by coenzyme Q10 deficiency." DSA03420,GSE33774,GPL6244,112,Peri-Implantitis,C2936258,Gingiva,GEO,Microarray,Homo sapiens,8|7,MSH:An inflammatory process with loss of supporting bone in the tissues surrounding functioning DENTAL IMPLANTS. DSA03421,GSE33774,GPL6244,0,Periodontitis,C0031099,Gingiva,GEO,Microarray,Homo sapiens,8|7,"EFO:Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology)" DSA03422,GSE33814,GPL6884,1000,Steatohepatitis,C2711227,Liver,GEO,Microarray,Homo sapiens,13|12,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA03423,GSE33814,GPL6884,1000,Steatosis,C2711227,Liver,GEO,Microarray,Homo sapiens,13|19,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA03424,GSE33855,GPL5188,0,Amyotrophic Lateral Sclerosis,C0002736,,GEO,Microarray,Homo sapiens,6|4,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA03425,GSE33855,GPL5188,5,Amyotrophic Lateral Sclerosis,C0002736,,GEO,Microarray,Homo sapiens,6|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA03426,GSE33855,GPL5188,0,Amyotrophic Lateral Sclerosis,C0002736,,GEO,Microarray,Homo sapiens,6|6,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA03427,GSE33886,GPL6244,1000,Spinal Cord Disorder,C0037928,Vastus lateralis,GEO,Microarray,Homo sapiens,4|3,EFO:A disease involving the spinal cord. DSA03428,GSE33940,GPL6244,1000,Coenzyme Q10 Deficiency,C1843920,,GEO,Microarray,Homo sapiens,3|4,"MONDO:A genetically heterogeneous condition, typically inherited in an autosomal recessive fashion, characterized by coenzyme Q10 deficiency." DSA03429,GSE33940,GPL6244,1000,Coenzyme Q10 Deficiency,C1843920,,GEO,Microarray,Homo sapiens,3|4,"MONDO:A genetically heterogeneous condition, typically inherited in an autosomal recessive fashion, characterized by coenzyme Q10 deficiency." DSA03430,GSE33943,GPL570,1000,Inflammatory Bowel Disease,C0021390,Peripheral blood,GEO,Microarray,Homo sapiens,13|45,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA03431,GSE34015,GPL6244,1000,Lymphoma,C0024299,Bone marrow,GEO,Microarray,Homo sapiens,5|5,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA03432,GSE34111,GPL570,26,Gastrointestinal Cancer,C0017185,Quadriceps,GEO,Microarray,Homo sapiens,6|12,DO:An organ system cancer located_in gastrointestinal tract that is manifested in organs of the gastrointestinal system. DSA03433,GSE34126,GPL1261,1000,Medulloblastoma,C0025149,Cerebellum,GEO,Microarray,Mus musculus,5|5,DO:An infratentorial cancer that is located_in the lower part of the brain and is a type of primitive neuroectodermal tumor. DSA03434,GSE34198,GPL6102,0,Myocardial Infarction,C0027051,Blood,GEO,Microarray,Homo sapiens,33|32,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA03435,GSE34198,GPL6102,0,Myocardial Infarction,C0027051,Blood,GEO,Microarray,Homo sapiens,15|13,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA03436,GSE34198,GPL6102,1000,Myocardial Infarction,C0027051,Blood,GEO,Microarray,Homo sapiens,33|2,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA03437,GSE34198,GPL6102,0,Myocardial Infarction,C0027051,Blood,GEO,Microarray,Homo sapiens,15|2,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA03438,GSE34201,GPL6884,118,Huntington's Disease,C0020179,,GEO,Microarray,Homo sapiens,30|42,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA03439,GSE34287,GPL7884,0,Multiple System Atrophy,C0393571,Blood,GEO,Microarray,Homo sapiens,12|4,"MONDO:Multiple system atrophy (MSA) is a neurodegenerative disorder characterized by autonomic failure (cardiovascular and/or urinary), parkinsonism, cerebellar impairment and corticospinal signs with a median survival of 6-9 years." DSA03440,GSE34287,GPL7884,0,Parkinson's Disease,C0030567,Blood,GEO,Microarray,Homo sapiens,12|19,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03441,GSE34287,GPL7884,0,Progressive Supranuclear Palsy,C0038868,Blood,GEO,Microarray,Homo sapiens,12|4,"DO:A movement disease that is characterized by serious and progressive problems with control of gait and balance, along with complex eye movement and thinking problems. It involves gradual deterioration and death of specific volumes of the brain." DSA03442,GSE41665,GPL1261,1000,Asthma,C0004096,Lung,GEO,Microarray,Mus musculus,61|62,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA03443,GSE41667,GPL1261,0,Atopic Dermatitis,C0011615,Lung,GEO,Microarray,Mus musculus,16|14,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA03444,GSE41667,GPL1261,1000,Atopic Dermatitis,C0011615,Lung,GEO,Microarray,Mus musculus,16|15,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA03445,GSE41667,GPL1261,1000,Atopic Dermatitis,C0011615,Lung,GEO,Microarray,Mus musculus,16|16,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA03446,GSE41667,GPL1261,1000,Atopic Dermatitis,C0011615,Lung,GEO,Microarray,Mus musculus,16|16,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA03447,GSE41667,GPL1261,2,Atopic Dermatitis,C0011615,Lung,GEO,Microarray,Mus musculus,15|15,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA03448,GSE34516,GPL5175,0,Parkinson's Disease,C0030567,Brain,GEO,Microarray,Homo sapiens,4|4,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03449,GSE34516,GPL5175,0,Parkinson's Disease,C0030567,Brain,GEO,Microarray,Homo sapiens,4|2,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03450,GSE34549,GPL6246,0,Fetal Alcohol Spectrum Disorder,C2985290,Brain,GEO,Microarray,Mus musculus,2|2,"MONDO:A group of disorders caused by a prenatal exposure to maternal consumption of alcohol leading to a range of behavioral, cognitive and neurological deficits in the offspring. It is characterized by physical growth problems, distinct facies, and varying psycho-neurological issues." DSA03451,GSE34553,GPL6885,1000,Colitis,C0009319,Colon,GEO,Microarray,Mus musculus,4|6,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA03452,GSE34573,GPL570,473,Nasopharyngeal Carcinoma,C2931822,Nasopharynx,GEO,Microarray,Homo sapiens,3|15,"DO:A pharynx cancer that is located in the nasopharynx, the uppermost region of the pharynx or throat, where the nasal passages and auditory tubes join the remainder of the upper respiratory tract." DSA03453,GSE34577,GPL6947,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,18|11,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03454,GSE34577,GPL6947,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,18|9,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03455,GSE34577,GPL6947,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,18|21,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03456,GSE34577,GPL6947,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,18|7,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03457,GSE34608,GPL6480,1000,Sarcoidosis,C0036202,Peripheral blood,GEO,Microarray,Homo sapiens,18|18,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA03458,GSE34608,GPL6480,1000,Tuberculosis,C0041296,Peripheral blood,GEO,Microarray,Homo sapiens,18|8,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA03459,GSE34781,GPL570,0,Angina,C0002962,Blood,GEO,Microarray,Homo sapiens,1|2,"EFO:The symptom of paroxysmal pain consequent to MYOCARDIAL ISCHEMIA usually of distinctive character, location and radiation. It is thought to be provoked by a transient stressful situation during which the oxygen requirements of the MYOCARDIUM exceed that supplied by the CORONARY CIRCULATION." DSA03460,GSE34861,GPL15088,209,Acute Lymphoblastic Leukemia,C0023449,,GEO,Microarray,Homo sapiens,3|191,DO:A acute leukemia that is characterized by over production of lymphoblasts. DSA03461,GSE34885,GPL570,0,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,Microarray,Homo sapiens,3|4,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03462,GSE34885,GPL570,0,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,Microarray,Homo sapiens,3|4,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03463,GSE35007,GPL10558,1000,Sickle Cell Disease,C0002895,Blood,GEO,Microarray,Homo sapiens,61|59,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA03464,GSE35007,GPL10558,1000,Sickle Cell Disease,C0002895,Blood,GEO,Microarray,Homo sapiens,61|190,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA03465,GSE35010,GPL6244,37,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,6|5,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03466,GSE35010,GPL6244,7,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,4|4,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03467,GSE35010,GPL6244,415,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,6|6,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03468,GSE35108,GPL6244,0,Dilated Cardiomyopathy,C0007193,,GEO,Microarray,Homo sapiens,3|4,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA03469,GSE35108,GPL6244,1000,Dilated Cardiomyopathy,C0007193,,GEO,Microarray,Homo sapiens,2|2,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA03470,GSE35108,GPL6244,1000,Dilated Cardiomyopathy,C0007193,,GEO,Microarray,Homo sapiens,2|2,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA03471,GSE35133,GPL4133,1000,Neuroblastoma,C0027819,Bone marrow,GEO,Microarray,Homo sapiens,12|12,DO:An autonomic nervous system neoplasm that derives_from immature nerve cells. DSA03472,GSE35138,GPL6246,0,Parkinson's Disease,C0030567,Thalamus,GEO,Microarray,Mus musculus,2|2,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03473,GSE35179,GPL6480,389,Chronic Lymphocytic Leukemia,C0023434,Peripheral blood,GEO,Microarray,Homo sapiens,5|5,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA03474,GSE35287,GPL6244,0,Endometriosis,C0014175,,GEO,Microarray,Homo sapiens,4|4,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA03475,GSE35287,GPL6244,0,Endometriosis,C0014175,,GEO,Microarray,Homo sapiens,4|4,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA03476,GSE35287,GPL6244,0,Endometriosis,C0014175,,GEO,Microarray,Homo sapiens,4|4,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA03477,GSE35287,GPL6244,10,Endometriosis,C0014175,,GEO,Microarray,Homo sapiens,4|4,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA03478,GSE35331,GPL570,1000,Follicular Lymphoma,C0024301,Bone marrow,GEO,Microarray,Homo sapiens,12|10,DO:A B-cell lymphoma that is characterized as an indolent non-Hodgkin's lymphoma and has_material_basis_in follicle center B-cells (centrocytes and centroblasts). DSA03479,GSE35338,GPL1261,58,Neurogenic Inflammation,C0600467,Brain,GEO,Microarray,Mus musculus,4|5,MSH:Inflammation caused by an injurious stimulus of peripheral neurons and resulting in release of neuropeptides which affect vascular permeability and help initiate proinflammatory and immune reactions at the site of injury. DSA03480,GSE35338,GPL1261,1000,Ischemic Stroke,C0948008,Brain,GEO,Microarray,Mus musculus,4|5,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA03481,GSE35338,GPL1261,0,Ischemic Stroke,C0948008,Brain,GEO,Microarray,Mus musculus,3|3,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA03482,GSE35338,GPL1261,129,Ischemic Stroke,C0948008,Brain,GEO,Microarray,Mus musculus,3|3,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA03483,GSE41667,GPL1261,18,Atopic Dermatitis,C0011615,Lung,GEO,Microarray,Mus musculus,15|14,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA03484,GSE35363,GPL6100,11,Experimental Autoimmune Encephalomyelitis,C0014072,Choroid plexus,GEO,Microarray,Mus musculus,3|8,"EFO:An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)" DSA03485,GSE35482,GPL6096,0,Diabetes,C0011847,Lymph node,GEO,Microarray,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA03486,GSE35487,GPL96,406,IgA Nephropathy,C0017661,Kidney,GEO,Microarray,Homo sapiens,6|25,DO:A glomerulonephritis characterized by build up of IgA antibody in the glomerulus. DSA03487,GSE35488,GPL14663,381,IgA Nephropathy,C0017661,Kidney,GEO,Microarray,Homo sapiens,6|25,DO:A glomerulonephritis characterized by build up of IgA antibody in the glomerulus. DSA03488,GSE35499,GPL2895,145,Neurocytoma,C1622510,Brain,GEO,Microarray,Homo sapiens,1|5,HPO:A benign brain tumor composed of neural elements which most often arise from the septum pellucidum and the walls of the lateral ventricles. DSA03489,GSE35499,GPL2895,1,Pineocytoma,C0917890,Brain,GEO,Microarray,Homo sapiens,1|4,"EFO:Pineocytoma is the least aggressive form of pineal parenchymal tumors, manifesting with symptoms such as Parinaud's syndrome (a group of eye movement abnormalities and pupil dysfunction, including deficiency in upward-gaze and convergence-retraction nystagmus), headaches, balance impairment, urinary incontinence, and changes in mood and that are not known to disseminate in a diffuse manner. They are usually associated with a good prognosis." DSA03490,GSE35609,GPL6885,8,Colitis,C0009319,Distal colon,GEO,Microarray,Mus musculus,4|5,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA03491,GSE35609,GPL6885,21,Colitis,C0009319,Distal colon,GEO,Microarray,Mus musculus,4|5,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA03492,GSE35609,GPL6885,359,Colitis,C0009319,Distal colon,GEO,Microarray,Mus musculus,4|5,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA03493,GSE35609,GPL6885,32,Colitis,C0009319,Distal colon,GEO,Microarray,Mus musculus,4|5,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA03494,GSE35609,GPL6885,255,Colitis,C0009319,Distal colon,GEO,Microarray,Mus musculus,4|5,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA03495,GSE35609,GPL6885,149,Colitis,C0009319,Distal colon,GEO,Microarray,Mus musculus,4|5,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA03496,GSE35643,GPL6244,0,Asthma,C0004096,Bronchial airway,GEO,Microarray,Homo sapiens,3|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA03497,GSE35643,GPL6244,0,Asthma,C0004096,Bronchial airway,GEO,Microarray,Homo sapiens,3|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA03498,GSE35665,GPL5175,38,Down Syndrome,C0013080,Peripheral blood,GEO,Microarray,Homo sapiens,15|10,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA03499,GSE35665,GPL5175,0,Down Syndrome,C0013080,Peripheral blood,GEO,Microarray,Homo sapiens,7|5,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA03500,GSE35711,GPL570,1000,Cystic Fibrosis,C0010674,,GEO,Microarray,Homo sapiens,24|20,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA03501,GSE35712,GPL570,46,H1N1 Influenza,C2076600,,GEO,Microarray,Homo sapiens,5|5,"EFO:An influenza that results_in infection located_in respiratory tract of pigs and humans, has_material_basis_in Influenza C virus, or has_material_basis_in Influenza A virus subtypes (H1N1, H1N2, H3N1, H3N2, and H2N3), which are transmitted_by direct contact with infected pigs. The infection in humans has_symptom fever, has_symptom lethargy, has_symptom lack of appetite, has_symptom coughing, has_symptom runny nose, has_symptom sore throat, has_symptom nausea, has_symptom vomiting, and has_symptom diarrhea." DSA03502,GSE35713,GPL570,1000,Bacterial Pneumonia,C0004626,,GEO,Microarray,Homo sapiens,18|10,DO:A pneumonia involving inflammation of the lungs caused by bacteria. DSA03503,GSE35713,GPL570,220,Type 1 Diabetes,C0011854,Plasma,GEO,Microarray,Homo sapiens,44|46,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA03504,GSE35713,GPL570,684,Type 1 Diabetes,C0011854,Plasma,GEO,Microarray,Homo sapiens,44|11,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA03505,GSE35713,GPL570,1000,Type 1 Diabetes,C0011854,Plasma,GEO,Microarray,Homo sapiens,44|5,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA03506,GSE35776,GPL5175,1000,Tetralogy of Fallot,C0039685,Right ventricle,GEO,Microarray,Homo sapiens,8|16,"HPO:A congenital cardiac malformation comprising pulmonary stenosis, overriding aorta, ventricular septum defect, and right ventricular hypertrophy. The diagnosis of TOF is made if at least three of the four above mentioned features are present." DSA03507,GSE35864,GPL570,0,AIDS Dementia,C0001849,White matter,GEO,Microarray,Homo sapiens,6|7,"EFO:A neurologic condition associated with the ACQUIRED IMMUNODEFICIENCY SYNDROME and characterized by impaired concentration and memory, slowness of hand movements, ATAXIA, incontinence, apathy, and gait difficulties associated with HIV-1 viral infection of the central nervous system. Pathologic examination of the brain reveals white matter rarefaction, perivascular infiltrates of lymphocytes, foamy macrophages, and multinucleated giant cells. (From Adams et al., Principles of Neurology, 6th ed, pp760-1; N Engl J Med, 1995 Apr 6;332(14):934-40)" DSA03508,GSE35864,GPL570,1000,AIDS Dementia,C0001849,White matter,GEO,Microarray,Homo sapiens,6|5,"EFO:A neurologic condition associated with the ACQUIRED IMMUNODEFICIENCY SYNDROME and characterized by impaired concentration and memory, slowness of hand movements, ATAXIA, incontinence, apathy, and gait difficulties associated with HIV-1 viral infection of the central nervous system. Pathologic examination of the brain reveals white matter rarefaction, perivascular infiltrates of lymphocytes, foamy macrophages, and multinucleated giant cells. (From Adams et al., Principles of Neurology, 6th ed, pp760-1; N Engl J Med, 1995 Apr 6;332(14):934-40)" DSA03509,GSE35864,GPL570,1000,AIDS Dementia,C0001849,Frontal cortex,GEO,Microarray,Homo sapiens,6|7,"EFO:A neurologic condition associated with the ACQUIRED IMMUNODEFICIENCY SYNDROME and characterized by impaired concentration and memory, slowness of hand movements, ATAXIA, incontinence, apathy, and gait difficulties associated with HIV-1 viral infection of the central nervous system. Pathologic examination of the brain reveals white matter rarefaction, perivascular infiltrates of lymphocytes, foamy macrophages, and multinucleated giant cells. (From Adams et al., Principles of Neurology, 6th ed, pp760-1; N Engl J Med, 1995 Apr 6;332(14):934-40)" DSA03510,GSE35864,GPL570,1000,AIDS Dementia,C0001849,Frontal cortex,GEO,Microarray,Homo sapiens,6|5,"EFO:A neurologic condition associated with the ACQUIRED IMMUNODEFICIENCY SYNDROME and characterized by impaired concentration and memory, slowness of hand movements, ATAXIA, incontinence, apathy, and gait difficulties associated with HIV-1 viral infection of the central nervous system. Pathologic examination of the brain reveals white matter rarefaction, perivascular infiltrates of lymphocytes, foamy macrophages, and multinucleated giant cells. (From Adams et al., Principles of Neurology, 6th ed, pp760-1; N Engl J Med, 1995 Apr 6;332(14):934-40)" DSA03511,GSE35864,GPL570,0,AIDS Dementia,C0001849,Basal ganglia,GEO,Microarray,Homo sapiens,6|7,"EFO:A neurologic condition associated with the ACQUIRED IMMUNODEFICIENCY SYNDROME and characterized by impaired concentration and memory, slowness of hand movements, ATAXIA, incontinence, apathy, and gait difficulties associated with HIV-1 viral infection of the central nervous system. Pathologic examination of the brain reveals white matter rarefaction, perivascular infiltrates of lymphocytes, foamy macrophages, and multinucleated giant cells. (From Adams et al., Principles of Neurology, 6th ed, pp760-1; N Engl J Med, 1995 Apr 6;332(14):934-40)" DSA03512,GSE35864,GPL570,1000,AIDS Dementia,C0001849,Basal ganglia,GEO,Microarray,Homo sapiens,6|5,"EFO:A neurologic condition associated with the ACQUIRED IMMUNODEFICIENCY SYNDROME and characterized by impaired concentration and memory, slowness of hand movements, ATAXIA, incontinence, apathy, and gait difficulties associated with HIV-1 viral infection of the central nervous system. Pathologic examination of the brain reveals white matter rarefaction, perivascular infiltrates of lymphocytes, foamy macrophages, and multinucleated giant cells. (From Adams et al., Principles of Neurology, 6th ed, pp760-1; N Engl J Med, 1995 Apr 6;332(14):934-40)" DSA03513,GSE35934,GPL6845,1000,Inflammation,C0021368,Brain,GEO,Microarray,Mus musculus,3|3,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA03514,GSE35934,GPL6845,1000,Inflammation,C0021368,Heart,GEO,Microarray,Mus musculus,3|3,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA03515,GSE35934,GPL6845,1000,Inflammation,C0021368,Kidney,GEO,Microarray,Mus musculus,3|3,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA03516,GSE35934,GPL6845,1000,Inflammation,C0021368,Liver,GEO,Microarray,Mus musculus,3|3,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA03517,GSE35956,GPL570,1,Osteoporosis,C0029456,Bone marrow,GEO,Microarray,Homo sapiens,5|5,DO:A bone resorption disease characterized by decreased density of normally mineralized bone which results_in the thinning of bone tissue and decreased mechanical strength. DSA03518,GSE35974,GPL6244,370,Bipolar Disorder,C0005586,Cerebellum,GEO,Microarray,Homo sapiens,50|37,DO:A mood disorder that involves alternating periods of mania and depression. DSA03519,GSE35974,GPL6244,0,Depression,C0011581,Cerebellum,GEO,Microarray,Homo sapiens,50|13,DO:A mood disorder that involves the presence of a low mood almost daily over a span of at least two years. DSA03520,GSE35974,GPL6244,442,Schizophrenia,C0036341,Cerebellum,GEO,Microarray,Homo sapiens,50|44,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA03521,GSE35977,GPL6244,2,Bipolar Disorder,C0005586,Brain,GEO,Microarray,Homo sapiens,50|45,DO:A mood disorder that involves alternating periods of mania and depression. DSA03522,GSE35977,GPL6244,0,Depression,C0011581,Parietal cortex,GEO,Microarray,Homo sapiens,50|14,DO:A mood disorder that involves the presence of a low mood almost daily over a span of at least two years. DSA03523,GSE35977,GPL6244,38,Schizophrenia,C0036341,Brain,GEO,Microarray,Homo sapiens,50|51,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA03524,GSE36076,GPL570,1000,Gastric Cancer,C0699791,Blood,GEO,Microarray,Homo sapiens,10|3,DO:A gastrointestinal system cancer that is located_in the stomach. DSA03525,GSE36076,GPL570,1000,Hepatocellular Carcinoma,C0334287,Blood,GEO,Microarray,Homo sapiens,10|10,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA03526,GSE41667,GPL1261,2,Atopic Dermatitis,C0011615,Lung,GEO,Microarray,Mus musculus,15|13,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA03527,GSE3624,GPL96,4,Polycystic Lipomembranous Osteodysplasia With Sclerosing Leukoencephalopathy 1,C4721893,,GEO,Microarray,Homo sapiens,3|5,DO:A syndrome that is characterized by progressive presenile dementia and recurrent bone fractures due to polycystic osseous lesions of the lower and upper extremities that has_material_basis_in homozygous mutation in the TYRO protein tyrosine kinase binding protein (TYROBP) gene on chromosome 19q13 or homozygous mutation in the triggering receptor expressed on myeloid cells 2 (TREM2) gene on chromosome 6p21. DSA03528,GSE36295,GPL6244,1000,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,5|45,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03529,GSE3634,GPL339,24,Huntington's Disease,C0020179,Retina,GEO,Microarray,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA03530,GSE3634,GPL339,317,Spinocerebellar Ataxia Type 7,C0752125,Retina,GEO,Microarray,Mus musculus,11|11,"DO:An autosomal dominant cerebellar ataxia that is characterized by ataxia, progressive vision loss, and failure to thrive, has_material_basis_in mutation in the ATXN7 gene." DSA03531,GSE36406,GPL6244,1,Epidermolysis Bullosa Simplex With Mottled Pigmentation,C0432316,Skin,GEO,Microarray,Homo sapiens,7|1,DO:An epidermolysis bullosa simplex characterized by generalized blistering with mottled hyper- and hypopigmentation of the skin that has_material_basis_in heterozygous mutation in KRT5 on chromosome 12q13.13. DSA03532,GSE36414,GPL1261,0,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Mus musculus,2|6,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA03533,GSE36418,GPL6884,0,Thrombotic Thrombocytopenic Purpura,C0034155,Blood,GEO,Microarray,Homo sapiens,39|39,"MONDO:Thrombotic thrombocytopenic purpura (TTP) is an aggressive and life-threatening form of thrombotic microangiopathy (TMA) characterized by profound peripheral thrombocytopenia, microangiopathic hemolytic anemia (MAHA) and organ failure of variable severity and is comprised of congenital TTP and acquired TTP." DSA03534,GSE41667,GPL1261,1000,Atopic Dermatitis,C0011615,Lung,GEO,Microarray,Mus musculus,15|15,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA03535,GSE36539,GPL6480,0,Hepatitis E,C0085293,Blood,GEO,Microarray,Homo sapiens,8|8,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis E virus, which is transmitted_by ingestion of contaminated food. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom dark urine, has_symptom joint pain, and has_symptom jaundice." DSA03536,GSE36539,GPL6480,0,Hepatitis E,C0085293,,GEO,Microarray,Homo sapiens,8|8,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis E virus, which is transmitted_by ingestion of contaminated food. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom dark urine, has_symptom joint pain, and has_symptom jaundice." DSA03537,GSE36584,GPL8321,0,Melanoma,C0025202,Lung,GEO,Microarray,Mus musculus,3|3,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA03538,GSE36584,GPL8321,0,Melanoma,C0025202,Lung,GEO,Microarray,Mus musculus,3|3,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA03539,GSE36701,GPL570,300,Irritable Bowel Syndrome,C0022104,Rectal colon,GEO,Microarray,Homo sapiens,40|34,"DO:An intestinal disease that is characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause." DSA03540,GSE36701,GPL570,339,Irritable Bowel Syndrome,C0022104,Rectal colon,GEO,Microarray,Homo sapiens,40|53,"DO:An intestinal disease that is characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause." DSA03541,GSE36701,GPL570,3,Irritable Bowel Syndrome,C0022104,Rectal colon,GEO,Microarray,Homo sapiens,37|28,"DO:An intestinal disease that is characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause." DSA03542,GSE36701,GPL570,208,Irritable Bowel Syndrome,C0022104,Rectal colon,GEO,Microarray,Homo sapiens,37|15,"DO:An intestinal disease that is characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause." DSA03543,GSE36701,GPL570,10,Irritable Bowel Syndrome,C0022104,Rectal colon,GEO,Microarray,Homo sapiens,37|14,"DO:An intestinal disease that is characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause." DSA03544,GSE36761,GPL9052,1000,Tetralogy of Fallot,C0039685,Heart,GEO,RNA-Seq,Homo sapiens,7|22,"HPO:A congenital cardiac malformation comprising pulmonary stenosis, overriding aorta, ventricular septum defect, and right ventricular hypertrophy. The diagnosis of TOF is made if at least three of the four above mentioned features are present." DSA03545,GSE36765,GPL570,7,Breast Cancer,C0678222,Peripheral blood,GEO,Microarray,Homo sapiens,4|10,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03546,GSE36809,GPL570,1000,Severe Blunt Trauma,,,GEO,Microarray,Homo sapiens,37|820, DSA03547,GSE36830,GPL570,4,Chronic Rhinosinusitis,C0149516,Uncinate tissue,GEO,Microarray,Homo sapiens,6|6,EFO:An acute or chronic inflammatory process affecting the mucous membranes of any sinus cavity. DSA03548,GSE36830,GPL570,0,Chronic Rhinosinusitis,C0149516,Uncinate tissue,GEO,Microarray,Homo sapiens,6|6,EFO:An acute or chronic inflammatory process affecting the mucous membranes of any sinus cavity. DSA03549,GSE36833,GPL1261,510,Glaucoma,C0017601,Optic nerve head,GEO,Microarray,Mus musculus,9|20,DO:An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. DSA03550,GSE36961,GPL15389,1000,Hypertrophic Cardiomyopathy,C0007194,Myocardium,GEO,Microarray,Homo sapiens,39|106,DO:A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations. DSA03551,GSE36981,GPL6246,1,Alzheimer's Disease,C0002395,Hippocampus,GEO,Microarray,Mus musculus,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03552,GSE36981,GPL6246,2,Alzheimer's Disease,C0002395,Hippocampus,GEO,Microarray,Mus musculus,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03553,GSE37013,GPL6947,19,Ischemia,C0022116,Jejunum,GEO,Microarray,Homo sapiens,7|7,DO:A vascular disease that is characterized by a restriction in blood supply to tissues. DSA03554,GSE37013,GPL6947,75,Ischemia Reperfusion Injury,C0035126,Jejunum,GEO,Microarray,Homo sapiens,7|7,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA03555,GSE37013,GPL6947,398,Ischemia Reperfusion Injury,C0035126,Jejunum,GEO,Microarray,Homo sapiens,7|7,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA03556,GSE37031,GPL14877,993,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Homo sapiens,7|8,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA03557,GSE37069,GPL570,1000,Burn,C0036280,,GEO,Microarray,Homo sapiens,37|553, DSA03558,GSE37084,GPL5175,295,Myotonic Dystrophy Type 2,C2931689,Biceps,GEO,Microarray,Homo sapiens,10|10,"DO:A myotonic disease that is characterized by myotonia and progressive, proximal muscle wasting and weakness affecting the skeletal and smooth muscles of the neck, shoulders, elbows and hips and has_material_basis_in the autosomal dominant inheritance of the CNBP (ZNF9) gene containing an expansion of a CCTG repeat in intron one." DSA03559,GSE37146,GPL6102,0,Allergic Rhinitis,C2607914,,GEO,Microarray,Homo sapiens,11|11,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA03560,GSE37155,GPL10558,0,Allergic Rhinitis,C2607914,,GEO,Microarray,Homo sapiens,4|4,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA03561,GSE37171,GPL570,1000,Uremia,C0041948,Blood,GEO,Microarray,Homo sapiens,40|75,DO:A kidney disease characterized by the failure of the kidneys to adequately filter waste products from the blood. DSA03562,GSE37191,GPL1261,1000,Experimental Autoimmune Encephalomyelitis,C0014072,,GEO,Microarray,Mus musculus,3|3,"EFO:An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)" DSA03563,GSE37191,GPL1261,1000,Experimental Autoimmune Encephalomyelitis,C0014072,,GEO,Microarray,Mus musculus,3|3,"EFO:An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)" DSA03564,GSE37258,GPL570,55,Klinefelter Syndrome,C0022735,,GEO,Microarray,Homo sapiens,3|6,DO:A chromosomal duplication syndrome that is characterized by infertility and that has_material_basis_in an extra X chromosome in cells in men. DSA03565,GSE37258,GPL570,104,Klinefelter Syndrome,C0022735,,GEO,Microarray,Homo sapiens,3|3,DO:A chromosomal duplication syndrome that is characterized by infertility and that has_material_basis_in an extra X chromosome in cells in men. DSA03566,GSE37263,GPL5175,0,Alzheimer's Disease,C0002395,Neocortex,GEO,Microarray,Homo sapiens,8|8,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03567,GSE37264,GPL5188,0,Alzheimer's Disease,C0002395,Neocortex,GEO,Microarray,Homo sapiens,8|8,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03568,GSE37265,GPL570,1000,Aphthous Stomatitis,C0038363,,GEO,Microarray,Homo sapiens,5|14,DO:A stomatitis characterized by the repeated formation of benign and non-contagious mouth ulcers. DSA03569,GSE37265,GPL570,1000,Aphthous Stomatitis,C0038363,,GEO,Microarray,Homo sapiens,14|14,DO:A stomatitis characterized by the repeated formation of benign and non-contagious mouth ulcers. DSA03570,GSE37307,GPL96,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,Microarray,Homo sapiens,17|30,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03571,GSE37356,GPL10558,0,Atherosclerosis,C0004153,,GEO,Microarray,Homo sapiens,7|9,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA03572,GSE37356,GPL10558,0,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,7|10,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03573,GSE37356,GPL10558,0,Atherosclerosis;Systemic Lupus Erythematosus,,,GEO,Microarray,Homo sapiens,7|10, DSA03574,GSE37356,GPL10558,0,Atherosclerosis,C0004153,,GEO,Microarray,Homo sapiens,7|9,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA03575,GSE37356,GPL10558,0,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,7|10,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03576,GSE37356,GPL10558,0,Atherosclerosis;Systemic Lupus Erythematosus,,,GEO,Microarray,Homo sapiens,7|10, DSA03577,GSE37450,GPL339,48,Type 1 Diabetes,C0011854,Spleen,GEO,Microarray,Mus musculus,5|5,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA03578,GSE37450,GPL339,63,Type 1 Diabetes,C0011854,Spleen,GEO,Microarray,Mus musculus,5|5,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA03579,GSE37450,GPL340,36,Type 1 Diabetes,C0011854,Spleen,GEO,Microarray,Mus musculus,5|5,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA03580,GSE37450,GPL340,32,Type 1 Diabetes,C0011854,Spleen,GEO,Microarray,Mus musculus,5|5,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA03581,GSE37455,GPL14663,0,Hypertensive Nephropathy,C0848548,Kidney,GEO,Microarray,Homo sapiens,3|20,EFO:Hardening of the walls of the small arteries and arterioles (small arteries that convey blood from arteries to the even smaller capillaries) of the kidney. This condition is caused by hypertension (high blood pressure) DSA03582,GSE37460,GPL14663,1000,IgA Nephropathy,C0017661,Kidney,GEO,Microarray,Homo sapiens,9|15,DO:A glomerulonephritis characterized by build up of IgA antibody in the glomerulus. DSA03583,GSE37460,GPL14663,1000,Hypertensive Nephropathy,C0848548,Kidney,GEO,Microarray,Homo sapiens,9|27,EFO:Hardening of the walls of the small arteries and arterioles (small arteries that convey blood from arteries to the even smaller capillaries) of the kidney. This condition is caused by hypertension (high blood pressure) DSA03584,GSE37468,GPL6246,138,Chronic Cholangitis,C0267918,Liver,GEO,Microarray,Mus musculus,3|4,MONDO:Cholangitis that is persistent and long-standing. DSA03585,GSE37517,GPL10739,0,Huntington's Disease,C0020179,,GEO,Microarray,Homo sapiens,2|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA03586,GSE37517,GPL10739,1000,Huntington's Disease,C0020179,,GEO,Microarray,Homo sapiens,3|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA03587,GSE37559,GPL6246,1000,Chronic Cholangitis,C0267918,Liver,GEO,Microarray,Mus musculus,3|5,MONDO:Cholangitis that is persistent and long-standing. DSA03588,GSE37573,GPL201,0,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,12|16,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03589,GSE37573,GPL201,1,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,12|16,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03590,GSE37573,GPL201,4,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,4|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03591,GSE37573,GPL201,2,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,4|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03592,GSE37573,GPL201,4,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,4|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03593,GSE37573,GPL201,10,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,4|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03594,GSE37573,GPL201,4,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,4|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03595,GSE37573,GPL201,6,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,4|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03596,GSE37582,GPL6947,1000,Ovarian Cancer,C1140680,,GEO,Microarray,Homo sapiens,47|74,DO:A female reproductive organ cancer that is located_in the ovary. DSA03597,GSE51927,GPL1261,1000,Epithelial Ovarian Cancer,C0677886,Ovary,GEO,Microarray,Mus musculus,3|56,DO:A female reproductive organ cancer that is located_in the ovary. DSA03598,GSE37635,GPL6885,1000,Pulmonary Fibrosis,C0034069,Lung,GEO,Microarray,Mus musculus,7|7,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA03599,GSE37635,GPL6885,1000,Pulmonary Fibrosis,C0034069,Lung,GEO,Microarray,Mus musculus,7|6,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA03600,GSE37635,GPL6885,748,Pulmonary Fibrosis,C0034069,Lung,GEO,Microarray,Mus musculus,7|6,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA03601,GSE37635,GPL6885,316,Pulmonary Fibrosis,C0034069,Lung,GEO,Microarray,Mus musculus,7|6,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA03602,GSE37635,GPL6885,4,Pulmonary Fibrosis,C0034069,Lung,GEO,Microarray,Mus musculus,7|6,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA03603,GSE55177,GPL1261,1000,Spinocerebellar Ataxia Type 2,C0752121,Cerebellum,GEO,Microarray,Mus musculus,4|4,"DO:An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene." DSA03604,GSE37689,GPL6883,0,Steatosis,C2711227,Dermis,GEO,Microarray,Homo sapiens,2|4,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA03605,GSE37749,GPL6246,1000,Colorectal Carcinoma,C0009402,Rectal mucosa,GEO,Microarray,Mus musculus,4|5,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA03606,GSE37749,GPL6246,1000,Inflammatory Bowel Disease,C0021390,Rectal mucosa,GEO,Microarray,Mus musculus,4|4,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA03607,GSE37750,GPL570,0,Multiple Sclerosis,C0026769,,GEO,Microarray,Homo sapiens,8|9,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA03608,GSE55177,GPL1261,331,Spinocerebellar Ataxia Type 2,C0752121,Midbrain,GEO,Microarray,Mus musculus,4|4,"DO:An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene." DSA03609,GSE37768,GPL570,0,Chronic Obstructive Pulmonary Disease,C0024117,Lung,GEO,Microarray,Homo sapiens,9|18,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA03610,GSE37768,GPL570,0,Chronic Obstructive Pulmonary Disease,C0024117,Lung,GEO,Microarray,Homo sapiens,11|18,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA03611,GSE37772,GPL6883,17,Autism,C1510586,,GEO,Microarray,Homo sapiens,206|233,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA03612,GSE3790,GPL96,1000,Huntington's Disease,C0020179,Caudate nucleus,GEO,Microarray,Homo sapiens,32|38,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA03613,GSE3790,GPL96,146,Huntington's Disease,C0020179,Cerebellum,GEO,Microarray,Homo sapiens,27|39,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA03614,GSE3790,GPL96,1,Huntington's Disease,C0020179,Frontal cortex,GEO,Microarray,Homo sapiens,28|37,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA03615,GSE3790,GPL97,1000,Huntington's Disease,C0020179,Caudate nucleus,GEO,Microarray,Homo sapiens,32|38,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA03616,GSE3790,GPL97,67,Huntington's Disease,C0020179,Cerebellum,GEO,Microarray,Homo sapiens,28|39,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA03617,GSE3790,GPL97,2,Huntington's Disease,C0020179,Frontal cortex,GEO,Microarray,Homo sapiens,29|37,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA03618,GSE37912,GPL5175,0,Sarcoidosis,C0036202,,GEO,Microarray,Homo sapiens,8|11,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA03619,GSE37912,GPL5175,47,Sarcoidosis,C0036202,,GEO,Microarray,Homo sapiens,8|18,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA03620,GSE37912,GPL5175,1000,Sarcoidosis,C0036202,,GEO,Microarray,Homo sapiens,27|6,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA03621,GSE37912,GPL5175,24,Sarcoidosis,C0036202,,GEO,Microarray,Homo sapiens,27|4,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA03622,GSE37981,GPL1352,0,Schizophrenia,C0036341,Superior temporal gyrus,GEO,Microarray,Homo sapiens,9|9,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA03623,GSE37985,GPL6244,0,Glioblastoma,C0017636,,GEO,Microarray,Homo sapiens,3|3,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA03624,GSE38003,GPL14603,0,Asthma,C0004096,Airway smooth muscle,GEO,RNA-Seq,Homo sapiens,6|12,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA03625,GSE38043,GPL570,0,Prostate Cancer,C0600139,Blood,GEO,Microarray,Homo sapiens,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03626,GSE38117,GPL4134,1000,Renal Fibrosis,C0151650,Kidney,GEO,Microarray,Mus musculus,3|3,HPO:Renal fibrosis is the consequence of an excessive accumulation of extracellular matrix that occurs in virtually every type of chronic kidney disease. DSA03627,GSE38153,GPL14550,1000,Parkinson's Disease,C0030567,Dermis,GEO,Microarray,Homo sapiens,2|4,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03628,GSE38153,GPL14550,27,Parkinson's Disease,C0030567,Peripheral blood,GEO,Microarray,Homo sapiens,2|4,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03629,GSE38174,GPL6480,1000,Liver Cancer,C2239176,Liver,GEO,Microarray,Homo sapiens,36|30,DO:A hepatobiliary system cancer that is located_in the liver. DSA03630,GSE38174,GPL6480,4,Liver Cancer,C2239176,Liver,GEO,Microarray,Homo sapiens,36|30,DO:A hepatobiliary system cancer that is located_in the liver. DSA03631,GSE38199,GPL6246,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Mus musculus,9|7,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA03632,GSE38218,GPL1261,1000,Huntington's Disease,C0020179,Cortex,GEO,Microarray,Mus musculus,9|9,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA03633,GSE38219,GPL1261,1000,Huntington's Disease,C0020179,Cortex,GEO,Microarray,Mus musculus,8|9,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA03634,GSE38226,GPL6947,164,Liver Tumor,C0345904,Liver,GEO,Microarray,Homo sapiens,4|6,DO:A hepatobiliary system cancer that is located_in the liver. DSA03635,GSE38226,GPL6947,952,Hepatitis C,C0019196,Liver,GEO,Microarray,Homo sapiens,4|4,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA03636,GSE38226,GPL6947,688,Hepatitis C,C0019196,Liver,GEO,Microarray,Homo sapiens,4|8,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA03637,GSE38267,GPL13607,1000,Cystic Fibrosis,C0010674,Blood,GEO,Microarray,Homo sapiens,28|23,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA03638,GSE38267,GPL13607,1000,Pulmonary Arterial Hypertension,C2973725,Blood,GEO,Microarray,Homo sapiens,28|13,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA03639,GSE38322,GPL10558,1000,Autism,C1510586,Brain,GEO,Microarray,Homo sapiens,12|14,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA03640,GSE38322,GPL10558,0,Autism,C1510586,Brain,GEO,Microarray,Homo sapiens,6|4,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA03641,GSE38351,GPL570,1000,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,11|4,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA03642,GSE38351,GPL96,488,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,12|14,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03643,GSE38351,GPL96,134,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,12|8,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA03644,GSE38396,GPL570,0,Type 2 Diabetes,C0011860,,GEO,Microarray,Homo sapiens,4|4,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA03645,GSE38417,GPL570,1000,Duchenne Muscular Dystrophy,C0013264,Skeletal muscle,GEO,Microarray,Homo sapiens,6|16,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA03646,GSE38481,GPL6883,0,Schizophrenia,C0036341,Blood,GEO,Microarray,Homo sapiens,22|15,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA03647,GSE38484,GPL6947,1000,Schizophrenia,C0036341,Blood,GEO,Microarray,Homo sapiens,96|106,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA03648,GSE38517,GPL570,0,Oral Squamous Cell Carcinoma,C0585362,,GEO,Microarray,Homo sapiens,2|2,"EFO:A squamous cell carcinoma arising from the oral cavity. It affects predominantly adults in their fifth and sixth decades of life and is associated with alcohol and tobacco use. Human papillomavirus is present in approximately half of the cases. It is characterized by a tendency to metastasize early to the lymph nodes. When the tumor is small, patients are often asymptomatic. Physical examination may reveal erythematous or white lesions or plaques. The majority of patients present with signs and symptoms of locally advanced disease including mucosal ulceration, pain, difficulty with speaking, chewing, and swallowing, bleeding, weight loss, and neck swelling. Patients may also present with swollen neck lymph nodes without any symptoms from the oropharyngeal tumor. The most significant prognostic factors are the size of the tumor and the lymph nodes status." DSA03649,GSE38517,GPL570,0,Dysphasia,C0973461,,GEO,Microarray,Homo sapiens,5|4,"MSH:A cognitive disorder marked by an impaired ability to comprehend or express language in its written or spoken form. This condition is caused by diseases which affect the language areas of the dominant hemisphere. Clinical features are used to classify the various subtypes of this condition. General categories include receptive, expressive, and mixed forms of aphasia." DSA03650,GSE38517,GPL570,122,Oral Squamous Cell Carcinoma,C0585362,,GEO,Microarray,Homo sapiens,5|7,"EFO:A squamous cell carcinoma arising from the oral cavity. It affects predominantly adults in their fifth and sixth decades of life and is associated with alcohol and tobacco use. Human papillomavirus is present in approximately half of the cases. It is characterized by a tendency to metastasize early to the lymph nodes. When the tumor is small, patients are often asymptomatic. Physical examination may reveal erythematous or white lesions or plaques. The majority of patients present with signs and symptoms of locally advanced disease including mucosal ulceration, pain, difficulty with speaking, chewing, and swallowing, bleeding, weight loss, and neck swelling. Patients may also present with swollen neck lymph nodes without any symptoms from the oropharyngeal tumor. The most significant prognostic factors are the size of the tumor and the lymph nodes status." DSA03651,GSE38537,GPL6480,1000,Tropical Spastic Paraparesis,C0030481,Peripheral blood,GEO,Microarray,Homo sapiens,4|4,"DO:A viral infectious disease that results in inflammation located in spinal cord, has_material_basis_in Human T-lymphotropic virus 1, which is transmitted by sexual contact, and transmitted by breast feeding. The infection has symptom spastic weakness of both legs, has symptom muscle stiffness, has symptom sensory disturbance, and has symptom spasms." DSA03652,GSE38543,GPL4685,1000,Myeloproliferative Neoplasm,C0027022,Peripheral blood,GEO,Microarray,Homo sapiens,11|18,"DO:A myeloid neoplasm that is characterized by a group of slow growing blood cancers in which large numbers of abnormal red blood cells, white blood cells, or platelets grow and spread in the bone marrow and the peripheral blood." DSA03653,GSE38543,GPL4685,1000,Myeloproliferative Neoplasm,C0027022,Peripheral blood,GEO,Microarray,Homo sapiens,11|24,"DO:A myeloid neoplasm that is characterized by a group of slow growing blood cancers in which large numbers of abnormal red blood cells, white blood cells, or platelets grow and spread in the bone marrow and the peripheral blood." DSA03654,GSE38543,GPL4685,1000,Myeloproliferative Neoplasm,C0027022,Peripheral blood,GEO,Microarray,Homo sapiens,11|13,"DO:A myeloid neoplasm that is characterized by a group of slow growing blood cancers in which large numbers of abnormal red blood cells, white blood cells, or platelets grow and spread in the bone marrow and the peripheral blood." DSA03655,GSE38597,GPL570,1000,Hepatitis C,C0019196,Liver,GEO,Microarray,Homo sapiens,2|6,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA03656,GSE3860,GPL96,850,Hutchinson-Gilford Progeria Syndrome,C0033300,,GEO,Microarray,Homo sapiens,9|9,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA03657,GSE3860,GPL97,456,Hutchinson-Gilford Progeria Syndrome,C0033300,,GEO,Microarray,Homo sapiens,9|9,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA03658,GSE38616,GPL6244,0,Oral Lichen Planus,C0206139,Oral mucosa,GEO,Microarray,Homo sapiens,7|7,EFO:Oral lichen planus is a chronic inflammatory oral condition of unknown aetiology characterized by T-cell-mediated chronic immune response and abnormal epithelial keratinization cycle. DSA03659,GSE38626,GPL13607,1000,Chronic Infantile Neurological Cutaneous And Articular Syndrome,C0409818,,GEO,Microarray,Homo sapiens,3|3,"DO:An autoimmune disease characterized by neonatal onset of cutaneous symptoms, chronic meningitis, and joint manifestations with recurrent fever and inflammation that has_material_basis_in heterozygous mutation in the NLRP3 gene on chromosome 1q." DSA03660,GSE38750,GPL571,235,Uremia,C0041948,Artery,GEO,Microarray,Homo sapiens,19|15,DO:A kidney disease characterized by the failure of the kidneys to adequately filter waste products from the blood. DSA03661,GSE38751,GPL571,0,Uremia,C0041948,Mammary gland,GEO,Microarray,Homo sapiens,5|5,DO:A kidney disease characterized by the failure of the kidneys to adequately filter waste products from the blood. DSA03662,GSE38792,GPL6244,0,Obstructive Sleep Apnea,C4237227,Visceral adipose tissue,GEO,Microarray,Homo sapiens,8|10,"DO:A sleep apnea that is characterized by repeated collapse and obstruction of the upper airway during sleep, which results in reduced airflow (hypopnea) or complete airflow cessation (apnea), oxygen desaturation, and arousals from sleep." DSA03663,GSE38931,GPL10558,397,Down Syndrome,C0013080,,GEO,Microarray,Homo sapiens,2|6,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA03664,GSE38948,GPL6096,160,Dysphasia,C0973461,Lung,GEO,Microarray,Mus musculus,4|4,"MSH:A cognitive disorder marked by an impaired ability to comprehend or express language in its written or spoken form. This condition is caused by diseases which affect the language areas of the dominant hemisphere. Clinical features are used to classify the various subtypes of this condition. General categories include receptive, expressive, and mixed forms of aphasia." DSA03665,GSE38948,GPL6096,17,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Mus musculus,4|4,DO:A respiratory system cancer that is located_in the lung. DSA03666,GSE38958,GPL5175,1000,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,Microarray,Homo sapiens,45|70,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA03667,GSE38961,GPL570,0,Loeys-Dietz Syndrome,C1836635,,GEO,Microarray,Homo sapiens,3|3,"DO:A syndrome that is characterized by increased risk of aortic aneurysm and dissection, elongated limbs, hypertelorism, bifid uvula and easy skin bruising due to mutations in TGFB3 that results in connective tissue defects." DSA03668,GSE38994,GPL14603,5,Asthma,C0004096,Airway wall,GEO,RNA-Seq,Homo sapiens,1|1,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA03669,GSE39001,GPL201,1000,Cervical Cancer,C4048328,Endocervix,GEO,Microarray,Homo sapiens,12|43,DO:A female reproductive organ cancer that is located_in the cervix. DSA03670,GSE39001,GPL6244,1000,Cervical Cancer,C4048328,Endocervix,GEO,Microarray,Homo sapiens,5|19,DO:A female reproductive organ cancer that is located_in the cervix. DSA03671,GSE39041,GPL6884,119,Sezary Syndrome,C0036920,,GEO,Microarray,Homo sapiens,3|6,"MONDO:Sezary syndrome (SS) is an aggressive form of cutaneous T-cell lymphoma characterized by a triad of erythroderma, lymphadenopathy and circulating atypical lymphocytes (Sezary cells)." DSA03672,GSE39117,GPL570,1000,Endotoxemia,C0376618,Adipose tissue,GEO,Microarray,Homo sapiens,14|14,"MSH:A condition characterized by the presence of ENDOTOXINS in the blood. On lysis, the outer cell wall of gram-negative bacteria enters the systemic circulation and initiates a pathophysiologic cascade of pro-inflammatory mediators." DSA03673,GSE39117,GPL570,335,Endotoxemia,C0376618,Adipose tissue,GEO,Microarray,Homo sapiens,14|14,"MSH:A condition characterized by the presence of ENDOTOXINS in the blood. On lysis, the outer cell wall of gram-negative bacteria enters the systemic circulation and initiates a pathophysiologic cascade of pro-inflammatory mediators." DSA03674,GSE39117,GPL570,1,Endotoxemia,C0376618,Adipose tissue,GEO,Microarray,Homo sapiens,14|12,"MSH:A condition characterized by the presence of ENDOTOXINS in the blood. On lysis, the outer cell wall of gram-negative bacteria enters the systemic circulation and initiates a pathophysiologic cascade of pro-inflammatory mediators." DSA03675,GSE39228,GPL6887,1000,Tumor,C0006826,Spleen,GEO,Microarray,Mus musculus,2|2,"DO:A disease of cellular proliferation that is malignant and primary, characterized by uncontrolled cellular proliferation, local cell invasion and metastasis." DSA03676,GSE39345,GPL6104,1000,Non-Small Cell Lung Cancer,C0007131,,GEO,Microarray,Homo sapiens,20|32,DO:A respiratory system cancer that is located_in the lung. DSA03677,GSE39400,GPL4133,1000,Head And Neck Squamous Cell Carcinoma,C1168401,,GEO,Microarray,Homo sapiens,11|28,"DO:A head and neck carcinoma that has_material_basis_in squamous cells that line the moist, mucosal surfaces inside the head and neck." DSA03678,GSE55177,GPL1261,471,Spinocerebellar Ataxia Type 2,C0752121,Midbrain,GEO,Microarray,Mus musculus,4|4,"DO:An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene." DSA03679,GSE55177,GPL1261,264,Spinocerebellar Ataxia Type 2,C0752121,Cerebellum,GEO,Microarray,Mus musculus,4|4,"DO:An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene." DSA03680,GSE39411,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,6|6,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA03681,GSE39411,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,6|6,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA03682,GSE39411,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,6|6,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA03683,GSE39411,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,6|6,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA03684,GSE39411,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,6|6,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA03685,GSE39411,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,6|6,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA03686,GSE39411,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,6|6,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA03687,GSE39411,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,6|6,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA03688,GSE39411,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,6|5,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA03689,GSE39411,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,6|5,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA03690,GSE39411,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,6|5,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA03691,GSE39411,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,6|5,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA03692,GSE39411,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,6|5,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA03693,GSE39411,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,6|5,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA03694,GSE39411,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,6|5,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA03695,GSE39411,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,6|5,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA03696,GSE39420,GPL11532,718,Alzheimer's Disease,C0002395,Brain,GEO,Microarray,Homo sapiens,7|7,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03697,GSE39420,GPL11532,1000,Alzheimer's Disease,C0002395,Brain,GEO,Microarray,Homo sapiens,7|7,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA03698,GSE39458,GPL1261,0,Arthritis,C0003864,Bone marrow,GEO,Microarray,Mus musculus,4|2,DO:A bone disease that is located_in the joint. DSA03699,GSE39488,GPL10332,82,Arteriovenous Fistula,C0003855,Venous segment,GEO,Microarray,Homo sapiens,4|6,HPO:An abnormal connection between an artery and vein. DSA03700,GSE39509,GPL13112,1000,Prostate Cancer,C0600139,Prostate,GEO,RNA-Seq,Mus musculus,6|5,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03701,GSE39509,GPL13112,1000,Prostate Cancer,C0600139,Prostate,GEO,RNA-Seq,Mus musculus,6|6,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03702,GSE39509,GPL13112,1000,Prostate Cancer,C0600139,Prostate,GEO,RNA-Seq,Mus musculus,5|6,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03703,GSE39509,GPL13112,1000,Prostate Cancer,C0600139,Prostate,GEO,RNA-Seq,Mus musculus,5|6,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03704,GSE3964,GPL3282,585,Colorectal Carcinoma,C0009402,Liver,GEO,Microarray,Homo sapiens,6|9,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA03705,GSE3964,GPL3282,483,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,6|14,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA03706,GSE39642,GPL15846,43,Amyotrophic Lateral Sclerosis,C0002736,,GEO,Microarray,Homo sapiens,10|10,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA03707,GSE39642,GPL15846,28,Amyotrophic Lateral Sclerosis,C0002736,,GEO,Microarray,Homo sapiens,10|4,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA03708,GSE39653,GPL10558,6,Bipolar Disorder,C0005586,,GEO,Microarray,Homo sapiens,24|8,DO:A mood disorder that involves alternating periods of mania and depression. DSA03709,GSE39653,GPL10558,1,Major Depressive Disorder,C1269683,,GEO,Microarray,Homo sapiens,24|21,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA03710,GSE39683,GPL16522,1000,Multiple Myeloma,C0026764,Bone marrow,GEO,Microarray,Homo sapiens,4|55,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA03711,GSE39683,GPL16522,1000,Plasma Cell Leukemia,C0023484,Bone marrow,GEO,Microarray,Homo sapiens,4|8,DO:A plasma cell neoplasm that is characterized by the presence of a circulating clonal plasma cell count that exceeds 2x10^9/L or is 20% of the leukocyte differential count. DSA03712,GSE39754,GPL5175,1000,Multiple Myeloma,C0026764,,GEO,Microarray,Homo sapiens,6|170,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA03713,GSE40033,GPL14550,0,Psoriasis,C0033860,Bone marrow,GEO,Microarray,Homo sapiens,4|7,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA03714,GSE40102,GPL6244,812,Schizophrenia,C0036341,,GEO,Microarray,Homo sapiens,12|12,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA03715,GSE40182,GPL570,1,Pre-Eclampsia,C0032914,Placenta,GEO,Microarray,Homo sapiens,5|5,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA03716,GSE40182,GPL570,3,Pre-Eclampsia,C0032914,Placenta,GEO,Microarray,Homo sapiens,5|5,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA03717,GSE40182,GPL570,2,Pre-Eclampsia,C0032914,Placenta,GEO,Microarray,Homo sapiens,5|5,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA03718,GSE40182,GPL570,0,Pre-Eclampsia,C0032914,Placenta,GEO,Microarray,Homo sapiens,4|5,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA03719,GSE40184,GPL96,0,Hepatitis C,C0019196,,GEO,Microarray,Homo sapiens,8|10,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA03720,GSE40223,GPL10558,25,Hepatitis C,C0019196,,GEO,Microarray,Homo sapiens,5|5,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA03721,GSE40225,GPL6246,1,Type 1 Diabetes,C0011854,Pancreas,GEO,Microarray,Mus musculus,3|3,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA03722,GSE40227,GPL5175,1000,Chuvash Polycythemia,C0032461,,GEO,Microarray,Homo sapiens,21|24,DO:A primary polycythemia that has_material_basis_in homozygous or compound heterozygous mutation in the VHL gene (608537) on chromosome 3p25. DSA03723,GSE40263,GPL6244,0,Psoriasis,C0033860,,GEO,Microarray,Homo sapiens,5|5,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA03724,GSE40263,GPL6244,0,Psoriasis,C0033860,,GEO,Microarray,Homo sapiens,5|5,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA03725,GSE40263,GPL6244,0,Psoriasis,C0033860,,GEO,Microarray,Homo sapiens,5|5,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA03726,GSE40378,GPL10558,904,Frontotemporal Dementia,C0338451,,GEO,Microarray,Homo sapiens,12|10,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA03727,GSE40378,GPL10558,543,Frontotemporal Dementia,C0338451,,GEO,Microarray,Homo sapiens,12|10,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA03728,GSE40445,GPL10097,206,Cystic Fibrosis,C0010674,,GEO,Microarray,Homo sapiens,5|5,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA03729,GSE55177,GPL1261,3,Spinocerebellar Ataxia Type 2,C0752121,Cerebellum,GEO,Microarray,Mus musculus,4|4,"DO:An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene." DSA03730,GSE55177,GPL1261,3,Spinocerebellar Ataxia Type 2,C0752121,Midbrain,GEO,Microarray,Mus musculus,4|4,"DO:An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene." DSA03731,GSE40531,GPL1261,718,Acute Myeloid Leukemia (Aml-M2),C1879321,Spleen,GEO,Microarray,Mus musculus,5|6,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA03732,GSE40561,GPL6947,55,Chronic Infantile Neurological Cutaneous And Articular Syndrome,C0409818,Blood,GEO,Microarray,Homo sapiens,41|2,"DO:An autoimmune disease characterized by neonatal onset of cutaneous symptoms, chronic meningitis, and joint manifestations with recurrent fever and inflammation that has_material_basis_in heterozygous mutation in the NLRP3 gene on chromosome 1q." DSA03733,GSE40561,GPL6947,395,Hoil1 Deficiency,,Blood,GEO,Microarray,Homo sapiens,41|1, DSA03734,GSE40561,GPL6947,58,Deficiency Disease,C0751753,Blood,GEO,Microarray,Homo sapiens,41|2,DO:A urea cycle disorder that involves accumulation of ammonia in the blood. DSA03735,GSE40561,GPL6947,205,Muckle-Wells Syndrome,C0268390,Blood,GEO,Microarray,Homo sapiens,41|5,"DO:A syndrome characterized by episodic skin rash, arthralgias, and fever associated with late-onset sensorineural deafness and renal amyloidosis that has_material_basis_in heterozygous mutation in NLRP3 on chromosome 1q44." DSA03736,GSE40568,GPL570,91,Sjogren's Syndrome,C1527336,Labial salivary gland,GEO,Microarray,Homo sapiens,3|5,DO:An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. DSA03737,GSE40568,GPL570,1000,IgG4-Related Disease,C3203653,Labial salivary gland,GEO,Microarray,Homo sapiens,3|5,"DO:An autoimmune disease that is characterized by tumefactive lesions, a dense lymphoplasmacytic infiltrate rich in IgG4-positive plasma cells, storiform fibrosis, obliterative phlebitis, autoimmune pancreatitis, and sometimes elevated serum IgG4 levels affecting various organs." DSA03738,GSE55177,GPL1261,0,Spinocerebellar Ataxia Type 2,C0752121,Liver,GEO,Microarray,Mus musculus,4|4,"DO:An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene." DSA03739,GSE40586,GPL6244,675,Bacterial Meningitis,C0085437,Peripheral blood,GEO,Microarray,Homo sapiens,18|7,DO:A meningitis that has_material_basis_in a bacterial infection. DSA03740,GSE40586,GPL6244,1000,Bacterial Meningitis,C0085437,Peripheral blood,GEO,Microarray,Homo sapiens,18|14,DO:A meningitis that has_material_basis_in a bacterial infection. DSA03741,GSE40611,GPL570,610,Primary Sjogren Syndrome,C0151449,Parotid,GEO,Microarray,Homo sapiens,18|17,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA03742,GSE40611,GPL570,315,Sicca,C0086981,Parotid,GEO,Microarray,Homo sapiens,18|14,DO:An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. DSA03743,GSE40732,GPL16025,0,Asthma,C0004096,,GEO,Microarray,Homo sapiens,97|97,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA03744,GSE40839,GPL96,1000,Scleroderma-Associated Interstitial Lung Disease,C0339904,,GEO,Microarray,Homo sapiens,10|8,HPO:It is a bilateral reticular pattern of linear or lineonodular densities that are most pronounced in basilar portions of the lungs on standard chest x-ray. It is the third minor criterion for scleroderma diagnosis. DSA03745,GSE40839,GPL96,1000,Usual Interstitial Pneumonia,C4721509,,GEO,Microarray,Homo sapiens,10|3,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA03746,GSE40889,GPL6244,0,Asthma,C0004096,Peripheral blood,GEO,Microarray,Homo sapiens,5|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA03747,GSE40889,GPL6244,5,Asthma,C0004096,Peripheral blood,GEO,Microarray,Homo sapiens,13|14,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA03748,GSE40889,GPL6244,0,Asthma,C0004096,Peripheral blood,GEO,Microarray,Homo sapiens,13|8,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA03749,GSE40889,GPL6244,0,Asthma,C0004096,Peripheral blood,GEO,Microarray,Homo sapiens,13|14,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA03750,GSE40889,GPL6244,1000,Asthma,C0004096,Peripheral blood,GEO,Microarray,Homo sapiens,14|8,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA03751,GSE40889,GPL6244,1000,Asthma,C0004096,Peripheral blood,GEO,Microarray,Homo sapiens,13|13,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA03752,GSE40889,GPL6244,1,Asthma,C0004096,Peripheral blood,GEO,Microarray,Homo sapiens,14|8,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA03753,GSE40911,GPL3985,459,Clear Cell Renal Cell Carcinoma,C0007134,Kidney,GEO,Microarray,Homo sapiens,22|22,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA03754,GSE41011,GPL6254,829,Colorectal Carcinoma,C0009402,Mucosa,GEO,Microarray,Homo sapiens,12|19,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA03755,GSE41030,GPL15950,4,Uremia,C0041948,,GEO,Microarray,Homo sapiens,3|3,DO:A kidney disease characterized by the failure of the kidneys to adequately filter waste products from the blood. DSA03756,GSE41038,GPL6883,0,Ankylosing Spondylitis,C0038013,Synovium,GEO,Microarray,Homo sapiens,4|2,"DO:A bone inflammation disease that results_in inflammation in the joints of the spine and pelvis. The disease has_symptom pain, has_symptom stiffness in the spine, has_symptom stiffness in the neck, has_symptom stiffness in the hips, has_symptom stiffness in the jaw and has_symptom stiffness in the rib cage." DSA03757,GSE41038,GPL6883,0,Osteoarthritis,C0157946,Synovium,GEO,Microarray,Homo sapiens,4|3,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA03758,GSE41038,GPL6883,0,Spondyloarthropathy,C0949690,Synovium,GEO,Microarray,Homo sapiens,4|6,"EFO:Heterogeneous group of arthritic diseases sharing clinical and radiologic features. They are associated with the HLA-B27 ANTIGEN and some with a triggering infection. Most involve the axial joints in the SPINE, particularly the SACROILIAC JOINT, but can also involve asymmetric peripheral joints. Subsets include ANKYLOSING SPONDYLITIS; REACTIVE ARTHRITIS; PSORIATIC ARTHRITIS; and others." DSA03759,GSE41039,GPL6885,405,Spondylitis,C0038012,Spine,GEO,Microarray,Mus musculus,4|4,MONDO:The inflammation of a vertebra. DSA03760,GSE41055,GPL5175,0,Tuberculosis,C0041296,Blood,GEO,Microarray,Homo sapiens,9|9,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA03761,GSE41055,GPL5175,0,Tuberculosis,C0041296,Blood,GEO,Microarray,Homo sapiens,9|9,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA03762,GSE41130,GPL16100,425,Myelodysplastic Syndrome,C3463824,,GEO,Microarray,Homo sapiens,7|6,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA03763,GSE41130,GPL16100,99,Myelodysplastic Syndrome,C3463824,,GEO,Microarray,Homo sapiens,7|5,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA03764,GSE41130,GPL16100,6,Myelodysplastic Syndrome,C3463824,,GEO,Microarray,Homo sapiens,7|7,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA03765,GSE4115,GPL96,1000,Lung Cancer,C0684249,Bronchial epithelium,GEO,Microarray,Homo sapiens,90|97,DO:A respiratory system cancer that is located_in the lung. DSA03766,GSE153923,GPL19057,1000,Heart Failure With Preserved Ejection Fraction,C4509226,Left ventricle,GEO,RNA-Seq,Mus musculus,4|4, DSA03767,GSE153946,GPL20301,658,Hepatitis B,C0019163,,GEO,RNA-Seq,Homo sapiens,5|4,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus, which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice." DSA03768,GSE153957,GPL26963,1000,Autoimmune Pulmonary Alveolar Proteinosis,C1970472,Left ventricle,GEO,Microarray,Homo sapiens,5|5,MONDO:Pulmonary alveolar proteinosis (PAP) is a rare lung disease characterized by the accumulation of a lipoproteinaceous substance in the distal air spaces which positively stains with periodic acid-Schiff (PAS). DSA03769,GSE153990,GPL18573,127,Aromatic L-Amino Acid Decarboxylase Deficiency,C1291564,Midbrain,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An inherited metabolic disorder that is characterized by reduced production of serotonin and dopamine resulting in hypotonia, hypokinesia, ptosis oculogyric crises, and signs of autonomic dysfunction, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the dopa decarboxylase gene (DDC) on chromosome 7p12." DSA03770,GSE153990,GPL18573,126,Aromatic L-Amino Acid Decarboxylase Deficiency,C1291564,Midbrain,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An inherited metabolic disorder that is characterized by reduced production of serotonin and dopamine resulting in hypotonia, hypokinesia, ptosis oculogyric crises, and signs of autonomic dysfunction, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the dopa decarboxylase gene (DDC) on chromosome 7p12." DSA03771,GSE55177,GPL1261,11,Spinocerebellar Ataxia Type 2,C0752121,Liver,GEO,Microarray,Mus musculus,4|4,"DO:An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene." DSA03772,GSE55177,GPL1261,1000,Spinocerebellar Ataxia Type 2,C0752121,Liver,GEO,Microarray,Mus musculus,4|4,"DO:An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene." DSA03773,GSE154046,GPL20301,1000,Primary Immunoglobulin A Nephropathy (Disorder),C3161650,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A glomerulonephritis characterized by build up of IgA antibody in the glomerulus. DSA03774,GSE154055,GPL16791,14,Hepatic Fibrosis,C0239946,Plasma,GEO,RNA-Seq,Homo sapiens,3|3,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA03775,GSE154084,GPL24676,1000,Atrial Fibrillation,C0004238,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A heart conduction disease that is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular and has symptoms palpitations, weakness, fatigue, lightheadedness, dizziness, confusion, shortness of breath and chest pain." DSA03776,GSE154084,GPL24676,1000,Atrial Fibrillation,C0004238,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A heart conduction disease that is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular and has symptoms palpitations, weakness, fatigue, lightheadedness, dizziness, confusion, shortness of breath and chest pain." DSA03777,GSE154096,GPL21273,156,Cardiomyopathy,C0878544,Heart,GEO,RNA-Seq,Mus musculus,3|3,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA03778,GSE60413,GPL1261,10,Parkinson's Disease,C0030567,Cerebellum,GEO,Microarray,Mus musculus,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03779,GSE60413,GPL1261,10,Parkinson's Disease,C0030567,Cerebellum,GEO,Microarray,Mus musculus,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03780,GSE154197,GPL18573,1000,Ciliopathy,C4551720,Retina,GEO,RNA-Seq,Homo sapiens,3|3,DO:A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer dynein arm defect and in about half of patients situs inversus and has_material_basis_in compound heterozygous mutation in the DNAI1 gene on chromosome 9p13. DSA03781,GSE154197,GPL18573,1000,Ciliopathy,C4551720,Retina,GEO,RNA-Seq,Homo sapiens,3|3,DO:A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer dynein arm defect and in about half of patients situs inversus and has_material_basis_in compound heterozygous mutation in the DNAI1 gene on chromosome 9p13. DSA03782,GSE154199,GPL20301,363,Neurodevelopmental Disorder,C1535926,,GEO,RNA-Seq,Homo sapiens,8|3,"MSH:These are a group of conditions with onset in the developmental period. The disorders typically manifest early in development, often before the child enters grade school, and are characterized by developmental deficits that produce impairments of personal, social, academic, or occupational functioning. (From DSM-5)." DSA03783,GSE154274,GPL16791,1000,Polycystic Ovary Syndrome,C0032460,Placenta,GEO,RNA-Seq,Homo sapiens,3|1,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA03784,GSE154311,GPL18573,1000,COVID-19,D8888888,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA03785,GSE154311,GPL18573,1000,COVID-19,D8888888,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA03786,GSE154377,GPL20301,3,Gestational Diabetes,C0085207,Plasma,GEO,RNA-Seq,Homo sapiens,7|7,DO:A diabetes mellitus that manifests during pregnancy. DSA03787,GSE154377,GPL20301,67,Gestational Hypertension,C0852036,Plasma,GEO,RNA-Seq,Homo sapiens,7|8,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA03788,GSE154377,GPL20301,1,Hypertension,C0020538,Plasma,GEO,RNA-Seq,Homo sapiens,7|2,DO:An artery disease characterized by chronic elevated blood pressure in the arteries. DSA03789,GSE154377,GPL20301,0,Gestational Diabetes,C0085207,Plasma,GEO,RNA-Seq,Homo sapiens,9|7,DO:A diabetes mellitus that manifests during pregnancy. DSA03790,GSE154377,GPL20301,3,Gestational Hypertension,C0852036,Plasma,GEO,RNA-Seq,Homo sapiens,9|8,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA03791,GSE154377,GPL20301,0,Hypertension,C0020538,Plasma,GEO,RNA-Seq,Homo sapiens,9|2,DO:An artery disease characterized by chronic elevated blood pressure in the arteries. DSA03792,GSE154377,GPL20301,11,Gestational Diabetes,C0085207,Plasma,GEO,RNA-Seq,Homo sapiens,9|6,DO:A diabetes mellitus that manifests during pregnancy. DSA03793,GSE154377,GPL20301,1000,Gestational Hypertension,C0852036,Plasma,GEO,RNA-Seq,Homo sapiens,9|8,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA03794,GSE154377,GPL20301,2,Hypertension,C0020538,Plasma,GEO,RNA-Seq,Homo sapiens,9|2,DO:An artery disease characterized by chronic elevated blood pressure in the arteries. DSA03795,GSE154377,GPL20301,181,Gestational Diabetes,C0085207,Plasma,GEO,RNA-Seq,Homo sapiens,9|7,DO:A diabetes mellitus that manifests during pregnancy. DSA03796,GSE154377,GPL20301,864,Gestational Hypertension,C0852036,Plasma,GEO,RNA-Seq,Homo sapiens,9|8,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA03797,GSE154377,GPL20301,0,Hypertension,C0020538,Plasma,GEO,RNA-Seq,Homo sapiens,9|2,DO:An artery disease characterized by chronic elevated blood pressure in the arteries. DSA03798,GSE154377,GPL20301,31,Gestational Diabetes,C0085207,Plasma,GEO,RNA-Seq,Homo sapiens,9|6,DO:A diabetes mellitus that manifests during pregnancy. DSA03799,GSE154377,GPL20301,0,Gestational Hypertension,C0852036,Plasma,GEO,RNA-Seq,Homo sapiens,9|8,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA03800,GSE154377,GPL20301,0,Hypertension,C0020538,Plasma,GEO,RNA-Seq,Homo sapiens,9|2,DO:An artery disease characterized by chronic elevated blood pressure in the arteries. DSA03801,GSE154400,GPL21103,1000,Diabetes Mellitus,C0011849,,GEO,snRNA-Seq,Mus musculus,1|1,"DO:A glucose metabolism disease that is characterized by chronic hyperglycaemia with disturbances of carbohydrate, fat and protein metabolism resulting from defects in insulin secretion, insulin action, or both." DSA03802,GSE154414,GPL20301,505,Gestational Diabetes Mellitus,C0085207,Placenta,GEO,RNA-Seq,Homo sapiens,4|4,DO:A diabetes mellitus that manifests during pregnancy. DSA03803,GSE154519,GPL24247,1000,Myocardial Disease,C0878544,,GEO,RNA-Seq,Mus musculus,3|2,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA03804,GSE154519,GPL24247,1000,Myocardial Disease,C0878544,,GEO,RNA-Seq,Mus musculus,3|1,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA03805,GSE154609,GPL17692,23,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,12|12,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA03806,GSE154650,GPL20301,47,Hemorrhoids,C0019112,Anal canal,GEO,RNA-Seq,Homo sapiens,9|8,"DO:A pelvic varices that is characterized by swollen, inflamed veins around the anus or lower rectum." DSA03807,GSE154650,GPL20301,1000,Hemorrhoids,C0019112,Anal canal,GEO,RNA-Seq,Homo sapiens,8|12,"DO:A pelvic varices that is characterized by swollen, inflamed veins around the anus or lower rectum." DSA03808,GSE154773,GPL18573,1000,Hidradenitis Suppurativa,C0162836,Skin,GEO,RNA-Seq,Homo sapiens,10|22,"DO:A hidradenitis that is characterized by chronic inflammation of the apocrine sweat glands, has_symptom painful nodules, abscesses, sinus tract formation, scarring, erythema, pruritis, and pain, and has_material_basis_in chronic inflammation of the apocrine sweat glands leading to recurrent folliculitis and an accompanying immune response that worsens inflammation." DSA03809,GSE154773,GPL18573,1000,Hidradenitis Suppurativa,C0162836,Whole blood,GEO,RNA-Seq,Homo sapiens,10|21,"DO:A hidradenitis that is characterized by chronic inflammation of the apocrine sweat glands, has_symptom painful nodules, abscesses, sinus tract formation, scarring, erythema, pruritis, and pain, and has_material_basis_in chronic inflammation of the apocrine sweat glands leading to recurrent folliculitis and an accompanying immune response that worsens inflammation." DSA03810,GSE154777,GPL16791,1000,Melanoma,C0025202,Bone marrow,GEO,RNA-Seq,Homo sapiens,3|8,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA03811,GSE154777,GPL16791,1000,Melanoma,C0025202,Bone marrow,GEO,RNA-Seq,Homo sapiens,3|5,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA03812,GSE154777,GPL16791,1000,Melanoma,C0025202,Bone marrow,GEO,RNA-Seq,Homo sapiens,3|8,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA03813,GSE154802,GPL16791,1000,Cystic Fibrosis,C0010674,Airway epithelium,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA03814,GSE154806,GPL13112,365,Obstructive Lung Disease,C0600260,,GEO,RNA-Seq,Mus musculus,3|3,DO:A lung disease that is characterized by narrowing of pulmonary airways. DSA03815,GSE154825,GPL18573,1000,Stroke-Like Episodes,C1857287,,GEO,RNA-Seq,Homo sapiens,3|2,"HPO:No consensus exists on what a stroke-like episode is, but these episodes can be functionally defined as a new neurological deficit, occurring with or without the context of seizures, which last longer than 24 hours." DSA03816,GSE154825,GPL18573,114,Stroke-Like Episodes,C1857287,,GEO,RNA-Seq,Homo sapiens,3|2,"HPO:No consensus exists on what a stroke-like episode is, but these episodes can be functionally defined as a new neurological deficit, occurring with or without the context of seizures, which last longer than 24 hours." DSA03817,GSE154851,GPL16699,880,Systemic Lupus Erythematosus,C0024141,Peripheral blood,GEO,Microarray,Homo sapiens,32|38,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03818,GSE154871,GPL19057,1000,Blister,C3814530,Skin,GEO,RNA-Seq,Mus musculus,3|3,"HPO:A circumscribed, fluid-containing, epidermal elevation generally considered less than 10mm in diameter at the widest point." DSA03819,GSE60413,GPL1261,372,Parkinson's Disease,C0030567,Cerebellum,GEO,Microarray,Mus musculus,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03820,GSE15489,GPL339,1000,Alveolar Rhabdomyosarcoma,C0206655,Skeletal muscle,GEO,Microarray,Mus musculus,3|6,EFO:A rapidly growing malignant mesenchymal neoplasm. It is characterized by the presence of round cells with myoblastic differentiation and a fibrovascular stroma resembling an alveolar growth pattern. The tumor usually presents in the extremities. DSA03821,GSE154916,GPL570,1000,Erythema Migrans,C0014740,Skin,GEO,Microarray,Homo sapiens,16|15,"DO:An atrophic glossitis that is characterized as an inflammatory condition of the mucous membrane of the tongue, usually on the dorsal surface." DSA03822,GSE154916,GPL571,1000,Erythema Migrans,C0014740,Skin,GEO,Microarray,Homo sapiens,11|3,"DO:An atrophic glossitis that is characterized as an inflammatory condition of the mucous membrane of the tongue, usually on the dorsal surface." DSA03823,GSE154918,GPL20301,1000,Septic Shock,C0036983,Blood,GEO,RNA-Seq,Homo sapiens,40|19,"DO:A commensal bacterial infectious disease that results_in infection, has_material_basis_in Streptococcus pyogenes or has_material_basis_in Staphylococcus aureus , which produce toxins that are absorbed systemically and produce the systemic manifestations. The infection has_symptom fever, has_symptom rash, has_symptom hypotension, has_symptom multiorgan failure, has_symptom desquamation, has_symptom vomiting, has_symptom diarrhea, has_symptom headache, and has_symptom nonfocal neurologic abnormalities." DSA03824,GSE154918,GPL20301,1000,Septic Shock,C0036983,Blood,GEO,RNA-Seq,Homo sapiens,40|10,"DO:A commensal bacterial infectious disease that results_in infection, has_material_basis_in Streptococcus pyogenes or has_material_basis_in Staphylococcus aureus , which produce toxins that are absorbed systemically and produce the systemic manifestations. The infection has_symptom fever, has_symptom rash, has_symptom hypotension, has_symptom multiorgan failure, has_symptom desquamation, has_symptom vomiting, has_symptom diarrhea, has_symptom headache, and has_symptom nonfocal neurologic abnormalities." DSA03825,GSE154918,GPL20301,1000,Sepsis,C0243026,Blood,GEO,RNA-Seq,Homo sapiens,40|20,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA03826,GSE154918,GPL20301,1000,Sepsis,C0243026,Blood,GEO,RNA-Seq,Homo sapiens,40|12,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA03827,GSE154918,GPL20301,1000,Sepsis,C0243026,Blood,GEO,RNA-Seq,Homo sapiens,40|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA03828,GSE154926,GPL18573,1,Primary Sjogren Syndrome,C0151449,,GEO,RNA-Seq,Homo sapiens,7|43,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA03829,GSE154928,GPL20301,1000,Autoimmune Lymphoproliferative Syndrome,C1328840,Peripheral blood,GEO,RNA-Seq,Homo sapiens,8|3,"DO:A hypersensitivity reaction type IV disease that is an inherited disorder in which the body cannot properly regulate the number of immune system cells (lymphocytes). It is characterized by the production of an abnormally large number of lymphocytes. Accumulation of excess lymphocytes results in enlargement of the lymph nodes, the liver, and the spleen." DSA03830,GSE155056,GPL28784,0,Prostate Cancer,C0600139,,GEO,Microarray,Homo sapiens,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03831,GSE155067,GPL21697,0,Schizophrenia,C0036341,,GEO,RNA-Seq,Homo sapiens,5|5,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA03832,GSE155067,GPL21697,0,Schizophrenia,C0036341,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA03833,GSE155099,GPL16791,1000,Cdags Syndrome,C1864186,,GEO,RNA-Seq,Homo sapiens,2|1,"MONDO:Craniosynostosis - anal anomalies - porokeratosis, or CDAGS, is a very rare condition characterized by craniosynostosis and clavicular hypoplasia, (C), delayed closure of the fontanel (D), anal anomalies (A), genitourinary malformations (G) and skin eruption (S)." DSA03834,GSE60413,GPL1261,1,Parkinson's Disease,C0030567,Cerebellum,GEO,Microarray,Mus musculus,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03835,GSE60413,GPL1261,4,Parkinson's Disease,C0030567,Midbrain,GEO,Microarray,Mus musculus,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03836,GSE60413,GPL1261,1,Parkinson's Disease,C0030567,Midbrain,GEO,Microarray,Mus musculus,2|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03837,GSE60413,GPL1261,1,Parkinson's Disease,C0030567,Midbrain,GEO,Microarray,Mus musculus,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03838,GSE155176,GPL11154,1000,Hidradenitis Suppurativa,C0162836,Skin,GEO,RNA-Seq,Homo sapiens,16|19,"DO:A hidradenitis that is characterized by chronic inflammation of the apocrine sweat glands, has_symptom painful nodules, abscesses, sinus tract formation, scarring, erythema, pruritis, and pain, and has_material_basis_in chronic inflammation of the apocrine sweat glands leading to recurrent folliculitis and an accompanying immune response that worsens inflammation." DSA03839,GSE155176,GPL11154,1000,Hidradenitis Suppurativa,C0162836,Skin,GEO,RNA-Seq,Homo sapiens,16|7,"DO:A hidradenitis that is characterized by chronic inflammation of the apocrine sweat glands, has_symptom painful nodules, abscesses, sinus tract formation, scarring, erythema, pruritis, and pain, and has_material_basis_in chronic inflammation of the apocrine sweat glands leading to recurrent folliculitis and an accompanying immune response that worsens inflammation." DSA03840,GSE155176,GPL11154,1000,Hidradenitis Suppurativa,C0162836,Skin,GEO,RNA-Seq,Homo sapiens,13|19,"DO:A hidradenitis that is characterized by chronic inflammation of the apocrine sweat glands, has_symptom painful nodules, abscesses, sinus tract formation, scarring, erythema, pruritis, and pain, and has_material_basis_in chronic inflammation of the apocrine sweat glands leading to recurrent folliculitis and an accompanying immune response that worsens inflammation." DSA03841,GSE155176,GPL11154,1000,Hidradenitis Suppurativa,C0162836,Skin,GEO,RNA-Seq,Homo sapiens,13|7,"DO:A hidradenitis that is characterized by chronic inflammation of the apocrine sweat glands, has_symptom painful nodules, abscesses, sinus tract formation, scarring, erythema, pruritis, and pain, and has_material_basis_in chronic inflammation of the apocrine sweat glands leading to recurrent folliculitis and an accompanying immune response that worsens inflammation." DSA03842,GSE155241,GPL24676,313,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA03843,GSE155301,GPL21103,0,Ulcerative Colitis,C0009324,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA03844,GSE155301,GPL21103,8,Ulcerative Colitis,C0009324,Blood,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA03845,GSE155326,GPL16686,1000,End-Stage Renal Disease,C0022661,,GEO,Microarray,Homo sapiens,3|3,DO:A kidney failure that is characterized by the gradual loss of kidney function. DSA03846,GSE155377,GPL23038,4,Diabetes Mellitus,C0011849,Myocardium,GEO,Microarray,Mus musculus,4|4,"DO:A glucose metabolism disease that is characterized by chronic hyperglycaemia with disturbances of carbohydrate, fat and protein metabolism resulting from defects in insulin secretion, insulin action, or both." DSA03847,GSE155423,GPL21103,173,Myocarditis,C0027059,Heart,GEO,RNA-Seq,Mus musculus,4|4,DO:An extrinsic cardiomyopathy that is characterized as an inflammation of the heart muscle. DSA03848,GSE155423,GPL21103,1000,Myocarditis,C0027059,Heart,GEO,RNA-Seq,Mus musculus,4|4,DO:An extrinsic cardiomyopathy that is characterized as an inflammation of the heart muscle. DSA03849,GSE155423,GPL21103,1000,Myocarditis,C0027059,Heart,GEO,RNA-Seq,Mus musculus,4|4,DO:An extrinsic cardiomyopathy that is characterized as an inflammation of the heart muscle. DSA03850,GSE155454,GPL20301,91,COVID-19,D8888888,Whole blood,GEO,RNA-Seq,Homo sapiens,6|26,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA03851,GSE155454,GPL20301,0,COVID-19,D8888888,Whole blood,GEO,RNA-Seq,Homo sapiens,6|26,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA03852,GSE155468,GPL24676,1000,Descending Thoracic Aorta Aneurysm,C1388233,Aorta,GEO,RNA-Seq,Homo sapiens,3|8,HPO:An abnormal localized widening (dilatation) of the descending thoracic aorta. DSA03853,GSE155489,GPL20795,1000,Polycystic Ovary Syndrome,C0032460,,GEO,RNA-Seq,Homo sapiens,6|6,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA03854,GSE155495,GPL21697,1000,Dilated Cardiomyopathy;Heart Failure,,,GEO,RNA-Seq,Homo sapiens,3|6, DSA03855,GSE155498,GPL21697|GPL30173,98,Steatosis,C2711227,,GEO,RNA-Seq,Homo sapiens,2|3,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA03856,GSE155498,GPL21697|GPL30173,79,Steatosis,C2711227,,GEO,RNA-Seq,Homo sapiens,2|3,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA03857,GSE155644,GPL15520,82,Sarcoidosis,C0036202,,GEO,RNA-Seq,Homo sapiens,14|14,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA03858,GSE60413,GPL1261,239,Parkinson's Disease,C0030567,Midbrain,GEO,Microarray,Mus musculus,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03859,GSE60413,GPL1261,2,Parkinson's Disease,C0030567,Striatum,GEO,Microarray,Mus musculus,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03860,GSE155697,GPL24676,148,H Syndrome,C1864445,Peripheral blood,GEO,RNA-Seq,Homo sapiens,5|4,"DO:A syndrome characterized by histiocytosis, hyperpigmentation, hypertrichosis, hepatosplenomegaly, heart anomalies, hearing loss, hypogonadism, and reduced height that has_material_basis_in homozygous or compound heterozygous mutation in SLC29A3 on 10q22.1. This syndrome comprises features from 4 histiocytic disorders that were previously considered distinct: Faisalabad histiocytosis, sinus histiocytosis with massive lymphadenopathy, H syndrome, and pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome." DSA03861,GSE155697,GPL24676,28,H Syndrome,C1864445,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A syndrome characterized by histiocytosis, hyperpigmentation, hypertrichosis, hepatosplenomegaly, heart anomalies, hearing loss, hypogonadism, and reduced height that has_material_basis_in homozygous or compound heterozygous mutation in SLC29A3 on 10q22.1. This syndrome comprises features from 4 histiocytic disorders that were previously considered distinct: Faisalabad histiocytosis, sinus histiocytosis with massive lymphadenopathy, H syndrome, and pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome." DSA03862,GSE155697,GPL24676,65,H Syndrome,C1864445,Peripheral blood,GEO,RNA-Seq,Homo sapiens,5|4,"DO:A syndrome characterized by histiocytosis, hyperpigmentation, hypertrichosis, hepatosplenomegaly, heart anomalies, hearing loss, hypogonadism, and reduced height that has_material_basis_in homozygous or compound heterozygous mutation in SLC29A3 on 10q22.1. This syndrome comprises features from 4 histiocytic disorders that were previously considered distinct: Faisalabad histiocytosis, sinus histiocytosis with massive lymphadenopathy, H syndrome, and pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome." DSA03863,GSE155697,GPL24676,45,H Syndrome,C1864445,Peripheral blood,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A syndrome characterized by histiocytosis, hyperpigmentation, hypertrichosis, hepatosplenomegaly, heart anomalies, hearing loss, hypogonadism, and reduced height that has_material_basis_in homozygous or compound heterozygous mutation in SLC29A3 on 10q22.1. This syndrome comprises features from 4 histiocytic disorders that were previously considered distinct: Faisalabad histiocytosis, sinus histiocytosis with massive lymphadenopathy, H syndrome, and pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome." DSA03864,GSE155697,GPL24676,1000,Autoinflammatory Disease,C3267073,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|1,MONDO:A group of disorders of the innate immune system characterized by attacks of seemingly unprovoked inflammation without significant levels of either autoantibodies or autoreactive T cells more characteristic of autoimmune disease. DSA03865,GSE155697,GPL24676,1000,Autoinflammatory Disease,C3267073,Peripheral blood,GEO,RNA-Seq,Homo sapiens,5|1,MONDO:A group of disorders of the innate immune system characterized by attacks of seemingly unprovoked inflammation without significant levels of either autoantibodies or autoreactive T cells more characteristic of autoimmune disease. DSA03866,GSE155697,GPL24676,1000,Autoinflammatory Disease,C3267073,Peripheral blood,GEO,RNA-Seq,Homo sapiens,2|1,MONDO:A group of disorders of the innate immune system characterized by attacks of seemingly unprovoked inflammation without significant levels of either autoantibodies or autoreactive T cells more characteristic of autoimmune disease. DSA03867,GSE155697,GPL24676,1000,Tnf Receptor-Associated Periodic Syndrome (Traps),C1275126,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|1,"DO:A primary immunodeficiency disease characterized by recurrent fever, abdominal pain, localized tender skin lesions, arthralgia and myalgia associated with skin, joint, ocular and serosal inflammation that has_material_basis_in heterozygous mutation in the TNFRSF1A gene on chromosome 12p13." DSA03868,GSE155697,GPL24676,1000,Tnf Receptor-Associated Periodic Syndrome (Traps),C1275126,Peripheral blood,GEO,RNA-Seq,Homo sapiens,5|1,"DO:A primary immunodeficiency disease characterized by recurrent fever, abdominal pain, localized tender skin lesions, arthralgia and myalgia associated with skin, joint, ocular and serosal inflammation that has_material_basis_in heterozygous mutation in the TNFRSF1A gene on chromosome 12p13." DSA03869,GSE155697,GPL24676,1000,Tnf Receptor-Associated Periodic Syndrome (Traps),C1275126,Peripheral blood,GEO,RNA-Seq,Homo sapiens,2|1,"DO:A primary immunodeficiency disease characterized by recurrent fever, abdominal pain, localized tender skin lesions, arthralgia and myalgia associated with skin, joint, ocular and serosal inflammation that has_material_basis_in heterozygous mutation in the TNFRSF1A gene on chromosome 12p13." DSA03870,GSE60413,GPL1261,1,Parkinson's Disease,C0030567,Striatum,GEO,Microarray,Mus musculus,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03871,GSE60413,GPL1261,1000,Parkinson's Disease,C0030567,Striatum,GEO,Microarray,Mus musculus,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03872,GSE155738,GPL23479,1000,Sepsis/Inflammation,,Liver,GEO,RNA-Seq,Mus musculus,3|3, DSA03873,GSE155738,GPL23479,1000,Sepsis/Inflammation,,,GEO,RNA-Seq,Mus musculus,3|3, DSA03874,GSE155750,GPL24676,29,Pre-Eclampsia,C0032914,,GEO,RNA-Seq,Homo sapiens,4|2,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA03875,GSE60413,GPL1261,1,Parkinson's Disease,C0030567,Striatum,GEO,Microarray,Mus musculus,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03876,GSE155763,GPL19057,1000,Leukemia,C0023418,Bone marrow,GEO,scRNA-Seq,Mus musculus,3|3,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA03877,GSE155763,GPL19057,1000,Leukemia,C0023418,Bone marrow,GEO,scRNA-Seq,Mus musculus,3|3,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA03878,GSE155776,GPL18573,1000,Pterygium,C0033999,Pterygium,GEO,RNA-Seq,Homo sapiens,8|8,DO:A corneal disease that is characterized by a triangular tissue growth located_in cornea of the eye that is the result of collagen degeneration and fibrovascular proliferation. DSA03879,GSE60413,GPL1261,2,Parkinson's Disease,C0030567,Liver,GEO,Microarray,Mus musculus,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03880,GSE155907,GPL21290,1000,Alcoholic Hepatitis,C0019187,Liver,GEO,RNA-Seq,Homo sapiens,4|5,MONDO:Acute hepatitis resulting from ingestion of alcohol. DSA03881,GSE156035,GPL20844,675,Type 1 Diabetes,C0011854,Peripheral blood,GEO,Microarray,Homo sapiens,20|20,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA03882,GSE156044,GPL24676,1000,Crohn's Disease,C0010346,Adipose tissue,GEO,RNA-Seq,Homo sapiens,4|4,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA03883,GSE156061,GPL16791,1000,Type 2 Diabetes,C0011860,Blood,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA03884,GSE156067,GPL20301,698,Polycystic Ovary Syndrome,C0032460,Subcutaneous adipose tissue,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA03885,GSE156067,GPL20301,1000,Polycystic Ovary Syndrome,C0032460,Subcutaneous adipose tissue,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA03886,GSE156067,GPL20301,315,Polycystic Ovary Syndrome,C0032460,Subcutaneous adipose tissue,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA03887,GSE156123,GPL20775,0,Cerebrovascular Disorders,C0007820,,GEO,Microarray,Mus musculus,4|3,DO:An vascular disease that is characterized by dysfunction of the blood vessels supplying the brain. DSA03888,GSE156123,GPL20775,0,Cerebrovascular Disorders,C0007820,,GEO,Microarray,Mus musculus,4|4,DO:An vascular disease that is characterized by dysfunction of the blood vessels supplying the brain. DSA03889,GSE156123,GPL20775,106,Cerebrovascular Disorders,C0007820,,GEO,Microarray,Mus musculus,4|4,DO:An vascular disease that is characterized by dysfunction of the blood vessels supplying the brain. DSA03890,GSE156173,GPL20301,20,Systemic Sclerosis [Scleroderma],C2364016,,GEO,RNA-Seq,Homo sapiens,5|3, DSA03891,GSE156181,GPL11202,1000,Ureteral Obstruction,C0041956,Kidney,GEO,Microarray,Mus musculus,2|2,HPO:Obstruction of the flow of urine through the ureter. DSA03892,GSE156181,GPL11202,1000,Ureteral Obstruction,C0041956,Kidney,GEO,Microarray,Mus musculus,2|3,HPO:Obstruction of the flow of urine through the ureter. DSA03893,GSE156202,GPL19057,51,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA03894,GSE156202,GPL19057,1000,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA03895,GSE156202,GPL19057,12,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA03896,GSE156202,GPL19057,692,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA03897,GSE156202,GPL19057,19,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA03898,GSE156230,GPL17021,1000,Pompe Disease,C0017921,Quadriceps,GEO,RNA-Seq,Mus musculus,3|3,DO:A glycogen storage disease that has_material_basis_in deficiency of the lysosomal acid alpha-glucosidase enzyme resulting in damage to muscle and nerve cells due to an accumulation of glycogen in the lysosome. DSA03899,GSE156230,GPL17021,1000,Pompe Disease,C0017921,Spinal cord,GEO,RNA-Seq,Mus musculus,3|3,DO:A glycogen storage disease that has_material_basis_in deficiency of the lysosomal acid alpha-glucosidase enzyme resulting in damage to muscle and nerve cells due to an accumulation of glycogen in the lysosome. DSA03900,GSE156243,GPL18573,1000,Devastating Woree Syndrome,,Cerebellum,GEO,RNA-Seq,Homo sapiens,2|4, DSA03901,GSE60413,GPL1261,1,Parkinson's Disease,C0030567,Liver,GEO,Microarray,Mus musculus,2|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03902,GSE156336,GPL16791,1000,Essential Thrombocythemia,C0040028,,GEO,RNA-Seq,Homo sapiens,4|3,"DO:A myeloproliferative neoplasm that is characterized by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocytes in the bone marrow, and episodes of thrombosis and/or hemorrhage and that results_in the overproduction of platelets." DSA03903,GSE156336,GPL16791,1000,Essential Thrombocythemia,C0040028,,GEO,RNA-Seq,Homo sapiens,4|3,"DO:A myeloproliferative neoplasm that is characterized by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocytes in the bone marrow, and episodes of thrombosis and/or hemorrhage and that results_in the overproduction of platelets." DSA03904,GSE156336,GPL16791,1000,Essential Thrombocythemia,C0040028,,GEO,RNA-Seq,Homo sapiens,4|12,"DO:A myeloproliferative neoplasm that is characterized by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocytes in the bone marrow, and episodes of thrombosis and/or hemorrhage and that results_in the overproduction of platelets." DSA03905,GSE156341,GPL16791,1000,Type 2 Diabetes,C0011860,,GEO,scRNA-Seq,Homo sapiens,6|4,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA03906,GSE156349,GPL1261,147,Breast Cancer,C0678222,Lung,GEO,Microarray,Mus musculus,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03907,GSE156349,GPL1261,105,Breast Cancer,C0678222,Lung,GEO,Microarray,Mus musculus,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03908,GSE156349,GPL1261,1000,Breast Cancer,C0678222,Lung,GEO,Microarray,Mus musculus,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03909,GSE156350,GPL1261,1000,Breast Cancer,C0678222,Lung,GEO,Microarray,Mus musculus,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03910,GSE156351,GPL1261,1000,Breast Cancer,C0678222,Lung,GEO,Microarray,Mus musculus,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03911,GSE156382,GPL20844,271,Acute-On-Chronic Liver Failure,C3850141,,GEO,Microarray,Homo sapiens,5|6,"EFO:Acute-on-chronic liver failure (ACLF) is an extreme condition during the natural history of chronic HBV infection, with a relatively high short-term mortality." DSA03912,GSE156382,GPL20844,0,Acute-On-Chronic Liver Failure,C3850141,,GEO,Microarray,Homo sapiens,5|6,"EFO:Acute-on-chronic liver failure (ACLF) is an extreme condition during the natural history of chronic HBV infection, with a relatively high short-term mortality." DSA03913,GSE156382,GPL20844,0,Chronic Liver Disease,C0341439,,GEO,Microarray,Homo sapiens,5|6,"NCI:Hepatic necrosis, inflammation, or scarring due to any cause that persists for more than 6 months. Manifestations may include signs and symptoms of cholestasis, portal hypertension, and/or abnormal liver function tests." DSA03914,GSE156429,GPL10787,1000,Colorectal Carcinoma,C0009402,,GEO,Microarray,Mus musculus,4|4,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA03915,GSE156429,GPL10787,24,Colorectal Carcinoma,C0009402,,GEO,Microarray,Mus musculus,4|4,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA03916,GSE156429,GPL10787,43,Colorectal Carcinoma,C0009402,,GEO,Microarray,Mus musculus,4|4,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA03917,GSE156441,GPL21697|GPL24676,1000,Diamond-Blackfan Anemia,C1260899,Bone marrow,GEO,scRNA-Seq,Homo sapiens,3|3,DO:A congenital hypoplastic anemia that is characterized by anemia (low red blood cell counts) with decreased erythroid progenitors in the bone marrow and has_material_basis_insufficient levels of red blood cells due to bone marrow dysfunction. DSA03918,GSE156441,GPL21697|GPL24676,1000,Diamond-Blackfan Anemia,C1260899,Bone marrow,GEO,scRNA-Seq,Homo sapiens,3|2,DO:A congenital hypoplastic anemia that is characterized by anemia (low red blood cell counts) with decreased erythroid progenitors in the bone marrow and has_material_basis_insufficient levels of red blood cells due to bone marrow dysfunction. DSA03919,GSE156441,GPL21697|GPL24676,1000,Diamond-Blackfan Anemia,C1260899,Bone marrow,GEO,scRNA-Seq,Homo sapiens,3|1,DO:A congenital hypoplastic anemia that is characterized by anemia (low red blood cell counts) with decreased erythroid progenitors in the bone marrow and has_material_basis_insufficient levels of red blood cells due to bone marrow dysfunction. DSA03920,GSE156542,GPL21103,58,Motor Deficit,C0521654,Spinal cord,GEO,RNA-Seq,Mus musculus,4|4,MSH:Clinical signs and symptoms caused by nervous system injury or dysfunction. DSA03921,GSE156542,GPL21103,1000,Motor Deficit,C0521654,Spinal cord,GEO,RNA-Seq,Mus musculus,4|4,MSH:Clinical signs and symptoms caused by nervous system injury or dysfunction. DSA03922,GSE60413,GPL1261,1,Parkinson's Disease,C0030567,Liver,GEO,Microarray,Mus musculus,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA03923,GSE156651,GPL16791,3,Eosinophilic Esophagitis,C0341106,Whole blood,GEO,RNA-Seq,Homo sapiens,5|5,DO:An esophagitis characterized by inflammation involving eosinophils located_in esophagus. DSA03924,GSE156651,GPL16791,505,Eosinophilic Esophagitis,C0341106,Esophagus,GEO,RNA-Seq,Homo sapiens,5|5,DO:An esophagitis characterized by inflammation involving eosinophils located_in esophagus. DSA03925,GSE156657,GPL16791,1000,Retinoblastoma,C0035335,,GEO,RNA-Seq,Homo sapiens,3|7,DO:A retinal cell cancer and malignant neoplasm of retina and neuroblastoma and neuroendocrine tumors that derives_from the tissues of the retina. DSA03926,GSE156686,GPL13112,1000,Nephropathy,C0022658,Kidney,GEO,RNA-Seq,Mus musculus,3|3,DO:A kidney disease that is characterized by an inflammation of the kidneys. DSA03927,GSE156751,GPL17077,1000,Systemic Lupus Erythematosus,C0024141,Whole blood,GEO,Microarray,Homo sapiens,4|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03928,GSE156751,GPL17077,1000,Systemic Lupus Erythematosus,C0024141,Whole blood,GEO,Microarray,Homo sapiens,4|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03929,GSE156751,GPL17077,1000,Systemic Lupus Erythematosus,C0024141,Whole blood,GEO,Microarray,Homo sapiens,4|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA03930,GSE7897,GPL1261,1000,Lymphoma,C0024299,,GEO,Microarray,Mus musculus,10|25,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA03931,GSE156776,GPL18573,1000,Crohn's Disease,C0010346,,GEO,scRNA-Seq,Homo sapiens,2|2,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA03932,GSE156815,GPL24247,1000,Lewis Lung Carcinoma,,Diaphragm muscle,GEO,RNA-Seq,Mus musculus,5|3, DSA03933,GSE156898,GPL17021,96,Intellectual Developmental Disorder With Cardiac Arrhythmia,C4310682,Atria,GEO,RNA-Seq,Mus musculus,6|6,"ORDO:A rare genetic disease characterized by intellectual disability, developmental delay, language deficits, and cardiac arrhythmia (most commonly sick sinus syndrome). Additional reported features include epilepsy, hypotonia, retinal abnormalities, nystagmus, attention deficit hyperactivity disorder, autism, and gastroesophageal reflux. The severity of the phenotype is highly variable." DSA03934,GSE156898,GPL17021,91,Intellectual Developmental Disorder With Cardiac Arrhythmia,C4310682,Ventricle,GEO,RNA-Seq,Mus musculus,6|6,"ORDO:A rare genetic disease characterized by intellectual disability, developmental delay, language deficits, and cardiac arrhythmia (most commonly sick sinus syndrome). Additional reported features include epilepsy, hypotonia, retinal abnormalities, nystagmus, attention deficit hyperactivity disorder, autism, and gastroesophageal reflux. The severity of the phenotype is highly variable." DSA03935,GSE156898,GPL17021,65,Intellectual Developmental Disorder With Cardiac Arrhythmia,C4310682,Cerebellum,GEO,RNA-Seq,Mus musculus,6|6,"ORDO:A rare genetic disease characterized by intellectual disability, developmental delay, language deficits, and cardiac arrhythmia (most commonly sick sinus syndrome). Additional reported features include epilepsy, hypotonia, retinal abnormalities, nystagmus, attention deficit hyperactivity disorder, autism, and gastroesophageal reflux. The severity of the phenotype is highly variable." DSA03936,GSE156898,GPL17021,31,Intellectual Developmental Disorder With Cardiac Arrhythmia,C4310682,Cerebral cortex,GEO,RNA-Seq,Mus musculus,6|6,"ORDO:A rare genetic disease characterized by intellectual disability, developmental delay, language deficits, and cardiac arrhythmia (most commonly sick sinus syndrome). Additional reported features include epilepsy, hypotonia, retinal abnormalities, nystagmus, attention deficit hyperactivity disorder, autism, and gastroesophageal reflux. The severity of the phenotype is highly variable." DSA03937,GSE156898,GPL17021,114,Intellectual Developmental Disorder With Cardiac Arrhythmia,C4310682,Hippocampus,GEO,RNA-Seq,Mus musculus,6|6,"ORDO:A rare genetic disease characterized by intellectual disability, developmental delay, language deficits, and cardiac arrhythmia (most commonly sick sinus syndrome). Additional reported features include epilepsy, hypotonia, retinal abnormalities, nystagmus, attention deficit hyperactivity disorder, autism, and gastroesophageal reflux. The severity of the phenotype is highly variable." DSA03938,GSE156898,GPL17021,8,Intellectual Developmental Disorder With Cardiac Arrhythmia,C4310682,,GEO,RNA-Seq,Mus musculus,6|6,"ORDO:A rare genetic disease characterized by intellectual disability, developmental delay, language deficits, and cardiac arrhythmia (most commonly sick sinus syndrome). Additional reported features include epilepsy, hypotonia, retinal abnormalities, nystagmus, attention deficit hyperactivity disorder, autism, and gastroesophageal reflux. The severity of the phenotype is highly variable." DSA03939,GSE156898,GPL17021,3,Intellectual Developmental Disorder With Cardiac Arrhythmia,C4310682,,GEO,RNA-Seq,Mus musculus,6|6,"ORDO:A rare genetic disease characterized by intellectual disability, developmental delay, language deficits, and cardiac arrhythmia (most commonly sick sinus syndrome). Additional reported features include epilepsy, hypotonia, retinal abnormalities, nystagmus, attention deficit hyperactivity disorder, autism, and gastroesophageal reflux. The severity of the phenotype is highly variable." DSA03940,GSE156906,GPL24676,995,Obesity,C0028754,Subcutaneous adipose tissue,GEO,RNA-Seq,Homo sapiens,25|27,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA03941,GSE156993,GPL570,1,Type 2 Diabetes Mellitus,C0011847,,GEO,Microarray,Homo sapiens,6|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA03942,GSE156993,GPL570,0,Type 2 Diabetes Mellitus,C0011847,,GEO,Microarray,Homo sapiens,6|7,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA03943,GSE156993,GPL570,0,Dyslipidemia,C0242339,,GEO,Microarray,Homo sapiens,6|6,HPO:Any deviation from the normal concentration of a lipid in the blood circulation. DSA03944,GSE156993,GPL570,0,Periodontitis,C0031099,,GEO,Microarray,Homo sapiens,6|6,"EFO:Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology)" DSA03945,GSE157047,GPL16791|GPL20301,1000,Rheumatoid Arthritis,C0003873,Blood,GEO,RNA-Seq,Homo sapiens,3|4,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA03946,GSE157047,GPL16791|GPL20301,1000,Rheumatoid Arthritis,C0003873,Blood,GEO,RNA-Seq,Homo sapiens,4|4,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA03947,GSE157047,GPL16791|GPL20301,1000,Rheumatoid Arthritis,C0003873,Blood,GEO,RNA-Seq,Homo sapiens,5|4,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA03948,GSE157047,GPL16791|GPL20301,43,Rheumatoid Arthritis,C0003873,Sinovial fluid,GEO,RNA-Seq,Homo sapiens,3|3,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA03949,GSE157047,GPL16791|GPL20301,47,Rheumatoid Arthritis,C0003873,Sinovial fluid,GEO,RNA-Seq,Homo sapiens,3|3,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA03950,GSE157047,GPL16791|GPL20301,154,Rheumatoid Arthritis,C0003873,Sinovial fluid,GEO,RNA-Seq,Homo sapiens,3|2,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA03951,GSE157057,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,5|5,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA03952,GSE157057,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,5|1,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA03953,GSE157057,GPL24676,17,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,2|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA03954,GSE157057,GPL24676,10,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,2|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA03955,GSE157148,GPL17303,8,Pre-Eclampsia,C0032914,Whole blood,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA03956,GSE157157,GPL16791|GPL24676,1000,Pulmonary Atresia With Intact Ventricular Septum,C0344975,,GEO,scRNA-Seq,Homo sapiens,2|2,"MONDO:Pulmonary atresia with intact ventricular septum (PA-IVS) is a rare form of cyanotic congenital heart malformation characterized by severe cyanosis and tachypnea. PA-IVS presents significant morphologic diversity: at the end of the spectrum are patients with a mildly hypoplastic and tripartite right ventricle (RV) and mild tricuspid valve (TV) hypoplasia, and at the other end are patients with severe RV and TV hypoplasia, often with RV-dependent coronary circulation." DSA03957,GSE157157,GPL16791|GPL24676,1000,Pulmonary Atresia With Intact Ventricular Septum,C0344975,,GEO,scRNA-Seq,Homo sapiens,2|2,"MONDO:Pulmonary atresia with intact ventricular septum (PA-IVS) is a rare form of cyanotic congenital heart malformation characterized by severe cyanosis and tachypnea. PA-IVS presents significant morphologic diversity: at the end of the spectrum are patients with a mildly hypoplastic and tripartite right ventricle (RV) and mild tricuspid valve (TV) hypoplasia, and at the other end are patients with severe RV and TV hypoplasia, often with RV-dependent coronary circulation." DSA03958,GSE157157,GPL16791|GPL24676,1000,Pulmonary Atresia With Intact Ventricular Septum,C0344975,,GEO,scRNA-Seq,Homo sapiens,2|2,"MONDO:Pulmonary atresia with intact ventricular septum (PA-IVS) is a rare form of cyanotic congenital heart malformation characterized by severe cyanosis and tachypnea. PA-IVS presents significant morphologic diversity: at the end of the spectrum are patients with a mildly hypoplastic and tripartite right ventricle (RV) and mild tricuspid valve (TV) hypoplasia, and at the other end are patients with severe RV and TV hypoplasia, often with RV-dependent coronary circulation." DSA03959,GSE157159,GPL24676,1000,Sjogren's Syndrome,C1527336,Salivary gland,GEO,RNA-Seq,Homo sapiens,8|9,DO:An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. DSA03960,GSE157205,GPL18573,1000,Acute Ischemic Heart Disease,C1510446,Heart,GEO,RNA-Seq,Homo sapiens,4|6,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA03961,GSE157236,GPL16791,64,Melanoma,C0025202,,GEO,RNA-Seq,Homo sapiens,4|5,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA03962,GSE7897,GPL1261,1000,Lymphoma,C0024299,,GEO,Microarray,Mus musculus,10|25,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA03963,GSE157293,GPL16791,83,Lupus Nephritis,C0024143,Kidney,GEO,RNA-Seq,Homo sapiens,3|3,DO:A glomerulonephritis that is characterized by inflammation of the kidneys resulting from systemic lupus erythematosus. DSA03964,GSE157331,GPL23038,4,Diabetes Mellitus,C0011849,Myocardium,GEO,Microarray,Mus musculus,4|4,"DO:A glucose metabolism disease that is characterized by chronic hyperglycaemia with disturbances of carbohydrate, fat and protein metabolism resulting from defects in insulin secretion, insulin action, or both." DSA03965,GSE8249,GPL1261,1,Female Infertility,C0021361,Ovary,GEO,Microarray,Mus musculus,9|6,EFO:Diminished or absent ability of a female to achieve conception. DSA03966,GSE9355,GPL1261,1000,Secretory Breast Carcinoma,C0334371,Breast,GEO,Microarray,Mus musculus,5|34,DO:A breast adenocarcinoma that has_material_basis_in cells with abundant granular or clear vacuolated cytoplasm. DSA03967,GSE157355,GPL17077,40,Melanoma,C0025202,Lymph node,GEO,Microarray,Homo sapiens,4|4,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA03968,GSE157356,GPL21103,130,Mandibulofacial Dysostosis-Microcephaly Syndrome,C1864652,Cranial nerve ganglia,GEO,RNA-Seq,Mus musculus,3|3,"DO:A syndrome characterized by progressive microcephaly, micrognathia, microtia, dysplastic ears, preauricular skin tags, speech delay, significant developmental delay, midface and malar hypoplasia." DSA03969,GSE157356,GPL21103,515,Mandibulofacial Dysostosis-Microcephaly Syndrome,C1864652,Cranial nerve ganglia,GEO,RNA-Seq,Mus musculus,3|3,"DO:A syndrome characterized by progressive microcephaly, micrognathia, microtia, dysplastic ears, preauricular skin tags, speech delay, significant developmental delay, midface and malar hypoplasia." DSA03970,GSE157376,GPL18573,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,scRNA-Seq,Homo sapiens,5|5,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA03971,GSE157379,GPL19057,1000,Pulmonary Fibrosis,C0034069,Lung,GEO,scRNA-Seq,Mus musculus,3|3,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA03972,GSE157440,GPL16791|GPL17021,30,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,RNA-Seq,Mus musculus,3|3,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA03973,GSE9355,GPL1261,1000,Secretory Breast Carcinoma,C0334371,Breast,GEO,Microarray,Mus musculus,3|34,DO:A breast adenocarcinoma that has_material_basis_in cells with abundant granular or clear vacuolated cytoplasm. DSA03974,GSE12610,GPL1261,0,Diabetic Retinopathy,C0011884,Retina,GEO,Microarray,Mus musculus,2|3,"EFO:Disease of the RETINA as a complication of DIABETES MELLITUS. It is characterized by the progressive microvascular complications, such as ANEURYSM, interretinal EDEMA, and intraocular PATHOLOGIC NEOVASCULARIZATION." DSA03975,GSE157509,GPL16791,1000,Bipolar Disorder,C0005586,,GEO,RNA-Seq,Homo sapiens,7|10,DO:A mood disorder that involves alternating periods of mania and depression. DSA03976,GSE157526,GPL24676,1000,COVID-19,D8888888,,GEO,scRNA-Seq,Homo sapiens,1|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA03977,GSE157538,GPL20301,1000,Chronic Graft-Versus-Host Disease,C0867389,Skin,GEO,RNA-Seq,Homo sapiens,6|8,"MONDO:Chronic graft versus host disease (GVHD) is a complication that can occur after a stem cell or bone marrow transplant in which the newly transplanted donor cells attack the transplant recipient's body. Symptoms may include skin rash, mouth sores, dry eyes, liver inflammation, development of scar tissue in the skin and joints, and damage to the lungs. The exact cause of chronic GVHD is unknown.It likely results from a complex immune-mediated interaction between the donor and recipient cells.Chronic GVHD is treated with prednisone or other similar anti-inflammatory or immunosuppressive medications." DSA03978,GSE157538,GPL20301,1000,Chronic Graft-Versus-Host Disease,C0867389,Skin,GEO,RNA-Seq,Homo sapiens,6|5,"MONDO:Chronic graft versus host disease (GVHD) is a complication that can occur after a stem cell or bone marrow transplant in which the newly transplanted donor cells attack the transplant recipient's body. Symptoms may include skin rash, mouth sores, dry eyes, liver inflammation, development of scar tissue in the skin and joints, and damage to the lungs. The exact cause of chronic GVHD is unknown.It likely results from a complex immune-mediated interaction between the donor and recipient cells.Chronic GVHD is treated with prednisone or other similar anti-inflammatory or immunosuppressive medications." DSA03979,GSE11343,GPL1261,0,Diabetic Kidney Disease,C0011881,Peripheral Nerve,GEO,Microarray,Mus musculus,4|5,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA03980,GSE157627,GPL24247,1000,Pneumocystis Pneumonia,C1535939,Lung,GEO,scRNA-Seq,Mus musculus,1|1,"DO:An opportunistic mycosis that is located in lungs, but can also occur in eyes, ears, skin, thyroid, pituitary, palate, parathyroid, esophagus, pleura, heart, liver, spleen, small intestine, adrenals, kidneys, bone marrow, and lymph nodes, has_material_basis_in Pneumocystis jirovecii that effects interstitial and alveolar tissues and has symptom nonproductive cough, has symptom shortness of breath, and has symptom fever." DSA03981,GSE157627,GPL24247,1000,Pneumocystis Pneumonia,C1535939,Lung,GEO,scRNA-Seq,Mus musculus,1|1,"DO:An opportunistic mycosis that is located in lungs, but can also occur in eyes, ears, skin, thyroid, pituitary, palate, parathyroid, esophagus, pleura, heart, liver, spleen, small intestine, adrenals, kidneys, bone marrow, and lymph nodes, has_material_basis_in Pneumocystis jirovecii that effects interstitial and alveolar tissues and has symptom nonproductive cough, has symptom shortness of breath, and has symptom fever." DSA03982,GSE157627,GPL24247,1000,Pneumocystis Pneumonia,C1535939,Lung,GEO,scRNA-Seq,Mus musculus,1|1,"DO:An opportunistic mycosis that is located in lungs, but can also occur in eyes, ears, skin, thyroid, pituitary, palate, parathyroid, esophagus, pleura, heart, liver, spleen, small intestine, adrenals, kidneys, bone marrow, and lymph nodes, has_material_basis_in Pneumocystis jirovecii that effects interstitial and alveolar tissues and has symptom nonproductive cough, has symptom shortness of breath, and has symptom fever." DSA03983,GSE157627,GPL24247,1000,Pneumocystis Pneumonia,C1535939,Lung,GEO,scRNA-Seq,Mus musculus,1|1,"DO:An opportunistic mycosis that is located in lungs, but can also occur in eyes, ears, skin, thyroid, pituitary, palate, parathyroid, esophagus, pleura, heart, liver, spleen, small intestine, adrenals, kidneys, bone marrow, and lymph nodes, has_material_basis_in Pneumocystis jirovecii that effects interstitial and alveolar tissues and has symptom nonproductive cough, has symptom shortness of breath, and has symptom fever." DSA03984,GSE157627,GPL24247,1000,Pneumocystis Pneumonia,C1535939,Lung,GEO,scRNA-Seq,Mus musculus,1|1,"DO:An opportunistic mycosis that is located in lungs, but can also occur in eyes, ears, skin, thyroid, pituitary, palate, parathyroid, esophagus, pleura, heart, liver, spleen, small intestine, adrenals, kidneys, bone marrow, and lymph nodes, has_material_basis_in Pneumocystis jirovecii that effects interstitial and alveolar tissues and has symptom nonproductive cough, has symptom shortness of breath, and has symptom fever." DSA03985,GSE157671,GPL11154,16,Coccidiosis Granuloma,,Lung,GEO,RNA-Seq,Homo sapiens,3|3, DSA03986,GSE157671,GPL11154,680,Sarcoidosis,C0036202,Lung,GEO,RNA-Seq,Homo sapiens,3|6,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA03987,GSE157671,GPL11154,273,Sarcoidosis,C0036202,Lymph node,GEO,RNA-Seq,Homo sapiens,3|12,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA03988,GSE157671,GPL11154,380,Tuberculosis Granuloma,,Lymph node,GEO,RNA-Seq,Homo sapiens,3|4, DSA03989,GSE157712,GPL20301,1000,Chronic Kidney Disease,C1561643,Muscle,GEO,RNA-Seq,Homo sapiens,7|7,DO:A kidney failure that is characterized by the gradual loss of kidney function. DSA03990,GSE157737,GPL6244,0,Breast Cancer,C0678222,,GEO,Microarray,Homo sapiens,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03991,GSE157737,GPL6244,0,Sepsis,C0243026,,GEO,Microarray,Homo sapiens,3|3,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA03992,GSE157737,GPL6244,1000,Breast Cancer,C0678222,,GEO,Microarray,Homo sapiens,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA03993,GSE157737,GPL6244,1000,Sepsis,C0243026,,GEO,Microarray,Homo sapiens,3|3,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA03994,GSE11343,GPL1261,0,Diabetic Kidney Disease,C0011881,Peripheral Nerve,GEO,Microarray,Mus musculus,4|5,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA03995,GSE9038,GPL1261,38,Huntington's Disease,C0020179,Striatum,GEO,Microarray,Mus musculus,12|12,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA03996,GSE157769,GPL17021,1000,Thymic Lymphoma,C1336745,,GEO,RNA-Seq,Mus musculus,3|14,DO:A thymus cancer that arises from the thymus. DSA03997,GSE157777,GPL24247,1000,Bile Duct Paucity,C1855284,Liver,GEO,RNA-Seq,Mus musculus,3|3,HPO:Atresia in the intrahepatic bile duct. DSA03998,GSE157777,GPL24247,1000,Bile Duct Paucity,C1855284,Liver,GEO,RNA-Seq,Mus musculus,3|3,HPO:Atresia in the intrahepatic bile duct. DSA03999,GSE19780,GPL1261,0,Huntington's Disease,C0020179,Striatum,GEO,Microarray,Mus musculus,6|6,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA04000,GSE157789,GPL24676,1000,COVID-19,D8888888,,GEO,scRNA-Seq,Homo sapiens,2|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04001,GSE157789,GPL24676,1000,COVID-19,D8888888,,GEO,scRNA-Seq,Homo sapiens,2|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04002,GSE157789,GPL24676,1000,COVID-19,D8888888,,GEO,scRNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04003,GSE157789,GPL24676,1000,COVID-19,D8888888,,GEO,scRNA-Seq,Homo sapiens,3|6,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04004,GSE18064,GPL1261,6,Rift Valley Fever,C0035613,,GEO,Microarray,Mus musculus,3|3,"DO:A viral infectious disease that results_in infection, has_material_basis_in Rift Valley fever virus, which is transmitted_by Aedes mosquitoes. The virus affects domestic animals (cattle, buffalo, sheep, goats, and camels) and humans. The infection has_symptom jaundice, has_symptom vomiting blood, has_symptom passing blood in the feces, has_symptom ecchymoses (caused by bleeding in the skin), has_symptom bleeding from the nose or gums, has_symptom menorrhagia and has_symptom bleeding from venepuncture sites." DSA04005,GSE157829,GPL16791,1000,Acquired Immunodeficiency Syndrome,C0001175,,GEO,scRNA-Seq,Homo sapiens,1|6,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA04006,GSE157840,GPL20301,1000,Systemic Sclerosis [Scleroderma],C2364016,,GEO,RNA-Seq,Homo sapiens,4|5, DSA04007,GSE157840,GPL20301,19,Systemic Sclerosis [Scleroderma],C2364016,,GEO,RNA-Seq,Homo sapiens,4|5, DSA04008,GSE157948,GPL18573,1000,Herpes Simplex Virus Encephalitis,C0276226,,GEO,RNA-Seq,Homo sapiens,2|2,"HPO:Infection of the brain parenchyma with herpes simplex virus, resulting in inflammation of the brain parenchyma with neurologic dysfunction." DSA04009,GSE157948,GPL18573,1000,Herpes Simplex Virus Encephalitis,C0276226,,GEO,RNA-Seq,Homo sapiens,2|2,"HPO:Infection of the brain parenchyma with herpes simplex virus, resulting in inflammation of the brain parenchyma with neurologic dysfunction." DSA04010,GSE157948,GPL18573,1000,Herpes Simplex Virus Encephalitis,C0276226,,GEO,RNA-Seq,Homo sapiens,2|2,"HPO:Infection of the brain parenchyma with herpes simplex virus, resulting in inflammation of the brain parenchyma with neurologic dysfunction." DSA04011,GSE157948,GPL18573,1000,Herpes Simplex Virus Encephalitis,C0276226,,GEO,RNA-Seq,Homo sapiens,2|2,"HPO:Infection of the brain parenchyma with herpes simplex virus, resulting in inflammation of the brain parenchyma with neurologic dysfunction." DSA04012,GSE157948,GPL18573,1000,Herpes Simplex Virus Encephalitis,C0276226,,GEO,RNA-Seq,Homo sapiens,2|2,"HPO:Infection of the brain parenchyma with herpes simplex virus, resulting in inflammation of the brain parenchyma with neurologic dysfunction." DSA04013,GSE157959,GPL11154,172,Acute Graft Versus Host Disease,C0856825,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|4,"MONDO:A syndrome of immunologically mediated tissue damage that may occur following an allogeneic transplant, usually affecting the skin, liver, and GI tract. The onset is usually within one hundred days of transplantation or immunologic manipulation." DSA04014,GSE157959,GPL11154,239,Acute Graft Versus Host Disease,C0856825,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|4,"MONDO:A syndrome of immunologically mediated tissue damage that may occur following an allogeneic transplant, usually affecting the skin, liver, and GI tract. The onset is usually within one hundred days of transplantation or immunologic manipulation." DSA04015,GSE157960,GPL19057,1000,Tumor of Fallopian Tube,C0015558,Oviduct,GEO,RNA-Seq,Mus musculus,3|3,DO:A fallopian tube cancer that is located_in the fallopian tube. DSA04016,GSE157960,GPL19057,1000,Tumor of Fallopian Tube,C0015558,Oviduct,GEO,RNA-Seq,Mus musculus,3|3,DO:A fallopian tube cancer that is located_in the fallopian tube. DSA04017,GSE157978,GPL20795,224,Systemic Lupus Erythematosus,C0024141,Peripheral blood,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA04018,GSE157987,GPL19057,88,Gaucher Disease,C0017205,Brain,GEO,RNA-Seq,Mus musculus,3|4,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA04019,GSE157987,GPL19057,1000,Gaucher Disease,C0017205,Brain,GEO,RNA-Seq,Mus musculus,3|3,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA04020,GSE157991,GPL19057,81,Gaucher Disease,C0017205,Brain,GEO,RNA-Seq,Mus musculus,3|3,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA04021,GSE157991,GPL19057,1000,Gaucher Disease,C0017205,Brain,GEO,RNA-Seq,Mus musculus,3|3,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA04022,GSE157996,GPL18573,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,scRNA-Seq,Homo sapiens,6|6,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA04023,GSE158030,GPL18573,1000,COVID-19,D8888888,Peripheral blood,GEO,scRNA-Seq,Homo sapiens,3|10,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04024,GSE18064,GPL1261,6,Rift Valley Fever,C0035613,,GEO,Microarray,Mus musculus,3|3,"DO:A viral infectious disease that results_in infection, has_material_basis_in Rift Valley fever virus, which is transmitted_by Aedes mosquitoes. The virus affects domestic animals (cattle, buffalo, sheep, goats, and camels) and humans. The infection has_symptom jaundice, has_symptom vomiting blood, has_symptom passing blood in the feces, has_symptom ecchymoses (caused by bleeding in the skin), has_symptom bleeding from the nose or gums, has_symptom menorrhagia and has_symptom bleeding from venepuncture sites." DSA04025,GSE14277,GPL1261,1000,Lung Cancer,C0684249,Lung,GEO,Microarray,Mus musculus,5|3,DO:A respiratory system cancer that is located_in the lung. DSA04026,GSE14277,GPL1261,1000,Lung Cancer,C0684249,Lung,GEO,Microarray,Mus musculus,4|3,DO:A respiratory system cancer that is located_in the lung. DSA04027,GSE10162,GPL1261,67,Dent Disease,C0878681,Kidney,GEO,Microarray,Mus musculus,3|3,"DO:A renal tubular transport disease that is characterized by tubular proteinuria, hypercalciuria, calcium nephrolithiasis, nephrocalcinosis and chronic kidney failure and has_material_basis_in X-linked recessive inheritance of mutations in the CLCN5 gene or OCRL1 gene." DSA04028,GSE158112,GPL21103,175,Psoriasis,C0033860,Skin,GEO,RNA-Seq,Mus musculus,2|2,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA04029,GSE158140,GPL16791,104,Shwachman-Diamond Syndrome,C0272170,,GEO,RNA-Seq,Homo sapiens,9|12,"DO:A syndrome characterized by exocrine pancreatic insufficiency, bone marrow failure and skeletal abnormalities." DSA04030,GSE158140,GPL16791,409,Shwachman-Diamond Syndrome,C0272170,,GEO,RNA-Seq,Homo sapiens,12|29,"DO:A syndrome characterized by exocrine pancreatic insufficiency, bone marrow failure and skeletal abnormalities." DSA04031,GSE158163,GPL16791,1000,Pharyngitis,C0031350,Whole blood,GEO,RNA-Seq,Homo sapiens,3|10,"DO:An upper respiratory tract disease involving inflammation of the throat or pharynx resulting from bacterial, viral, fungal infections or irritants like pollutants or chemical substances and smoking. The infection is often referred to as sore throat. The symptoms include pain during swallowing, enlarged tonsils coated with a white discharge, runny nose, cough and slight fever." DSA04032,GSE158163,GPL16791,1000,Pharyngitis,C0031350,Whole blood,GEO,RNA-Seq,Homo sapiens,13|10,"DO:An upper respiratory tract disease involving inflammation of the throat or pharynx resulting from bacterial, viral, fungal infections or irritants like pollutants or chemical substances and smoking. The infection is often referred to as sore throat. The symptoms include pain during swallowing, enlarged tonsils coated with a white discharge, runny nose, cough and slight fever." DSA04033,GSE158163,GPL16791,1000,Pharyngitis,C0031350,Whole blood,GEO,RNA-Seq,Homo sapiens,5|10,"DO:An upper respiratory tract disease involving inflammation of the throat or pharynx resulting from bacterial, viral, fungal infections or irritants like pollutants or chemical substances and smoking. The infection is often referred to as sore throat. The symptoms include pain during swallowing, enlarged tonsils coated with a white discharge, runny nose, cough and slight fever." DSA04034,GSE158163,GPL16791,527,Pharyngitis,C0031350,Whole blood,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An upper respiratory tract disease involving inflammation of the throat or pharynx resulting from bacterial, viral, fungal infections or irritants like pollutants or chemical substances and smoking. The infection is often referred to as sore throat. The symptoms include pain during swallowing, enlarged tonsils coated with a white discharge, runny nose, cough and slight fever." DSA04035,GSE158163,GPL16791,479,Pharyngitis,C0031350,Whole blood,GEO,RNA-Seq,Homo sapiens,13|3,"DO:An upper respiratory tract disease involving inflammation of the throat or pharynx resulting from bacterial, viral, fungal infections or irritants like pollutants or chemical substances and smoking. The infection is often referred to as sore throat. The symptoms include pain during swallowing, enlarged tonsils coated with a white discharge, runny nose, cough and slight fever." DSA04036,GSE158163,GPL16791,368,Pharyngitis,C0031350,Whole blood,GEO,RNA-Seq,Homo sapiens,5|3,"DO:An upper respiratory tract disease involving inflammation of the throat or pharynx resulting from bacterial, viral, fungal infections or irritants like pollutants or chemical substances and smoking. The infection is often referred to as sore throat. The symptoms include pain during swallowing, enlarged tonsils coated with a white discharge, runny nose, cough and slight fever." DSA04037,GSE158163,GPL16791,1000,Pharyngitis,C0031350,Whole blood,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An upper respiratory tract disease involving inflammation of the throat or pharynx resulting from bacterial, viral, fungal infections or irritants like pollutants or chemical substances and smoking. The infection is often referred to as sore throat. The symptoms include pain during swallowing, enlarged tonsils coated with a white discharge, runny nose, cough and slight fever." DSA04038,GSE158163,GPL16791,450,Pharyngitis,C0031350,Whole blood,GEO,RNA-Seq,Homo sapiens,13|3,"DO:An upper respiratory tract disease involving inflammation of the throat or pharynx resulting from bacterial, viral, fungal infections or irritants like pollutants or chemical substances and smoking. The infection is often referred to as sore throat. The symptoms include pain during swallowing, enlarged tonsils coated with a white discharge, runny nose, cough and slight fever." DSA04039,GSE158163,GPL16791,360,Pharyngitis,C0031350,Whole blood,GEO,RNA-Seq,Homo sapiens,5|3,"DO:An upper respiratory tract disease involving inflammation of the throat or pharynx resulting from bacterial, viral, fungal infections or irritants like pollutants or chemical substances and smoking. The infection is often referred to as sore throat. The symptoms include pain during swallowing, enlarged tonsils coated with a white discharge, runny nose, cough and slight fever." DSA04040,GSE158216,GPL24676,1000,Myotonic Dystrophy 1,C3250443,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA04041,GSE158241,GPL19057,1000,Diet-Induced Obese Non-Alcoholic Steatohepatitis ,,Liver,GEO,scRNA-Seq,Mus musculus,4|2, DSA04042,GSE158264,GPL16686,0,Amyotrophic Lateral Sclerosis,C0002736,,GEO,Microarray,Homo sapiens,4|4,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA04043,GSE158264,GPL16686,0,Amyotrophic Lateral Sclerosis,C0002736,,GEO,Microarray,Homo sapiens,4|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA04044,GSE158312,GPL18573,276,Stroke,C0948008,Whole blood,GEO,RNA-Seq,Homo sapiens,4|20,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA04045,GSE158356,GPL24247,747,Pancreatic Cancer,C0235974,,GEO,scRNA-Seq,Mus musculus,1|1,DO:An endocrine gland cancer located_in the pancreas. DSA04046,GSE158356,GPL24247,620,Pancreatic Cancer,C0235974,,GEO,scRNA-Seq,Mus musculus,1|1,DO:An endocrine gland cancer located_in the pancreas. DSA04047,GSE158384,GPL16570,0,Global Glomerulosclerosis,C1865276,Glomerulus,GEO,Microarray,Mus musculus,2|2,"HPO:Obliteration of the glomerular capillary lumen by increased collagenous matrix, with or without hyalinosis or foam cells. Sclerosis involves 100% of the glomerular tuft. Relative to other patent glomeruli in the sample, glomerular size is preserved, or increased/decreased by no more than 50%." DSA04048,GSE158395,GPL24676,1000,Keloid,C0022548,Skin,GEO,RNA-Seq,Homo sapiens,6|7,"EFO:An irregularly shaped, elevated mark on the skin caused by deposits of excessive amounts of collagen during wound healing. It extends beyond the original boundaries of the wound and may enlarge progressively." DSA04049,GSE158415,GPL23479,1000,Myocardial Infarction,C0027051,Heart,GEO,RNA-Seq,Mus musculus,6|5,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA04050,GSE19286,GPL1261,0,Atherosclerosis,C0004153,Aorta,GEO,Microarray,Mus musculus,2|2,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA04051,GSE15852,GPL96,1000,Mucinous Carcinoma,C0007130,Breast,GEO,Microarray,Homo sapiens,43|43,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which produce mucin." DSA04052,GSE158558,GPL20301,1000,Intracranial Aneurysm,C0007766,Arterial vessel,GEO,RNA-Seq,Homo sapiens,4|4,EFO:Outpouching of BASILAR ARTERY at the base of the skull. The basilar artery is the most important artery in the posterior cerebral circulation. DSA04053,GSE11494,GPL1261,0,Pharyngitis,C0031350,,GEO,Microarray,Mus musculus,4|12,"DO:An upper respiratory tract disease involving inflammation of the throat or pharynx resulting from bacterial, viral, fungal infections or irritants like pollutants or chemical substances and smoking. The infection is often referred to as sore throat. The symptoms include pain during swallowing, enlarged tonsils coated with a white discharge, runny nose, cough and slight fever." DSA04054,GSE6461,GPL1261,1000,Rhabdomyosarcoma,C0035412,,GEO,Microarray,Mus musculus,4|5,DO:A skeletal muscle cancer that arise from skeletal muscle progenitors. DSA04055,GSE6399,GPL1261,4,Striated Muscle Laminopathies,,Heart,GEO,Microarray,Mus musculus,8|6, DSA04056,GSE6980,GPL1261,1000,Multiple Myeloma,C0026764,,GEO,Microarray,Mus musculus,4|6,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA04057,GSE6980,GPL1261,857,Multiple Myeloma,C0026764,,GEO,Microarray,Mus musculus,5|6,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA04058,GSE10006,GPL570,575,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,12|14,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA04059,GSE10006,GPL570,756,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,12|13,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA04060,GSE158712,GPL20795|GPL23227,81,Hemorrhagic Fever With Renal Syndrome,C0019101,,GEO,RNA-Seq,Homo sapiens,3|27,"DO:A viral infectious disease that is a hemorrhagic fever, located in kidney, has_material_basis_in Hantaan virus, has_material_basis_in Dobrava-Belgrade orthohantavirus has_material_basis_in Seoul virus, or has_material_basis_in Puumala virus, which are carried and transmitted by rodents. The infection has symptom headache, has symptom fever, has symptom muscle pains, has symptom facial flush, has symptom petechiae, has symptom proteinuria, and has symptom renal failure." DSA04061,GSE158752,GPL18573,1000,Asthma,C0004096,Lung,GEO,RNA-Seq,Homo sapiens,17|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA04062,GSE158752,GPL18573,687,Asthma,C0004096,Lung,GEO,RNA-Seq,Homo sapiens,17|25,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA04063,GSE158754,GPL21290,625,CTBP1 Mutations,C0600433,,GEO,RNA-Seq,Homo sapiens,6|6,HPO:Poor anticoagulant response to activated protein C. A plasma is termed 'APC resistant' when the addition of exogenous APC fails to prolong its clotting time in an activated partial thromboplastin time assay. DSA04064,GSE158799,GPL18635,404,Retinopathy,C0035309,Retina,GEO,RNA-Seq,Mus musculus,2|2,DO:An eye disease that is located_in the retina. DSA04065,GSE158799,GPL18635,1000,Retinopathy,C0035309,Retina,GEO,RNA-Seq,Mus musculus,3|3,DO:An eye disease that is located_in the retina. DSA04066,GSE158799,GPL18635,1000,Retinopathy,C0035309,Retina,GEO,RNA-Seq,Mus musculus,3|3,DO:An eye disease that is located_in the retina. DSA04067,GSE158807,GPL21163,73,Tuberculosis,C0041296,Whole blood,GEO,Microarray,Mus musculus,7|13,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA04068,GSE158807,GPL21163,1000,Tuberculosis,C0041296,Whole blood,GEO,Microarray,Mus musculus,7|29,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA04069,GSE158807,GPL21163,1000,Tuberculosis,C0041296,Whole blood,GEO,Microarray,Mus musculus,7|25,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA04070,GSE158859,GPL21103,278,Inflammation,C0021368,Colon,GEO,scRNA-Seq,Mus musculus,1|1,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA04071,GSE158923,GPL20301,1000,Granuloma Annulare,C0085074,Skin,GEO,RNA-Seq,Homo sapiens,2|5,"MONDO:Granuloma annulare is a long-term (chronic) skin disease consisting of a rash with reddish bumps arranged in a circle or ring. The most commonly affected areas are the forearms, hands and feet. The lesions associated with granuloma annulare usually resolve without treatment. Strong steroids (applied as a cream or injection) are sometimes used to clear the rash more quickly. Most symptoms will disappear within 2 years (even without treatment), but recurrence is common. The underlying cause of granuloma annulare is unknown." DSA04072,GSE158924,GPL20301,1000,Granuloma Annulare,C0085074,Skin,GEO,scRNA-Seq,Homo sapiens,3|3,"MONDO:Granuloma annulare is a long-term (chronic) skin disease consisting of a rash with reddish bumps arranged in a circle or ring. The most commonly affected areas are the forearms, hands and feet. The lesions associated with granuloma annulare usually resolve without treatment. Strong steroids (applied as a cream or injection) are sometimes used to clear the rash more quickly. Most symptoms will disappear within 2 years (even without treatment), but recurrence is common. The underlying cause of granuloma annulare is unknown." DSA04073,GSE10334,GPL570,1000,Periodontitis,C0031099,Gingiva,GEO,Microarray,Homo sapiens,64|183,"EFO:Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology)" DSA04074,GSE158951,GPL23479,0,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,1|1,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA04075,GSE158986,GPL16791|GPL29219,0,Chagas Disease,C0041234,,GEO,RNA-Seq,Homo sapiens,6|6,DO:A parasitic protozoa infectious disease that involves infection caused by parasitic protozoan of the genus Trypanosoma in animals and humans. DSA04076,GSE159007,GPL20301,167,Collagenous Colitis,C0238067,Colon,GEO,RNA-Seq,Homo sapiens,9|8,DO:A colitis characterized by a distinctive thickening of the subepithelial collagen table. DSA04077,GSE159007,GPL20301,562,Collagenous Colitis,C0238067,Colon,GEO,RNA-Seq,Homo sapiens,9|9,DO:A colitis characterized by a distinctive thickening of the subepithelial collagen table. DSA04078,GSE159008,GPL20301,258,Collagenous Colitis,C0238067,Colon,GEO,RNA-Seq,Homo sapiens,13|9,DO:A colitis characterized by a distinctive thickening of the subepithelial collagen table. DSA04079,GSE159008,GPL20301,768,Collagenous Colitis,C0238067,Colon,GEO,RNA-Seq,Homo sapiens,13|9,DO:A colitis characterized by a distinctive thickening of the subepithelial collagen table. DSA04080,GSE159062,GPL13112|GPL15228,90,Glycogen Storage Disease,C0017919,Engineered skeletal muscle,GEO,RNA-Seq,Homo sapiens,4|3,DO:A glycogen storage disease IX that is characterized by X-linked inheritance of variable exercise-induced muscle weakness or stiffness that has_material_basis_in mutation in the PHKA1 gene on chromosome Xq13. DSA04081,GSE10406,GPL570,118,Chronic Rhinosinusitis,C0149516,Sinus mucosa,GEO,Microarray,Homo sapiens,9|5,EFO:An acute or chronic inflammatory process affecting the mucous membranes of any sinus cavity. DSA04082,GSE159225,GPL20795,1000,Multiple Sclerosis,C0026769,Blood,GEO,RNA-Seq,Homo sapiens,20|20,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA04083,GSE159225,GPL20795,1000,Multiple Sclerosis,C0026769,Blood,GEO,RNA-Seq,Homo sapiens,20|10,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA04084,GSE159243,GPL11154,460,Cardiac Hypertrophy,C1383860,Heart,GEO,RNA-Seq,Homo sapiens,5|5,"EFO:an increase in size of the cardiac tissue, not due to increased cell number" DSA04085,GSE159260,GPL18573,1000,Glioma,C0017638,Brain,GEO,RNA-Seq,Homo sapiens,5|14,DO:A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine. DSA04086,GSE159354,GPL20301,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,scRNA-Seq,Homo sapiens,1|1,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA04087,GSE159354,GPL20301,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,scRNA-Seq,Homo sapiens,3|3,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA04088,GSE159354,GPL20301,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,scRNA-Seq,Homo sapiens,3|3,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA04089,GSE159354,GPL20301,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,scRNA-Seq,Homo sapiens,3|4,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA04090,GSE159354,GPL20301,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,scRNA-Seq,Homo sapiens,3|4,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA04091,GSE159354,GPL20301,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,scRNA-Seq,Homo sapiens,2|3,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA04092,GSE159354,GPL20301,1000,Systemic Sclerosis With Lung Involvement,C0339904,Lung,GEO,scRNA-Seq,Homo sapiens,3|2,HPO:It is a bilateral reticular pattern of linear or lineonodular densities that are most pronounced in basilar portions of the lungs on standard chest x-ray. It is the third minor criterion for scleroderma diagnosis. DSA04093,GSE159354,GPL20301,1000,Systemic Sclerosis With Lung Involvement,C0339904,Lung,GEO,scRNA-Seq,Homo sapiens,3|3,HPO:It is a bilateral reticular pattern of linear or lineonodular densities that are most pronounced in basilar portions of the lungs on standard chest x-ray. It is the third minor criterion for scleroderma diagnosis. DSA04094,GSE159354,GPL20301,1000,Systemic Sclerosis With Lung Involvement,C0339904,Lung,GEO,scRNA-Seq,Homo sapiens,3|3,HPO:It is a bilateral reticular pattern of linear or lineonodular densities that are most pronounced in basilar portions of the lungs on standard chest x-ray. It is the third minor criterion for scleroderma diagnosis. DSA04095,GSE159354,GPL20301,1000,Systemic Sclerosis With Lung Involvement,C0339904,Lung,GEO,scRNA-Seq,Homo sapiens,3|2,HPO:It is a bilateral reticular pattern of linear or lineonodular densities that are most pronounced in basilar portions of the lungs on standard chest x-ray. It is the third minor criterion for scleroderma diagnosis. DSA04096,GSE159354,GPL20301,1000,Systemic Sclerosis With Lung Involvement,C0339904,Lung,GEO,scRNA-Seq,Homo sapiens,1|1,HPO:It is a bilateral reticular pattern of linear or lineonodular densities that are most pronounced in basilar portions of the lungs on standard chest x-ray. It is the third minor criterion for scleroderma diagnosis. DSA04097,GSE159356,GPL19057,1000,Type I Tyrosinemia,C0268490,Liver,GEO,RNA-Seq,Mus musculus,8|16,DO:A tyrosinemia that has_material_basis_in deficiency of the enzyme fumarylacetoacetate hydrolase resulting in an increase in fumarylacetoacetate which inhibits previous steps in tyrosine degradation leading to an accumulation of tyrosine in the body. DSA04098,GSE159392,GPL24676,1000,Pitt-Hopkins Syndrome,C1970431,,GEO,RNA-Seq,Homo sapiens,12|9,"DO:A syndrome characterized by intellectual disability and developmental delay, breathing problems, recurrent seizures, and distinctive facial features and that has_material_basis_in heterozygous de novo mutations in the TCF4 gene in chromosome 18q21." DSA04099,GSE159392,GPL24676,1000,Pitt-Hopkins Syndrome,C1970431,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A syndrome characterized by intellectual disability and developmental delay, breathing problems, recurrent seizures, and distinctive facial features and that has_material_basis_in heterozygous de novo mutations in the TCF4 gene in chromosome 18q21." DSA04100,GSE159417,GPL24676,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,scRNA-Seq,Homo sapiens,1|1,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA04101,GSE159495,GPL16791|GPL18573|GPL24676,1000,Environmental Enteric Dysfunction,,Duodenum,GEO,RNA-Seq,Homo sapiens,24|52, DSA04102,GSE159495,GPL16791|GPL18573|GPL24676,1000,Coeliac Disease,C0007570,Duodenum,GEO,RNA-Seq,Homo sapiens,24|17,"DO:An autoimmune disease of gastrointestinal tract that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite." DSA04103,GSE179209,GPL20301,1000,Hutchinson-Gilford Progeria Syndrome,C0033300,,GEO,RNA-Seq,Homo sapiens,6|3,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA04104,GSE179209,GPL20301,1000,Hutchinson-Gilford Progeria Syndrome,C0033300,,GEO,RNA-Seq,Homo sapiens,6|3,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA04105,GSE179209,GPL20301,1000,Hutchinson-Gilford Progeria Syndrome,C0033300,,GEO,RNA-Seq,Homo sapiens,6|3,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA04106,GSE179209,GPL20301,1000,Hutchinson-Gilford Progeria Syndrome,C0033300,,GEO,RNA-Seq,Homo sapiens,6|3,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA04107,GSE179209,GPL20301,1000,Hutchinson-Gilford Progeria Syndrome,C0033300,,GEO,RNA-Seq,Homo sapiens,6|3,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA04108,GSE179209,GPL20301,1000,Hutchinson-Gilford Progeria Syndrome,C0033300,,GEO,RNA-Seq,Homo sapiens,6|3,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA04109,GSE179221,GPL24676,1000,Monoclonal Gammopathy of Undetermined Significance,C0026470,,GEO,scRNA-Seq,Homo sapiens,4|7,DO:A blood protein disease that is characterized by the presence of an abnormal protein called monoclonal protein in the blood. DSA04110,GSE179221,GPL24676,1000,Waldenstrom Macroglobulinemia,C0024419,,GEO,scRNA-Seq,Homo sapiens,4|7,DO:A B-cell lymphocytic neoplasm characterized by an uncontrolled increase of B-cells. DSA04111,GSE179233,GPL19057,1000,Colitis,C0009319,Cecum,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA04112,GSE179233,GPL19057,1000,Colitis,C0009319,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA04113,GSE179233,GPL19057,50,Colitis,C0009319,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA04114,GSE179233,GPL19057,1000,Colitis,C0009319,Cecum,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA04115,GSE179233,GPL19057,195,Colitis,C0009319,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA04116,GSE179233,GPL19057,204,Colitis,C0009319,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA04117,GSE179285,GPL6480,318,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,23|32,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA04118,GSE179285,GPL6480,1000,Crohn's Disease,C0010346,Colon,GEO,Microarray,Homo sapiens,23|72,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04119,GSE179285,GPL6480,0,Crohn's Disease,C0010346,Colon,GEO,Microarray,Homo sapiens,8|49,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04120,GSE10406,GPL570,225,Chronic Rhinosinusitis,C0149516,Sinus mucosa,GEO,Microarray,Homo sapiens,9|9,EFO:An acute or chronic inflammatory process affecting the mucous membranes of any sinus cavity. DSA04121,GSE10650,GPL570,1000,Colon Cancer,C0699790,Colon,GEO,Microarray,Homo sapiens,2|2,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA04122,GSE10714,GPL570,52,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,3|3,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA04123,GSE10714,GPL570,358,Colorectal Adenoma,C1302401,Colon,GEO,Microarray,Homo sapiens,3|5,"EFO:An adenoma that arises from the colon or rectum. The group of colorectal adenomas includes tubular, villous, and tubulovillous adenomas, traditional serrated adenomas, sessile serrated adenomas/polyps, and familial adenomatous polyposis." DSA04124,GSE179441,GPL19057,65,Graft Versus Host Disease,C0018133,,GEO,RNA-Seq,Mus musculus,3|3,MONDO:An immune system disorder that occurs after allogeneic hematopoietic stem cell transplant and is a reaction of donor immune cells against host tissues. Activated donor T cells damage host epithelial cells after an inflammatory cascade that begins with the preparative regimen. DSA04125,GSE179441,GPL19057,610,Graft Versus Host Disease,C0018133,Hippocampus,GEO,RNA-Seq,Mus musculus,3|3,MONDO:An immune system disorder that occurs after allogeneic hematopoietic stem cell transplant and is a reaction of donor immune cells against host tissues. Activated donor T cells damage host epithelial cells after an inflammatory cascade that begins with the preparative regimen. DSA04126,GSE179445,GPL16686,27,Lung Injury,C0273115,Lung,GEO,Microarray,Homo sapiens,5|5,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA04127,GSE179445,GPL16686,19,Lung Injury,C0273115,Lung,GEO,Microarray,Homo sapiens,5|4,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA04128,GSE10714,GPL570,0,Crohn's Disease,C0010346,Colon,GEO,Microarray,Homo sapiens,3|4,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04129,GSE10714,GPL570,0,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,3|3,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA04130,GSE10714,GPL570,1,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,3|4,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA04131,GSE10714,GPL570,1,Hyperplastic Polyp,C0333983,Colon,GEO,Microarray,Homo sapiens,3|11,"EFO:A polyp found mainly in the stomach and colon. Microscopically, it is characterized by elongated, serrated crypts lined by proliferative epithelium. Hyperplastic polyps are traditionally considered non-neoplastic, but ras mutation is common, clonality has been demonstrated and biochemical abnormalities and epidemiological associations that occur in colorectal adenomas and carcinomas have been found (WHO Tumors of the Digestive System, 2000)." DSA04132,GSE10780,GPL570,1000,Ductal Breast Carcinoma,C1527349,Breast,GEO,Microarray,Homo sapiens,143|42,DO:A breast ductal carcinoma that is characterized by infiltration into the fibrous or fatty tissue of the breast outside of the duct where it originated. DSA04133,GSE10799,GPL570,1000,Lung Adenocarcinoma,C0152013,,GEO,Microarray,Homo sapiens,3|16,DO:A respiratory system cancer that is located_in the lung. DSA04134,GSE179509,GPL18573,70,Breast Cancer,C0678222,Breast,GEO,RNA-Seq,Homo sapiens,2|2,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA04135,GSE10810,GPL570,1000,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,27|31,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA04136,GSE10927,GPL570,714,Adrenocortical Adenoma,C0206667,,GEO,Microarray,Homo sapiens,10|22,DO:An endocrine organ benign neoplasm that is a benign tumor of the glandular type (adenoma) in the adrenal gland. DSA04137,GSE10927,GPL570,1000,Adrenocortical Carcinoma,C0206686,,GEO,Microarray,Homo sapiens,10|33,DO:An adrenal cortex cancer that forms in the outer layer of tissue of the adrenal gland and that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA04138,GSE10961,GPL570,0,Liver Metastatic,C0494165,,GEO,Microarray,Homo sapiens,10|8,"NCI:A malignant neoplasm that has spread to the liver from another (primary) anatomic site. Representative examples include carcinomas, lymphomas, melanomas, or sarcomas." DSA04139,GSE179895,GPL24676,762,Pleomorphic Adenoma Carcinoma,C0344460,Salivary gland,GEO,RNA-Seq,Homo sapiens,5|5,"EFO:A carcinoma that arises from a pleomorphic adenoma in the salivary glands. It usually originates in the parotid gland. Patients usually present with a history of a long-standing tumor mass which grew rapidly in the past few months. Patients with non-invasive or minimally invasive carcinoma have an excellent prognosis. In cases where there is invasion of the surrounding tissues, the clinical course is aggressive." DSA04140,GSE10971,GPL570,1000,High Grade Serous Carcinoma,C3839280,,GEO,Microarray,Homo sapiens,24|13, DSA04141,GSE11151,GPL570,0,Clear Cell Sarcoma of The Kidney,C0334488,Kidney,GEO,Microarray,Homo sapiens,2|1,DO:A kidney sarcoma that has_material_basis_in clear cells that are characterized as cells that look clear when viewed under a microscope. DSA04142,GSE11151,GPL570,0,Collecting Duct Carcinoma,C1266044,Kidney,GEO,Microarray,Homo sapiens,2|2,DO:A renal cell carcinoma that begins in distal collecting ducts of the kidney with a tubulopapillary morphology and intracytoplasmic mucicarminophilic material. DSA04143,GSE11151,GPL570,1000,Chromophobe Renal Cell Carcinoma,C1266042,Kidney,GEO,Microarray,Homo sapiens,2|4,"DO:A renal cell carcinoma that has_material_basis_in chromophobe cell that appear pale when viewed under microscope, but that are larger and display different features than clear cells." DSA04144,GSE11151,GPL570,1000,Chromophobe Renal Cell Carcinoma,C1266042,Kidney,GEO,Microarray,Homo sapiens,2|26,"DO:A renal cell carcinoma that has_material_basis_in chromophobe cell that appear pale when viewed under microscope, but that are larger and display different features than clear cells." DSA04145,GSE11151,GPL570,0,Renal Lipoma,,Kidney,GEO,Microarray,Homo sapiens,2|1, DSA04146,GSE11151,GPL570,1000,Papillary Renal Cell Carcinoma,C1306837,Kidney,GEO,Microarray,Homo sapiens,2|19,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA04147,GSE11151,GPL570,1000,Renal Oncocytoma,C0346255,Kidney,GEO,Microarray,Homo sapiens,2|4,"EFO:A benign tumor of the kidney, characterized by the presence of large cells with abundant eosinophilic granular cytoplasm. The majority of these tumors are discovered incidentally, during work-up of other conditions." DSA04148,GSE179987,GPL16791,31,Leprosy,C0023343,Peripheral blood,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A primary bacterial infectious disease that results_in infection located_in superficial peripheral nerves, located_in skin, located_in mucous membranes of the upper respiratory tract, located_in anterior chamber of the eyes, or located_in testes, has_material_basis_in Mycobacterium leprae, which is transmitted_by aerosol spread from infected nasal secretions to exposed nasal and oral mucosa. The infection has_symptom skin lesions, has_symptom sensory loss, has_symptom motor loss and has_symptom eye damage." DSA04149,GSE179987,GPL16791,1000,Leprosy,C0023343,Peripheral blood,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A primary bacterial infectious disease that results_in infection located_in superficial peripheral nerves, located_in skin, located_in mucous membranes of the upper respiratory tract, located_in anterior chamber of the eyes, or located_in testes, has_material_basis_in Mycobacterium leprae, which is transmitted_by aerosol spread from infected nasal secretions to exposed nasal and oral mucosa. The infection has_symptom skin lesions, has_symptom sensory loss, has_symptom motor loss and has_symptom eye damage." DSA04150,GSE179993,GPL19057,1000,Primary Biliary Cholangitis,C0008312,Liver,GEO,RNA-Seq,Mus musculus,4|3,DO:A liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts. DSA04151,GSE179993,GPL19057,1000,Primary Sclerosing Cholangitis,C0566602,Liver,GEO,RNA-Seq,Mus musculus,4|3,"DO:A sclerosing cholangitis characterized by fibroobliterative inflammation of the biliary tract, leading to cirrhosis and portal hypertension." DSA04152,GSE180014,GPL24676,1000,Acute-On-Chronic Liver Failure,C3850141,,GEO,RNA-Seq,Homo sapiens,5|8,"EFO:Acute-on-chronic liver failure (ACLF) is an extreme condition during the natural history of chronic HBV infection, with a relatively high short-term mortality." DSA04153,GSE180014,GPL24676,1000,Acute Decompensation,,,GEO,RNA-Seq,Homo sapiens,5|5, DSA04154,GSE180226,GPL6480,1000,COVID-19,D8888888,Lung,GEO,Microarray,Homo sapiens,3|20,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04155,GSE11151,GPL570,0,Rhabdoid Tumor of The Kidney,C0854917,Kidney,GEO,Microarray,Homo sapiens,2|1,DO:A embryonal cancer that is located in the kidney. DSA04156,GSE11151,GPL570,2,Wilms Tumor,C2930471,Kidney,GEO,Microarray,Homo sapiens,2|4,"MSH:A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN." DSA04157,GSE180329,GPL24676,301,TAB2 haploinsufficiency,,,GEO,RNA-Seq,Homo sapiens,10|12, DSA04158,GSE180415,GPL20301,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,RNA-Seq,Homo sapiens,4|5,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA04159,GSE180574,GPL16791,1000,Cutaneous T Cell Lymphoma,C0079773,,GEO,RNA-Seq,Homo sapiens,1|1,DO:A non-Hodgkin's lymphoma that has_material_basis_in a mutation of T cells. DSA04160,GSE180574,GPL16791,1000,Cutaneous T Cell Lymphoma,C0079773,,GEO,RNA-Seq,Homo sapiens,1|1,DO:A non-Hodgkin's lymphoma that has_material_basis_in a mutation of T cells. DSA04161,GSE180574,GPL16791,1000,Cutaneous T Cell Lymphoma,C0079773,,GEO,RNA-Seq,Homo sapiens,1|1,DO:A non-Hodgkin's lymphoma that has_material_basis_in a mutation of T cells. DSA04162,GSE180574,GPL16791,1000,Cutaneous T Cell Lymphoma,C0079773,,GEO,RNA-Seq,Homo sapiens,1|1,DO:A non-Hodgkin's lymphoma that has_material_basis_in a mutation of T cells. DSA04163,GSE11151,GPL570,1000,Wilms Tumor,C2930471,Kidney,GEO,Microarray,Homo sapiens,3|4,"MSH:A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN." DSA04164,GSE11190,GPL570,140,"Hepatitis C, Chronic",C0524910,Kidney,GEO,Microarray,Homo sapiens,2|8,EFO:INFLAMMATION of the LIVER in humans that is caused by HEPATITIS C VIRUS lasting six months or more. Chronic hepatitis C can lead to LIVER CIRRHOSIS. DSA04165,GSE11199,GPL570,390,Latent Tuberculosis,C1609538,,GEO,Microarray,Homo sapiens,4|4,"MONDO:Mycobacterium tuberculosis infection that does not induce infectious expression of the disease in the affected person, although it can cause continuous immune response generated towards TB antigens; person having LTBI are asymptomatic and acting as a reservoir of active tuberculosis tuberculosis cases and Mycobacterium tuberculosis and run a 5-10% risk of reactivating tuberculosis throughout their lives." DSA04166,GSE11199,GPL570,12,Pulmonary Tuberculosis,C0041327,,GEO,Microarray,Homo sapiens,4|4,"DO:A tuberculosis that is a contagious disease located_in lungs. The infection has_symptom fever, has_symptom cough, has_symptom difficulty in breathing, has_symptom inflammatory infiltrations, has_symptom formation of tubercles, has_symptom caseation, has_symptom pleural effusion, and has_symptom fibrosis." DSA04167,GSE11199,GPL570,268,Meningeal Tuberculosis,C0041318,,GEO,Microarray,Homo sapiens,4|4,EFO:A bacterial infection of the membranes covering the brain and the spinal cord caused by Mycobacterium tuberculosis. DSA04168,GSE11309,GPL570,0,Autoimmune Polyendocrinopathy,C4316913,,GEO,Microarray,Homo sapiens,3|3,"MONDO:A group of diverse conditions that are characterized by spontaneous, multi-organ autoimmunity, which target both endocrine (adrenal, gonad, pancreatic islet cells, parathyroid, pituitary, thyroid) and non-endocrine (gastrointestinal, integumentary, lymphatic) tissues." DSA04169,GSE11309,GPL570,1,Autoimmune Polyendocrinopathy,C4316913,,GEO,Microarray,Homo sapiens,3|3,"MONDO:A group of diverse conditions that are characterized by spontaneous, multi-organ autoimmunity, which target both endocrine (adrenal, gonad, pancreatic islet cells, parathyroid, pituitary, thyroid) and non-endocrine (gastrointestinal, integumentary, lymphatic) tissues." DSA04170,GSE11524,GPL570,346,Sickle Cell Disease,C0002895,Peripheral blood,GEO,Microarray,Homo sapiens,12|18,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA04171,GSE11622,GPL570,1000,Vaginal Atrophy,,Vaginal tissue,GEO,Microarray,Homo sapiens,19|19, DSA04172,GSE11784,GPL570,284,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,66|22,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA04173,GSE11784,GPL570,1000,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,53|22,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA04174,GSE11886,GPL570,0,Ankylosing Spondylitis,C0038013,,GEO,Microarray,Homo sapiens,9|7,"DO:A bone inflammation disease that results_in inflammation in the joints of the spine and pelvis. The disease has_symptom pain, has_symptom stiffness in the spine, has_symptom stiffness in the neck, has_symptom stiffness in the hips, has_symptom stiffness in the jaw and has_symptom stiffness in the rib cage." DSA04175,GSE11886,GPL570,0,Ankylosing Spondylitis,C0038013,,GEO,Microarray,Homo sapiens,9|8,"DO:A bone inflammation disease that results_in inflammation in the joints of the spine and pelvis. The disease has_symptom pain, has_symptom stiffness in the spine, has_symptom stiffness in the neck, has_symptom stiffness in the hips, has_symptom stiffness in the jaw and has_symptom stiffness in the rib cage." DSA04176,GSE180706,GPL20301,1000,Odontogenic Keratocysts of The Jaw,C1708604,Dental Follicle,GEO,RNA-Seq,Homo sapiens,6|6,"HPO:A benign uni- or multicystic, intraosseous tumor of odontogenic origin, with a characteristic lining of parakeratinized stratified squamous epithelium and potential for aggressive, infiltrative behaviour." DSA04177,GSE180706,GPL20301,1000,Odontogenic Keratocyst,C1708604,Dental Follicle,GEO,RNA-Seq,Homo sapiens,6|6,"HPO:A benign uni- or multicystic, intraosseous tumor of odontogenic origin, with a characteristic lining of parakeratinized stratified squamous epithelium and potential for aggressive, infiltrative behaviour." DSA04178,GSE180722,GPL23126,0,Alcohol Use Disorder,C0001956,Amygdala,GEO,Microarray,Homo sapiens,8|8,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04179,GSE180722,GPL23126,0,Alcohol Use Disorder,C0001956,Caudate nucleus,GEO,Microarray,Homo sapiens,8|8,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04180,GSE180722,GPL23126,0,Alcohol Use Disorder,C0001956,Cerebellum,GEO,Microarray,Homo sapiens,8|8,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04181,GSE180722,GPL23126,0,Alcohol Use Disorder,C0001956,Hippocampus,GEO,Microarray,Homo sapiens,8|8,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04182,GSE180722,GPL23126,0,Alcohol Use Disorder,C0001956,Prefrontal cortex,GEO,Microarray,Homo sapiens,8|8,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04183,GSE180722,GPL23126,0,Alcohol Use Disorder,C0001956,Putamen,GEO,Microarray,Homo sapiens,8|8,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04184,GSE11917,GPL570,0,Cardiovascular Disease,C0007222,,GEO,Microarray,Homo sapiens,2|3,"DO:A disease of anatomical entity which occurs in the blood, heart, blood vessels or the lymphatic system that passes nutrients (such as amino acids and electrolytes), gases, hormones, blood cells or lymph to and from cells in the body to help fight diseases and help stabilize body temperature and pH to maintain homeostasis." DSA04185,GSE12090,GPL570,485,Chromophobe Renal Cell Carcinoma,C1266042,,GEO,Microarray,Homo sapiens,9|9,"DO:A renal cell carcinoma that has_material_basis_in chromophobe cell that appear pale when viewed under microscope, but that are larger and display different features than clear cells." DSA04186,GSE12102,GPL570,0,Ewing Sarcoma,C0553580,,GEO,Microarray,Homo sapiens,13|17,"DO:A connective tissue cancer that has_material_basis_in neural crest cells derives_from undeveloped, undifferentiated neuroectoderm." DSA04187,GSE12102,GPL570,0,Ewing Sarcoma,C0553580,,GEO,Microarray,Homo sapiens,13|7,"DO:A connective tissue cancer that has_material_basis_in neural crest cells derives_from undeveloped, undifferentiated neuroectoderm." DSA04188,GSE180882,GPL24676,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Homo sapiens,15|18,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA04189,GSE180882,GPL24676,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Homo sapiens,15|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA04190,GSE180882,GPL24676,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Homo sapiens,15|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA04191,GSE180882,GPL24676,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Homo sapiens,15|6,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA04192,GSE180885,GPL20301,1000,Atopic Dermatitis,C0011615,Skin,GEO,scRNA-Seq,Homo sapiens,3|4,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA04193,GSE180928,GPL24676,1000,Huntington's Disease,C0020179,Brain,GEO,scRNA-Seq,Homo sapiens,3|6,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA04194,GSE12195,GPL570,1000,Diffuse Large B-Cell Lymphoma,C0079744,Lymph node,GEO,Microarray,Homo sapiens,10|73,DO:A B-cell lymphoma that is a cancer of B cells presenting as an aggressive tumour which can arise in virtually any part of the body. DSA04195,GSE180928,GPL24676,1000,Huntington's Disease,C0020179,Brain,GEO,scRNA-Seq,Homo sapiens,3|6,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA04196,GSE181029,GPL18573,1000,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,8|9,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA04197,GSE181029,GPL18573,1000,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,6|9,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA04198,GSE181179,GPL11154,53,Malaria,C0024530,Peripheral blood,GEO,RNA-Seq,Homo sapiens,6|5,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA04199,GSE181179,GPL11154,1000,Malaria,C0024530,Peripheral blood,GEO,RNA-Seq,Homo sapiens,6|6,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA04200,GSE181238,GPL24676,0,COVID-19,D8888888,Placenta,GEO,RNA-Seq,Homo sapiens,4|17,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04201,GSE181279,GPL24676,1000,Alzheimer's Disease,C0002395,,GEO,scRNA-Seq,Homo sapiens,2|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA04202,GSE181364,GPL24676,74,Ankylosing Spondylitis,C0038013,Whole blood,GEO,RNA-Seq,Homo sapiens,3|5,"DO:A bone inflammation disease that results_in inflammation in the joints of the spine and pelvis. The disease has_symptom pain, has_symptom stiffness in the spine, has_symptom stiffness in the neck, has_symptom stiffness in the hips, has_symptom stiffness in the jaw and has_symptom stiffness in the rib cage." DSA04203,GSE181549,GPL13497,1000,Systemic Sclerosis [Scleroderma],C2364016,Skin,GEO,Microarray,Homo sapiens,44|295, DSA04204,GSE181646,GPL30209,209,Metabolic Syndrome,C0524620,,GEO,RNA-Seq,Homo sapiens,9|11,"DO:An abdominal obesity-metabolic syndrome characterized by insulin resistance and hyperinsulinemia, dyslipidemia, essential hypertension, abdominal obesity, glucose intolerance or noninsulin-dependent diabetes mellitus and an increased risk of cardiovascular events." DSA04205,GSE181678,GPL24247,104,Type 1 Diabetes,C0011854,Islet,GEO,RNA-Seq,Mus musculus,8|7,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA04206,GSE181716,GPL13497,40,Ossification of Ligamentun Flavum(Olf),C4285709,Whole blood,GEO,Microarray,Homo sapiens,5|5, DSA04207,GSE181741,GPL16791,0,Alcohol Use Disorder,C0001956,Caudate nucleus,GEO,RNA-Seq,Homo sapiens,12|12,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04208,GSE181804,GPL16791,0,Alcohol Use Disorder,C0001956,Caudate nucleus,GEO,RNA-Seq,Homo sapiens,11|12,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04209,GSE181813,GPL16791,14,Alcohol Use Disorder,C0001956,Caudate nucleus,GEO,RNA-Seq,Homo sapiens,12|12,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04210,GSE181959,GPL24247,1000,Inflammatory Bowel Disease,C0021390,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA04211,GSE181959,GPL24247,1000,Inflammatory Bowel Disease,C0021390,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA04212,GSE181981,GPL16791,0,Alcohol Use Disorder,C0001956,Amygdala,GEO,RNA-Seq,Homo sapiens,9|5,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04213,GSE181981,GPL16791,2,Alcohol Use Disorder,C0001956,Amygdala,GEO,RNA-Seq,Homo sapiens,3|7,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04214,GSE12195,GPL570,1000,Diffuse Large B-Cell Lymphoma,C0079744,Lymph node,GEO,Microarray,Homo sapiens,5|73,DO:A B-cell lymphoma that is a cancer of B cells presenting as an aggressive tumour which can arise in virtually any part of the body. DSA04215,GSE181994,GPL16791,150,Generalized Pustular Psoriasis,C0343055,,GEO,RNA-Seq,Homo sapiens,4|3,"DO:A psoriasis characterized by sudden, repeated episodes of high-grade fever, generalized rash, and disseminated pustules, with hyperleukocytosis and elevated serum levels of C-reactive protein that has_material_basis_in homozygous or compound heterozygous mutation in the IL36RN gene on chromosome 2q14." DSA04216,GSE182071,GPL17400,0,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,Microarray,Mus musculus,4|4,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA04217,GSE12195,GPL570,1000,Diffuse Large B-Cell Lymphoma,C0079744,Lymph node,GEO,Microarray,Homo sapiens,5|73,DO:A B-cell lymphoma that is a cancer of B cells presenting as an aggressive tumour which can arise in virtually any part of the body. DSA04218,GSE12195,GPL570,1000,Diffuse Large B-Cell Lymphoma,C0079744,,GEO,Microarray,Homo sapiens,5|5,DO:A B-cell lymphoma that is a cancer of B cells presenting as an aggressive tumour which can arise in virtually any part of the body. DSA04219,GSE12368,GPL570,136,Adrenocortical Adenoma,C0206667,Adrenal cortex,GEO,Microarray,Homo sapiens,6|16,DO:An endocrine organ benign neoplasm that is a benign tumor of the glandular type (adenoma) in the adrenal gland. DSA04220,GSE12368,GPL570,735,Adrenocortical Carcinoma,C0206686,Adrenal cortex,GEO,Microarray,Homo sapiens,6|12,DO:An adrenal cortex cancer that forms in the outer layer of tissue of the adrenal gland and that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA04221,GSE12452,GPL570,1000,Nasopharyngeal Carcinoma,C2931822,Nasopharynx,GEO,Microarray,Homo sapiens,10|31,"DO:A pharynx cancer that is located in the nasopharynx, the uppermost region of the pharynx or throat, where the nasal passages and auditory tubes join the remainder of the upper respiratory tract." DSA04222,GSE12644,GPL570,0,Aortic Stenosis,C0003507,Calcified aortic valve,GEO,Microarray,Homo sapiens,10|10,DO:A bicuspid aortic valve disease that has_material_basis_in heterozygous mutation in the SMAD6 gene on chromosome 15q22. DSA04223,GSE12734,GPL570,7,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,7|7,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA04224,GSE12814,GPL570,587,Uterine Leiomyoma,C0042133,,GEO,Microarray,Homo sapiens,11|11,DO:An uterine benign neoplasm derived from the smooth muscle layer of the uterus. DSA04225,GSE182173,GPL16791,165,Alcohol Use Disorder,C0001956,Prefrontal cortex,GEO,RNA-Seq,Homo sapiens,9|5,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04226,GSE182173,GPL16791,18,Alcohol Use Disorder,C0001956,Prefrontal cortex,GEO,RNA-Seq,Homo sapiens,2|6,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04227,GSE182223,GPL16791,1,Alcohol Use Disorder,C0001956,Nucleus accumbens,GEO,RNA-Seq,Homo sapiens,9|6,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04228,GSE182223,GPL16791,13,Alcohol Use Disorder,C0001956,Nucleus accumbens,GEO,RNA-Seq,Homo sapiens,2|7,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04229,GSE182244,GPL16791,1000,Generalized Pustular Psoriasis,C0343055,,GEO,scRNA-Seq,Homo sapiens,3|2,"DO:A psoriasis characterized by sudden, repeated episodes of high-grade fever, generalized rash, and disseminated pustules, with hyperleukocytosis and elevated serum levels of C-reactive protein that has_material_basis_in homozygous or compound heterozygous mutation in the IL36RN gene on chromosome 2q14." DSA04230,GSE182256,GPL21103,1000,Ureteral Obstruction,C0041956,Kidney,GEO,scRNA-Seq,Mus musculus,6|2,HPO:Obstruction of the flow of urine through the ureter. DSA04231,GSE12814,GPL570,852,Uterine Leiomyoma,C0042133,,GEO,Microarray,Homo sapiens,11|11,DO:An uterine benign neoplasm derived from the smooth muscle layer of the uterus. DSA04232,GSE182279,GPL30524,209,COVID-19,D8888888,Skin,GEO,Microarray,Homo sapiens,4|10,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04233,GSE182279,GPL30524,144,Chilblains,C0008058,Skin,GEO,Microarray,Homo sapiens,4|4,"HPO:Chilblains, also called perniosis, are an inflammatory skin condition related to an abnormal vascular response to the cold. We are unaware of a reliable estimate of incidence. It typically presents as tender, pruritic red or bluish lesions located symmetrically on the dorsal aspect of the fingers, toes, ears and nose. Less commonly, reports describe involvement of the thighs and buttocks. The lesions present hours after exposure to cold and usually resolve spontaneously in one to three weeks." DSA04234,GSE182347,GPL23227,1000,Cystic Fibrosis,C0010674,Liver,GEO,RNA-Seq,Homo sapiens,1|1,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA04235,GSE182347,GPL23227,1000,Cystic Fibrosis,C0010674,Ileum,GEO,RNA-Seq,Homo sapiens,1|1,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA04236,GSE182440,GPL16791,15,Alcohol Use Disorder,C0001956,Putamen,GEO,RNA-Seq,Homo sapiens,9|5,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04237,GSE182440,GPL16791,818,Alcohol Use Disorder,C0001956,Putamen,GEO,RNA-Seq,Homo sapiens,2|7,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04238,GSE182477,GPL24247,1000,Diabetes,C0011847,Corneal epithelium,GEO,scRNA-Seq,Mus musculus,1|1,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA04239,GSE182494,GPL23159,0,Type 1 Diabetes,C0011854,Muscle,GEO,Microarray,Homo sapiens,4|4,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA04240,GSE182494,GPL23159,0,Type 1 Diabetes,C0011854,Vastus lateralis,GEO,Microarray,Homo sapiens,4|4,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA04241,GSE182503,GPL21185,1000,Adult Onset Asthma,C0741260,,GEO,Microarray,Homo sapiens,36|50, DSA04242,GSE182503,GPL21185,1000,Idiopathic Environmental Intolerance,,,GEO,Microarray,Homo sapiens,36|16, DSA04243,GSE182522,GPL24676,0,Sepsis,C0243026,,GEO,RNA-Seq,Homo sapiens,18|18,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA04244,GSE182522,GPL24676,1000,Sepsis,C0243026,,GEO,RNA-Seq,Homo sapiens,18|18,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA04245,GSE13205,GPL570,1000,Septicemia,C0036690,Vastus lateralis,GEO,Microarray,Homo sapiens,8|13,HPO:Systemic inflammatory response to infection. DSA04246,GSE13319,GPL570,1000,Leiomyoma,C0042133,,GEO,Microarray,Homo sapiens,27|50,DO:An uterine benign neoplasm derived from the smooth muscle layer of the uterus. DSA04247,GSE182649,GPL16791,1,Alcohol Use Disorder,C0001956,Ventral tegmental area,GEO,RNA-Seq,Homo sapiens,9|5,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04248,GSE182649,GPL16791,3,Alcohol Use Disorder,C0001956,Ventral tegmental area,GEO,RNA-Seq,Homo sapiens,2|7,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA04249,GSE182797,GPL21185,1000,Adult Onset Asthma,C0741260,Nasal,GEO,Microarray,Homo sapiens,21|45, DSA04250,GSE182797,GPL21185,1000,Idiopathic Environmental Intolerance,,Nasal,GEO,Microarray,Homo sapiens,21|14, DSA04251,GSE182824,GPL20301,18,Liver Cancer,C2239176,Plasma,GEO,RNA-Seq,Homo sapiens,20|8,DO:A hepatobiliary system cancer that is located_in the liver. DSA04252,GSE182824,GPL20301,104,Cirrhosis,C1623038,Plasma,GEO,RNA-Seq,Homo sapiens,20|4,"MSH:Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury." DSA04253,GSE182824,GPL20301,608,Monoclonal Gammopathy of Undetermined Significance,C0026470,Plasma,GEO,RNA-Seq,Homo sapiens,20|9,DO:A blood protein disease that is characterized by the presence of an abnormal protein called monoclonal protein in the blood. DSA04254,GSE182824,GPL20301,396,Multiple Myeloma,C0026764,Plasma,GEO,RNA-Seq,Homo sapiens,20|10,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA04255,GSE182824,GPL20301,7,Liver Cancer,C2239176,Plasma,GEO,RNA-Seq,Homo sapiens,10|20,DO:A hepatobiliary system cancer that is located_in the liver. DSA04256,GSE182824,GPL20301,336,Multiple Myeloma,C0026764,Plasma,GEO,RNA-Seq,Homo sapiens,10|9,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA04257,GSE182866,GPL11154,1,Huntington's Disease,C0020179,,GEO,RNA-Seq,Homo sapiens,7|7,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA04258,GSE182866,GPL11154,2,Huntington's Disease,C0020179,,GEO,RNA-Seq,Homo sapiens,7|7,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA04259,GSE13353,GPL570,598,Ruptured Aneurysm,C0162869,,GEO,Microarray,Homo sapiens,8|11,"MSH:The tearing or bursting of the weakened wall of the aneurysmal sac, usually heralded by sudden worsening pain. The great danger of a ruptured aneurysm is the large amount of blood spilling into the surrounding tissues and cavities, causing HEMORRHAGIC SHOCK." DSA04260,GSE13355,GPL570,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,64|58,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA04261,GSE182923,GPL20301,20,Diabetes,C0011847,Craniofacial bone,GEO,RNA-Seq,Homo sapiens,6|7,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA04262,GSE182923,GPL20301,1000,Diabetes,C0011847,Craniofacial bone,GEO,RNA-Seq,Homo sapiens,4|1,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA04263,GSE182974,GPL24676,1000,Non-Erosive Reflux Disease,,Esophagus,GEO,RNA-Seq,Homo sapiens,6|9, DSA04264,GSE182986,GPL21273,1000,Type 1 Diabetes,C0011854,Bone marrow,GEO,RNA-Seq,Mus musculus,1|1,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA04265,GSE183021,GPL29703,1,Cerebral Palsy,C0007789,Whole blood,GEO,Microarray,Homo sapiens,5|5,"DO:A spastic cerebral palsy that affects lower extremities resulting in tight leg and hip muscles. The legs cross at the knees, making it difficult to walk." DSA04266,GSE13355,GPL570,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,58|58,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA04267,GSE13367,GPL570,0,Ulcerative Colitis,C0009324,Colon mucosa,GEO,Microarray,Homo sapiens,10|10,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA04268,GSE13367,GPL570,0,Ulcerative Colitis,C0009324,Colon mucosa,GEO,Microarray,Homo sapiens,10|9,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA04269,GSE183071,GPL30569,87,COVID-19,D8888888,Blood,GEO,Microarray,Homo sapiens,13|41,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04270,GSE183071,GPL30569,2,COVID-19,D8888888,Nasal,GEO,Microarray,Homo sapiens,11|38,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04271,GSE183071,GPL30569,1,COVID-19,D8888888,Saliva,GEO,Microarray,Homo sapiens,12|41,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04272,GSE183098,GPL24247,1000,Particulate Matter,,,GEO,RNA-Seq,Mus musculus,3|3, DSA04273,GSE18312,GPL5175,0,Bipolar Disorder,C0005586,,GEO,Microarray,Homo sapiens,8|9,DO:A mood disorder that involves alternating periods of mania and depression. DSA04274,GSE18312,GPL5175,0,Schizophrenia,C0036341,,GEO,Microarray,Homo sapiens,8|13,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04275,GSE13367,GPL570,270,Ulcerative Colitis,C0009324,Colon mucosa,GEO,Microarray,Homo sapiens,10|8,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA04276,GSE183252,GPL20301,678,Juvenile Myelomonocytic Leukemia,C0349639,Bone marrow,GEO,RNA-Seq,Homo sapiens,3|5,DO:A myelodysplastic/myeloproliferative neoplasm that is characterized by the uncontrolled growth of monocytes. DSA04277,GSE183252,GPL20301,1000,Juvenile Myelomonocytic Leukemia,C0349639,Bone marrow,GEO,RNA-Seq,Homo sapiens,4|5,DO:A myelodysplastic/myeloproliferative neoplasm that is characterized by the uncontrolled growth of monocytes. DSA04278,GSE183252,GPL20301,692,Juvenile Myelomonocytic Leukemia,C0349639,Bone marrow,GEO,RNA-Seq,Homo sapiens,5|2,DO:A myelodysplastic/myeloproliferative neoplasm that is characterized by the uncontrolled growth of monocytes. DSA04279,GSE183252,GPL20301,1000,Juvenile Myelomonocytic Leukemia,C0349639,Bone marrow,GEO,RNA-Seq,Homo sapiens,4|5,DO:A myelodysplastic/myeloproliferative neoplasm that is characterized by the uncontrolled growth of monocytes. DSA04280,GSE183252,GPL20301,1000,Juvenile Myelomonocytic Leukemia,C0349639,Bone marrow,GEO,RNA-Seq,Homo sapiens,1|2,DO:A myelodysplastic/myeloproliferative neoplasm that is characterized by the uncontrolled growth of monocytes. DSA04281,GSE13367,GPL570,1000,Ulcerative Colitis,C0009324,Colon mucosa,GEO,Microarray,Homo sapiens,10|8,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA04282,GSE13396,GPL570,1000,Acquired Immunodeficiency Syndrome,C0001175,,GEO,Microarray,Homo sapiens,5|5,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA04283,GSE13396,GPL570,1000,Acquired Immunodeficiency Syndrome,C0001175,,GEO,Microarray,Homo sapiens,6|6,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA04284,GSE13396,GPL201,1000,Acquired Immunodeficiency Syndrome,C0001175,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA04285,GSE13396,GPL201,0,Acquired Immunodeficiency Syndrome,C0001175,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA04286,GSE13471,GPL570,583,Colon Tumor,C0009375,Colon,GEO,Microarray,Homo sapiens,4|4,DO:A colorectal cancer that is located_in the colon. DSA04287,GSE13576,GPL570,39,B-Cell Pediatric Acute Lymphoblastic Leukemia,C0279584,Bone marrow,GEO,Microarray,Homo sapiens,157|26,DO:A childhood acute lymphoblastic leukemia that has_material_basis_in B-cells. DSA04288,GSE13576,GPL570,1,B-Cell Pediatric Acute Lymphoblastic Leukemia,C0279584,Bone marrow,GEO,Microarray,Homo sapiens,157|14,DO:A childhood acute lymphoblastic leukemia that has_material_basis_in B-cells. DSA04289,GSE13732,GPL570,1000,Clinically Isolated Syndrome,C2921627,,GEO,Microarray,Homo sapiens,30|39, DSA04290,GSE13732,GPL570,927,Clinically Isolated Syndrome,C2921627,,GEO,Microarray,Homo sapiens,10|34, DSA04291,GSE13785,GPL570,0,Bronchoconstriction,,Sputum,GEO,Microarray,Homo sapiens,3|3, DSA04292,GSE13785,GPL570,6,Bronchoconstriction,,Sputum,GEO,Microarray,Homo sapiens,3|3, DSA04293,GSE183325,GPL18573,332,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,RNA-Seq,Homo sapiens,8|12,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA04294,GSE183327,GPL18573,384,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,RNA-Seq,Homo sapiens,6|2,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA04295,GSE183349,GPL21185,0,Hepatocellular Carcinoma,C0334287,,GEO,Microarray,Homo sapiens,6|11,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA04296,GSE183484,GPL23159,3,Gaucher Disease,C0017205,,GEO,Microarray,Homo sapiens,2|2,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA04297,GSE183484,GPL23159,84,Gaucher Disease,C0017205,,GEO,Microarray,Homo sapiens,2|2,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA04298,GSE183533,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|30,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04299,GSE183607,GPL20301,112,Echinococcosis,C0013502,Serum exosomes,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A parasitic helminthiasis infectious disease that involves parasitic infection of humans and domestic animals caused by the larval stages of tapeworms of the genus Echinococcus in the liver, lungs, spleen, brain, heart and kidneys." DSA04300,GSE183701,GPL30173,1000,Down Syndrome,C0013080,Whole blood,GEO,RNA-Seq,Homo sapiens,26|23,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA04301,GSE183701,GPL30173,3,Type 1 Diabetes,C0011854,Whole blood,GEO,RNA-Seq,Homo sapiens,26|26,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA04302,GSE183787,GPL17586,0,Multidrug-Resistant Tuberculosis,C0206526,,GEO,Microarray,Homo sapiens,4|4,"DO:A tuberculosis that is resistant to isoniazid and rifampicin, the two most powerful first-line anti-TB drugs." DSA04303,GSE183787,GPL17586,0,Drug-Sensitive Tuberculosis(Ds-Tb),C0206526,,GEO,Microarray,Homo sapiens,4|4,"DO:A tuberculosis that is resistant to isoniazid and rifampicin, the two most powerful first-line anti-TB drugs." DSA04304,GSE183817,GPL20301,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,RNA-Seq,Homo sapiens,3|4,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA04305,GSE183817,GPL20301,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA04306,GSE183817,GPL20301,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA04307,GSE183837,GPL24676,1000,Recurrent Implantation Failure,,Endometrium,GEO,scRNA-Seq,Homo sapiens,3|6, DSA04308,GSE183854,GPL18573,1000,Head And Neck Squamous Cell Carcinoma,C1168401,,GEO,RNA-Seq,Homo sapiens,2|5,"DO:A head and neck carcinoma that has_material_basis_in squamous cells that line the moist, mucosal surfaces inside the head and neck." DSA04309,GSE183973,GPL24676,488,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA04310,GSE183973,GPL24676,24,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA04311,GSE183973,GPL24676,398,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA04312,GSE183973,GPL24676,55,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA04313,GSE183973,GPL24676,24,Chronic Obstructive Pulmonary Disease,C0024117,Blood,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA04314,GSE183973,GPL24676,7,Chronic Obstructive Pulmonary Disease,C0024117,Blood,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA04315,GSE13785,GPL96,0,Bronchoconstriction,,Sputum,GEO,Microarray,Homo sapiens,2|3, DSA04316,GSE13785,GPL96,0,Bronchoconstriction,,Sputum,GEO,Microarray,Homo sapiens,2|3, DSA04317,GSE184050,GPL11154,1,Type 2 Diabetes,C0011860,Peripheral blood,GEO,RNA-Seq,Homo sapiens,33|25,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA04318,GSE184050,GPL11154,1,Type 2 Diabetes,C0011860,Peripheral blood,GEO,RNA-Seq,Homo sapiens,33|25,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA04319,GSE184053,GPL16791,1000,Non-Small Cell Lung Cancer,C0007131,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|3,DO:A respiratory system cancer that is located_in the lung. DSA04320,GSE13791,GPL570,1000,Chagas Disease,C0041234,,GEO,Microarray,Homo sapiens,2|2,DO:A parasitic protozoa infectious disease that involves infection caused by parasitic protozoan of the genus Trypanosoma in animals and humans. DSA04321,GSE13791,GPL570,0,Chagas Disease,C0041234,,GEO,Microarray,Homo sapiens,2|2,DO:A parasitic protozoa infectious disease that involves infection caused by parasitic protozoan of the genus Trypanosoma in animals and humans. DSA04322,GSE184102,GPL21697,1000,Schizophrenia,C0036341,,GEO,RNA-Seq,Homo sapiens,4|5,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04323,GSE184200,GPL16791,115,Cirrhosis,C1623038,,GEO,RNA-Seq,Homo sapiens,8|6,"MSH:Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury." DSA04324,GSE184237,GPL23227,59,Atopic Dermatitis,C0011615,,GEO,RNA-Seq,Homo sapiens,6|6,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA04325,GSE184256,GPL24247,113,Non-Alcoholic Steatohepatitis,C3241937,Kidney cortex,GEO,RNA-Seq,Mus musculus,3|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA04326,GSE184256,GPL24247,0,Non-Alcoholic Steatohepatitis,C3241937,Kidney cortex,GEO,RNA-Seq,Mus musculus,3|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA04327,GSE184382,GPL21185,1000,Allergic Rhinitis,C2607914,Sputum,GEO,Microarray,Homo sapiens,8|8,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA04328,GSE184673,GPL24247,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Mus musculus,2|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04329,GSE184673,GPL24247,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Mus musculus,2|4,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04330,GSE184699,GPL21493,54,Icf Syndrome,,Spleen,GEO,RNA-Seq,Mus musculus,3|3, DSA04331,GSE184699,GPL21493,38,Icf Syndrome,,Spleen,GEO,RNA-Seq,Mus musculus,3|3, DSA04332,GSE184875,GPL20795,0,Immune Dysregulation,C1844666,,GEO,RNA-Seq,Homo sapiens,3|4,"HPO:Altered immune function characterized by lymphoid proliferation, immune activation, and excessive autoreactivity often leading to autoimmune/inflammatory complications." DSA04333,GSE184875,GPL20795,6,Immune Dysregulation,C1844666,,GEO,RNA-Seq,Homo sapiens,4|3,"HPO:Altered immune function characterized by lymphoid proliferation, immune activation, and excessive autoreactivity often leading to autoimmune/inflammatory complications." DSA04334,GSE184875,GPL20795,4,Immune Dysregulation,C1844666,,GEO,RNA-Seq,Homo sapiens,4|3,"HPO:Altered immune function characterized by lymphoid proliferation, immune activation, and excessive autoreactivity often leading to autoimmune/inflammatory complications." DSA04335,GSE184875,GPL20795,69,Immune Dysregulation,C1844666,,GEO,RNA-Seq,Homo sapiens,4|4,"HPO:Altered immune function characterized by lymphoid proliferation, immune activation, and excessive autoreactivity often leading to autoimmune/inflammatory complications." DSA04336,GSE184875,GPL20795,91,Immune Dysregulation,C1844666,,GEO,RNA-Seq,Homo sapiens,4|4,"HPO:Altered immune function characterized by lymphoid proliferation, immune activation, and excessive autoreactivity often leading to autoimmune/inflammatory complications." DSA04337,GSE184876,GPL20301,517,Immune Dysregulation,C1844666,Whole blood,GEO,RNA-Seq,Homo sapiens,6|4,"HPO:Altered immune function characterized by lymphoid proliferation, immune activation, and excessive autoreactivity often leading to autoimmune/inflammatory complications." DSA04338,GSE184898,GPL10558,0,Granulomatosis With Polyangiitis,C3495801,,GEO,Microarray,Homo sapiens,4|6,"DO:An autoimmune disease that is characterized by necrotizing granulomatous inflammation of the upper and lower respiratory tract, glomerulonephritis, vasculitis, and the presence of antineutrophil cytoplasmatic autoantibodies (ANCAs) in patient sera, and is located_in lung, located_in kidney, located_in skin resulting from an autoimmune attack by antineutrophil cytoplasmic antibodies against small and medium-size blood vessels." DSA04339,GSE184898,GPL10558,0,Granulomatosis With Polyangiitis,C3495801,,GEO,Microarray,Homo sapiens,4|6,"DO:An autoimmune disease that is characterized by necrotizing granulomatous inflammation of the upper and lower respiratory tract, glomerulonephritis, vasculitis, and the presence of antineutrophil cytoplasmatic autoantibodies (ANCAs) in patient sera, and is located_in lung, located_in kidney, located_in skin resulting from an autoimmune attack by antineutrophil cytoplasmic antibodies against small and medium-size blood vessels." DSA04340,GSE184906,GPL23126,118,Sandhoff Disease,C0036161,,GEO,Microarray,Homo sapiens,3|2,"DO:A GM2 gangliosidosis that is characterized by an accumulation of GM2 gangliosides, particularly in neurons, and that has_material_basis_in mutation in the beta subunit of hexosaminidase (HEXB) on chromosome 5q13." DSA04341,GSE184906,GPL23126,291,Tay-Sachs Disease,C0039373,,GEO,Microarray,Homo sapiens,3|4,"DO:A GM2 gangliosidosis that is characterized onset in infancy of developmental retardation, followed by paralysis, dementia and blindness, with death in the second or third year of life and has_material_basis_in homozygous or compound heterozygous mutation in the alpha subunit of the hexosaminidase A gene (HEXA) on chromosome 15q23." DSA04342,GSE184906,GPL23126,217,Tay-Sachs Disease; Juvenile,C1848913,,GEO,Microarray,Homo sapiens,3|3,"DO:A GM2 gangliosidosis that is characterized onset in infancy of developmental retardation, followed by paralysis, dementia and blindness, with death in the second or third year of life and has_material_basis_in homozygous or compound heterozygous mutation in the alpha subunit of the hexosaminidase A gene (HEXA) on chromosome 15q23." DSA04343,GSE184942,GPL11154,14,Alzheimer's Disease,C0002395,Hippocampus,GEO,RNA-Seq,Homo sapiens,5|5,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA04344,GSE13791,GPL570,0,Chagas Disease,C0041234,,GEO,Microarray,Homo sapiens,2|2,DO:A parasitic protozoa infectious disease that involves infection caused by parasitic protozoan of the genus Trypanosoma in animals and humans. DSA04345,GSE13791,GPL570,175,Chagas Disease,C0041234,,GEO,Microarray,Homo sapiens,2|2,DO:A parasitic protozoa infectious disease that involves infection caused by parasitic protozoan of the genus Trypanosoma in animals and humans. DSA04346,GSE184956,GPL18460,41,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,4|5,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA04347,GSE185011,GPL24676,508,Type 2 Diabetes Mellitus,C0011847,,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA04348,GSE185011,GPL24676,121,Type 2 Diabetes Mellitus,C0011847,,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA04349,GSE185011,GPL24676,768,Type 2 Diabetes Mellitus,C0011847,,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA04350,GSE185011,GPL24676,16,Type 2 Diabetes Mellitus,C0011847,,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA04351,GSE185028,GPL16791,1000,Smith-Lemli-Opitz Syndrome,C0175694,,GEO,RNA-Seq,Homo sapiens,4|6,"MONDO:Smith-Lemli-Opitz syndrome (SLOS) is characterized by multiple congenital anomalies, intellectual deficit, and behavioral problems." DSA04352,GSE185028,GPL16791,1000,Smith-Lemli-Opitz Syndrome,C0175694,,GEO,RNA-Seq,Homo sapiens,4|6,"MONDO:Smith-Lemli-Opitz syndrome (SLOS) is characterized by multiple congenital anomalies, intellectual deficit, and behavioral problems." DSA04353,GSE185051,GPL24676,1000,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,RNA-Seq,Homo sapiens,5|22,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA04354,GSE185051,GPL24676,1000,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,RNA-Seq,Homo sapiens,5|15,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA04355,GSE185051,GPL24676,1000,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,RNA-Seq,Homo sapiens,5|15,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA04356,GSE185064,GPL24676,93,Osteoarthritis,C0157946,Meniscus,GEO,RNA-Seq,Homo sapiens,4|4,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA04357,GSE185193,GPL24676,12,Juvenile Idiopathic Arthritis,C3890205,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA04358,GSE13791,GPL570,0,Chagas Disease,C0041234,,GEO,Microarray,Homo sapiens,2|2,DO:A parasitic protozoa infectious disease that involves infection caused by parasitic protozoan of the genus Trypanosoma in animals and humans. DSA04359,GSE185645,GPL6244,22,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,1|15,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA04360,GSE13791,GPL570,144,Chagas Disease,C0041234,,GEO,Microarray,Homo sapiens,3|3,DO:A parasitic protozoa infectious disease that involves infection caused by parasitic protozoan of the genus Trypanosoma in animals and humans. DSA04361,GSE13827,GPL570,3,Melanoma,C0025202,,GEO,Microarray,Homo sapiens,2|2,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA04362,GSE13849,GPL570,752,Polyarticular Juvenile Idiopathic Arthritis,C0409667,,GEO,Microarray,Homo sapiens,59|12,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA04363,GSE13849,GPL570,119,Polyarticular Juvenile Idiopathic Arthritis,C0409667,,GEO,Microarray,Homo sapiens,59|49,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA04364,GSE185919,GPL24676,0,Behcet's Disease,C0004943,,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis." DSA04365,GSE13887,GPL570,0,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,17|10,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA04366,GSE13896,GPL570,1000,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,34|12,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA04367,GSE14001,GPL570,1000,Ovarian Serous Carcinoma,C1335177,Ovarian surface epithelia,GEO,Microarray,Homo sapiens,3|10,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA04368,GSE186054,GPL20795,1000,Sepsis,C0243026,Blood,GEO,RNA-Seq,Homo sapiens,3|3,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA04369,GSE186143,GPL16791,1000,Melanoma,C0025202,Blood,GEO,RNA-Seq,Homo sapiens,5|61,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA04370,GSE186280,GPL11154,6,COVID-19,D8888888,Blood,GEO,RNA-Seq,Homo sapiens,10|6,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04371,GSE14001,GPL570,1000,Ovarian Serous Carcinoma,C1335177,Ovarian surface epithelia,GEO,Microarray,Homo sapiens,3|10,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA04372,GSE186360,GPL24247,1000,COVID-19,D8888888,Lung,GEO,scRNA-Seq,Mus musculus,4|4,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04373,GSE186444,GPL16791|GPL24676,337,Biliary Atresia,C0005411,Liver,GEO,RNA-Seq,Homo sapiens,2|14,DO:A cholestasis characterized by blockage of the ducts that carry bile from the liver to the gallbladder. DSA04374,GSE186476,GPL24676,1000,Cutaneous Lupus Erythematosus,C0024137,Skin,GEO,scRNA-Seq,Homo sapiens,14|7,DO:A lupus erythematosus that causes skin lesions on parts of the body that are exposed to sunlight. DSA04375,GSE186477,GPL18573,1000,Trichohepatoenteric Syndrome 2,C3281289,,GEO,RNA-Seq,Homo sapiens,2|1,DO:A trichohepatoenteric syndrome that has_material_basis_in homozygous or compound heterozygous mutation in SKIV2L on chromosome 6p21.33. DSA04376,GSE186505,GPL24676,0,Trigeminal Neuralgia,C0040997,Whole blood,GEO,RNA-Seq,Homo sapiens,10|10,"HPO:A neuropathic disorder characterized by episodes of intense pain in the face, originating from the trigeminal nerve. One, two, or all three branches of the nerve may be affected." DSA04377,GSE186803,GPL16791,624,Transposition of The Great Arteries,C0040761,,GEO,RNA-Seq,Homo sapiens,2|2,DO:A congenital heart disease characterized by complete inversion of the great vessels where the aorta incorrectly arises from the right ventricle and the pulmonary artery incorrectly arises from the left ventricle. DSA04378,GSE186882,GPL24247,1000,Periodontitis,C0031099,Gingiva,GEO,RNA-Seq,Mus musculus,3|3,"EFO:Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology)" DSA04379,GSE186895,GPL28337,1000,Radiologically Isolated Syndrom,,,GEO,RNA-Seq,Homo sapiens,8|8, DSA04380,GSE187420,GPL18573,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04381,GSE187429,GPL24676,0,Non-Bacterial Osteomyelitis,C0410422,Whole blood,GEO,RNA-Seq,Homo sapiens,9|11,"DO:An osteomyelitis characterized by multiple foci of painful swelling of bones, mainly in the metaphyses of the long bones, in addition to the pelvis, the shoulder girdle and the spine." DSA04382,GSE188479,GPL24247,1000,Cachexia,C0006625,White adipose tissue,GEO,RNA-Seq,Mus musculus,3|3,"HPO:Severe weight loss, wasting of muscle, loss of appetite, and general debility related to a chronic disease." DSA04383,GSE14001,GPL570,1000,High Grade Ovarian Serous Carcinoma,C1335177,Ovarian surface epithelia,GEO,Microarray,Homo sapiens,10|10,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA04384,GSE188740,GPL24676,221,Polycystic Ovary Syndrome,C0032460,Muscle,GEO,RNA-Seq,Homo sapiens,5|8,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA04385,GSE188740,GPL24676,10,Polycystic Ovary Syndrome,C0032460,,GEO,RNA-Seq,Homo sapiens,6|5,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA04386,GSE188799,GPL28038,4,Gestational Diabetes,C0085207,Adipose tissue,GEO,RNA-Seq,Homo sapiens,5|5,DO:A diabetes mellitus that manifests during pregnancy. DSA04387,GSE188799,GPL28038,0,Gestational Diabetes,C0085207,Adipose tissue,GEO,RNA-Seq,Homo sapiens,5|5,DO:A diabetes mellitus that manifests during pregnancy. DSA04388,GSE18885,GPL6104,0,Wegener's Granulomatosis,C3495801,,GEO,Microarray,Homo sapiens,23|18,"DO:An autoimmune disease that is characterized by necrotizing granulomatous inflammation of the upper and lower respiratory tract, glomerulonephritis, vasculitis, and the presence of antineutrophil cytoplasmatic autoantibodies (ANCAs) in patient sera, and is located_in lung, located_in kidney, located_in skin resulting from an autoimmune attack by antineutrophil cytoplasmic antibodies against small and medium-size blood vessels." DSA04389,GSE18885,GPL6104,1000,Wegener's Granulomatosis,C3495801,,GEO,Microarray,Homo sapiens,23|23,"DO:An autoimmune disease that is characterized by necrotizing granulomatous inflammation of the upper and lower respiratory tract, glomerulonephritis, vasculitis, and the presence of antineutrophil cytoplasmatic autoantibodies (ANCAs) in patient sera, and is located_in lung, located_in kidney, located_in skin resulting from an autoimmune attack by antineutrophil cytoplasmic antibodies against small and medium-size blood vessels." DSA04390,GSE18885,GPL6104,0,Wegener's Granulomatosis,C3495801,,GEO,Microarray,Homo sapiens,23|16,"DO:An autoimmune disease that is characterized by necrotizing granulomatous inflammation of the upper and lower respiratory tract, glomerulonephritis, vasculitis, and the presence of antineutrophil cytoplasmatic autoantibodies (ANCAs) in patient sera, and is located_in lung, located_in kidney, located_in skin resulting from an autoimmune attack by antineutrophil cytoplasmic antibodies against small and medium-size blood vessels." DSA04391,GSE18885,GPL6104,1000,Wegener's Granulomatosis,C3495801,,GEO,Microarray,Homo sapiens,23|23,"DO:An autoimmune disease that is characterized by necrotizing granulomatous inflammation of the upper and lower respiratory tract, glomerulonephritis, vasculitis, and the presence of antineutrophil cytoplasmatic autoantibodies (ANCAs) in patient sera, and is located_in lung, located_in kidney, located_in skin resulting from an autoimmune attack by antineutrophil cytoplasmic antibodies against small and medium-size blood vessels." DSA04392,GSE188905,GPL21103,1000,Psoriasis,C0033860,Lymph node,GEO,RNA-Seq,Mus musculus,3|3,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA04393,GSE188905,GPL21103,1000,Psoriasis,C0033860,Spleen,GEO,RNA-Seq,Mus musculus,3|3,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA04394,GSE188938,GPL23227,35,Chronic Thromboembolic Pulmonary Hypertension,C2363973,Blood,GEO,RNA-Seq,Homo sapiens,5|7,MONDO:Chronic thromboembolic pulmonary hypertension (CTEPH) is characterized by the persistence of thromboemboli in the form of organized tissue obstructing the pulmonary arteries. The consequence is an increase in pulmonary vascular resistance (PVR) resulting in pulmonary hypertension (PH) and progressive right heart failure. DSA04395,GSE188943,GPL23038,0,Metabolic Ectopic Mineralization Disorder Pseudoxanthoma Elsaticum,,Annulus fibrosus,GEO,Microarray,Mus musculus,4|4, DSA04396,GSE189066,GPL17021,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,3|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA04397,GSE189112,GPL23479,8,Type 1 Diabetes,C0011854,Tibia,GEO,RNA-Seq,Mus musculus,3|3,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA04398,GSE189136,GPL24676,10,Rheumatoid Arthritis,C0003873,,GEO,RNA-Seq,Homo sapiens,2|2,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04399,GSE189150,GPL21145|GPL24676,121,Food Allergy,C0016470,,GEO,RNA-Seq,Homo sapiens,18|13,"DO:A hypersensitivity reaction type I disease that is an abnormal response to a food, triggered by the body's immune system." DSA04400,GSE189150,GPL21145|GPL24676,1,Food Allergy,C0016470,,GEO,RNA-Seq,Homo sapiens,18|4,"DO:A hypersensitivity reaction type I disease that is an abnormal response to a food, triggered by the body's immune system." DSA04401,GSE189150,GPL21145|GPL24676,1000,Food Allergy,C0016470,,GEO,RNA-Seq,Homo sapiens,18|1,"DO:A hypersensitivity reaction type I disease that is an abnormal response to a food, triggered by the body's immune system." DSA04402,GSE189150,GPL21145|GPL24676,1,Food Allergy,C0016470,,GEO,RNA-Seq,Homo sapiens,18|3,"DO:A hypersensitivity reaction type I disease that is an abnormal response to a food, triggered by the body's immune system." DSA04403,GSE189150,GPL21145|GPL24676,973,Food Allergy,C0016470,,GEO,RNA-Seq,Homo sapiens,18|1,"DO:A hypersensitivity reaction type I disease that is an abnormal response to a food, triggered by the body's immune system." DSA04404,GSE189150,GPL21145|GPL24676,1000,Food Allergy,C0016470,,GEO,RNA-Seq,Homo sapiens,18|1,"DO:A hypersensitivity reaction type I disease that is an abnormal response to a food, triggered by the body's immune system." DSA04405,GSE189150,GPL21145|GPL24676,1,Food Allergy,C0016470,,GEO,RNA-Seq,Homo sapiens,18|6,"DO:A hypersensitivity reaction type I disease that is an abnormal response to a food, triggered by the body's immune system." DSA04406,GSE189202,GPL24676,1000,Lewy Body Disease,C0752347,,GEO,scRNA-Seq,Homo sapiens,1|1,"DO:A dementia that is characterized by the development of abnormal proteinaceous (alpha-synuclein) cytoplasmic inclusions, called Lewy bodies, throughout the brain that results in progressive decline in mental abilities." DSA04407,GSE14245,GPL570,0,Pancreatic Cancer,C0235974,Saliva,GEO,Microarray,Homo sapiens,12|12,DO:An endocrine gland cancer located_in the pancreas. DSA04408,GSE189255,GPL13534,1,Multiple Sclerosis,C0026769,,GEO,Microarray,Homo sapiens,8|6,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA04409,GSE189256,GPL13534,0,Multiple Sclerosis,C0026769,,GEO,Microarray,Homo sapiens,8|6,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA04410,GSE189263,GPL30173,834,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,5|5,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04411,GSE189377,GPL19057,1000,Chronic Kidney Disease,C1561643,Kidney,GEO,RNA-Seq,Mus musculus,4|4,DO:A kidney failure that is characterized by the gradual loss of kidney function. DSA04412,GSE14668,GPL570,1000,Acute Liver Failure,C0162557,Liver,GEO,Microarray,Homo sapiens,8|12,"HPO:Hepatic failure refers to the inability of the liver to perform its normal synthetic and metabolic functions, which can result in coagulopathy and alteration in the mental status of a previously healthy individual. Hepatic failure is defined as fulminant if there is onset of encephalopathy within 4 weeks of the onset of symptoms in a patient with a previously healthy liver." DSA04413,GSE189555,GPL17021,144,Subretinal Fibrosis,,,GEO,RNA-Seq,Mus musculus,3|3, DSA04414,GSE14668,GPL570,1000,Acute Liver Failure,C0162557,Liver,GEO,Microarray,Homo sapiens,8|8,"HPO:Hepatic failure refers to the inability of the liver to perform its normal synthetic and metabolic functions, which can result in coagulopathy and alteration in the mental status of a previously healthy individual. Hepatic failure is defined as fulminant if there is onset of encephalopathy within 4 weeks of the onset of symptoms in a patient with a previously healthy liver." DSA04415,GSE189909,GPL20301,1000,Nedamss Syndrome,,,GEO,RNA-Seq,Homo sapiens,24|24, DSA04416,GSE189909,GPL20301,1000,Nedamss Syndrome,,,GEO,RNA-Seq,Homo sapiens,24|24, DSA04417,GSE14924,GPL570,1000,Acute Myeloid Leukemia,C0023467,,GEO,Microarray,Homo sapiens,10|10,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA04418,GSE14924,GPL570,1000,Acute Myeloid Leukemia,C0023467,,GEO,Microarray,Homo sapiens,11|10,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA04419,GSE189990,GPL18573,1000,COVID-19,D8888888,Peripheral venous blood,GEO,RNA-Seq,Homo sapiens,4|20,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04420,GSE190013,GPL24676,1000,Nasu-Hakola Disease,C1857316,Occipital cortex,GEO,RNA-Seq,Homo sapiens,10|1,DO:A syndrome that is characterized by progressive presenile dementia and recurrent bone fractures due to polycystic osseous lesions of the lower and upper extremities that has_material_basis_in homozygous mutation in the TYRO protein tyrosine kinase binding protein (TYROBP) gene on chromosome 19q13 or homozygous mutation in the triggering receptor expressed on myeloid cells 2 (TREM2) gene on chromosome 6p21. DSA04421,GSE190053,GPL24676,1000,Down Syndrome,C0013080,,GEO,RNA-Seq,Homo sapiens,9|6,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA04422,GSE190085,GPL18573,1000,Tendinopathy,C1568272,,GEO,RNA-Seq,Homo sapiens,12|12,"MONDO:Inflammation of a tendon, usually resulting from an overuse injury. It is characterized by swelling of the tendon, tenderness around the inflamed tendon, and pain while moving the affected area of the body." DSA04423,GSE190085,GPL18573,1000,Tendinopathy,C1568272,,GEO,RNA-Seq,Homo sapiens,12|12,"MONDO:Inflammation of a tendon, usually resulting from an overuse injury. It is characterized by swelling of the tendon, tenderness around the inflamed tendon, and pain while moving the affected area of the body." DSA04424,GSE190123,GPL11202,230,Neurotoxoplasmosis,C0751631,Cerebellum,GEO,Microarray,Mus musculus,15|15,"MSH:Infections of the BRAIN caused by the protozoan TOXOPLASMA gondii that primarily arise in individuals with IMMUNOLOGIC DEFICIENCY SYNDROMES (see also AIDS-RELATED OPPORTUNISTIC INFECTIONS). The infection may involve the brain diffusely or form discrete abscesses. Clinical manifestations include SEIZURES, altered mentation, headache, focal neurologic deficits, and INTRACRANIAL HYPERTENSION. (From Joynt, Clinical Neurology, 1998, Ch27, pp41-3)" DSA04425,GSE190123,GPL11202,33,Neurotoxoplasmosis,C0751631,Cerebellum,GEO,Microarray,Mus musculus,15|15,"MSH:Infections of the BRAIN caused by the protozoan TOXOPLASMA gondii that primarily arise in individuals with IMMUNOLOGIC DEFICIENCY SYNDROMES (see also AIDS-RELATED OPPORTUNISTIC INFECTIONS). The infection may involve the brain diffusely or form discrete abscesses. Clinical manifestations include SEIZURES, altered mentation, headache, focal neurologic deficits, and INTRACRANIAL HYPERTENSION. (From Joynt, Clinical Neurology, 1998, Ch27, pp41-3)" DSA04426,GSE190123,GPL11202,149,Neurotoxoplasmosis,C0751631,Cerebrum,GEO,Microarray,Mus musculus,15|15,"MSH:Infections of the BRAIN caused by the protozoan TOXOPLASMA gondii that primarily arise in individuals with IMMUNOLOGIC DEFICIENCY SYNDROMES (see also AIDS-RELATED OPPORTUNISTIC INFECTIONS). The infection may involve the brain diffusely or form discrete abscesses. Clinical manifestations include SEIZURES, altered mentation, headache, focal neurologic deficits, and INTRACRANIAL HYPERTENSION. (From Joynt, Clinical Neurology, 1998, Ch27, pp41-3)" DSA04427,GSE190123,GPL11202,1,Neurotoxoplasmosis,C0751631,Cerebrum,GEO,Microarray,Mus musculus,15|15,"MSH:Infections of the BRAIN caused by the protozoan TOXOPLASMA gondii that primarily arise in individuals with IMMUNOLOGIC DEFICIENCY SYNDROMES (see also AIDS-RELATED OPPORTUNISTIC INFECTIONS). The infection may involve the brain diffusely or form discrete abscesses. Clinical manifestations include SEIZURES, altered mentation, headache, focal neurologic deficits, and INTRACRANIAL HYPERTENSION. (From Joynt, Clinical Neurology, 1998, Ch27, pp41-3)" DSA04428,GSE190134,GPL18573,7,Ovarian Cancer,C1140680,,GEO,RNA-Seq,Homo sapiens,6|6,DO:A female reproductive organ cancer that is located_in the ovary. DSA04429,GSE190510,GPL24676,1000,Interstitial Lung Disease,C0206062,,GEO,scRNA-Seq,Homo sapiens,3|5,"DO:A lung disease that is characterized by inflammation and altered lung interstitium compromising pulmonary function and often has_symptom shortness of breath, dyspnea, and/or cough." DSA04430,GSE190635,GPL570,0,Aortic Dissection,C0340643,Artery,GEO,Microarray,Homo sapiens,4|4,HPO:Aortic dissection refers to a tear in the intimal layer of the aorta causing a separation between the intima and the medial layers of the aorta. DSA04431,GSE190639,GPL31059,68,Pre-Eclampsia,C0032914,Placenta,GEO,Microarray,Homo sapiens,13|13,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA04432,GSE190639,GPL31059,0,Pre-Eclampsia,C0032914,Placenta,GEO,Microarray,Homo sapiens,13|6,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA04433,GSE14951,GPL570,1000,Ischemia Reperfusion Injury,C0035126,Liver,GEO,Microarray,Homo sapiens,5|5,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA04434,GSE14951,GPL570,841,Ischemia Reperfusion Injury,C0035126,Liver,GEO,Microarray,Homo sapiens,5|5,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA04435,GSE14975,GPL570,4,Atrial Fibrillation,C0004238,Left atrial appendage,GEO,Microarray,Homo sapiens,5|5,"DO:A heart conduction disease that is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular and has symptoms palpitations, weakness, fatigue, lightheadedness, dizziness, confusion, shortness of breath and chest pain." DSA04436,GSE190752,GPL27644,1000,Non-Obstructive Azoospermia,C4021107,Testis,GEO,RNA-Seq,Homo sapiens,3|3,"HPO:Absence of any measurable level of sperm in his semen, resulting from a defect in the production of spermatozoa in the testes. This can be differentiated from obstructive azoospermia on the basis of testicular biopsy." DSA04437,GSE190786,GPL20795,1000,Periodontal Ehlers-Danlos Syndrome,C0268347,,GEO,RNA-Seq,Homo sapiens,3|2,"MONDO:Ehlers-Danlos syndromes (EDS) form a heterogeneous group of hereditary connective tissue diseases characterized by joint hyperlaxity, cutaneous hyperelasticity and tissue fragility." DSA04438,GSE190847,GPL23126,64,Primary Progressive Multiple Sclerosis,C0751964,Peripheral blood,GEO,Microarray,Homo sapiens,28|13,"DO:A multiple sclerosis that is characterized by steady worsening of neurologic functioning, without any distinct relapses or periods of remission. The rate of progression may vary over time, with occasional plateaus or temporary improvements, but the progression is continuous." DSA04439,GSE190869,GPL16791,1000,Large Artery Atherosclerotic Stroke,,,GEO,RNA-Seq,Homo sapiens,1|1, DSA04440,GSE15061,GPL570,1000,Acute Myeloid Leukemia,C0023467,Bone marrow,GEO,Microarray,Homo sapiens,69|199,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA04441,GSE191246,GPL24247,44,Crohn's Disease,C0010346,Colon,GEO,RNA-Seq,Mus musculus,8|8,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04442,GSE191246,GPL24247,171,Ulcerative Colitis,C0009324,Colon,GEO,RNA-Seq,Mus musculus,8|8,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA04443,GSE191246,GPL24247,367,Crohn's Disease,C0010346,Ileum,GEO,RNA-Seq,Mus musculus,2|2,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04444,GSE191246,GPL24247,110,Crohn's Disease,C0010346,Colon,GEO,RNA-Seq,Mus musculus,6|6,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04445,GSE191246,GPL24247,448,Ulcerative Colitis,C0009324,Colon,GEO,RNA-Seq,Mus musculus,6|8,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA04446,GSE191246,GPL24247,537,Crohn's Disease,C0010346,Ileum,GEO,RNA-Seq,Mus musculus,2|4,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04447,GSE191274,GPL23227,338,Sotos Syndrome,C4551477,Whole blood,GEO,RNA-Seq,Homo sapiens,10|5,DO:A syndrome that occurs rarely and is characterized by excessive physical growth during the first 2 to 3 years of life. DSA04448,GSE191274,GPL23227,112,Sotos Syndrome,C4551477,Whole blood,GEO,RNA-Seq,Homo sapiens,5|5,DO:A syndrome that occurs rarely and is characterized by excessive physical growth during the first 2 to 3 years of life. DSA04449,GSE191279,GPL24676,113,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,RNA-Seq,Homo sapiens,19|9,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA04450,GSE191279,GPL24676,324,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,RNA-Seq,Homo sapiens,18|9,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA04451,GSE191283,GPL19057,1000,Colorectal Carcinoma,C0009402,Heart,GEO,RNA-Seq,Mus musculus,1|1,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA04452,GSE191283,GPL19057,1000,Colorectal Carcinoma,C0009402,Heart,GEO,RNA-Seq,Mus musculus,1|1,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA04453,GSE191284,GPL19057,1000,Colorectal Carcinoma,C0009402,Lung,GEO,RNA-Seq,Mus musculus,1|1,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA04454,GSE191284,GPL19057,1000,Colorectal Carcinoma,C0009402,Lung,GEO,RNA-Seq,Mus musculus,1|1,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA04455,GSE19147,GPL96,175,B-Cell Chronic Lymphocytic Leukemia,C1868683,,GEO,Microarray,Homo sapiens,8|25,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA04456,GSE19151,GPL571,1000,Venous Thromboembolism,C1861172,Blood,GEO,Microarray,Homo sapiens,63|38,DO:A blood coagulation disease that is characterized by an increased tendency to form clots. DSA04457,GSE19151,GPL571,1000,Venous Thromboembolism,C1861172,Blood,GEO,Microarray,Homo sapiens,63|32,DO:A blood coagulation disease that is characterized by an increased tendency to form clots. DSA04458,GSE19187,GPL6244,3,Rhinitis,C0035455,Nasal airway epithelium,GEO,Microarray,Homo sapiens,11|14,"DO:A upper respiratory infectious disease which involves irritation and inflammation of the mucous membrane of the nose due to viruses, bacteria or irritants. The inflammation results in generation of excessive amounts of mucus leading to runny nose, as well as nasal congestion and post-nasal drip." DSA04459,GSE19187,GPL6244,19,Rhinitis,C0035455,Nasal airway epithelium,GEO,Microarray,Homo sapiens,11|7,"DO:A upper respiratory infectious disease which involves irritation and inflammation of the mucous membrane of the nose due to viruses, bacteria or irritants. The inflammation results in generation of excessive amounts of mucus leading to runny nose, as well as nasal congestion and post-nasal drip." DSA04460,GSE19187,GPL6244,211,Asthma,C0004096,Nasal airway epithelium,GEO,Microarray,Homo sapiens,11|6,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA04461,GSE19188,GPL570,1000,Non-Small Cell Lung Cancer,C0007131,,GEO,Microarray,Homo sapiens,65|45,DO:A respiratory system cancer that is located_in the lung. DSA04462,GSE19188,GPL570,1000,Non-Small Cell Lung Cancer,C0007131,,GEO,Microarray,Homo sapiens,65|19,DO:A respiratory system cancer that is located_in the lung. DSA04463,GSE19188,GPL570,1000,Non-Small Cell Lung Cancer,C0007131,,GEO,Microarray,Homo sapiens,65|27,DO:A respiratory system cancer that is located_in the lung. DSA04464,GSE19205,GPL571,0,Werner Syndrome,C0043119,,GEO,Microarray,Homo sapiens,3|3,"DO:A progeroid syndrome characterized by premature aging and age-related phenotypes such as atherosclerosis, arteriosclerosis, cataracts, osteoporosis, soft tissue calcification, premature thinning, graying, and loss of hair, as well as a high incidence of some types of cancers and that has_material_basis_in mutations in the WRN gene, on chromosome 8." DSA04465,GSE19205,GPL571,0,Bloom Syndrome,C0005859,,GEO,Microarray,Homo sapiens,3|3,"DO:A syndrome characterized by sun sensitivity, short stature, predisposition to the development of cancer and genomic instability." DSA04466,GSE19205,GPL571,0,Rubinstein-Taybi Syndrome,C0035934,,GEO,Microarray,Homo sapiens,3|3,DO:A syndrome characterized by congenital anomalies located_in heart and located_in upper limb. DSA04467,GSE192364,GPL24676,1000,Infant Acute Respiratory Distress Syndrome,C0035220,Bronchus,GEO,RNA-Seq,Homo sapiens,3|2,"DO:A respiratory failure that is characterized by deficiency of the surfactant coating the inner surface of the lungs, by failure of the lungs to expand and contract properly during breathing with resulting collapse, and by the accumulation of a protein-containing film lining the alveoli and their ducts." DSA04468,GSE192364,GPL24676,35,Infant Acute Respiratory Distress Syndrome,C0035220,Nasal mucosa,GEO,RNA-Seq,Homo sapiens,14|33,"DO:A respiratory failure that is characterized by deficiency of the surfactant coating the inner surface of the lungs, by failure of the lungs to expand and contract properly during breathing with resulting collapse, and by the accumulation of a protein-containing film lining the alveoli and their ducts." DSA04469,GSE192364,GPL24676,593,Infant Acute Respiratory Distress Syndrome,C0035220,Nasal mucosa,GEO,RNA-Seq,Homo sapiens,3|15,"DO:A respiratory failure that is characterized by deficiency of the surfactant coating the inner surface of the lungs, by failure of the lungs to expand and contract properly during breathing with resulting collapse, and by the accumulation of a protein-containing film lining the alveoli and their ducts." DSA04470,GSE192364,GPL24676,491,Infant Acute Respiratory Distress Syndrome,C0035220,Nasal mucosa,GEO,RNA-Seq,Homo sapiens,10|29,"DO:A respiratory failure that is characterized by deficiency of the surfactant coating the inner surface of the lungs, by failure of the lungs to expand and contract properly during breathing with resulting collapse, and by the accumulation of a protein-containing film lining the alveoli and their ducts." DSA04471,GSE192364,GPL24676,11,Infant Acute Respiratory Distress Syndrome,C0035220,Nasal mucosa,GEO,RNA-Seq,Homo sapiens,8|27,"DO:A respiratory failure that is characterized by deficiency of the surfactant coating the inner surface of the lungs, by failure of the lungs to expand and contract properly during breathing with resulting collapse, and by the accumulation of a protein-containing film lining the alveoli and their ducts." DSA04472,GSE15061,GPL570,1000,Myelodysplastic Syndrome,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,69|164,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA04473,GSE15061,GPL570,1000,Acute Myeloid Leukemia,C0023467,Bone marrow,GEO,Microarray,Homo sapiens,69|68,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA04474,GSE192707,GPL24676,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,5|10,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA04475,GSE192709,GPL24676,5,Familial Hypercholesterolemia,C0020445,,GEO,RNA-Seq,Homo sapiens,9|20,DO:A familial hyperlipidemia characterized by very high levels of low-density lipoprotein (LDL) and early cardiovascular disease. DSA04476,GSE192755,GPL24676,1000,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,2|4,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA04477,GSE57736,GPL13497,0,Tuberculosis,C0041296,Lung,GEO,Microarray,Homo sapiens,8|7,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA04478,GSE57772,GPL13912,0,Allergic Asthma,C0155877,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA04479,GSE57772,GPL13912,0,Allergic Asthma,C0155877,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA04480,GSE57803,GPL11154,711,Acromegaly,C0001206,Adipose tissue,GEO,RNA-Seq,Homo sapiens,11|7,DO:A disease of metabolism that has_material_basis_in excessive growth hormone production which results_in enlargement located_in limb. DSA04481,GSE57821,GPL17303,1000,Disrupted-In-Schizophrenia-1,,,GEO,RNA-Seq,Homo sapiens,3|6, DSA04482,GSE15072,GPL96,1000,Chronic Kidney Disease,C1561643,,GEO,Microarray,Homo sapiens,3|12,DO:A kidney failure that is characterized by the gradual loss of kidney function. DSA04483,GSE57944,GPL570,962,Hepatosplenic T-Cell Lymphoma,C1333984,Spleen,GEO,Microarray,Homo sapiens,3|4,"MONDO:An extranodal, mature T-cell non-Hodgkin lymphoma that originates from cytotoxic T-cells, usually of gamma/delta T-cell type. It is characterized by the presence of medium-size neoplastic lymphocytes infiltrating the hepatic sinusoids. A similar infiltrating pattern is also present in the spleen and bone marrow that are usually involved at the time of the diagnosis." DSA04484,GSE15072,GPL96,0,Chronic Kidney Disease,C1561643,,GEO,Microarray,Homo sapiens,3|9,DO:A kidney failure that is characterized by the gradual loss of kidney function. DSA04485,GSE58067,GPL18734,1000,Cockayne Syndrome,C0009207,Cerebellum,GEO,Microarray,Homo sapiens,6|6,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA04486,GSE5808,GPL96,19,Measles,C0025007,Blood,GEO,Microarray,Homo sapiens,3|15,"DO:A viral infectious disease that results_in infection located_in skin, has_material_basis_in Measles virus, which is transmitted_by contact with oronasal secretions, or semen of an infected person. The infection has_symptom fever, has_symptom cough, has_symptom coryza, has_symptom conjunctivitis, and has_symptom maculopapular, erythematous rash." DSA04487,GSE58178,GPL6947,772,Endometriosis,C0014175,Endometrium,GEO,Microarray,Homo sapiens,6|6,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA04488,GSE58291,GPL10558,1000,Infectious Keratitis,C3898765,Cornea,GEO,Microarray,Homo sapiens,12|7,NCI:Inflammation of the cornea secondary to an infectious process. DSA04489,GSE58291,GPL10558,1000,Infectious Keratitis,C3898765,Cornea,GEO,Microarray,Homo sapiens,12|8,NCI:Inflammation of the cornea secondary to an infectious process. DSA04490,GSE58430,GPL14550,1,Depression,C0011581,Peripheral blood,GEO,Microarray,Homo sapiens,6|6,DO:A mood disorder that involves the presence of a low mood almost daily over a span of at least two years. DSA04491,GSE58463,GPL6887,0,Monosomy 21,C0795875,Gastrocnemius muscle,GEO,Microarray,Mus musculus,6|6,"MONDO:Monosomy 21 is a chromosomal anomaly characterized by the loss of variable portions of a segment of the long arm of chromosome 21 that leads to an increased risk of birth defects, developmental delay and intellectual deficit." DSA04492,GSE58463,GPL6887,0,Down Syndrome,C0013080,Gastrocnemius muscle,GEO,Microarray,Mus musculus,5|6,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA04493,GSE15090,GPL570,0,Facioscapulohumeral Muscular Dystrophy,C0238288,Biceps,GEO,Microarray,Homo sapiens,5|5,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA04494,GSE5850,GPL570,0,Polycystic Ovary Syndrome,C0032460,,GEO,Microarray,Homo sapiens,6|6,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA04495,GSE58539,GPL10558,0,IgA Nephropathy,C0017661,,GEO,Microarray,Homo sapiens,9|8,DO:A glomerulonephritis characterized by build up of IgA antibody in the glomerulus. DSA04496,GSE58545,GPL96,1000,Papillary Thyroid Carcinoma,C0238463,Thyroid,GEO,Microarray,Homo sapiens,18|18,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA04497,GSE58545,GPL96,1000,Papillary Thyroid Carcinoma,C0238463,Thyroid,GEO,Microarray,Homo sapiens,18|8,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA04498,GSE58545,GPL96,1000,Papillary Thyroid Carcinoma,C0238463,Thyroid,GEO,Microarray,Homo sapiens,18|1,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA04499,GSE58625,GPL10332,0,Systemic Inflammatory Response Syndrome,C0242966,Blood,GEO,Microarray,Homo sapiens,22|22,"MSH:A systemic inflammatory response to a variety of clinical insults, characterized by two or more of the following conditions: (1) fever >38 degrees C or HYPOTHERMIA <36 degrees C; (2) TACHYCARDIA >90 beat/minute; (3) tachypnea >24 breaths/minute; (4) LEUKOCYTOSIS >12,000 cells/cubic mm or 10% immature forms. While usually related to infection, SIRS can also be associated with noninfectious insults such as TRAUMA; BURNS; or PANCREATITIS. If infection is involved, a patient with SIRS is said to have SEPSIS." DSA04500,GSE58640,GPL11154,1000,Eosinophilic Esophagitis,C0341106,Esophagus,GEO,RNA-Seq,Homo sapiens,6|9,DO:An esophagitis characterized by inflammation involving eosinophils located_in esophagus. DSA04501,GSE58667,GPL570,0,Juvenile Spondyloarthropathy,C0409676,Whole blood,GEO,Microarray,Homo sapiens,4|11,"MONDO:A group of chronic, inflammatory childhood diseases characterized by arthritis and enthesitis. This disorder can affect the axial skeleton in late childhood or young adulthood." DSA04502,GSE58831,GPL570,1000,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,17|159,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA04503,GSE58933,GPL16791,28,Bipolar Disorder,C0005586,Brain,GEO,RNA-Seq,Homo sapiens,4|6,DO:A mood disorder that involves alternating periods of mania and depression. DSA04504,GSE58934,GPL570,0,Frontal Fibrosing Alopecia,C4255374,Frontal scalp,GEO,Microarray,Homo sapiens,2|3,"EFO:A lichenoid and scarring inflammatory skin disorder associated with widespread cutaneous inflammation and irreversible hair loss, which occurs predominantly in women of post-menopausal age." DSA04505,GSE5900,GPL570,1000,Monoclonal Gammopathy of Undetermined Significance,C0026470,Bone marrow,GEO,Microarray,Homo sapiens,22|44,DO:A blood protein disease that is characterized by the presence of an abnormal protein called monoclonal protein in the blood. DSA04506,GSE5900,GPL570,1000,Smoldering Multiple Myeloma,C1531608,Bone marrow,GEO,Microarray,Homo sapiens,22|12,EFO:A plasma cell myeloma lacking clinical manifestations and organ impairment. DSA04507,GSE59019,GPL15207,0,Asthma,C0004096,,GEO,Microarray,Homo sapiens,6|7,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA04508,GSE59019,GPL15207,0,Asthma,C0004096,,GEO,Microarray,Homo sapiens,6|6,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA04509,GSE59051,GPL570,0,Huntington's Disease,C0020179,,GEO,Microarray,Homo sapiens,2|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA04510,GSE59085,GPL570,0,Clinically Isolated Syndrome,C2921627,Cerebrospinal fluid,GEO,Microarray,Homo sapiens,7|15, DSA04511,GSE59131,GPL570,0,Central Centrifugal Cicatricial Alopecia,C1274708,Frontal scalp,GEO,Microarray,Homo sapiens,3|3, DSA04512,GSE59131,GPL570,0,Lichen Planopilaris,C0023645,Occipital scalp,GEO,Microarray,Homo sapiens,7|7,"EFO:Lichen planopilaris (LPP) is an inflammatory condition that causes patchy hair loss, mainly on the scalp. It is a form of lichen planus that most often affects women in young adulthood. There are 3 forms of LPP, distinguished by specific patterns and locations of symptoms: classic LPP, frontal fibrosing alopecia, and Lassueur Graham-Little Piccardi syndrome." DSA04513,GSE59259,GPL18451,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,8|8,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA04514,GSE59307,GPL570,1000,Cutaneous T Cell Lymphoma,C0079773,Skin,GEO,Microarray,Homo sapiens,8|7,DO:A non-Hodgkin's lymphoma that has_material_basis_in a mutation of T cells. DSA04515,GSE59307,GPL570,1000,Cutaneous T Cell Lymphoma,C0079773,Skin,GEO,Microarray,Homo sapiens,8|2,DO:A non-Hodgkin's lymphoma that has_material_basis_in a mutation of T cells. DSA04516,GSE59307,GPL570,1000,Cutaneous T Cell Lymphoma,C0079773,Skin,GEO,Microarray,Homo sapiens,8|4,DO:A non-Hodgkin's lymphoma that has_material_basis_in a mutation of T cells. DSA04517,GSE59307,GPL570,1000,Cutaneous T Cell Lymphoma,C0079773,Skin,GEO,Microarray,Homo sapiens,8|1,DO:A non-Hodgkin's lymphoma that has_material_basis_in a mutation of T cells. DSA04518,GSE59337,GPL1261,0,Leukemia,C0023418,,GEO,Microarray,Mus musculus,2|2,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA04519,GSE59337,GPL1261,0,Leukemia,C0023418,,GEO,Microarray,Mus musculus,2|2,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA04520,GSE59363,GPL6244,2,Type 2 Diabetes,C0011860,Skeletal muscle,GEO,Microarray,Homo sapiens,7|7,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA04521,GSE59363,GPL6244,0,Type 2 Diabetes,C0011860,Skeletal muscle,GEO,Microarray,Homo sapiens,7|7,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA04522,GSE59363,GPL6244,0,Type 2 Diabetes,C0011860,Skeletal muscle,GEO,Microarray,Homo sapiens,7|7,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA04523,GSE59446,GPL18887,39,Kashin-Beck Disease,C2745963,,GEO,Microarray,Homo sapiens,100|100,"MONDO:Disabling osteochondrodysplasia with osteosclerosis, cone-shaped metaphysis, and shortening of the diaphysis. It is endemic in parts of Siberia and northern China. Mineral deficiencies (e.g., selenium, iodine), fungal cereal contamination, and water contamination may be contributing factors in its etiology." DSA04524,GSE60000,GPL6887,0,Fetal Alcohol Spectrum Disorder,C2985290,Hippocampus,GEO,Microarray,Mus musculus,6|6,"MONDO:A group of disorders caused by a prenatal exposure to maternal consumption of alcohol leading to a range of behavioral, cognitive and neurological deficits in the offspring. It is characterized by physical growth problems, distinct facies, and varying psycho-neurological issues." DSA04525,GSE15090,GPL570,0,Facioscapulohumeral Muscular Dystrophy,C0238288,Biceps,GEO,Microarray,Homo sapiens,5|5,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA04526,GSE15209,GPL570,1000,Glioma,C0017638,Brain,GEO,Microarray,Homo sapiens,6|9,DO:A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine. DSA04527,GSE60052,GPL11154,1000,Small Cell Lung Cancer,C0149925,Lung,GEO,RNA-Seq,Homo sapiens,7|79,DO:A lung carcinoma that has_material_basis_in primitive-appearing cells that are smaller than normal cells and is located_in the lung. DSA04528,GSE60083,GPL6884,0,Crohn's Disease,C0010346,,GEO,Microarray,Homo sapiens,42|58,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04529,GSE60088,GPL1261,1000,Multiple Organ Failure,C0026766,Lung,GEO,Microarray,Mus musculus,4|5,"MONDO:Fracture in the proximal half of the shaft of the ulna, with dislocation of the head of the radius." DSA04530,GSE60088,GPL1261,585,Multiple Organ Failure,C0026766,Liver,GEO,Microarray,Mus musculus,3|5,"MONDO:Fracture in the proximal half of the shaft of the ulna, with dislocation of the head of the radius." DSA04531,GSE60088,GPL1261,1000,Multiple Organ Failure,C0026766,Kidney,GEO,Microarray,Mus musculus,5|5,"MONDO:Fracture in the proximal half of the shaft of the ulna, with dislocation of the head of the radius." DSA04532,GSE60399,GPL18451,0,Chronic Obstructive Pulmonary Disease,C0024117,Peripheral blood,GEO,Microarray,Homo sapiens,1|4,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA04533,GSE60436,GPL6884,1000,Proliferative Diabetic Retinopathy,C0154830,Retina,GEO,Microarray,Homo sapiens,3|3,"EFO:Later stage of diabetic retinopathy, characterized by neovascularisation of the retina" DSA04534,GSE60436,GPL6884,1000,Proliferative Diabetic Retinopathy,C0154830,Retina,GEO,Microarray,Homo sapiens,3|3,"EFO:Later stage of diabetic retinopathy, characterized by neovascularisation of the retina" DSA04535,GSE6044,GPL201,288,Adenocarcinoma,C0001418,Lung,GEO,Microarray,Homo sapiens,5|10,"DO:A carcinoma that has_material_basis_in abnormally proliferating cells, derives_from epithelial cells, which originate in glandular tissue." DSA04536,GSE6044,GPL201,1000,Small Cell Lung Cancer,C0149925,Lung,GEO,Microarray,Homo sapiens,5|9,DO:A lung carcinoma that has_material_basis_in primitive-appearing cells that are smaller than normal cells and is located_in the lung. DSA04537,GSE6044,GPL201,315,Squamous Cell Carcinoma,C0007137,Lung,GEO,Microarray,Homo sapiens,5|10,DO:A carcinoma that derives_from squamous epithelial cells. DSA04538,GSE60460,GPL10787,49,Alzheimer's Disease,C0002395,Subventricular zone,GEO,Microarray,Mus musculus,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA04539,GSE60542,GPL570,1000,Papillary Thyroid Carcinoma,C0238463,Thyroid,GEO,Microarray,Homo sapiens,25|33,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA04540,GSE60601,GPL570,0,Pancreatic Ductal Adenocarcinoma,C1335302,,GEO,Microarray,Homo sapiens,3|5,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA04541,GSE60674,GPL10739,1000,Chronic Graft-Versus-Host Disease,C0867389,,GEO,Microarray,Homo sapiens,10|26,"MONDO:Chronic graft versus host disease (GVHD) is a complication that can occur after a stem cell or bone marrow transplant in which the newly transplanted donor cells attack the transplant recipient's body. Symptoms may include skin rash, mouth sores, dry eyes, liver inflammation, development of scar tissue in the skin and joints, and damage to the lungs. The exact cause of chronic GVHD is unknown.It likely results from a complex immune-mediated interaction between the donor and recipient cells.Chronic GVHD is treated with prednisone or other similar anti-inflammatory or immunosuppressive medications." DSA04542,GSE60709,GPL6947,390,Atopic Dermatitis,C0011615,Skin,GEO,Microarray,Homo sapiens,7|12,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA04543,GSE60709,GPL6947,894,Atopic Dermatitis,C0011615,Skin,GEO,Microarray,Homo sapiens,14|12,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA04544,GSE60762,GPL6244,0,Osteoarthritis,C0157946,Acetabular labrum,GEO,Microarray,Homo sapiens,3|5,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA04545,GSE15209,GPL570,852,Glioma,C0017638,Brain,GEO,Microarray,Homo sapiens,5|9,DO:A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine. DSA04546,GSE15296,GPL570,1000,Chronic Rejection of Renal Transplant,C0403592,Peripheral Blood,GEO,Microarray,Homo sapiens,24|51,"MONDO:Crouzon syndrome with acanthosis nigricans (CAN) is a very rare, clinically heterogeneous form of faciocraniostenosis with Crouzon-like features and premature synostosis of cranial sutures (Crouzon disease), associated with acanthosis nigricans (AN)." DSA04547,GSE60925,GPL19138,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Mus musculus,5|5,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA04548,GSE60925,GPL19138,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Mus musculus,5|6,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA04549,GSE60993,GPL6884,0,Acute Coronary Syndrome,C0948089,Blood,GEO,Microarray,Homo sapiens,7|10,EFO:Signs and symptoms related to acute ischemia of the myocardium secondary to coronary artery disease. The clinical presentation covers a spectrum of heart diseases from unstable angina to myocardial infarction. DSA04550,GSE60993,GPL6884,1000,Acute Coronary Syndrome,C0948089,Blood,GEO,Microarray,Homo sapiens,7|7,EFO:Signs and symptoms related to acute ischemia of the myocardium secondary to coronary artery disease. The clinical presentation covers a spectrum of heart diseases from unstable angina to myocardial infarction. DSA04551,GSE60993,GPL6884,0,Acute Coronary Syndrome,C0948089,Blood,GEO,Microarray,Homo sapiens,7|9,EFO:Signs and symptoms related to acute ischemia of the myocardium secondary to coronary artery disease. The clinical presentation covers a spectrum of heart diseases from unstable angina to myocardial infarction. DSA04552,GSE61019,GPL10558,1000,Ataxia-Telangiectasia,C0004135,Cerebellum,GEO,Microarray,Homo sapiens,4|3,"DO:An autosomal recessive cerebellar ataxia that is characterized by cerebellar ataxia, telangiectases, immune defects, and a predisposition to malignancy and that has_material_basis_in homozygous or compound heterozygous mutation in the ATM gene on chromosome 11q22." DSA04553,GSE61120,GPL13667,1,Silver-Russell Syndrome,C0175693,Skin,GEO,Microarray,Homo sapiens,4|8,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA04554,GSE61120,GPL13667,0,Silver-Russell Syndrome,C0175693,Skin,GEO,Microarray,Homo sapiens,4|4,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA04555,GSE61140,GPL6246,4,Rheumatoid Arthritis,C0003873,Tarsal joint,GEO,Microarray,Mus musculus,3|3,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04556,GSE61140,GPL6246,1000,Rheumatoid Arthritis,C0003873,Tarsal joint,GEO,Microarray,Mus musculus,3|3,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04557,GSE61140,GPL6246,12,Rheumatoid Arthritis,C0003873,Tarsal joint,GEO,Microarray,Mus musculus,3|3,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04558,GSE61140,GPL6246,0,Rheumatoid Arthritis,C0003873,Tarsal joint,GEO,Microarray,Mus musculus,3|3,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04559,GSE15471,GPL570,1000,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,Microarray,Homo sapiens,39|39,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA04560,GSE15578,GPL570,932,Ovarian Cancer,C1140680,,GEO,Microarray,Homo sapiens,6|4,DO:A female reproductive organ cancer that is located_in the ovary. DSA04561,GSE61144,GPL6106,1000,Acute Coronary Syndrome,C0948089,Peripheral blood,GEO,Microarray,Homo sapiens,10|7,EFO:Signs and symptoms related to acute ischemia of the myocardium secondary to coronary artery disease. The clinical presentation covers a spectrum of heart diseases from unstable angina to myocardial infarction. DSA04562,GSE61203,GPL5175,178,Smith-Lemli-Opitz Syndrome,C0175694,,GEO,Microarray,Homo sapiens,4|4,"MONDO:Smith-Lemli-Opitz syndrome (SLOS) is characterized by multiple congenital anomalies, intellectual deficit, and behavioral problems." DSA04563,GSE61203,GPL5175,417,Smith-Lemli-Opitz Syndrome,C0175694,,GEO,Microarray,Homo sapiens,4|4,"MONDO:Smith-Lemli-Opitz syndrome (SLOS) is characterized by multiple congenital anomalies, intellectual deficit, and behavioral problems." DSA04564,GSE61203,GPL5175,490,Smith-Lemli-Opitz Syndrome,C0175694,,GEO,Microarray,Homo sapiens,4|4,"MONDO:Smith-Lemli-Opitz syndrome (SLOS) is characterized by multiple congenital anomalies, intellectual deficit, and behavioral problems." DSA04565,GSE61203,GPL5175,1000,Smith-Lemli-Opitz Syndrome,C0175694,,GEO,Microarray,Homo sapiens,4|4,"MONDO:Smith-Lemli-Opitz syndrome (SLOS) is characterized by multiple congenital anomalies, intellectual deficit, and behavioral problems." DSA04566,GSE61203,GPL5175,1000,Smith-Lemli-Opitz Syndrome,C0175694,,GEO,Microarray,Homo sapiens,4|4,"MONDO:Smith-Lemli-Opitz syndrome (SLOS) is characterized by multiple congenital anomalies, intellectual deficit, and behavioral problems." DSA04567,GSE61203,GPL5175,1000,Smith-Lemli-Opitz Syndrome,C0175694,,GEO,Microarray,Homo sapiens,4|4,"MONDO:Smith-Lemli-Opitz syndrome (SLOS) is characterized by multiple congenital anomalies, intellectual deficit, and behavioral problems." DSA04568,GSE61218,GPL19061,1000,Nasopharyngeal Carcinoma,C2931822,Nasopharynx,GEO,Microarray,Homo sapiens,6|10,"DO:A pharynx cancer that is located in the nasopharynx, the uppermost region of the pharynx or throat, where the nasal passages and auditory tubes join the remainder of the upper respiratory tract." DSA04569,GSE6136,GPL8321,203,Lymphoma,C0024299,,GEO,Microarray,Mus musculus,5|6,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA04570,GSE6136,GPL8321,1000,Lymphoma,C0024299,,GEO,Microarray,Mus musculus,5|7,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA04571,GSE6136,GPL8321,739,Lymphoma,C0024299,,GEO,Microarray,Mus musculus,5|5,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA04572,GSE61399,GPL570,1,Behcet's Disease,C0004943,Peripheral blood,GEO,Microarray,Homo sapiens,3|9,"DO:A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis." DSA04573,GSE61399,GPL570,1000,Behcet's Disease,C0004943,Peripheral blood,GEO,Microarray,Homo sapiens,9|8,"DO:A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis." DSA04574,GSE61405,GPL9115,138,Huntington's Disease,C0020179,Peripheral blood,GEO,RNA-Seq,Homo sapiens,8|11,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA04575,GSE61490,GPL11154,4,Chronic Periodontitis,C0266929,Peripheral blood,GEO,RNA-Seq,Homo sapiens,5|5,"EFO:Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology)" DSA04576,GSE61651,GPL6244,761,Waldenstrom Macroglobulinemia,C0024419,Bone marrow,GEO,Microarray,Homo sapiens,17|4,DO:A B-cell lymphocytic neoplasm characterized by an uncontrolled increase of B-cells. DSA04577,GSE61651,GPL6244,1000,Waldenstrom Macroglobulinemia,C0024419,Bone marrow,GEO,Microarray,Homo sapiens,17|6,DO:A B-cell lymphocytic neoplasm characterized by an uncontrolled increase of B-cells. DSA04578,GSE61651,GPL6244,95,Waldenstrom Macroglobulinemia,C0024419,Bone marrow,GEO,Microarray,Homo sapiens,17|4,DO:A B-cell lymphocytic neoplasm characterized by an uncontrolled increase of B-cells. DSA04579,GSE62013,GPL8321,0,Diabetes,C0011847,Hypothalamus,GEO,Microarray,Mus musculus,6|6,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA04580,GSE62014,GPL18281,881,Blastic Plasmacytoid Dendritic Cell Neoplasm (Bpdcn),C4509017,,GEO,Microarray,Homo sapiens,4|25, DSA04581,GSE62019,GPL10558,0,Focal Cortical Dysplasia,C2938983,Brain,GEO,Microarray,Homo sapiens,3|5,"HPO:A type of malformation of cortical development that primarily affects areas of neocortex. It can be identified on conventional magnetic resonance imaging as focal cortical thickening, abnormal gyration, and blurring between gray and white matter, often associated with clusters of heterotopic neurons." DSA04582,GSE62019,GPL10558,0,Tuberous Sclerosis,C0041341,Brain,GEO,Microarray,Homo sapiens,3|3,DO:A tuberous sclerosis that is characterized by hamartomas in multiple organ systems and has_material_basis_in heterozygous mutation in the TSC1 gene on chromosome 9q34. DSA04583,GSE62333,GPL11532,26,Schizophrenia,C0036341,Skin,GEO,Microarray,Homo sapiens,20|20,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04584,GSE62525,GPL16951,1000,Tuberculosis,C0041296,Peripheral blood,GEO,Microarray,Homo sapiens,14|14,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA04585,GSE62525,GPL16951,1000,Tuberculosis,C0041296,Peripheral blood,GEO,Microarray,Homo sapiens,14|14,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA04586,GSE62584,GPL571,0,Optic Neuritis,C0029134,,GEO,Microarray,Homo sapiens,9|6,DO:An optic nerve disease that results_in inflammation located_in optic nerve which may cause a complete or partial loss of vision. DSA04587,GSE62584,GPL571,2,Optic Neuritis,C0029134,,GEO,Microarray,Homo sapiens,9|6,DO:An optic nerve disease that results_in inflammation located_in optic nerve which may cause a complete or partial loss of vision. DSA04588,GSE62584,GPL571,13,Optic Neuritis,C0029134,,GEO,Microarray,Homo sapiens,9|6,DO:An optic nerve disease that results_in inflammation located_in optic nerve which may cause a complete or partial loss of vision. DSA04589,GSE62584,GPL571,0,Optic Neuritis,C0029134,,GEO,Microarray,Homo sapiens,9|6,DO:An optic nerve disease that results_in inflammation located_in optic nerve which may cause a complete or partial loss of vision. DSA04590,GSE62594,GPL13912,207,Autism,C1510586,Cerebellum,GEO,Microarray,Mus musculus,4|4,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA04591,GSE62594,GPL13912,221,Autism,C1510586,Cerebellum,GEO,Microarray,Mus musculus,4|4,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA04592,GSE62642,GPL16791,786,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,4|2,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA04593,GSE62642,GPL16791,751,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,4|4,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA04594,GSE62646,GPL6244,1000,St Segment Elevation Myocardial Infarction,C1536220,Peripheral blood,GEO,Microarray,Homo sapiens,14|28,"MSH:A clinical syndrome defined by MYOCARDIAL ISCHEMIA symptoms; persistent elevation in the ST segments of the ELECTROCARDIOGRAM; and release of BIOMARKERS of myocardial NECROSIS (e.g., elevated TROPONIN levels). ST segment elevation in the ECG is often used in determining the treatment protocol (see also NON-ST ELEVATION MYOCARDIAL INFARCTION)." DSA04595,GSE62646,GPL6244,1000,St Segment Elevation Myocardial Infarction,C1536220,Peripheral blood,GEO,Microarray,Homo sapiens,14|28,"MSH:A clinical syndrome defined by MYOCARDIAL ISCHEMIA symptoms; persistent elevation in the ST segments of the ELECTROCARDIOGRAM; and release of BIOMARKERS of myocardial NECROSIS (e.g., elevated TROPONIN levels). ST segment elevation in the ECG is often used in determining the treatment protocol (see also NON-ST ELEVATION MYOCARDIAL INFARCTION)." DSA04596,GSE62646,GPL6244,1000,St Segment Elevation Myocardial Infarction,C1536220,Peripheral blood,GEO,Microarray,Homo sapiens,14|28,"MSH:A clinical syndrome defined by MYOCARDIAL ISCHEMIA symptoms; persistent elevation in the ST segments of the ELECTROCARDIOGRAM; and release of BIOMARKERS of myocardial NECROSIS (e.g., elevated TROPONIN levels). ST segment elevation in the ECG is often used in determining the treatment protocol (see also NON-ST ELEVATION MYOCARDIAL INFARCTION)." DSA04597,GSE62732,GPL1261,0,Acute Kidney Injury,C2609414,Kidney,GEO,Microarray,Mus musculus,3|5,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA04598,GSE62747,GPL4133,1000,Liposarcoma,C0023827,,GEO,Microarray,Homo sapiens,1|7,DO:A connective tissue cancer that arises in fat cells in deep soft tissue retroperitoneum and the extremities. DSA04599,GSE62764,GPL5188,0,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,3|5,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA04600,GSE62764,GPL5188,0,Lupus Nephritis,C0024143,Blood,GEO,Microarray,Homo sapiens,3|3,DO:A glomerulonephritis that is characterized by inflammation of the kidneys resulting from systemic lupus erythematosus. DSA04601,GSE62792,GPL10558,1000,Chronic Kidney Disease,C1561643,Blood,GEO,Microarray,Homo sapiens,3|3,DO:A kidney failure that is characterized by the gradual loss of kidney function. DSA04602,GSE62792,GPL10558,1000,Chronic Kidney Disease,C1561643,Blood,GEO,Microarray,Homo sapiens,3|3,DO:A kidney failure that is characterized by the gradual loss of kidney function. DSA04603,GSE62792,GPL10558,1000,Chronic Kidney Disease,C1561643,Blood,GEO,Microarray,Homo sapiens,3|3,DO:A kidney failure that is characterized by the gradual loss of kidney function. DSA04604,GSE62792,GPL10558,1000,Chronic Kidney Disease,C1561643,Blood,GEO,Microarray,Homo sapiens,3|3,DO:A kidney failure that is characterized by the gradual loss of kidney function. DSA04605,GSE6281,GPL570,0,Allergic Contact Dermatitis,C0162820,Skin,GEO,Microarray,Homo sapiens,3|4,"DO:A contact dermatitis that is an allergic skin reaction to foreign chemical or substances leading to red, itchy, weepy reaction where the skin has come into contact with a substance that the immune system recognizes as foreign." DSA04606,GSE6281,GPL570,0,Allergic Contact Dermatitis,C0162820,Skin,GEO,Microarray,Homo sapiens,4|3,"DO:A contact dermatitis that is an allergic skin reaction to foreign chemical or substances leading to red, itchy, weepy reaction where the skin has come into contact with a substance that the immune system recognizes as foreign." DSA04607,GSE6281,GPL570,999,Allergic Contact Dermatitis,C0162820,Skin,GEO,Microarray,Homo sapiens,5|5,"DO:A contact dermatitis that is an allergic skin reaction to foreign chemical or substances leading to red, itchy, weepy reaction where the skin has come into contact with a substance that the immune system recognizes as foreign." DSA04608,GSE6281,GPL570,1000,Allergic Contact Dermatitis,C0162820,Skin,GEO,Microarray,Homo sapiens,4|6,"DO:A contact dermatitis that is an allergic skin reaction to foreign chemical or substances leading to red, itchy, weepy reaction where the skin has come into contact with a substance that the immune system recognizes as foreign." DSA04609,GSE6283,GPL570,0,Patau Syndrome,C0152095,,GEO,Microarray,Homo sapiens,3|3,"MONDO:Trisomy 13 is a chromosomal anomaly caused by the presence of an extra chromosome 13 and is characterized by brain malformations (holoprosencephaly), facial dysmorphism, ocular anomalies, postaxial polydactyly, visceral malformations (cardiopathy) and severe psychomotor retardation." DSA04610,GSE6283,GPL570,0,Down Syndrome,C0013080,,GEO,Microarray,Homo sapiens,3|3,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA04611,GSE6283,GPL570,5,Edwards Syndrome,C4317091,,GEO,Microarray,Homo sapiens,6|3,DO:A chromosomal duplciation syndrome that is characterized by slow growth before birth and a low birth weight and that has_material_basis_in three copies of chromosome 18. DSA04612,GSE6283,GPL570,5,Down Syndrome,C0013080,,GEO,Microarray,Homo sapiens,6|3,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA04613,GSE62932,GPL570,1000,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,4|12,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA04614,GSE62932,GPL570,532,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,4|17,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA04615,GSE62932,GPL570,1000,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,4|20,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA04616,GSE62932,GPL570,809,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,4|15,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA04617,GSE62935,GPL10558,0,Frontotemporal Dementia,C0338451,,GEO,Microarray,Homo sapiens,3|2,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA04618,GSE62935,GPL10558,61,Frontotemporal Dementia,C0338451,,GEO,Microarray,Homo sapiens,6|6,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA04619,GSE63040,GPL19389,0,7Q31 Microdeletion Syndrome,C4750783,,GEO,Microarray,Homo sapiens,4|3,"ORDO:7q31 microdeletion syndrome is a rare chromosomal anomaly characterized by speech and language disorder, predominantly presenting as an apraxia of speech, sometimes associated with oral motor dyspraxia, dysarthria, receptive and expressive language disorder, and hearing loss. Individuals with larger deletions in this region have also been reported to display intellectual disability and autism." DSA04620,GSE63040,GPL19389,0,Williams-Beuren Syndrome,C0175702,,GEO,Microarray,Homo sapiens,4|3,"DO:A syndrome that is characterized by mild to moderate intellectual disability, a broad forehead, a short nose with a broad tip, full cheeks, and a wide mouth with full lips and difficulty with visual-spatial tasks and has_material_basis_in hemizygous deletion of 1.5 to 1.8 Mb on chromosome 7q11.23." DSA04621,GSE63040,GPL19389,0,7Q31 Microdeletion Syndrome,C4750783,,GEO,Microarray,Homo sapiens,4|4,"ORDO:7q31 microdeletion syndrome is a rare chromosomal anomaly characterized by speech and language disorder, predominantly presenting as an apraxia of speech, sometimes associated with oral motor dyspraxia, dysarthria, receptive and expressive language disorder, and hearing loss. Individuals with larger deletions in this region have also been reported to display intellectual disability and autism." DSA04622,GSE63040,GPL19389,0,Williams-Beuren Syndrome,C0175702,,GEO,Microarray,Homo sapiens,4|5,"DO:A syndrome that is characterized by mild to moderate intellectual disability, a broad forehead, a short nose with a broad tip, full cheeks, and a wide mouth with full lips and difficulty with visual-spatial tasks and has_material_basis_in hemizygous deletion of 1.5 to 1.8 Mb on chromosome 7q11.23." DSA04623,GSE63045,GPL10558,408,Mitral Regurgitation,C0026266,Atria,GEO,Microarray,Homo sapiens,3|7,HPO:An abnormality of the mitral valve characterized by insufficiency or incompetence of the mitral valve resulting in retrograde leaking of blood through the mitral valve upon ventricular contraction. DSA04624,GSE15578,GPL570,72,Ovarian Cancer,C1140680,,GEO,Microarray,Homo sapiens,7|4,DO:A female reproductive organ cancer that is located_in the ovary. DSA04625,GSE15605,GPL570,1000,Melanoma,C0025202,,GEO,Microarray,Homo sapiens,16|46,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA04626,GSE63055,GPL11154,337,7Q31 Microdeletion Syndrome,C4750783,Skin,GEO,RNA-Seq,Homo sapiens,2|2,"ORDO:7q31 microdeletion syndrome is a rare chromosomal anomaly characterized by speech and language disorder, predominantly presenting as an apraxia of speech, sometimes associated with oral motor dyspraxia, dysarthria, receptive and expressive language disorder, and hearing loss. Individuals with larger deletions in this region have also been reported to display intellectual disability and autism." DSA04627,GSE63055,GPL11154,872,Williams-Beuren Syndrome,C0175702,Skin,GEO,RNA-Seq,Homo sapiens,2|5,"DO:A syndrome that is characterized by mild to moderate intellectual disability, a broad forehead, a short nose with a broad tip, full cheeks, and a wide mouth with full lips and difficulty with visual-spatial tasks and has_material_basis_in hemizygous deletion of 1.5 to 1.8 Mb on chromosome 7q11.23." DSA04628,GSE63068,GPL1261,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Mus musculus,5|5,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA04629,GSE63068,GPL1261,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Mus musculus,5|4,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA04630,GSE63068,GPL8321,74,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Mus musculus,5|5,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA04631,GSE63068,GPL570,0,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Homo sapiens,7|9,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA04632,GSE63085,GPL11154,1000,Lyme Disease,C0024198,,GEO,RNA-Seq,Homo sapiens,13|28,"DO:A primary bacterial infectious disease that results_in infection, has_material_basis_in Borrelia burgdorferi, which is transmitted_by blacklegged tick (Ixodes scapularis) or transmitted_by western blacklegged tick (Ixodes pacificus). The infection has_symptom fever, has_symptom headache, has_symptom fatigue, and has_symptom skin rash called erythema migrans. If left untreated, infection can spread to joints, the heart, and the nervous system." DSA04633,GSE63161,GPL11154,1000,Left Ventricular Noncompaction,C1960469,,GEO,RNA-Seq,Homo sapiens,2|2,DO:An intrinsic cardiomyopathy characterized by distinctive (spongy) morphological appearance of the LV myocardium. DSA04634,GSE63214,GPL19407,1000,Hepatocellular Carcinoma,C0334287,,GEO,Microarray,Homo sapiens,12|12,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA04635,GSE63264,GPL1261,1000,Peripheral T-Cell Lymphoma,C0079774,,GEO,Microarray,Mus musculus,3|4,DO:A mature T-cell and NK-cell lymphoma includes a group of T-cell lymphomas that develop away from the thymus. DSA04636,GSE63264,GPL1261,1000,Thymic Lymphoma,C1336745,,GEO,Microarray,Mus musculus,3|3,DO:A thymus cancer that arises from the thymus. DSA04637,GSE63272,GPL6246,108,Focal Segmental Glomerulosclerosis,C0017668,,GEO,Microarray,Mus musculus,3|3,"EFO:A renal disorder characterized by sclerotic lesions in the glomeruli. Causes include drugs, viruses, and malignancies (lymphomas), or it may be idiopathic. It presents with asymptomatic proteinuria or nephritic syndrome and it may lead to renal failure." DSA04638,GSE63272,GPL6246,242,Focal Segmental Glomerulosclerosis,C0017668,,GEO,Microarray,Mus musculus,3|3,"EFO:A renal disorder characterized by sclerotic lesions in the glomeruli. Causes include drugs, viruses, and malignancies (lymphomas), or it may be idiopathic. It presents with asymptomatic proteinuria or nephritic syndrome and it may lead to renal failure." DSA04639,GSE63272,GPL6246,0,Focal Segmental Glomerulosclerosis,C0017668,,GEO,Microarray,Mus musculus,3|3,"EFO:A renal disorder characterized by sclerotic lesions in the glomeruli. Causes include drugs, viruses, and malignancies (lymphomas), or it may be idiopathic. It presents with asymptomatic proteinuria or nephritic syndrome and it may lead to renal failure." DSA04640,GSE63311,GPL10999,502,Sepsis,C0243026,Whole blood,GEO,RNA-Seq,Homo sapiens,11|36,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA04641,GSE63359,GPL96,1000,Osteoarthritis of Knee,C0409959,Peripheral blood,GEO,Microarray,Homo sapiens,26|46,"EFO:Noninflammatory degenerative disease of the knee joint consisting of three large categories: conditions that block normal synchronous movement, conditions that produce abnormal pathways of motion, and conditions that cause stress concentration resulting in changes to articular cartilage. (Crenshaw, Campbell's Operative Orthopaedics, 8th ed, p2019)" DSA04642,GSE63379,GPL17586,0,Irritable Bowel Syndrome,C0022104,Blood,GEO,Microarray,Homo sapiens,32|35,"DO:An intestinal disease that is characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause." DSA04643,GSE6338,GPL570,1000,Peripheral T-Cell Lymphoma; Not Otherwise Specified,C0279702,Lymph node,GEO,Microarray,Homo sapiens,20|40,DO:A hereditary renal cell carcinoma that has_material_basis_in a loss of 3p13-pter sequences. DSA04644,GSE63383,GPL6244,0,Asthma,C0004096,Airway smooth muscle,GEO,Microarray,Homo sapiens,3|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA04645,GSE63425,GPL19433,0,Giant Cell Arteritis,C0039483,Temporal artery,GEO,Microarray,Homo sapiens,4|4,"DO:A central nervous system vasculitis that is characterized by inflammation of the lining of arteries, often arteries in the head." DSA04646,GSE63548,GPL10558,1000,Tuberculosis,C0041296,Lymph node,GEO,Microarray,Homo sapiens,4|22,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA04647,GSE63569,GPL11154,1000,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,RNA-Seq,Homo sapiens,5|8,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA04648,GSE63569,GPL11154,139,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,RNA-Seq,Homo sapiens,5|4,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA04649,GSE63571,GPL5175,145,Lung Cancer,C0684249,Lung,GEO,Microarray,Homo sapiens,2|6,DO:A respiratory system cancer that is located_in the lung. DSA04650,GSE63571,GPL5175,1000,Metastatic Lung Cancer,C0684249,Lung,GEO,Microarray,Homo sapiens,2|4,DO:A respiratory system cancer that is located_in the lung. DSA04651,GSE15605,GPL570,1000,Melanoma,C0025202,,GEO,Microarray,Homo sapiens,16|12,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA04652,GSE63627,GPL1261,1000,Mammary Tumor,C1512981,Mammary gland,GEO,Microarray,Mus musculus,3|11,NCI:Production of a new growth or growths in the mammary gland. DSA04653,GSE63627,GPL1261,1000,Lung Metastases,C0153676,Lung,GEO,Microarray,Mus musculus,3|9,"NCI:The spread of a malignant neoplasm to the lung. This may be from a primary lung malignant neoplasm, or from a malignant neoplasm at a distant site." DSA04654,GSE63687,GPL6887,1000,Liver Tumor,C0345904,Liver,GEO,Microarray,Mus musculus,10|29,DO:A hepatobiliary system cancer that is located_in the liver. DSA04655,GSE63687,GPL6887,1000,T-Cell Acute Lymphoblastic Leukemia,C1961099,Thymus,GEO,Microarray,Mus musculus,5|9,DO:An acute lymphoblastic leukemia that is characterized by too many T-cell lymphoblasts found in the bone marrow and blood. DSA04656,GSE63744,GPL18460,5,Asthma,C0004096,Lung,GEO,RNA-Seq,Homo sapiens,6|8,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA04657,GSE63816,GPL11154,72,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA04658,GSE63816,GPL11154,899,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,RNA-Seq,Homo sapiens,4|8,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA04659,GSE63870,GPL17077,0,Severe Cognitive Disability And Early Dementia,,Blood,GEO,Microarray,Homo sapiens,28|7, DSA04660,GSE63870,GPL17077,0,Cognitive Dysfunction,C1270972,Blood,GEO,Microarray,Homo sapiens,5|8,"EFO:mild neurocognitive disorder (MND) is a mild form of HIV-associated neurocognitive disorder (HAND), defined as mild neuropsychological impairment in two or more domains with at least mildly decreased everyday functioning" DSA04661,GSE63903,GPL10558,0,Systemic Sclerosis [Scleroderma],C2364016,,GEO,Microarray,Homo sapiens,5|9, DSA04662,GSE64003,GPL10558,0,Facioscapulohumeral Muscular Dystrophy,C0238288,Skeletal muscle,GEO,Microarray,Homo sapiens,9|9,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA04663,GSE64003,GPL10558,9,Becker Muscular Dystrophy,C0917713,Skeletal muscle,GEO,Microarray,Homo sapiens,9|3,"DO:A muscular dystrophy that involves slowly worsening muscle weakness of the legs and pelvis, and has_material_basis_in X-linked recessive inheritance of mutation in the dystrophin gene on chromosome Xp21." DSA04664,GSE64018,GPL11154,1000,Autism,C1510586,Brain,GEO,RNA-Seq,Homo sapiens,12|12,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA04665,GSE64031,GPL17810,1000,CHOPS Syndrome,C4085597,,GEO,Microarray,Homo sapiens,6|4,"EFO:A multiple congenital anomaly syndrome with delayed psychomotor development with intellectual disability, short stature, obesity, variable dysmorphic facial features (round face, proptosis, hypertelorism, thick eyebrows and hair, long eyelashes, short nose and downturned corners of the mouth), heart defects, increased chance of chronic lung disease, skeletal defects such as brachydactyly, gastroesophageal reflux." DSA04666,GSE64034,GPL17889,205,Cornelia De Lange Syndrome,C0270972,,GEO,Microarray,Homo sapiens,8|8,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA04667,GSE64041,GPL6244,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,5|60,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA04668,GSE64041,GPL6244,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,60|60,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA04669,GSE64271,GPL6885,1000,Tongue Tumor,C0040411,Tongue,GEO,Microarray,Mus musculus,5|7,EFO:Tumors or cancer of the TONGUE. DSA04670,GSE64387,GPL17077,308,Prolidase Deficiency,C0268532,,GEO,Microarray,Homo sapiens,3|17,"MONDO:An inherited disorder of peptide metabolism characterized by severe skin lesions, recurrent infections (involving mainly the skin and respiratory system), dysmorphic facial features, variable cognitive impairment, and splenomegaly." DSA04671,GSE64392,GPL16686,1000,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,15|22,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA04672,GSE64457,GPL570,1000,Sepsis,C0243026,,GEO,Microarray,Homo sapiens,8|15,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA04673,GSE64486,GPL11154,962,Kawasaki Disease,C0026691,Coronary artery,GEO,RNA-Seq,Homo sapiens,7|4,"DO:A lymphadenitis characterized by swelling of cervical lymph nodes in infants and young children and inflammation of medium-sized blood vessels located_in body, has_symptom fever, has_symptom congestion of ocular conjunctivae, has_symptom reddening of lips, has_symptom reddening of oral cavity, has_symptom protuberance of tongue papillae and has_symptom edema of extremities." DSA04674,GSE64566,GPL6947,0,Coronary Artery Disease,C1956346,Subcutaneous adipose tissue,GEO,Microarray,Homo sapiens,10|13,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA04675,GSE64566,GPL6947,0,Coronary Artery Disease,C1956346,Epicardial adipose tissue,GEO,Microarray,Homo sapiens,10|13,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA04676,GSE15605,GPL570,1000,Metastatic Melanoma,C0025202,,GEO,Microarray,Homo sapiens,46|12,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA04677,GSE64634,GPL570,147,Nasopharyngeal Carcinoma,C2931822,Nasopharynx,GEO,Microarray,Homo sapiens,4|12,"DO:A pharynx cancer that is located in the nasopharynx, the uppermost region of the pharynx or throat, where the nasal passages and auditory tubes join the remainder of the upper respiratory tract." DSA04678,GSE64801,GPL11154,9,Necrotizing Enterocolitis,C0520459,Ileum,GEO,RNA-Seq,Homo sapiens,5|9,"EFO:Necrotizing enterocolitis (NEC) is a devastating disease that affects mostly the intestine of premature infants. The wall of the intestine is invaded by bacteria, which cause local infection and inflammation that can ultimately destroy the wall of the bowel (intestine). Such bowel wall destruction can lead to perforation of the intestine and spillage of stool into the infant's abdomen, which can result in an overwhelming infection and death." DSA04679,GSE64810,GPL11154,1000,Huntington's Disease,C0020179,Brain,GEO,RNA-Seq,Homo sapiens,49|20,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA04680,GSE64814,GPL11154,1000,Post-Traumatic Stress Disorder,C0038436,Peripheral blood,GEO,RNA-Seq,Homo sapiens,47|47,DO:An anxiety disorder which results from a traumatic experience that results in psychological trauma. DSA04681,GSE15645,GPL570,505,Polyarticular Juvenile Idiopathic Arthritis,C0409667,Peripheral Blood,GEO,Microarray,Homo sapiens,13|14,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA04682,GSE64823,GPL6096,1,Progressive Myoclonus Epilepsy,C0751778,,GEO,Microarray,Mus musculus,4|4,DO:An autosomal dominant cerebellar ataxia that has_material_basis_in expansion of CAG triplet repeats (glutamine) encoding a polyglutamine tract in the atrophin-1 protein. DSA04683,GSE64912,GPL11154,1000,Papillary Thyroid Carcinoma,C0238463,Thyroid,GEO,RNA-Seq,Homo sapiens,4|18,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA04684,GSE64913,GPL570,45,Asthma,C0004096,Airway,GEO,Microarray,Homo sapiens,23|13,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA04685,GSE64913,GPL570,50,Asthma,C0004096,Airway,GEO,Microarray,Homo sapiens,19|15,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA04686,GSE64916,GPL13497,0,Gastric Cancer,C0699791,Whole blood,GEO,Microarray,Homo sapiens,1|4,DO:A gastrointestinal system cancer that is located_in the stomach. DSA04687,GSE64998,GPL11532,0,Type 2 Diabetes,C0011860,Liver,GEO,Microarray,Homo sapiens,8|7,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA04688,GSE64998,GPL11532,0,Obesity,C0028754,Liver,GEO,Microarray,Homo sapiens,6|8,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA04689,GSE65010,GPL570,0,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,12|12,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04690,GSE65010,GPL570,0,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,12|12,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04691,GSE65106,GPL6244,201,Autism Spectrum Disorder,C1510586,,GEO,Microarray,Homo sapiens,6|6,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA04692,GSE65106,GPL6244,1000,Autism Spectrum Disorder,C1510586,,GEO,Microarray,Homo sapiens,6|4,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA04693,GSE65106,GPL6244,0,Autism Spectrum Disorder,C1510586,,GEO,Microarray,Homo sapiens,5|5,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA04694,GSE65106,GPL6244,0,Autism Spectrum Disorder,C1510586,,GEO,Microarray,Homo sapiens,5|3,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA04695,GSE65106,GPL6244,0,Autism Spectrum Disorder,C1510586,,GEO,Microarray,Homo sapiens,5|5,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA04696,GSE65106,GPL6244,0,Autism Spectrum Disorder,C1510586,,GEO,Microarray,Homo sapiens,5|3,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA04697,GSE65106,GPL6244,0,Autism Spectrum Disorder,C1510586,,GEO,Microarray,Homo sapiens,5|5,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA04698,GSE65106,GPL6244,0,Autism Spectrum Disorder,C1510586,,GEO,Microarray,Homo sapiens,5|3,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA04699,GSE65114,GPL16686,1000,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,12|16,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA04700,GSE65127,GPL570,262,Vitiligo,C0042900,Skin,GEO,Microarray,Homo sapiens,10|10,DO:An autoimmune disease that causes depigmentation of patches of skin resulting from loss of function or death of melanoctyes. DSA04701,GSE65134,GPL96,25,Follicular Lymphoma,C0024301,,GEO,Microarray,Homo sapiens,6|1,DO:A B-cell lymphoma that is characterized as an indolent non-Hodgkin's lymphoma and has_material_basis_in follicle center B-cells (centrocytes and centroblasts). DSA04702,GSE65135,GPL570,1000,Follicular Lymphoma,C0024301,Lymph node,GEO,Microarray,Homo sapiens,10|14,DO:A B-cell lymphoma that is characterized as an indolent non-Hodgkin's lymphoma and has_material_basis_in follicle center B-cells (centrocytes and centroblasts). DSA04703,GSE65152,GPL15207,0,Mastitis,C0024894,,GEO,Microarray,Homo sapiens,3|7,DO:A breast disease characterized by painful infection of the breast tissue. DSA04704,GSE65170,GPL5175,0,Nestor-Guillermo Progeria Syndrome,C3151446,,GEO,Microarray,Homo sapiens,1|2,"ORDO:Nestor-Guillermo progeria syndrome is a rare, genetic, progeroid syndrome characterized by a prematurely aged appearance associated with severe osteolysis (notably on mandible, clavicles, ribs, distal phalanges, and long bones), osteoporosis, generalized lipoatrophy and absence of cardiovascular, atherosclerotic and metabolic complications, presenting a relatively long survival. Additional characteristics include growth retardation, joint stiffness (mainly of fingers, hands, knees, and elbows), wide cranial sutures, dysmorphic facial features (prominent eyes, convex nasal ridge, malocclusion, dental crowding, thin lip vermillion, microretrognathia) and persistent eyebrows, eyelashes and scalp hair." DSA04705,GSE65170,GPL5175,0,Nestor-Guillermo Progeria Syndrome,C3151446,,GEO,Microarray,Homo sapiens,2|4,"ORDO:Nestor-Guillermo progeria syndrome is a rare, genetic, progeroid syndrome characterized by a prematurely aged appearance associated with severe osteolysis (notably on mandible, clavicles, ribs, distal phalanges, and long bones), osteoporosis, generalized lipoatrophy and absence of cardiovascular, atherosclerotic and metabolic complications, presenting a relatively long survival. Additional characteristics include growth retardation, joint stiffness (mainly of fingers, hands, knees, and elbows), wide cranial sutures, dysmorphic facial features (prominent eyes, convex nasal ridge, malocclusion, dental crowding, thin lip vermillion, microretrognathia) and persistent eyebrows, eyelashes and scalp hair." DSA04706,GSE65204,GPL14550,70,Asthma,C0004096,Nasal epithelium,GEO,Microarray,Homo sapiens,33|36,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA04707,GSE65368,GPL10904,1,Adult-Onset Autosomal Dominant Leukodystrophy,C3164344,Whole blood,GEO,Microarray,Homo sapiens,8|4,"DO:A leukodystrophy characterized by onset in the 4th or 5th decade of life of autonomic abnormalities, pyramidal and cerebellar dysfunction, and symmetric demyelination of the CNS that has_material_basis_in heterozygous tandem genomic duplication resulting in an extra copy of the LMNB1 gene on chromosome 5q." DSA04708,GSE65368,GPL10904,0,Adult-Onset Autosomal Dominant Leukodystrophy,C3164344,,GEO,Microarray,Homo sapiens,3|4,"DO:A leukodystrophy characterized by onset in the 4th or 5th decade of life of autonomic abnormalities, pyramidal and cerebellar dysfunction, and symmetric demyelination of the CNS that has_material_basis_in heterozygous tandem genomic duplication resulting in an extra copy of the LMNB1 gene on chromosome 5q." DSA04709,GSE65368,GPL10904,4,Adult-Onset Autosomal Dominant Leukodystrophy,C3164344,,GEO,Microarray,Homo sapiens,2|4,"DO:A leukodystrophy characterized by onset in the 4th or 5th decade of life of autonomic abnormalities, pyramidal and cerebellar dysfunction, and symmetric demyelination of the CNS that has_material_basis_in heterozygous tandem genomic duplication resulting in an extra copy of the LMNB1 gene on chromosome 5q." DSA04710,GSE65409,GPL6947,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,Microarray,Homo sapiens,8|30,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA04711,GSE6551,GPL570,0,Intracranial Aneurysm,C0007766,Intracranial artery,GEO,Microarray,Homo sapiens,3|2,EFO:Outpouching of BASILAR ARTERY at the base of the skull. The basilar artery is the most important artery in the posterior cerebral circulation. DSA04712,GSE65517,GPL10558,0,Breast Cancer,C0678222,,GEO,Microarray,Homo sapiens,3|4,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA04713,GSE65517,GPL10558,0,Gram-Negative Sepsis,C0036685,,GEO,Microarray,Homo sapiens,3|3, DSA04714,GSE65517,GPL10558,0,Tuberculosis,C0041296,,GEO,Microarray,Homo sapiens,3|3,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA04715,GSE175649,GPL17021,1000,Sjogren's Syndrome,C1527336,Salivary gland,GEO,RNA-Seq,Mus musculus,3|3,DO:An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. DSA04716,GSE93170,GPL14550,1000,Primary Biliary Cholangitis,C0008312,,GEO,Microarray,Homo sapiens,6|6,DO:A liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts. DSA04717,GSE93215,GPL6244,1000,Acutely Injured,,Whole venous blood,GEO,Microarray,Homo sapiens,19|9, DSA04718,GSE15645,GPL570,462,Polyarticular Juvenile Idiopathic Arthritis,C0409667,Peripheral Blood,GEO,Microarray,Homo sapiens,13|9,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA04719,GSE15645,GPL570,0,Polyarticular Juvenile Idiopathic Arthritis,C0409667,Peripheral Blood,GEO,Microarray,Homo sapiens,13|6,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA04720,GSE93311,GPL6887,52,Alcohol Use Disorder,C0001973,Basolateral amygdala,GEO,Microarray,Mus musculus,12|12,"DO:A substance dependence that is characterized by tolerance, withdrawal symptoms, increasing use, persistent desire to decrease consumption, time spent obtaining or recovering from alcohol caused by a physical and psychological dependence on alcohol." DSA04721,GSE93311,GPL6887,65,Alcohol Use Disorder,C0001973,Bed nucleus of the stria terminalis,GEO,Microarray,Mus musculus,12|11,"DO:A substance dependence that is characterized by tolerance, withdrawal symptoms, increasing use, persistent desire to decrease consumption, time spent obtaining or recovering from alcohol caused by a physical and psychological dependence on alcohol." DSA04722,GSE93311,GPL6887,56,Alcohol Use Disorder,C0001973,Central nucleus,GEO,Microarray,Mus musculus,12|12,"DO:A substance dependence that is characterized by tolerance, withdrawal symptoms, increasing use, persistent desire to decrease consumption, time spent obtaining or recovering from alcohol caused by a physical and psychological dependence on alcohol." DSA04723,GSE93311,GPL6887,39,Alcohol Use Disorder,C0001973,Nucleus accumbens,GEO,Microarray,Mus musculus,12|11,"DO:A substance dependence that is characterized by tolerance, withdrawal symptoms, increasing use, persistent desire to decrease consumption, time spent obtaining or recovering from alcohol caused by a physical and psychological dependence on alcohol." DSA04724,GSE93311,GPL6887,48,Alcohol Use Disorder,C0001973,Nucleus accumbens,GEO,Microarray,Mus musculus,12|12,"DO:A substance dependence that is characterized by tolerance, withdrawal symptoms, increasing use, persistent desire to decrease consumption, time spent obtaining or recovering from alcohol caused by a physical and psychological dependence on alcohol." DSA04725,GSE93311,GPL6887,13,Alcohol Use Disorder,C0001973,Prefrontal cortex,GEO,Microarray,Mus musculus,12|12,"DO:A substance dependence that is characterized by tolerance, withdrawal symptoms, increasing use, persistent desire to decrease consumption, time spent obtaining or recovering from alcohol caused by a physical and psychological dependence on alcohol." DSA04726,GSE93311,GPL6887,64,Alcohol Use Disorder,C0001973,Ventral tegmental area,GEO,Microarray,Mus musculus,12|12,"DO:A substance dependence that is characterized by tolerance, withdrawal symptoms, increasing use, persistent desire to decrease consumption, time spent obtaining or recovering from alcohol caused by a physical and psychological dependence on alcohol." DSA04727,GSE15773,GPL570,0,Type 2 Diabetes,C0011860,Subcutaneous adipose tissue,GEO,Microarray,Homo sapiens,5|4,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA04728,GSE93577,GPL13667,44,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04729,GSE93577,GPL13667,34,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04730,GSE93577,GPL13667,61,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04731,GSE93577,GPL13667,64,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04732,GSE93577,GPL13667,2,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|4,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04733,GSE93577,GPL13667,5,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|4,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04734,GSE93577,GPL13667,12,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04735,GSE93577,GPL13667,48,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|3,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04736,GSE93577,GPL13667,1000,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04737,GSE93577,GPL13667,53,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04738,GSE93577,GPL13667,48,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04739,GSE93577,GPL13667,35,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04740,GSE93577,GPL13667,51,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04741,GSE93577,GPL13667,198,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04742,GSE93577,GPL13667,3,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|10,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04743,GSE93577,GPL13667,164,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04744,GSE93577,GPL13667,20,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04745,GSE93577,GPL13667,25,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04746,GSE93577,GPL13667,537,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04747,GSE93577,GPL13667,85,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|4,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04748,GSE93577,GPL13667,23,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|4,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04749,GSE93577,GPL13667,0,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|4,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04750,GSE93577,GPL13667,145,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04751,GSE93577,GPL13667,61,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|2,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04752,GSE93577,GPL13667,42,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,71|3,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA04753,GSE93597,GPL16570,705,Hypertension,C0020538,Aorta,GEO,Microarray,Mus musculus,7|8,DO:An artery disease characterized by chronic elevated blood pressure in the arteries. DSA04754,GSE93606,GPL11532,1000,Idiopathic Pulmonary Fibrosis,C1800706,Whole blood,GEO,Microarray,Homo sapiens,20|57,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA04755,GSE93624,GPL11154,1000,Crohn's Disease,C0010346,Ileum,GEO,RNA-Seq,Homo sapiens,35|210,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04756,GSE93683,GPL570,0,Primary Sjogren Syndrome,C0151449,,GEO,Microarray,Homo sapiens,6|6,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA04757,GSE93683,GPL570,0,Primary Sjogren Syndrome,C0151449,,GEO,Microarray,Homo sapiens,6|6,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA04758,GSE93683,GPL570,0,Primary Sjogren Syndrome,C0151449,,GEO,Microarray,Homo sapiens,6|6,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA04759,GSE93683,GPL570,1,Primary Sjogren Syndrome,C0151449,,GEO,Microarray,Homo sapiens,6|6,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA04760,GSE93767,GPL10558,1000,Huntington's Disease,C0020179,,GEO,Microarray,Homo sapiens,3|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA04761,GSE93767,GPL10558,1000,Huntington's Disease,C0020179,,GEO,Microarray,Homo sapiens,3|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA04762,GSE93776,GPL570,0,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,6|6,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04763,GSE93776,GPL570,0,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,6|6,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04764,GSE93776,GPL570,0,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,6|6,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04765,GSE93776,GPL570,0,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,6|6,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04766,GSE93776,GPL570,0,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,6|6,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04767,GSE93776,GPL570,0,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,6|6,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04768,GSE93776,GPL570,0,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,6|6,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04769,GSE93776,GPL570,0,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,6|6,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04770,GSE93776,GPL570,0,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,6|6,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04771,GSE93776,GPL570,3,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,6|6,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04772,GSE93776,GPL570,0,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,6|9,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04773,GSE93776,GPL570,57,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,6|7,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04774,GSE93776,GPL570,10,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,6|7,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04775,GSE15773,GPL570,0,Type 2 Diabetes,C0011860,Omental adipose tissue,GEO,Microarray,Homo sapiens,5|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA04776,GSE93885,GPL16686,0,Alzheimer's Disease,C0002395,Olfactory bulb,GEO,Microarray,Homo sapiens,4|5,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA04777,GSE93885,GPL16686,0,Alzheimer's Disease,C0002395,Olfactory bulb,GEO,Microarray,Homo sapiens,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA04778,GSE93885,GPL16686,0,Alzheimer's Disease,C0002395,Olfactory bulb,GEO,Microarray,Homo sapiens,4|5,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA04779,GSE15824,GPL570,1000,Astrocytoma,C0004114,Brain,GEO,Microarray,Homo sapiens,3|8,"DO:A malignant glioma that is has_material_basis_in astrocyte cells, a type of star-shaped glial cell, located in the brain and spinal cord." DSA04780,GSE93987,GPL13158,0,Disorganized Schizophrenia,C0036347,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|2,"MSH:A type of schizophrenia characterized by frequent incoherence; marked loosening of associations, or grossly disorganized behavior and flat or grossly inappropriate affect that does not meet the criteria for the catatonic type; associated features include extreme social withdrawal, grimacing, mannerisms, mirror gazing, inappropriate giggling, and other odd behavior. (Dorland, 27th ed)" DSA04781,GSE93987,GPL13158,2,Paranoid Schizophrenia,C0036349,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|2,"DO:A schizophrenia characterized by delusions or auditory hallucinations of persecution or being plotted against without thought disorder, disorganized behavior, or affective flattening." DSA04782,GSE93987,GPL13158,53,Paranoid Schizophrenia,C0036349,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|2,"DO:A schizophrenia characterized by delusions or auditory hallucinations of persecution or being plotted against without thought disorder, disorganized behavior, or affective flattening." DSA04783,GSE93987,GPL13158,0,Paranoid Schizophrenia,C0036349,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|2,"DO:A schizophrenia characterized by delusions or auditory hallucinations of persecution or being plotted against without thought disorder, disorganized behavior, or affective flattening." DSA04784,GSE93987,GPL13158,2,Undifferentiated Schizophrenia,C0392322,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|4,"NCI:A subtype of schizophrenia in which the individual exhibits the characteristic symptoms of schizophrenia but the overall picture is not one of catatonic type, paranoid type, or disorganized type schizophrenia." DSA04785,GSE93987,GPL13158,106,Undifferentiated Schizophrenia,C0392322,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|4,"NCI:A subtype of schizophrenia in which the individual exhibits the characteristic symptoms of schizophrenia but the overall picture is not one of catatonic type, paranoid type, or disorganized type schizophrenia." DSA04786,GSE93987,GPL13158,16,Undifferentiated Schizophrenia,C0392322,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|2,"NCI:A subtype of schizophrenia in which the individual exhibits the characteristic symptoms of schizophrenia but the overall picture is not one of catatonic type, paranoid type, or disorganized type schizophrenia." DSA04787,GSE93987,GPL13158,109,Disorganized Schizophrenia,C0036347,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|6,"MSH:A type of schizophrenia characterized by frequent incoherence; marked loosening of associations, or grossly disorganized behavior and flat or grossly inappropriate affect that does not meet the criteria for the catatonic type; associated features include extreme social withdrawal, grimacing, mannerisms, mirror gazing, inappropriate giggling, and other odd behavior. (Dorland, 27th ed)" DSA04788,GSE93987,GPL13158,2,Disorganized Schizophrenia,C0036347,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|1,"MSH:A type of schizophrenia characterized by frequent incoherence; marked loosening of associations, or grossly disorganized behavior and flat or grossly inappropriate affect that does not meet the criteria for the catatonic type; associated features include extreme social withdrawal, grimacing, mannerisms, mirror gazing, inappropriate giggling, and other odd behavior. (Dorland, 27th ed)" DSA04789,GSE93987,GPL13158,505,Disorganized Schizophrenia,C0036347,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|4,"MSH:A type of schizophrenia characterized by frequent incoherence; marked loosening of associations, or grossly disorganized behavior and flat or grossly inappropriate affect that does not meet the criteria for the catatonic type; associated features include extreme social withdrawal, grimacing, mannerisms, mirror gazing, inappropriate giggling, and other odd behavior. (Dorland, 27th ed)" DSA04790,GSE93987,GPL13158,59,Disorganized Schizophrenia,C0036347,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|2,"MSH:A type of schizophrenia characterized by frequent incoherence; marked loosening of associations, or grossly disorganized behavior and flat or grossly inappropriate affect that does not meet the criteria for the catatonic type; associated features include extreme social withdrawal, grimacing, mannerisms, mirror gazing, inappropriate giggling, and other odd behavior. (Dorland, 27th ed)" DSA04791,GSE93987,GPL13158,280,Disorganized Schizophrenia,C0036347,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|4,"MSH:A type of schizophrenia characterized by frequent incoherence; marked loosening of associations, or grossly disorganized behavior and flat or grossly inappropriate affect that does not meet the criteria for the catatonic type; associated features include extreme social withdrawal, grimacing, mannerisms, mirror gazing, inappropriate giggling, and other odd behavior. (Dorland, 27th ed)" DSA04792,GSE93987,GPL13158,1000,Paranoid Schizophrenia,C0036349,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|4,"DO:A schizophrenia characterized by delusions or auditory hallucinations of persecution or being plotted against without thought disorder, disorganized behavior, or affective flattening." DSA04793,GSE93987,GPL13158,1000,Paranoid Schizophrenia,C0036349,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|4,"DO:A schizophrenia characterized by delusions or auditory hallucinations of persecution or being plotted against without thought disorder, disorganized behavior, or affective flattening." DSA04794,GSE93987,GPL13158,1,Schizoaffective Disorder,C0036337,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|16,DO:A psychotic disorder that is characterized by recurring episodes of mood fluctuations and a loss of contact with reality. DSA04795,GSE93987,GPL13158,238,Schizoaffective Disorder,C0036337,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|4,DO:A psychotic disorder that is characterized by recurring episodes of mood fluctuations and a loss of contact with reality. DSA04796,GSE93987,GPL13158,15,Schizoaffective Disorder,C0036337,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|2,DO:A psychotic disorder that is characterized by recurring episodes of mood fluctuations and a loss of contact with reality. DSA04797,GSE93987,GPL13158,4,Schizoaffective Disorder,C0036337,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|2,DO:A psychotic disorder that is characterized by recurring episodes of mood fluctuations and a loss of contact with reality. DSA04798,GSE93987,GPL13158,252,Schizoaffective Disorder,C0036337,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|2,DO:A psychotic disorder that is characterized by recurring episodes of mood fluctuations and a loss of contact with reality. DSA04799,GSE93987,GPL13158,631,Schizoaffective Disorder,C0036337,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|3,DO:A psychotic disorder that is characterized by recurring episodes of mood fluctuations and a loss of contact with reality. DSA04800,GSE93987,GPL13158,4,Schizoaffective Disorder,C0036337,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|6,DO:A psychotic disorder that is characterized by recurring episodes of mood fluctuations and a loss of contact with reality. DSA04801,GSE93987,GPL13158,1000,Undifferentiated Schizophrenia,C0392322,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|8,"NCI:A subtype of schizophrenia in which the individual exhibits the characteristic symptoms of schizophrenia but the overall picture is not one of catatonic type, paranoid type, or disorganized type schizophrenia." DSA04802,GSE93987,GPL13158,112,Undifferentiated Schizophrenia,C0392322,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|8,"NCI:A subtype of schizophrenia in which the individual exhibits the characteristic symptoms of schizophrenia but the overall picture is not one of catatonic type, paranoid type, or disorganized type schizophrenia." DSA04803,GSE93987,GPL13158,1000,Undifferentiated Schizophrenia,C0392322,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|4,"NCI:A subtype of schizophrenia in which the individual exhibits the characteristic symptoms of schizophrenia but the overall picture is not one of catatonic type, paranoid type, or disorganized type schizophrenia." DSA04804,GSE93987,GPL13158,1000,Undifferentiated Schizophrenia,C0392322,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,106|4,"NCI:A subtype of schizophrenia in which the individual exhibits the characteristic symptoms of schizophrenia but the overall picture is not one of catatonic type, paranoid type, or disorganized type schizophrenia." DSA04805,GSE94035,GPL11154,1000,Neuroblastoma,C0027819,,GEO,RNA-Seq,Homo sapiens,28|16,DO:An autonomic nervous system neoplasm that derives_from immature nerve cells. DSA04806,GSE94044,GPL8321,1000,Hyperlipidemia,C0020473,Abdominal aorta,GEO,Microarray,Mus musculus,4|4,EFO:Conditions with excess LIPIDS in the blood. DSA04807,GSE94087,GPL17021,215,Obesity,C0028754,Bone marrow,GEO,RNA-Seq,Mus musculus,48|48,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA04808,GSE94087,GPL17021,118,Obesity,C0028754,Bone marrow,GEO,RNA-Seq,Mus musculus,53|43,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA04809,GSE94116,GPL20301,1000,Tuberculosis,C0041296,,GEO,RNA-Seq,Homo sapiens,19|19,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA04810,GSE94116,GPL20301,1000,Tuberculosis,C0041296,,GEO,RNA-Seq,Homo sapiens,6|6,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA04811,GSE94335,GPL16791,1,Asthma,C0004096,Airway smooth muscle,GEO,RNA-Seq,Homo sapiens,8|9,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA04812,GSE94335,GPL16791,1,Asthma,C0004096,Airway smooth muscle,GEO,RNA-Seq,Homo sapiens,8|9,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA04813,GSE94510,GPL570,0,Primary Sjogren Syndrome,C0151449,,GEO,Microarray,Homo sapiens,6|6,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA04814,GSE94510,GPL570,0,Primary Sjogren Syndrome,C0151449,,GEO,Microarray,Homo sapiens,6|6,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA04815,GSE94510,GPL570,0,Primary Sjogren Syndrome,C0151449,,GEO,Microarray,Homo sapiens,6|6,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA04816,GSE15824,GPL570,1000,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,10|12,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA04817,GSE94643,GPL16686,0,Pre-Eclampsia,C0032914,Decidua basalis,GEO,Microarray,Homo sapiens,4|4,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA04818,GSE94643,GPL16686,0,Pre-Eclampsia,C0032914,,GEO,Microarray,Homo sapiens,4|4,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA04819,GSE94648,GPL19109,0,Ulcerative Colitis,C0009324,Peripheral blood,GEO,Microarray,Homo sapiens,22|2,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA04820,GSE94648,GPL19109,2,Ulcerative Colitis,C0009324,Peripheral blood,GEO,Microarray,Homo sapiens,22|2,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA04821,GSE94648,GPL19109,22,Crohn's Disease,C0010346,Peripheral blood,GEO,Microarray,Homo sapiens,22|11,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04822,GSE94648,GPL19109,9,Crohn's Disease,C0010346,Peripheral blood,GEO,Microarray,Homo sapiens,22|1,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04823,GSE94683,GPL10630,1000,Heterotopic Ossification,C0029396,Bone marrow,GEO,Microarray,Homo sapiens,9|7,"HPO:Formation of abnormal, extraskeletal bony tissue, i.e., the presence of bone in soft tissue where bone normally does not exist." DSA04824,GSE94754,GPL6246,3,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,Microarray,Mus musculus,4|4,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA04825,GSE94754,GPL6246,8,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,Microarray,Mus musculus,4|4,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA04826,GSE15824,GPL570,1000,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,10|3,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA04827,GSE94907,GPL16791|GPL20301,40,Tuberculosis Infection,C1609538,Serum exosomes,GEO,RNA-Seq,Homo sapiens,2|2,"MONDO:Mycobacterium tuberculosis infection that does not induce infectious expression of the disease in the affected person, although it can cause continuous immune response generated towards TB antigens; person having LTBI are asymptomatic and acting as a reservoir of active tuberculosis tuberculosis cases and Mycobacterium tuberculosis and run a 5-10% risk of reactivating tuberculosis throughout their lives." DSA04828,GSE94907,GPL16791|GPL20301,1000,Active Tuberculosis,C0151332,Serum exosomes,GEO,RNA-Seq,Homo sapiens,2|2,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA04829,GSE94916,GPL20844,22,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,6|6,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA04830,GSE94916,GPL20844,0,Malaria,C0024530,,GEO,Microarray,Homo sapiens,6|6,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA04831,GSE94916,GPL20844,0,Pneumonia,C0032285,,GEO,Microarray,Homo sapiens,6|6,"DO:A lung disease that involves lung parenchyma or alveolar inflammation and abnormal alveolar filling with fluid (consolidation and exudation). It results from a variety of causes including infection with bacteria, viruses, fungi or parasites, and chemical or physical injury to the lungs. It is accompanied by fever, chills, cough, and difficulty in breathing." DSA04832,GSE95065,GPL23080,1000,Systemic Sclerosis [Scleroderma],C2364016,Skin,GEO,Microarray,Homo sapiens,15|18, DSA04833,GSE95078,GPL18573,1000,Autoinflammatory Disease,C3267073,,GEO,RNA-Seq,Homo sapiens,3|3,MONDO:A group of disorders of the innate immune system characterized by attacks of seemingly unprovoked inflammation without significant levels of either autoantibodies or autoreactive T cells more characteristic of autoimmune disease. DSA04834,GSE95078,GPL18573,1000,Autoinflammatory Disease,C3267073,,GEO,RNA-Seq,Homo sapiens,3|3,MONDO:A group of disorders of the innate immune system characterized by attacks of seemingly unprovoked inflammation without significant levels of either autoantibodies or autoreactive T cells more characteristic of autoimmune disease. DSA04835,GSE95095,GPL14951,1000,Crohn's Disease,C0010346,Intestine,GEO,Microarray,Homo sapiens,12|24,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04836,GSE95095,GPL14951,139,Crohn's Disease,C0010346,Intestine,GEO,Microarray,Homo sapiens,12|24,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04837,GSE95120,GPL11154,312,Cardiomyopathy,C0878544,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA04838,GSE95132,GPL16791,1000,Colon Cancer,C0699790,Colon,GEO,RNA-Seq,Homo sapiens,10|10,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA04839,GSE95277,GPL11154,1000,Childhood Gliosarcoma,C3899658,Brain,GEO,RNA-Seq,Homo sapiens,3|4,NCI:A gliosarcoma that occurs during childhood. DSA04840,GSE95343,GPL11154,1000,Huntington's Disease,C0020179,,GEO,RNA-Seq,Homo sapiens,4|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA04841,GSE95437,GPL11154,1000,Crohn's Disease,C0010346,Colon,GEO,RNA-Seq,Homo sapiens,29|20,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04842,GSE95437,GPL11154,320,Crohn's Disease,C0010346,Colon,GEO,RNA-Seq,Homo sapiens,29|3,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04843,GSE95437,GPL11154,1000,Ulcerative Colitis,C0009324,Colon,GEO,RNA-Seq,Homo sapiens,29|25,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA04844,GSE95437,GPL11154,13,Ulcerative Colitis,C0009324,Colon,GEO,RNA-Seq,Homo sapiens,29|17,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA04845,GSE95474,GPL16699,1000,Discoid Lupus Erythematosus,C0024138,Skin,GEO,Microarray,Homo sapiens,5|6,"DO:An autoimmune disease that is characterized by a constellation of findings that include elevated antibodies to nuclear antigens, antiphospholipids, low complement levels, ulcers, non-scarring alopecia, renal or neurologic damage, and low white blood cell and platelet counts, has_symptom rashes, fatigue, arthritis, hair loss, seizures, and symptoms related to affected organs." DSA04846,GSE95474,GPL16699,266,Subacute Cutaneous Lupus Erythematosus,C0024140,Skin,GEO,Microarray,Homo sapiens,5|5,"MONDO:Subacute cutaneous lupus erythematosus (SCLE) is a form of cutaneous lupus erythematosus (CLE) that can present either as a non-scarring, annular photo-distributed dermatosis or psoriasiform plaques. SCLE is associated with anti-Ro/SSA antibodies and can be drug-induced." DSA04847,GSE95482,GPL16686,11,Tangier Disease,C0039292,,GEO,Microarray,Homo sapiens,3|3,"DO:A hypolipoproteinemia that is characterized by an inablility to fully absorb dietary fats, cholesterol and fat-soluble vitamins, has_material_basis_in an autosomal recessive disorder of lipid metabolism that has_material_basis_in mutation in the microsomal triglyceride transfer protein that catalyzes the transport of lipids and is required in the secretion of BETA-LIPOPROTEINS." DSA04848,GSE95587,GPL16791,2,Alzheimer's Disease,C0002395,Fusiform gyrus,GEO,RNA-Seq,Homo sapiens,16|6,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA04849,GSE95587,GPL16791,1000,Alzheimer's Disease,C0002395,Fusiform gyrus,GEO,RNA-Seq,Homo sapiens,12|37,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA04850,GSE95698,GPL17077,0,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,3|3,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA04851,GSE95743,GPL11154,790,ICF-specific DNMT3B dysfunction,,,GEO,RNA-Seq,Homo sapiens,4|4, DSA04852,GSE95849,GPL22448,1000,Diabetes Mellitus,C0011849,,GEO,Microarray,Homo sapiens,6|6,"DO:A glucose metabolism disease that is characterized by chronic hyperglycaemia with disturbances of carbohydrate, fat and protein metabolism resulting from defects in insulin secretion, insulin action, or both." DSA04853,GSE95849,GPL22448,1000,Diabetic Peripheral Angiopathy,C0011871,,GEO,Microarray,Homo sapiens,6|6,MONDO:Diabetic angiopathy is a form of angiopathy associated with diabetic complications. DSA04854,GSE96099,GPL11154|GPL13112|GPL15520,19,Huntington's Disease,C0020179,Motor cortex,GEO,RNA-Seq,Homo sapiens,4|6,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA04855,GSE96099,GPL11154|GPL13112|GPL15520,0,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Homo sapiens,6|9,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA04856,GSE9624,GPL570,0,Obesity,C0028754,Omental adipose tissue,GEO,Microarray,Homo sapiens,6|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA04857,GSE96668,GPL10558,1000,Gastroesophageal Junction Adenocarcinoma,C1332166,,GEO,Microarray,Homo sapiens,11|19,MONDO:A carcinoma that arises from glandular epithelial cells of the esophagogastric junction. DSA04858,GSE96854,GPL18943,475,Hirschsprung Disease,C0019569,Colon,GEO,Microarray,Homo sapiens,3|3,DO:A megacolon that is characterized by a blockage of the large intestine due to improper muscle movement in the bowel. DSA04859,GSE9686,GPL5760,9,Crohn's Disease,C0010346,Colon,GEO,Microarray,Homo sapiens,8|11,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04860,GSE9686,GPL5760,1000,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,8|5,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA04861,GSE96936,GPL4134,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Mus musculus,3|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA04862,GSE97001,GPL10332,372,Thyroid Tumor,C0040136,Left lobe of the thyroid gland,GEO,Microarray,Homo sapiens,4|4,DO:An endocrine gland cancer located in the thryoid gland located in the neck below the thyroid cartilage. DSA04863,GSE97003,GPL16791,868,Pancreatic Cancer,C0235974,Pancreas,GEO,RNA-Seq,Homo sapiens,2|9,DO:An endocrine gland cancer located_in the pancreas. DSA04864,GSE97012,GPL13607,1000,Crohn's Disease,C0010346,Intestine,GEO,Microarray,Homo sapiens,27|7,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04865,GSE97012,GPL13607,1000,Ulcerative Colitis,C0009324,Intestine,GEO,Microarray,Homo sapiens,27|7,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA04866,GSE97012,GPL13607,1000,Crohn's Disease,C0010346,Intestine,GEO,Microarray,Homo sapiens,27|2,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04867,GSE97012,GPL13607,1000,Ulcerative Colitis,C0009324,Intestine,GEO,Microarray,Homo sapiens,27|7,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA04868,GSE97012,GPL13607,1000,Crohn's Disease,C0010346,Intestine,GEO,Microarray,Homo sapiens,27|10,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA04869,GSE97012,GPL13607,1000,Ulcerative Colitis,C0009324,Intestine,GEO,Microarray,Homo sapiens,27|8,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA04870,GSE97038,GPL11154,187,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,RNA-Seq,Homo sapiens,4|4,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA04871,GSE97038,GPL11154,261,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,RNA-Seq,Homo sapiens,4|4,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA04872,GSE15824,GPL570,573,Brain Tumor,C0006118,Brain,GEO,Microarray,Homo sapiens,2|7,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA04873,GSE97156,GPL20301,1000,Multiple Symmetric Lipomatosis,C0023804,Subcutaneous adipose tissue,GEO,RNA-Seq,Homo sapiens,6|14,MONDO:A neoplastic process characterized by diffuse overgrowth of mature adipose tissue. DSA04874,GSE97234,GPL13112,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,4|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA04875,GSE97234,GPL13112,1000,Alcoholic Hepatitis,C0019187,Liver,GEO,RNA-Seq,Mus musculus,4|3,MONDO:Acute hepatitis resulting from ingestion of alcohol. DSA04876,GSE97236,GPL15207,1000,Pleuropulmonary Blastoma,C1266144,Lung,GEO,Microarray,Homo sapiens,2|4,DO:A pulmonary blastoma that derives_from the lung or pleural cavity. DSA04877,GSE97320,GPL570,1000,Acute Myocardial Infarction,C0155626,Peripheral blood,GEO,Microarray,Homo sapiens,3|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA04878,GSE97372,GPL6885,2,Dyt6 Dystonia Disorders,,Brain,GEO,Microarray,Mus musculus,4|4, DSA04879,GSE97372,GPL6885,8,Dyt6 Dystonia Disorders,,Brain,GEO,Microarray,Mus musculus,4|4, DSA04880,GSE97372,GPL6885,3,Dyt6 Dystonia Disorders,,Brain,GEO,Microarray,Mus musculus,4|4, DSA04881,GSE97485,GPL6244,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,Microarray,Homo sapiens,10|10,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA04882,GSE97546,GPL6887,1000,Kidney Fibrosis,C0151650,Kidney,GEO,Microarray,Mus musculus,3|2,HPO:Renal fibrosis is the consequence of an excessive accumulation of extracellular matrix that occurs in virtually every type of chronic kidney disease. DSA04883,GSE97546,GPL6887,1000,Pulmonary Fibrosis,C0034069,Lung,GEO,Microarray,Mus musculus,3|3,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA04884,GSE97562,GPL6244,1000,Chronic Myeloid Leukemia,C0023473,Bone marrow,GEO,Microarray,Homo sapiens,5|5,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA04885,GSE97562,GPL6244,265,Chronic Myeloid Leukemia,C0023473,Bone marrow,GEO,Microarray,Homo sapiens,5|5,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA04886,GSE97562,GPL6244,0,Chronic Myeloid Leukemia,C0023473,Bone marrow,GEO,Microarray,Homo sapiens,5|5,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA04887,GSE97562,GPL6244,1,Chronic Myeloid Leukemia,C0023473,Bone marrow,GEO,Microarray,Homo sapiens,5|5,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA04888,GSE97760,GPL16699,1000,Alzheimer's Disease,C0002395,Whole blood,GEO,Microarray,Homo sapiens,10|9,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA04889,GSE97779,GPL570,1000,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,5|9,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04890,GSE97910,GPL6885,1000,Liposarcoma,C0023827,Brown adipose tissue,GEO,Microarray,Mus musculus,5|5,DO:A connective tissue cancer that arises in fat cells in deep soft tissue retroperitoneum and the extremities. DSA04891,GSE97910,GPL6885,134,Liposarcoma,C0023827,Brown adipose tissue,GEO,Microarray,Mus musculus,4|4,DO:A connective tissue cancer that arises in fat cells in deep soft tissue retroperitoneum and the extremities. DSA04892,GSE97910,GPL6885,229,Liposarcoma,C0023827,Brown adipose tissue,GEO,Microarray,Mus musculus,4|4,DO:A connective tissue cancer that arises in fat cells in deep soft tissue retroperitoneum and the extremities. DSA04893,GSE97910,GPL6885,0,Liposarcoma,C0023827,White adipose tissue,GEO,Microarray,Mus musculus,3|4,DO:A connective tissue cancer that arises in fat cells in deep soft tissue retroperitoneum and the extremities. DSA04894,GSE98139,GPL16791,0,Chronic Fatigue Syndrome,C0015674,Whole Blood,GEO,RNA-Seq,Homo sapiens,19|28,"DO:A syndrome that involves prolonged and severe tiredness or weariness that is unrelated to exertion, is not relieved by rest and for a minimum of six months and is not directly caused by other conditions." DSA04895,GSE98289,GPL16791,123,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA04896,GSE98289,GPL16791,108,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,3|2,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA04897,GSE98461,GPL6480,1000,Tuberculosis,C0041296,,GEO,Microarray,Homo sapiens,4|4,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA04898,GSE15932,GPL570,935,Pancreatic Cancer,C0235974,Peripheral blood,GEO,Microarray,Homo sapiens,8|8,DO:An endocrine gland cancer located_in the pancreas. DSA04899,GSE15932,GPL570,407,Diabetes Mellitus,C0011849,Peripheral blood,GEO,Microarray,Homo sapiens,8|8,"DO:A glucose metabolism disease that is characterized by chronic hyperglycaemia with disturbances of carbohydrate, fat and protein metabolism resulting from defects in insulin secretion, insulin action, or both." DSA04900,GSE15932,GPL570,1,Pancreatic Cancer,C0235974,Peripheral blood,GEO,Microarray,Homo sapiens,8|8,DO:An endocrine gland cancer located_in the pancreas. DSA04901,E-MTAB-2312,A-GEOD-10558,0,Obesity,C0028754,Blood,ArrayExpress,Microarray,Homo sapiens,6|6,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA04902,E-MTAB-2312,A-GEOD-10558,0,Stroke,C0948008,Blood,ArrayExpress,Microarray,Homo sapiens,6|6,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA04903,E-MTAB-2312,A-GEOD-10558,15,Obesity;Stroke,,Blood,ArrayExpress,Microarray,Homo sapiens,6|6, DSA04904,E-MTAB-11415,A-MEXP-931,142,Clinically Isolated Syndrome,C2921627,Peripheral blood,ArrayExpress,Microarray,Homo sapiens,40|49, DSA04905,E-MTAB-11415,A-MEXP-931,852,Primary Progressive Multiple Sclerosis,C0751964,Peripheral blood,ArrayExpress,Microarray,Homo sapiens,40|23,"DO:A multiple sclerosis that is characterized by steady worsening of neurologic functioning, without any distinct relapses or periods of remission. The rate of progression may vary over time, with occasional plateaus or temporary improvements, but the progression is continuous." DSA04906,GSE98624,GPL18573,1000,RelA haploinsufficiency,,Skin,GEO,RNA-Seq,Homo sapiens,3|4, DSA04907,GSE98624,GPL18573,1000,RelA haploinsufficiency,,Skin,GEO,RNA-Seq,Homo sapiens,3|4, DSA04908,GSE98742,GPL10558,0,Microcystic Lymphatic Malformation,,Skin,GEO,Microarray,Homo sapiens,5|6, DSA04909,GSE98742,GPL10558,0,Macrocystic Lymphatic Malformation,,Skin,GEO,Microarray,Homo sapiens,5|7, DSA04910,GSE98750,GPL10558,3,Tuberculosis,C0041296,,GEO,Microarray,Homo sapiens,4|3,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA04911,GSE98784,GPL17021,1000,Neuromyelitis Optica,C0027873,,GEO,RNA-Seq,Mus musculus,3|3,DO:A central nervous system disease characterized by inflammation of the optic nerve (optic neuritis) and inflammation of the spinal cord (myelitis). DSA04912,GSE98793,GPL570,27,Major Depressive Disorder,C1269683,Whole blood,GEO,Microarray,Homo sapiens,64|64,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA04913,GSE98895,GPL6947,1000,Metabolic Syndrome,C0524620,,GEO,Microarray,Homo sapiens,20|20,"DO:An abdominal obesity-metabolic syndrome characterized by insulin resistance and hyperinsulinemia, dyslipidemia, essential hypertension, abdominal obesity, glucose intolerance or noninsulin-dependent diabetes mellitus and an increased risk of cardiovascular events." DSA04914,GSE98905,GPL13667,1000,Double Hit Lymphoma,C4285066,,GEO,Microarray,Homo sapiens,3|4,"NCI:A rare B-cell non-Hodgkin lymphoma that is characterized by the abnormal rearrangement of two genes, MYC gene and either BCL2 or BCL6 genes. Patients with this type of lymphoma usually respond poorly to standard treatments and have a poor prognosis." DSA04915,GSE98950,GPL18573,1000,Arthritis,C0003864,Peripheral blood,GEO,RNA-Seq,Homo sapiens,5|6,DO:A bone disease that is located_in the joint. DSA04916,GSE99006,GPL21290,1000,Rheumatoid Arthritis,C0003873,Blood,GEO,RNA-Seq,Homo sapiens,4|4,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04917,GSE99006,GPL21290,1000,Rheumatoid Arthritis,C0003873,Blood,GEO,RNA-Seq,Homo sapiens,4|4,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA04918,GSE99039,GPL570,0,Corticobasal Degeneration,C0393570,Whole blood,GEO,Microarray,Homo sapiens,3|1,MONDO:A progressive neurodegenerative condition affecting the cerebral cortex and basal ganglia. The disorder is characterized by varying degrees of cognitive and motor impairment. DSA04919,GSE99039,GPL570,0,Dopa-Responsive Dystonia Disorders,C1851920,Whole blood,GEO,Microarray,Homo sapiens,6|2,DO:A dystonia characterized by childhood-onset dystonia that responds to low doses of levodopa (L-dopa) and may be associated with parkinsonism at an older age and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the gene enconding GTP cyclohydrolase 1 (GCH1) on chromosome 14q13. DSA04920,GSE99039,GPL570,1,Parkinson's Disease,C0030567,Whole blood,GEO,Microarray,Homo sapiens,184|40,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA04921,GSE99039,GPL570,0,Huntington's Disease,C0020179,Whole blood,GEO,Microarray,Homo sapiens,105|19,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA04922,GSE99039,GPL570,1000,Idiopathic Parkinsonism Or Parkinson's Disease,C0865475,Whole blood,GEO,Microarray,Homo sapiens,221|201,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA04923,GSE99039,GPL570,0,Multiple System Atrophy,C0393571,Whole blood,GEO,Microarray,Homo sapiens,20|8,"MONDO:Multiple system atrophy (MSA) is a neurodegenerative disorder characterized by autonomic failure (cardiovascular and/or urinary), parkinsonism, cerebellar impairment and corticospinal signs with a median survival of 6-9 years." DSA04924,GSE99039,GPL570,0,Progressive Supranuclear Palsy,C0038868,Whole blood,GEO,Microarray,Homo sapiens,65|8,"DO:A movement disease that is characterized by serious and progressive problems with control of gait and balance, along with complex eye movement and thinking problems. It involves gradual deterioration and death of specific volumes of the brain." DSA04925,E-MTAB-11415,A-MEXP-931,24,Relapsing-Remitting Multiple Sclerosis,C0751967,Peripheral blood,ArrayExpress,Microarray,Homo sapiens,40|53,"DO:A multiple sclerosis that is characterized by relapse (attacks of symptom flare-ups) followed by remission (periods of recovery). Symptoms may vary from mild to severe, and relapses and remissions may last for days or months. More than 80 percent of people who have MS begin with relapsing-remitting cycles." DSA04926,GSE99277,GPL16570,0,Autism,C1510586,Cortex,GEO,Microarray,Mus musculus,5|5,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA04927,GSE99321,GPL16791,1000,Idiopathic Dilated Cardiomyopathy,C1449563,Heart left ventricle,GEO,RNA-Seq,Homo sapiens,7|7,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LMNA gene on chromosome 1q21. DSA04928,GSE99373,GPL16791,1000,Tuberculosis,C0041296,,GEO,RNA-Seq,Homo sapiens,19|20,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA04929,GSE99374,GPL16791,8,Tuberculosis,C0041296,,GEO,RNA-Seq,Homo sapiens,19|21,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA04930,GSE99531,GPL20301,1000,Non-Small Cell Lung Cancer,C0007131,Blood,GEO,RNA-Seq,Homo sapiens,4|11,DO:A respiratory system cancer that is located_in the lung. DSA04931,GSE99531,GPL20301,1000,Non-Small Cell Lung Cancer,C0007131,Blood,GEO,RNA-Seq,Homo sapiens,4|11,DO:A respiratory system cancer that is located_in the lung. DSA04932,GSE99531,GPL20301,1000,Non-Small Cell Lung Cancer,C0007131,Blood,GEO,RNA-Seq,Homo sapiens,4|11,DO:A respiratory system cancer that is located_in the lung. DSA04933,GSE99621,GPL16791,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,RNA-Seq,Homo sapiens,8|10,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA04934,GSE99967,GPL21970,1000,Systemic Lupus Erythematosus,C0024141,Peripheral blood,GEO,Microarray,Homo sapiens,17|29,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA04935,GSE99967,GPL21970,63,Systemic Lupus Erythematosus,C0024141,Peripheral blood,GEO,Microarray,Homo sapiens,17|13,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA04936,GSE101900,GPL11002,1000,Muscle Injury,,Tibialis anterior,GEO,RNA-Seq,Mus musculus,7|7, DSA04937,GSE101900,GPL11002,1000,Muscle Injury,,Tibialis anterior,GEO,RNA-Seq,Mus musculus,5|5, DSA04938,GSE101900,GPL11002,422,Muscle Injury,,Tibialis anterior,GEO,RNA-Seq,Mus musculus,3|4, DSA04939,GSE101900,GPL11002,1000,Muscle Injury,,Tibialis anterior,GEO,RNA-Seq,Mus musculus,6|6, DSA04940,GSE101900,GPL11002,612,Muscle Injury,,Tibialis anterior,GEO,RNA-Seq,Mus musculus,5|5, DSA04941,GSE101900,GPL11002,1000,Muscle Injury,,Tibialis anterior,GEO,RNA-Seq,Mus musculus,5|4, DSA04942,GSE101900,GPL11002,1000,Muscle Injury,,Tibialis anterior,GEO,RNA-Seq,Mus musculus,4|3, DSA04943,GSE101900,GPL11002,202,Muscle Injury,,Tibialis anterior,GEO,RNA-Seq,Mus musculus,6|6, DSA04944,GSE101900,GPL11002,1000,Muscle Injury,,Tibialis anterior,GEO,RNA-Seq,Mus musculus,5|5, DSA04945,GSE101906,GPL21103,11,Obesity,C0028754,Ovary,GEO,RNA-Seq,Mus musculus,3|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA04946,E-MTAB-11415,A-MEXP-931,471,Secondary Progressive Multiple Sclerosis,C0751965,Peripheral blood,ArrayExpress,Microarray,Homo sapiens,40|21,"DO:A multiple sclerosis that is characterised by a worsening of disability, rather than by relapses followed by recovery, which progressively worsens until a steady progression of disability replaces the cycles of attacks." DSA04947,E-MTAB-11240,A-GEOD-23159,1000,Severe Acute Respiratory Syndrome,C1175175,Blood,ArrayExpress,Microarray,Homo sapiens,12|14,"DO:A Coronavirus infection that results_in infection located_in respiratory tract, has_material_basis_in SARS coronavirus (SARS-CoV), which is transmitted_by droplet spread of respiratory secretions, transmitted_by ingestion of contaminated food, or transmitted_by fomites. The infection has_symptom fever, has_symptom headache, has_symptom body aches, has_symptom dry cough, and has_symptom hypoxia." DSA04948,GSE102416,GPL11533,6,Liver Cancer,C2239176,Liver,GEO,Microarray,Mus musculus,5|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA04949,GSE102416,GPL11533,236,Liver Cancer,C2239176,Liver,GEO,Microarray,Mus musculus,3|5,DO:A hepatobiliary system cancer that is located_in the liver. DSA04950,GSE102558,GPL20710,1000,Ischemic Stroke,C0948008,Heart,GEO,Microarray,Mus musculus,6|6,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA04951,GSE102558,GPL20710,1000,Ischemic Stroke,C0948008,Heart,GEO,Microarray,Mus musculus,6|6,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA04952,GSE102642,GPL19057,123,Obesity,C0028754,Ectoplacental cone,GEO,RNA-Seq,Mus musculus,4|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA04953,GSE102642,GPL19057,230,Obesity,C0028754,Ectoplacental cone,GEO,RNA-Seq,Mus musculus,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA04954,GSE102675,GPL13112,1000,Pancreatitis,C0030305,Pancreas,GEO,RNA-Seq,Mus musculus,3|3,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA04955,GSE102675,GPL13112,1000,Pancreatitis,C0030305,Pancreas,GEO,RNA-Seq,Mus musculus,3|3,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA04956,E-MTAB-11240,A-GEOD-23159,48,Severe Acute Respiratory Syndrome,C1175175,Blood,ArrayExpress,Microarray,Homo sapiens,12|12,"DO:A Coronavirus infection that results_in infection located_in respiratory tract, has_material_basis_in SARS coronavirus (SARS-CoV), which is transmitted_by droplet spread of respiratory secretions, transmitted_by ingestion of contaminated food, or transmitted_by fomites. The infection has_symptom fever, has_symptom headache, has_symptom body aches, has_symptom dry cough, and has_symptom hypoxia." DSA04957,E-MTAB-11240,A-GEOD-23159,45,Severe Acute Respiratory Syndrome,C1175175,Blood,ArrayExpress,Microarray,Homo sapiens,12|14,"DO:A Coronavirus infection that results_in infection located_in respiratory tract, has_material_basis_in SARS coronavirus (SARS-CoV), which is transmitted_by droplet spread of respiratory secretions, transmitted_by ingestion of contaminated food, or transmitted_by fomites. The infection has_symptom fever, has_symptom headache, has_symptom body aches, has_symptom dry cough, and has_symptom hypoxia." DSA04958,E-MTAB-11240,A-GEOD-23159,1000,Severe Acute Respiratory Syndrome,C1175175,Blood,ArrayExpress,Microarray,Homo sapiens,12|14,"DO:A Coronavirus infection that results_in infection located_in respiratory tract, has_material_basis_in SARS coronavirus (SARS-CoV), which is transmitted_by droplet spread of respiratory secretions, transmitted_by ingestion of contaminated food, or transmitted_by fomites. The infection has_symptom fever, has_symptom headache, has_symptom body aches, has_symptom dry cough, and has_symptom hypoxia." DSA04959,GSE103888,GPL570,0,Non-Small Cell Lung Cancer,C0007131,,GEO,Microarray,Homo sapiens,4|1,DO:A respiratory system cancer that is located_in the lung. DSA04960,GSE103888,GPL570,10,Non-Small Cell Lung Cancer,C0007131,,GEO,Microarray,Homo sapiens,4|1,DO:A respiratory system cancer that is located_in the lung. DSA04961,GSE103888,GPL570,0,Non-Small Cell Lung Cancer,C0007131,,GEO,Microarray,Homo sapiens,4|3,DO:A respiratory system cancer that is located_in the lung. DSA04962,GSE103888,GPL570,26,Non-Small Cell Lung Cancer,C0007131,,GEO,Microarray,Homo sapiens,6|2,DO:A respiratory system cancer that is located_in the lung. DSA04963,GSE104627,GPL13912,1000,Liver Tumor,C0345904,Liver,GEO,Microarray,Mus musculus,3|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA04964,GSE105117,GPL13912,36,Vitamin D Deficiency,C0042870,Colon,GEO,Microarray,Mus musculus,3|3,"EFO:A nutritional condition produced by a deficiency of VITAMIN D in the diet, insufficient production of vitamin D in the skin, inadequate absorption of vitamin D from the diet, or abnormal conversion of vitamin D to its bioactive metabolites. It is manifested clinically as RICKETS in children and OSTEOMALACIA in adults. (From Cecil Textbook of Medicine, 19th ed, p1406)" DSA04965,GSE105117,GPL13912,0,Vitamin D Deficiency,C0042870,Colon,GEO,Microarray,Mus musculus,3|3,"EFO:A nutritional condition produced by a deficiency of VITAMIN D in the diet, insufficient production of vitamin D in the skin, inadequate absorption of vitamin D from the diet, or abnormal conversion of vitamin D to its bioactive metabolites. It is manifested clinically as RICKETS in children and OSTEOMALACIA in adults. (From Cecil Textbook of Medicine, 19th ed, p1406)" DSA04966,GSE105147,GPL13112,1000,Liver Tumor,C0345904,Liver,GEO,RNA-Seq,Mus musculus,3|2,DO:A hepatobiliary system cancer that is located_in the liver. DSA04967,GSE105147,GPL13112,1000,Liver Tumor,C0345904,Liver,GEO,RNA-Seq,Mus musculus,3|2,DO:A hepatobiliary system cancer that is located_in the liver. DSA04968,GSE10535,GPL1261,5,Retina Degeneration,C0035304,Retina,GEO,Microarray,Mus musculus,3|3,DO:A retinal disease that is characterized by deterioration of the retina caused by the progressive and eventual death of the cells of the retina. DSA04969,GSE105763,GPL1261,1000,T-Cell Acute Lymphoblastic Leukemia,C1961099,,GEO,Microarray,Mus musculus,3|3,DO:An acute lymphoblastic leukemia that is characterized by too many T-cell lymphoblasts found in the bone marrow and blood. DSA04970,GSE105763,GPL1261,1000,T-Cell Acute Lymphoblastic Leukemia,C1961099,,GEO,Microarray,Mus musculus,3|3,DO:An acute lymphoblastic leukemia that is characterized by too many T-cell lymphoblasts found in the bone marrow and blood. DSA04971,GSE10598,GPL1261,601,Atrial Fibrillation,C0004238,,GEO,Microarray,Mus musculus,2|2,"DO:A heart conduction disease that is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular and has symptoms palpitations, weakness, fatigue, lightheadedness, dizziness, confusion, shortness of breath and chest pain." DSA04972,E-MTAB-8887,A-MEXP-2320,328,Cholangiocellular Carcinoma,C0206698,Liver,ArrayExpress,Microarray,Homo sapiens,2|1,DO:A bile duct carcinoma that derives_from epithelial cells of glandular origin. DSA04973,GSE106316,GPL16570,1000,Gata6 Deficiency,,Pancreatic islet,GEO,Microarray,Mus musculus,3|4, DSA04974,GSE106362,GPL17021,0,Ovarian Tumor,C1140680,Oviduct,GEO,RNA-Seq,Mus musculus,3|3,DO:A female reproductive organ cancer that is located_in the ovary. DSA04975,GSE107214,GPL10558,924,Obesity,C0028754,,GEO,Microarray,Homo sapiens,21|21,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA04976,E-MTAB-8887,A-MEXP-2320,0,Hepatocellular Carcinoma,C0334287,Liver,ArrayExpress,Microarray,Homo sapiens,7|6,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA04977,GSE107374,GPL18802,25,Liver Tumor,C0345904,Liver,GEO,Microarray,Mus musculus,5|8,DO:A hepatobiliary system cancer that is located_in the liver. DSA04978,GSE107374,GPL18802,8,Liver Tumor,C0345904,Liver,GEO,Microarray,Mus musculus,3|8,DO:A hepatobiliary system cancer that is located_in the liver. DSA04979,GSE107412,GPL21103,62,Hypercholesterolemia,C0020443,,GEO,RNA-Seq,Mus musculus,3|3,HPO:An increased concentration of cholesterol in the blood. DSA04980,GSE107412,GPL21103,77,Hypercholesterolemia,C0020443,,GEO,RNA-Seq,Mus musculus,3|3,HPO:An increased concentration of cholesterol in the blood. DSA04981,GSE107915,GPL19057,1000,Lymphoma,C0024299,Thymus,GEO,RNA-Seq,Mus musculus,3|6,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA04982,GSE108933,GPL20301,1000,Tendon Injury,,Tendon,GEO,RNA-Seq,Homo sapiens,3|3, DSA04983,E-MTAB-8887,A-MEXP-2320,2,Hepatocellular Carcinoma,C0334287,Liver,ArrayExpress,Microarray,Homo sapiens,6|11,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA04984,GSE109234,GPL10999|GPL11154,1000,T-Lymphoblastic Lymphoma,C1292758,Thymus,GEO,RNA-Seq,Homo sapiens,2|8,"MONDO:The most frequent type of lymphoblastic lymphoma. It comprises approximately 85-90% of cases. It is more frequently seen in adolescent males. It frequently presents with a mass lesion in the mediastinum. Pleural effusions are common. (WHO, 2001)" DSA04985,GSE109431,GPL21103,553,Hepatic Steatosis,C2711227,Liver,GEO,RNA-Seq,Mus musculus,3|3,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA04986,GSE109431,GPL21103,359,Hepatic Steatosis,C2711227,Liver,GEO,RNA-Seq,Mus musculus,4|2,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA04987,E-MTAB-8887,A-MEXP-2320,1,Hepatocellular Carcinoma,C0334287,Liver,ArrayExpress,Microarray,Homo sapiens,2|1,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA04988,E-MTAB-8588,A-MEXP-1173,1000,Carcinoma of The Base of The Tongue,C0346564,Tongue,ArrayExpress,Microarray,Homo sapiens,17|20,"NCI:A carcinoma that arises from the base of the tongue. Representative examples include squamous cell carcinoma, adenoid cystic carcinoma, and mucoepidermoid carcinoma." DSA04989,E-MTAB-8588,A-MEXP-1173,0,Piriformal Recessus Carcinoma,,Hypopharynx,ArrayExpress,Microarray,Homo sapiens,5|6, DSA04990,E-MTAB-8588,A-MEXP-1173,1000,Glottic Carcinoma,C0740083,Larynx,ArrayExpress,Microarray,Homo sapiens,24|9,MONDO:A carcinoma that arises from epithelial cells of the glottis. DSA04991,E-MTAB-8588,A-MEXP-1173,1000,Subglottic Carcinoma,,Larynx,ArrayExpress,Microarray,Homo sapiens,24|2, DSA04992,GSE110188,GPL15103,1000,Encephalitis,C0014038,Olfactory bulb,GEO,RNA-Seq,Mus musculus,3|3,DO:A brain disease that is characterized as an acute inflammation of the brain with flu-like symptoms. DSA04993,GSE110384,GPL11202,678,Influenza,C0021400,Blood,GEO,Microarray,Mus musculus,34|6,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA04994,GSE110384,GPL11202,1000,Influenza,C0021400,Blood,GEO,Microarray,Mus musculus,34|28,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA04995,E-MTAB-8588,A-MEXP-1173,1000,Supraglottic Carcinoma,C1299240,Larynx,ArrayExpress,Microarray,Homo sapiens,24|12,MONDO:A carcinoma of the larynx that arises from the supraglottic area. DSA04996,E-MTAB-8588,A-MEXP-1173,1000,Transglottic Carcinoma,,Larynx,ArrayExpress,Microarray,Homo sapiens,24|6, DSA04997,E-MTAB-8588,A-MEXP-1173,1000,Malignant Tumor of Floor of Mouth,C0153368,Oral cavity,ArrayExpress,Microarray,Homo sapiens,18|9,DO:A gastrointestinal system cancer that is located_in the oral cavity. DSA04998,GSE111734,GPL19057,1000,Medulloblastoma,C0025149,,GEO,RNA-Seq,Mus musculus,4|4,DO:An infratentorial cancer that is located_in the lower part of the brain and is a type of primitive neuroectodermal tumor. DSA04999,GSE111734,GPL19057,1000,Medulloblastoma,C0025149,,GEO,RNA-Seq,Mus musculus,4|4,DO:An infratentorial cancer that is located_in the lower part of the brain and is a type of primitive neuroectodermal tumor. DSA05000,GSE112373,GPL13112,476,Pten Deficiency,,Brain,GEO,RNA-Seq,Mus musculus,2|2, DSA05001,E-MTAB-8588,A-MEXP-1173,761,Carcinoma of The Retromolar Trigonu,,Oral cavity,ArrayExpress,Microarray,Homo sapiens,18|3, DSA05002,E-MTAB-8588,A-MEXP-1173,1000,Tongue Carcinoma,C0558353,Oral cavity,ArrayExpress,Microarray,Homo sapiens,18|9,NCI:A malignant tumor arising from the epithelium that covers the tongue. The vast majority of tongue carcinomas are moderately or poorly differentiated squamous cell carcinomas. DSA05003,E-MTAB-8588,A-MEXP-1173,45,Pharyngeal Carcinoma,C0747548,Oropharynx part,ArrayExpress,Microarray,Homo sapiens,8|3,MONDO:A carcinoma that involves the pharynx. DSA05004,E-MTAB-8588,A-MEXP-1173,561,Pharyngeal Carcinoma,C0747548,Oropharynx part,ArrayExpress,Microarray,Homo sapiens,8|2,MONDO:A carcinoma that involves the pharynx. DSA05005,E-MTAB-8588,A-MEXP-1173,354,Soft Palate Carcinoma,,Oropharynx part,ArrayExpress,Microarray,Homo sapiens,8|4, DSA05006,E-MTAB-8588,A-MEXP-1173,1000,Tonsillar Carcinoma,C0558355,Tonsil,ArrayExpress,Microarray,Homo sapiens,26|29,MONDO:A carcinoma that involves the tonsil. DSA05007,E-MTAB-8018,A-GEOD-10558,244,Bipolar Disorder,C0005586,Blood,ArrayExpress,Microarray,Homo sapiens,391|84,DO:A mood disorder that involves alternating periods of mania and depression. DSA05008,E-MTAB-8018,A-GEOD-10558,37,Schizoaffective Disorder,C0036337,Blood,ArrayExpress,Microarray,Homo sapiens,391|13,DO:A psychotic disorder that is characterized by recurring episodes of mood fluctuations and a loss of contact with reality. DSA05009,GSE115810,GPL96,0,Endometrial Cancer,C0476089,Endometrium,GEO,Microarray,Homo sapiens,3|7,DO:A uterine cancer that is located_in tissues lining the uterus. DSA05010,GSE115810,GPL96,654,Endometrial Cancer,C0476089,Endometrium,GEO,Microarray,Homo sapiens,3|11,DO:A uterine cancer that is located_in tissues lining the uterus. DSA05011,GSE115810,GPL96,104,Endometrial Cancer,C0476089,Endometrium,GEO,Microarray,Homo sapiens,3|6,DO:A uterine cancer that is located_in tissues lining the uterus. DSA05012,GSE115840,GPL1261,1000,Glioma,C0017638,Brain,GEO,Microarray,Mus musculus,24|6,DO:A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine. DSA05013,GSE115840,GPL1261,1000,Medulloblastoma,C0025149,Brain,GEO,Microarray,Mus musculus,24|22,DO:An infratentorial cancer that is located_in the lower part of the brain and is a type of primitive neuroectodermal tumor. DSA05014,GSE116236,GPL19057,3,Leukemia,C0023418,Intraepithelium,GEO,RNA-Seq,Mus musculus,6|5,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA05015,GSE116236,GPL19057,83,Leukemia,C0023418,Lamina propria,GEO,RNA-Seq,Mus musculus,6|5,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA05016,E-MTAB-8018,A-GEOD-10558,194,Schizophrenia,C0036341,Blood,ArrayExpress,Microarray,Homo sapiens,391|58,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA05017,E-MTAB-6986,A-AFFY-45,0,Spinal And Bulbar Muscular Atrophy,C1839259,Spinal cord,ArrayExpress,Microarray,Mus musculus,4|4,DO:A spinal muscular dystrophy that has_material_basis_in an X-linked recessive expansion of CAG triplet repeats (glutamine) in exon 1 of AR gene encoding the androgen receptor. DSA05018,GSE117029,GPL17021,56,Influenza,C0021400,Lung,GEO,RNA-Seq,Mus musculus,6|6,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA05019,GSE117029,GPL17021,1000,Influenza,C0021400,Lung,GEO,RNA-Seq,Mus musculus,6|7,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA05020,E-MTAB-7853,A-GEOD-16570,0,Arthritis,C0003864,Dorsal root ganglion,ArrayExpress,Microarray,Mus musculus,3|4,DO:A bone disease that is located_in the joint. DSA05021,GSE118349,GPL17021,1000,Kidney Fibrosis,C0151650,Kidney,GEO,RNA-Seq,Mus musculus,3|4,HPO:Renal fibrosis is the consequence of an excessive accumulation of extracellular matrix that occurs in virtually every type of chronic kidney disease. DSA05022,GSE118349,GPL17021,1000,Kidney Fibrosis,C0151650,Kidney,GEO,RNA-Seq,Mus musculus,3|4,HPO:Renal fibrosis is the consequence of an excessive accumulation of extracellular matrix that occurs in virtually every type of chronic kidney disease. DSA05023,GSE118349,GPL17021,1000,Kidney Fibrosis,C0151650,Kidney,GEO,RNA-Seq,Mus musculus,3|4,HPO:Renal fibrosis is the consequence of an excessive accumulation of extracellular matrix that occurs in virtually every type of chronic kidney disease. DSA05024,GSE192767,GPL15207,124,Alpha Thalassemia-Intellectual Disability Syndrome Type 1,C2873754,,GEO,Microarray,Homo sapiens,20|28,"DO:An alpha thalassemia that has_material_basis_in a deletion in chromosome 16p that involves the alpha-1 (HBA1) and alpha-2 (HBA2) genes, among others." DSA05025,GSE192829,GPL18573,1000,Pulmonary Sarcoidosis,C0036205,Blood,GEO,RNA-Seq,Homo sapiens,11|8,"DO:A sarcoidosis that is characterized by noncaseating granulomatous infiltration of the lungs and supporting lymph nodes, bilateral hilar adenopathy, and pulmonary issues, has_symptom shortness of breath, fatigue, wheezing, and chronic cough, and develops_from a type IV hypersensitivity reaction." DSA05026,GSE192832,GPL20301,1000,Ichthyosis,C0020757,Skin,GEO,RNA-Seq,Homo sapiens,40|18,DO:A skin disease characterized by drying and scaling of skin with the accumulation of thick scales and cracks that may be painful or bleed. DSA05027,GSE192832,GPL20301,1000,Ichthyosis,C0020757,Skin,GEO,RNA-Seq,Homo sapiens,40|13,DO:A skin disease characterized by drying and scaling of skin with the accumulation of thick scales and cracks that may be painful or bleed. DSA05028,GSE192832,GPL20301,1000,Ichthyosis,C0020757,Skin,GEO,RNA-Seq,Homo sapiens,40|16,DO:A skin disease characterized by drying and scaling of skin with the accumulation of thick scales and cracks that may be painful or bleed. DSA05029,GSE192832,GPL20301,1000,Ichthyosis,C0020757,Skin,GEO,RNA-Seq,Homo sapiens,40|7,DO:A skin disease characterized by drying and scaling of skin with the accumulation of thick scales and cracks that may be painful or bleed. DSA05030,GSE192867,GPL23126,1000,Psoriasis,C0033860,Venous blood,GEO,Microarray,Homo sapiens,10|23,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA05031,GSE192867,GPL23126,1000,Psoriasis,C0033860,Venous blood,GEO,Microarray,Homo sapiens,10|16,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA05032,GSE192867,GPL23126,1000,Psoriasis,C0033860,Venous blood,GEO,Microarray,Homo sapiens,10|23,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA05033,GSE192886,GPL24676,20,Heart Failure With Preserved Ejection Fraction,C4509226,Adipose tissue,GEO,RNA-Seq,Homo sapiens,5|5, DSA05034,E-MTAB-7853,A-GEOD-16570,0,Arthritis,C0003864,Dorsal root ganglion,ArrayExpress,Microarray,Mus musculus,3|4,DO:A bone disease that is located_in the joint. DSA05035,E-MTAB-7671,A-MEXP-2320,0,Chronic Obstructive Pulmonary Disease,C0024117,Lung blood vessel,ArrayExpress,Microarray,Homo sapiens,3|4,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA05036,GSE193016,GPL21047,1000,Sinonasal Inverted Papilloma,,Nasal,GEO,Microarray,Homo sapiens,4|4, DSA05037,GSE193037,GPL18573,1000,Atr-X Syndrome,C1845055,Peripheral blood,GEO,scRNA-Seq,Homo sapiens,1|1,DO:An alpha thalassemia that has_material_basis_in mutation in the ATRX gene on Xq21. DSA05038,E-MTAB-7406,A-AFFY-44,0,Asthma,C0004096,Bronchus,ArrayExpress,Microarray,Homo sapiens,3|1,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA05039,GSE193113,GPL20301,654,X-Linked Acrogigantism,C3891556,Pituitary gland,GEO,RNA-Seq,Homo sapiens,3|4,"ORDO:A rare, genetic pituitary disease characterized by infantile-onset, rapid and excessive acceleration of linear growth and body size due to mixed growth hormone (GH)- and prolactin-secreting adenomas and/or pituitary hyperplasia. Patients present with gigantism and may have associated acromegalic features (e.g. coarse facial features, frontal bossing, prognathism, increased interdental space) as well as marked enlargement of hands and feet, soft tissue swelling, increased appetite and acanthosis nigricans." DSA05040,E-MTAB-7406,A-AFFY-44,0,Asthma,C0004096,Bronchus,ArrayExpress,Microarray,Homo sapiens,3|1,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA05041,E-MTAB-7406,A-AFFY-44,0,Asthma,C0004096,Bronchus,ArrayExpress,Microarray,Homo sapiens,3|1,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA05042,GSE193123,GPL24676,89,Polycystic Ovary Syndrome,C0032460,Ovary,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA05043,GSE193193,GPL24676,1000,Rheumatoid Arthritis,C0003873,,GEO,RNA-Seq,Homo sapiens,5|5,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA05044,GSE193238,GPL24247,1000,Multiple Sclerosis,C0026769,Spinal cord,GEO,scRNA-Seq,Mus musculus,1|1,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA05045,GSE193260,GPL24676,1000,Multiple Sclerosis,C0026769,,GEO,RNA-Seq,Homo sapiens,3|5,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA05046,GSE193260,GPL24676,1000,Multiple Sclerosis,C0026769,,GEO,RNA-Seq,Homo sapiens,3|5,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA05047,GSE193260,GPL24676,1000,Multiple Sclerosis,C0026769,,GEO,RNA-Seq,Homo sapiens,3|5,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA05048,GSE193273,GPL20844,675,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,20|20,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA05049,GSE193309,GPL24676,1000,Atopic Dermatitis,C0011615,Skin,GEO,RNA-Seq,Homo sapiens,45|91,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA05050,GSE193309,GPL24676,393,Atopic Dermatitis,C0011615,Skin,GEO,RNA-Seq,Homo sapiens,13|44,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA05051,GSE193309,GPL24676,175,Atopic Dermatitis,C0011615,Skin,GEO,RNA-Seq,Homo sapiens,15|27,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA05052,GSE193309,GPL24676,253,Atopic Dermatitis,C0011615,Skin,GEO,RNA-Seq,Homo sapiens,15|25,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA05053,GSE193309,GPL24676,475,Atopic Dermatitis,C0011615,Skin,GEO,RNA-Seq,Homo sapiens,15|27,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA05054,GSE193351,GPL20301,1000,Lichen Planus,C0023646,Skin,GEO,RNA-Seq,Homo sapiens,10|37,"DO:A lichen disease that is located_in skin, located_in tongue or located_in oral mucosa, which presents itself in the form of papules, lesions or rashes." DSA05055,GSE193391,GPL31198,31,Alzheimer's Disease,C0002395,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,8|8,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05056,GSE193391,GPL31198,303,Frontotemporal Lobar Degeneration,C0751072,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,8|8,"MSH:Heterogeneous group of neurodegenerative disorders characterized by frontal and temporal lobe atrophy associated with neuronal loss, gliosis, and dementia. Patients exhibit progressive changes in social, behavioral, and/or language function. Multiple subtypes or forms are recognized based on presence or absence of TAU PROTEIN inclusions. FTLD includes three clinical syndromes: FRONTOTEMPORAL DEMENTIA, semantic dementia, and PRIMARY PROGRESSIVE NONFLUENT APHASIA." DSA05057,GSE193417,GPL15520,96,Major Depressive Disorder,C1269683,Anterior cingulate cortex,GEO,RNA-Seq,Homo sapiens,6|6,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA05058,GSE193438,GPL18573,1000,Alzheimer's Disease,C0002395,Basal ganglia,GEO,RNA-Seq,Homo sapiens,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05059,GSE193438,GPL18573,1000,Lewy Body Dementia,C0752347,Basal ganglia,GEO,RNA-Seq,Homo sapiens,4|3,"DO:A dementia that is characterized by the development of abnormal proteinaceous (alpha-synuclein) cytoplasmic inclusions, called Lewy bodies, throughout the brain that results in progressive decline in mental abilities." DSA05060,GSE193438,GPL18573,818,Alzheimer's Disease,C0002395,Hippocampus,GEO,RNA-Seq,Homo sapiens,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05061,GSE193438,GPL18573,1000,Lewy Body Dementia,C0752347,Hippocampus,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A dementia that is characterized by the development of abnormal proteinaceous (alpha-synuclein) cytoplasmic inclusions, called Lewy bodies, throughout the brain that results in progressive decline in mental abilities." DSA05062,GSE193438,GPL18573,1000,Alzheimer's Disease,C0002395,Parietal lobe,GEO,RNA-Seq,Homo sapiens,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05063,GSE193438,GPL18573,1000,Lewy Body Dementia,C0752347,Parietal lobe,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A dementia that is characterized by the development of abnormal proteinaceous (alpha-synuclein) cytoplasmic inclusions, called Lewy bodies, throughout the brain that results in progressive decline in mental abilities." DSA05064,GSE193438,GPL18573,1000,Alzheimer's Disease,C0002395,Substantia nigra,GEO,RNA-Seq,Homo sapiens,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05065,GSE193438,GPL18573,1000,Lewy Body Dementia,C0752347,Substantia nigra,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A dementia that is characterized by the development of abnormal proteinaceous (alpha-synuclein) cytoplasmic inclusions, called Lewy bodies, throughout the brain that results in progressive decline in mental abilities." DSA05066,GSE193531,GPL16791,1000,Multiple Myeloma,C0026764,,GEO,scRNA-Seq,Homo sapiens,9|6,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA05067,GSE193531,GPL16791,1000,Multiple Myeloma,C0026764,,GEO,scRNA-Seq,Homo sapiens,9|12,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA05068,GSE193531,GPL16791,1000,Multiple Myeloma,C0026764,,GEO,scRNA-Seq,Homo sapiens,9|8,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA05069,E-MTAB-7406,A-AFFY-44,0,Asthma,C0004096,Bronchus,ArrayExpress,Microarray,Homo sapiens,3|2,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA05070,GSE193662,GPL21697,386,Limb-Girdle Muscular Dystrophy,C0686353,,GEO,RNA-Seq,Homo sapiens,10|10,DO:A muscular dystrophy that is characterized by weakening of the muscles of the hip and shoulders which comprise the limb girdle muscles. DSA05071,GSE193677,GPL16791,1000,Crohn's Disease,C0010346,Bowel,GEO,RNA-Seq,Homo sapiens,459|419,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA05072,GSE193677,GPL16791,1000,Ulcerative Colitis,C0009324,Bowel,GEO,RNA-Seq,Homo sapiens,458|872,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA05073,GSE193682,GPL16791,4,Pulmonary Fibrosis,C0034069,Lung,GEO,RNA-Seq,Homo sapiens,4|4,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA05074,GSE193682,GPL16791,10,Pulmonary Fibrosis,C0034069,Lung,GEO,RNA-Seq,Homo sapiens,4|4,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA05075,GSE193682,GPL16791,0,Pulmonary Fibrosis,C0034069,Lung,GEO,RNA-Seq,Homo sapiens,4|4,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA05076,GSE193682,GPL16791,64,Pulmonary Fibrosis,C0034069,Lung,GEO,RNA-Seq,Homo sapiens,4|4,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA05077,E-MTAB-7406,A-AFFY-44,1,Asthma,C0004096,Bronchus,ArrayExpress,Microarray,Homo sapiens,3|2,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA05078,GSE193770,GPL20301,1000,Multiple Sclerosis,C0026769,,GEO,scRNA-Seq,Homo sapiens,4|6,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA05079,GSE193776,GPL18573,1000,Idiopathic Pulmonary Arterial Hypertension,C3203102,Pulmonary artery,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A chronic pulmonary heart disease characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein, or pulmonary capillaries, among others, has symptoms shortness of breath, dizziness, fainting, leg swelling." DSA05080,E-MTAB-7406,A-AFFY-44,0,Asthma,C0004096,Bronchus,ArrayExpress,Microarray,Homo sapiens,3|2,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA05081,E-MTAB-7140,A-MEXP-2183,0,Chronic Obstructive Pulmonary Disease,C0024117,Lung,ArrayExpress,Microarray,Homo sapiens,3|4,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA05082,E-MTAB-5638,A-MEXP-2183,1000,Pneumonia,C0032285,Blood,ArrayExpress,Microarray,Homo sapiens,15|24,"DO:A lung disease that involves lung parenchyma or alveolar inflammation and abnormal alveolar filling with fluid (consolidation and exudation). It results from a variety of causes including infection with bacteria, viruses, fungi or parasites, and chemical or physical injury to the lungs. It is accompanied by fever, chills, cough, and difficulty in breathing." DSA05083,GSE194071,GPL19057,1000,Multiple Sclerosis,C0026769,Spinal cord,GEO,RNA-Seq,Mus musculus,3|3,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA05084,GSE194071,GPL19057,1000,Multiple Sclerosis,C0026769,Spinal cord,GEO,RNA-Seq,Mus musculus,3|3,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA05085,GSE194071,GPL19057,1000,Multiple Sclerosis,C0026769,Spinal cord,GEO,RNA-Seq,Mus musculus,3|3,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA05086,GSE194119,GPL22120,0,Gestational Diabetes Mellitus,C0085207,Cord blood,GEO,Microarray,Homo sapiens,3|3,DO:A diabetes mellitus that manifests during pregnancy. DSA05087,GSE194234,GPL11154,1000,Primary Sjogren Syndrome,C0151449,,GEO,RNA-Seq,Homo sapiens,6|7,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA05088,E-MTAB-5385,A-MEXP-2072,1000,Breast Cancer,C0678222,Dermis,ArrayExpress,Microarray,Homo sapiens,19|4,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05089,GSE194245,GPL24676,799,Parkinson's Disease,C0030567,,GEO,scRNA-Seq,Homo sapiens,6|8,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05090,GSE194261,GPL17077,0,Gastric Cancer,C0699791,,GEO,Microarray,Homo sapiens,4|4,DO:A gastrointestinal system cancer that is located_in the stomach. DSA05091,GSE194261,GPL17077,0,Gastric Cancer,C0699791,,GEO,Microarray,Homo sapiens,6|6,DO:A gastrointestinal system cancer that is located_in the stomach. DSA05092,GSE194282,GPL17692,480,Chronic Rhinosinusitis,C0149516,,GEO,Microarray,Homo sapiens,7|7,EFO:An acute or chronic inflammatory process affecting the mucous membranes of any sinus cavity. DSA05093,E-MTAB-5385,A-MEXP-2072,224,Melanoma,C0025202,Dermis,ArrayExpress,Microarray,Homo sapiens,19|10,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA05094,GSE194331,GPL16791,1000,Acute Pancreatitis,C0001339,Blood,GEO,RNA-Seq,Homo sapiens,32|57,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA05095,GSE194331,GPL16791,1000,Acute Pancreatitis,C0001339,Blood,GEO,RNA-Seq,Homo sapiens,32|20,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA05096,GSE194331,GPL16791,1000,Acute Pancreatitis,C0001339,Blood,GEO,RNA-Seq,Homo sapiens,32|10,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA05097,GSE194368,GPL24676,146,Opioid Use Disorder,C4324621,,GEO,RNA-Seq,Homo sapiens,21|21, DSA05098,GSE19443,GPL6947,0,Tuberculosis,C0041296,Blood,GEO,Microarray,Homo sapiens,4|6,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05099,GSE19443,GPL6947,0,Tuberculosis,C0041296,Blood,GEO,Microarray,Homo sapiens,4|6,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05100,GSE19443,GPL6947,0,Tuberculosis,C0041296,Blood,GEO,Microarray,Homo sapiens,4|6,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05101,GSE19443,GPL6947,0,Tuberculosis,C0041296,Blood,GEO,Microarray,Homo sapiens,4|5,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05102,GSE19444,GPL6947,0,Tuberculosis,C0041296,Blood,GEO,Microarray,Homo sapiens,12|21,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05103,GSE19444,GPL6947,1000,Tuberculosis,C0041296,Blood,GEO,Microarray,Homo sapiens,12|21,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05104,GSE195442,GPL31275,1,Ischemic Stroke,C0948008,,GEO,Microarray,Homo sapiens,10|10,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA05105,GSE195452,GPL18573|GPL24676,292,Systemic Sclerosis [Scleroderma],C2364016,Peripheral blood,GEO,RNA-Seq,Homo sapiens,21|82, DSA05106,GSE195452,GPL18573|GPL24676,317,Systemic Sclerosis [Scleroderma],C2364016,Skin,GEO,RNA-Seq,Homo sapiens,97|219, DSA05107,GSE195460,GPL24676,1000,Diabetic Kidney Disease,C0011881,Kidney cortex,GEO,snRNA-Seq,Homo sapiens,1|2,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA05108,GSE195501,GPL18573,95,Active Uveitis,,Blood,GEO,RNA-Seq,Homo sapiens,13|10, DSA05109,GSE195501,GPL18573,63,Active Uveitis,,Blood,GEO,RNA-Seq,Homo sapiens,13|8, DSA05110,GSE195501,GPL18573,121,Active Uveitis,,Blood,GEO,RNA-Seq,Homo sapiens,13|5, DSA05111,GSE195599,GPL16791,1000,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,3|4,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA05112,E-MTAB-5385,A-MEXP-2072,132,Melanoma,C0025202,Dermis,ArrayExpress,Microarray,Homo sapiens,19|2,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA05113,GSE195872,GPL23126,0,Alzheimer's Disease,C0002395,Prefrontal cortex,GEO,Microarray,Homo sapiens,5|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05114,GSE195872,GPL23126,0,Alzheimer's Disease,C0002395,Prefrontal cortex,GEO,Microarray,Homo sapiens,5|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05115,GSE195872,GPL23126,0,Frontotemporal Dementia,C0338451,Prefrontal cortex,GEO,Microarray,Homo sapiens,5|5,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA05116,GSE195872,GPL23126,0,Frontotemporal Dementia,C0338451,Prefrontal cortex,GEO,Microarray,Homo sapiens,5|3,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA05117,GSE195872,GPL23126,8,Frontotemporal Dementia,C0338451,Prefrontal cortex,GEO,Microarray,Homo sapiens,5|5,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA05118,GSE195872,GPL23126,0,Frontotemporal Dementia,C0338451,Prefrontal cortex,GEO,Microarray,Homo sapiens,5|5,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA05119,GSE195872,GPL23126,0,Frontotemporal Dementia,C0338451,Prefrontal cortex,GEO,Microarray,Homo sapiens,5|5,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA05120,GSE195872,GPL23126,0,Alzheimer's Disease,C0002395,,GEO,Microarray,Homo sapiens,5|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05121,GSE195872,GPL23126,0,Alzheimer's Disease,C0002395,,GEO,Microarray,Homo sapiens,5|5,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05122,GSE195872,GPL23126,0,Frontotemporal Dementia,C0338451,,GEO,Microarray,Homo sapiens,5|5,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA05123,GSE195872,GPL23126,0,Frontotemporal Dementia,C0338451,,GEO,Microarray,Homo sapiens,5|3,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA05124,GSE195938,GPL23159,0,COVID-19,D8888888,Umbilical cord blood,GEO,Microarray,Homo sapiens,8|8,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05125,E-MTAB-3950,A-MEXP-2246,1000,Lung Squamous Cell Carcinoma,C0149782,Lung,ArrayExpress,Microarray,Homo sapiens,21|15,DO:A non-small cell lung carcinoma that has_material_basis_in the squamous cell. DSA05126,GSE196070,GPL16791,7,Systemic Sclerosis [Scleroderma],C2364016,,GEO,RNA-Seq,Homo sapiens,18|16, DSA05127,GSE196264,GPL18281,1000,Medullary Thyroid Cancer,C0238462,Thyroid,GEO,Microarray,Homo sapiens,3|9,DO:A thyroid gland carcinoma that has_material_basis_in parafollicular cells. DSA05128,GSE196264,GPL18281,1000,Medullary Thyroid Cancer,C0238462,Thyroid,GEO,Microarray,Homo sapiens,3|8,DO:A thyroid gland carcinoma that has_material_basis_in parafollicular cells. DSA05129,GSE196266,GPL24242,0,Ischemic Stroke,C0948008,Brain,GEO,Microarray,Mus musculus,4|8,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA05130,GSE196266,GPL24242,61,Ischemic Stroke,C0948008,Brain,GEO,Microarray,Mus musculus,4|8,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA05131,GSE196266,GPL24242,0,Ischemic Stroke,C0948008,Brain,GEO,Microarray,Mus musculus,4|8,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA05132,GSE196266,GPL24242,1,Ischemic Stroke,C0948008,Brain,GEO,Microarray,Mus musculus,4|8,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA05133,GSE196266,GPL24242,0,Ischemic Stroke,C0948008,Brain,GEO,Microarray,Mus musculus,4|8,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA05134,GSE196266,GPL24242,1,Ischemic Stroke,C0948008,Brain,GEO,Microarray,Mus musculus,4|8,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA05135,GSE196266,GPL24242,0,Ischemic Stroke,C0948008,Brain,GEO,Microarray,Mus musculus,4|8,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA05136,GSE196266,GPL24242,14,Ischemic Stroke,C0948008,Brain,GEO,Microarray,Mus musculus,4|8,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA05137,GSE196292,GPL20301,1000,Melanoma,C0025202,Skin,GEO,RNA-Seq,Homo sapiens,8|4,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA05138,GSE196292,GPL20301,1000,Basal Cell Carcinoma,C0007117,Skin,GEO,RNA-Seq,Homo sapiens,8|13,DO:A skin carcinoma affecting basal cells. DSA05139,GSE196292,GPL20301,18,Melanoma,C0025202,Skin,GEO,RNA-Seq,Homo sapiens,5|6,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA05140,GSE196292,GPL20301,18,Basal Cell Carcinoma,C0007117,Skin,GEO,RNA-Seq,Homo sapiens,5|4,DO:A skin carcinoma affecting basal cells. DSA05141,GSE19637,GPL7363,1,Hernia,C0019270,,GEO,Microarray,Homo sapiens,8|9,DO:A prolapse of female genital organ that is characterized by the descent of a peritoneal sac containing small bowel into the rectovagnial space causing a bulge in the posterior vaginal wall. DSA05142,GSE19637,GPL7363,0,Hernia,C0019270,Skin,GEO,Microarray,Homo sapiens,8|9,DO:A prolapse of female genital organ that is characterized by the descent of a peritoneal sac containing small bowel into the rectovagnial space causing a bulge in the posterior vaginal wall. DSA05143,GSE196399,GPL24676,1000,Community Acquired Pneumonia,C0694549,,GEO,RNA-Seq,Homo sapiens,21|56,NCI:Pneumonia that is not acquired in a hospital or long-term care facility setting. DSA05144,E-MTAB-3950,A-MEXP-2246,819,Lung Squamous Cell Carcinoma,C0149782,Lung,ArrayExpress,Microarray,Homo sapiens,21|8,DO:A non-small cell lung carcinoma that has_material_basis_in the squamous cell. DSA05145,GSE196652,GPL16791,500,Neurofibromatosis Type 1,C0027831,,GEO,RNA-Seq,Homo sapiens,46|41,"DO:A neurofibromatosis classically characterized by cafe-au-lait spots, Lisch nodules in the eye, and fibromatous tumors of the skin or in some cases by a high load of spinal tumors that has_material_basis_in heterozygous mutation in NF1 on 17q11.2." DSA05146,GSE196652,GPL16791,532,Neurofibromatosis Type 1,C0027831,,GEO,RNA-Seq,Homo sapiens,46|46,"DO:A neurofibromatosis classically characterized by cafe-au-lait spots, Lisch nodules in the eye, and fibromatous tumors of the skin or in some cases by a high load of spinal tumors that has_material_basis_in heterozygous mutation in NF1 on 17q11.2." DSA05147,GSE196652,GPL16791,795,Neurofibromatosis Type 1,C0027831,,GEO,RNA-Seq,Homo sapiens,46|46,"DO:A neurofibromatosis classically characterized by cafe-au-lait spots, Lisch nodules in the eye, and fibromatous tumors of the skin or in some cases by a high load of spinal tumors that has_material_basis_in heterozygous mutation in NF1 on 17q11.2." DSA05148,GSE196656,GPL20301,705,Myocardial Fibrosis,C0151654,Blood,GEO,RNA-Seq,Homo sapiens,3|3,DO:An extrinsic cardiomyopathy that is characterized as an inflammation of the heart muscle. DSA05149,GSE196656,GPL20301,5,Heart Failure,C0018801,Blood,GEO,RNA-Seq,Homo sapiens,3|3,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA05150,E-MTAB-3950,A-MEXP-2246,702,Lung Squamous Cell Carcinoma,C0149782,Lung,ArrayExpress,Microarray,Homo sapiens,21|12,DO:A non-small cell lung carcinoma that has_material_basis_in the squamous cell. DSA05151,GSE196694,GPL16791,1000,Astrocytoma,C0004114,Brain,GEO,RNA-Seq,Homo sapiens,5|15,"DO:A malignant glioma that is has_material_basis_in astrocyte cells, a type of star-shaped glial cell, located in the brain and spinal cord." DSA05152,GSE196822,GPL20301,1000,COVID-19,D8888888,Whole blood,GEO,RNA-Seq,Homo sapiens,9|8,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05153,GSE196822,GPL20301,1000,COVID-19,D8888888,Whole blood,GEO,RNA-Seq,Homo sapiens,9|9,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05154,GSE196822,GPL20301,1000,COVID-19,D8888888,Whole blood,GEO,RNA-Seq,Homo sapiens,9|10,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05155,GSE196822,GPL20301,1000,COVID-19,D8888888,Whole blood,GEO,RNA-Seq,Homo sapiens,9|7,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05156,GSE196822,GPL20301,1000,COVID-19,D8888888,Whole blood,GEO,RNA-Seq,Homo sapiens,9|6,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05157,GSE197342,GPL23479,1000,Colitis,C0009319,Colorectum,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA05158,GSE197342,GPL23479,423,Colitis,C0009319,Colorectum,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA05159,GSE197344,GPL24676,1000,Microcephalic Osteodysplastic Primordial Dwarfism; Type 1,C1859452,,GEO,RNA-Seq,Homo sapiens,2|4,"DO:A microcephalic osteodysplastic primordial dwarfism that is characterized by dwarfism, microcephaly, mental retardation, brain malformations, and ocular, auditory sensory deficits and that has_material_basis_in homozygous or compound heterozygous mutation in the RNU4ATAC gene, encoding a small nuclear RNA component of the U12-dependent spliceosome, on chromosome 2q14.2." DSA05160,GSE19743,GPL570,1000,Burn,C0036280,Blood,GEO,Microarray,Homo sapiens,63|57, DSA05161,GSE19743,GPL570,1000,Burn,C0036280,Blood,GEO,Microarray,Homo sapiens,63|57, DSA05162,GSE197443,GPL20795,1000,Papillary Thyroid Carcinoma,C0238463,Thyroid,GEO,RNA-Seq,Homo sapiens,4|4,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA05163,GSE197463,GPL23479,377,Chronic Obstructive Pulmonary Disease,C0024117,Gastrocnemius,GEO,RNA-Seq,Mus musculus,5|5,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA05164,GSE197505,GPL21290,74,Alzheimer's Disease,C0002395,Frontal cortex,GEO,RNA-Seq,Homo sapiens,10|8,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05165,GSE197514,GPL16791,34,Esophageal Squamous Cell Carcinoma,C0279626,,GEO,RNA-Seq,Homo sapiens,25|71,DO:An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus. DSA05166,E-MTAB-4257,A-MEXP-2104,1000,Active Tuberculosis,C0151332,Blood,ArrayExpress,Microarray,Homo sapiens,24|32,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05167,GSE197626,GPL21103,1000,Acute Kidney Injury,C2609414,Kidney,GEO,scRNA-Seq,Mus musculus,2|6,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA05168,GSE197637,GPL20301,688,Grover's Disease,C0263325,,GEO,RNA-Seq,Homo sapiens,4|5, DSA05169,GSE197727,GPL20301,1000,Peripheral Artery Disease,C4025272,,GEO,RNA-Seq,Homo sapiens,1|2,"HPO:Narrowing of peripheral arteries with reduction of blood flow to the limbs. This feature may be quantified as an ankle-brachial index of less than 0.9, and may be manifested clinically as claudication." DSA05170,GSE197727,GPL20301,1000,Peripheral Artery Disease,C4025272,,GEO,RNA-Seq,Homo sapiens,1|2,"HPO:Narrowing of peripheral arteries with reduction of blood flow to the limbs. This feature may be quantified as an ankle-brachial index of less than 0.9, and may be manifested clinically as claudication." DSA05171,GSE197727,GPL20301,1000,Peripheral Artery Disease,C4025272,,GEO,RNA-Seq,Homo sapiens,1|2,"HPO:Narrowing of peripheral arteries with reduction of blood flow to the limbs. This feature may be quantified as an ankle-brachial index of less than 0.9, and may be manifested clinically as claudication." DSA05172,GSE197906,GPL16791,8,Colorectal Carcinoma,C0009402,Colon,GEO,RNA-Seq,Homo sapiens,4|6,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA05173,GSE197906,GPL16791,3,Colorectal Carcinoma,C0009402,Colon,GEO,RNA-Seq,Homo sapiens,4|6,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA05174,GSE197907,GPL24676,1000,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA05175,GSE197907,GPL24676,1000,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA05176,GSE197907,GPL24676,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,RNA-Seq,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA05177,E-MTAB-4257,A-MEXP-2104,1000,Active Tuberculosis,C0151332,Blood,ArrayExpress,Microarray,Homo sapiens,24|31,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05178,GSE198121,GPL20301,27,Opioid Use Disorder; Severe,C4237239,Blood,GEO,RNA-Seq,Homo sapiens,7|7, DSA05179,E-MTAB-4257,A-MEXP-2104,1000,Fever,C0015967,Blood,ArrayExpress,Microarray,Homo sapiens,24|32,HPO:Body temperature elevated above the normal range. DSA05180,E-MTAB-4257,A-MEXP-2104,1000,Pneumonia,C0032285,Blood,ArrayExpress,Microarray,Homo sapiens,24|10,"DO:A lung disease that involves lung parenchyma or alveolar inflammation and abnormal alveolar filling with fluid (consolidation and exudation). It results from a variety of causes including infection with bacteria, viruses, fungi or parasites, and chemical or physical injury to the lungs. It is accompanied by fever, chills, cough, and difficulty in breathing." DSA05181,GSE198321,GPL16791,3,Myotonic Dystrophy Type 1,C0027126,Brain,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA05182,GSE198321,GPL16791,22,Myotonic Dystrophy Type 1,C0027126,Brain,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA05183,GSE198321,GPL16791,49,Myotonic Dystrophy Type 1,C0027126,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA05184,E-MTAB-4257,A-MEXP-2104,1000,Active Tuberculosis,C0151332,Blood,ArrayExpress,Microarray,Homo sapiens,24|10,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05185,GSE198391,GPL18573,285,Obesity,C0028754,,GEO,RNA-Seq,Homo sapiens,8|8,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA05186,GSE198391,GPL18573,224,Obesity,C0028754,,GEO,RNA-Seq,Homo sapiens,8|8,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA05187,GSE198533,GPL24676,1000,Behcet's Disease,C0004943,,GEO,RNA-Seq,Homo sapiens,10|9,"DO:A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis." DSA05188,E-MTAB-4257,A-MEXP-2104,1000,Active Tuberculosis,C0151332,Blood,ArrayExpress,Microarray,Homo sapiens,24|10,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05189,E-MTAB-1791,A-MEXP-2271,1000,Cystic Tumor,C1333190,Pancreas,ArrayExpress,Microarray,Homo sapiens,22|24,"MONDO:A benign or malignant neoplasm that contains a single or multiple cystic spaces. Examples include cystadenoma, mucinous cystadenocarcinoma, and serous cystadenocarcinoma." DSA05190,GSE198676,GPL20301,0,Fanconi-Bickel Syndrome,C3495427,Whole blood,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A lysosomal storage disease characterized by the abnormal accumulation of cystine in the lysosomes. It follows an autosomal recessive inheritance pattern and that has_material_basis_in mutations in the CTNS gene, located on chromosome 17." DSA05191,GSE198781,GPL17021,12,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA05192,E-MTAB-1791,A-MEXP-2271,1,Endocrine Tumor,C0014132,Pancreas,ArrayExpress,Microarray,Homo sapiens,2|18,DO:An organ system cancer located_in endocrine system that is characterized by uncontrolled cellular proliferation of the hormone producing glands of the endocrine system. DSA05193,GSE198896,GPL21697|GPL24676,1000,Osteosarcoma,C0029463,,GEO,scRNA-Seq,Homo sapiens,1|4,DO:A bone sarcoma that is located_in bone that has_material_basis_in cells of mesenchymal origin. DSA05194,GSE198896,GPL21697|GPL24676,1000,Ewing Sarcoma,C0553580,,GEO,scRNA-Seq,Homo sapiens,1|1,"DO:A connective tissue cancer that has_material_basis_in neural crest cells derives_from undeveloped, undifferentiated neuroectoderm." DSA05195,GSE198950,GPL20301,33,Chronic Rhinosinusitis,C0149516,Ethmoidal tissue,GEO,RNA-Seq,Homo sapiens,4|16,EFO:An acute or chronic inflammatory process affecting the mucous membranes of any sinus cavity. DSA05196,GSE199105,GPL24247,1000,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,RNA-Seq,Mus musculus,6|6,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA05197,GSE199152,GPL16791,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,RNA-Seq,Homo sapiens,4|20,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA05198,GSE199152,GPL16791,277,Arthritis-Associated Interstitial Diseases,,Lung,GEO,RNA-Seq,Homo sapiens,4|3, DSA05199,GSE199225,GPL24676,79,Polycystic Ovary Syndrome,C0032460,Myotube,GEO,RNA-Seq,Homo sapiens,10|10,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA05200,GSE199225,GPL24676,127,Polycystic Ovary Syndrome,C0032460,Myotube,GEO,RNA-Seq,Homo sapiens,15|15,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA05201,GSE199258,GPL16791,34,Multiple System Atrophy,C0393571,Cerebellum,GEO,RNA-Seq,Homo sapiens,19|19,"MONDO:Multiple system atrophy (MSA) is a neurodegenerative disorder characterized by autonomic failure (cardiovascular and/or urinary), parkinsonism, cerebellar impairment and corticospinal signs with a median survival of 6-9 years." DSA05202,E-MTAB-1791,A-MEXP-2271,1000,Neoplasm,C0027651,Pancreas,ArrayExpress,Microarray,Homo sapiens,30|195,"DO:A disease of cellular proliferation that is malignant and primary, characterized by uncontrolled cellular proliferation, local cell invasion and metastasis." DSA05203,E-MTAB-1791,A-MEXP-2271,1000,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,ArrayExpress,Microarray,Homo sapiens,15|68,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA05204,E-MTAB-1791,A-MEXP-2271,7,Pancreatitis,C0030305,Pancreas,ArrayExpress,Microarray,Homo sapiens,11|31,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA05205,GSE199324,GPL24676,1000,Breast Cancer,C0678222,Breast,GEO,RNA-Seq,Homo sapiens,2|1,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05206,GSE199324,GPL24676,1000,Colorectal Carcinoma,C0009402,Colon,GEO,RNA-Seq,Homo sapiens,2|1,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA05207,GSE199329,GPL20301,1000,Pulmonary Alveolar Microlithiasis,C0155912,Lung,GEO,scRNA-Seq,Homo sapiens,1|2,DO:A lung disease that is characterized the accumulation of tiny fragments of calcium phosphate gradually accumulate in the alveoli of the lungs. DSA05208,GSE199403,GPL24676,516,Lung Disease,C0024115,Lung,GEO,RNA-Seq,Homo sapiens,10|14,"DO:A lower respiratory tract disease in which the function of the lungs is adversely affected by narrowing or blockage of the airways resulting in poor air flow, a loss of elasticity in the lungs that produces a decrease in the total volume of air that the lungs are able to hold, and clotting, scarring, or inflammation of the blood vessels that affect the ability of the lungs to take up oxygen and to release carbon dioxide." DSA05209,GSE199403,GPL24676,32,Lung Disease,C0024115,Lung,GEO,RNA-Seq,Homo sapiens,15|14,"DO:A lower respiratory tract disease in which the function of the lungs is adversely affected by narrowing or blockage of the airways resulting in poor air flow, a loss of elasticity in the lungs that produces a decrease in the total volume of air that the lungs are able to hold, and clotting, scarring, or inflammation of the blood vessels that affect the ability of the lungs to take up oxygen and to release carbon dioxide." DSA05210,GSE199403,GPL24676,48,Lung Disease,C0024115,Lung,GEO,RNA-Seq,Homo sapiens,10|15,"DO:A lower respiratory tract disease in which the function of the lungs is adversely affected by narrowing or blockage of the airways resulting in poor air flow, a loss of elasticity in the lungs that produces a decrease in the total volume of air that the lungs are able to hold, and clotting, scarring, or inflammation of the blood vessels that affect the ability of the lungs to take up oxygen and to release carbon dioxide." DSA05211,GSE199403,GPL24676,53,Lung Disease,C0024115,Lung,GEO,RNA-Seq,Homo sapiens,15|15,"DO:A lower respiratory tract disease in which the function of the lungs is adversely affected by narrowing or blockage of the airways resulting in poor air flow, a loss of elasticity in the lungs that produces a decrease in the total volume of air that the lungs are able to hold, and clotting, scarring, or inflammation of the blood vessels that affect the ability of the lungs to take up oxygen and to release carbon dioxide." DSA05212,GSE199403,GPL24676,99,Lung Disease,C0024115,Lung,GEO,RNA-Seq,Homo sapiens,10|15,"DO:A lower respiratory tract disease in which the function of the lungs is adversely affected by narrowing or blockage of the airways resulting in poor air flow, a loss of elasticity in the lungs that produces a decrease in the total volume of air that the lungs are able to hold, and clotting, scarring, or inflammation of the blood vessels that affect the ability of the lungs to take up oxygen and to release carbon dioxide." DSA05213,GSE199403,GPL24676,82,Lung Disease,C0024115,Lung,GEO,RNA-Seq,Homo sapiens,15|15,"DO:A lower respiratory tract disease in which the function of the lungs is adversely affected by narrowing or blockage of the airways resulting in poor air flow, a loss of elasticity in the lungs that produces a decrease in the total volume of air that the lungs are able to hold, and clotting, scarring, or inflammation of the blood vessels that affect the ability of the lungs to take up oxygen and to release carbon dioxide." DSA05214,GSE199403,GPL24676,1000,Lung Disease,C0024115,Lung,GEO,RNA-Seq,Homo sapiens,10|14,"DO:A lower respiratory tract disease in which the function of the lungs is adversely affected by narrowing or blockage of the airways resulting in poor air flow, a loss of elasticity in the lungs that produces a decrease in the total volume of air that the lungs are able to hold, and clotting, scarring, or inflammation of the blood vessels that affect the ability of the lungs to take up oxygen and to release carbon dioxide." DSA05215,GSE199403,GPL24676,62,Lung Disease,C0024115,Lung,GEO,RNA-Seq,Homo sapiens,15|14,"DO:A lower respiratory tract disease in which the function of the lungs is adversely affected by narrowing or blockage of the airways resulting in poor air flow, a loss of elasticity in the lungs that produces a decrease in the total volume of air that the lungs are able to hold, and clotting, scarring, or inflammation of the blood vessels that affect the ability of the lungs to take up oxygen and to release carbon dioxide." DSA05216,GSE199403,GPL24676,991,Lung Disease,C0024115,Lung,GEO,RNA-Seq,Homo sapiens,10|15,"DO:A lower respiratory tract disease in which the function of the lungs is adversely affected by narrowing or blockage of the airways resulting in poor air flow, a loss of elasticity in the lungs that produces a decrease in the total volume of air that the lungs are able to hold, and clotting, scarring, or inflammation of the blood vessels that affect the ability of the lungs to take up oxygen and to release carbon dioxide." DSA05217,GSE199403,GPL24676,19,Lung Disease,C0024115,Lung,GEO,RNA-Seq,Homo sapiens,15|15,"DO:A lower respiratory tract disease in which the function of the lungs is adversely affected by narrowing or blockage of the airways resulting in poor air flow, a loss of elasticity in the lungs that produces a decrease in the total volume of air that the lungs are able to hold, and clotting, scarring, or inflammation of the blood vessels that affect the ability of the lungs to take up oxygen and to release carbon dioxide." DSA05218,GSE199460,GPL24247,1000,Experimental Autoimmune Encephalomyelitis,C0014072,Brain,GEO,scRNA-Seq,Mus musculus,3|2,"EFO:An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)" DSA05219,GSE199460,GPL24247,1000,Experimental Autoimmune Encephalomyelitis,C0014072,Brain,GEO,scRNA-Seq,Mus musculus,3|3,"EFO:An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)" DSA05220,GSE199468,GPL18573,413,Increased Intracranial Pressure,C0151740,,GEO,RNA-Seq,Homo sapiens,4|3,"DO:A brain disease that is characterized by high pressure inside the skull, the brain tissue and cerebrospinal fluid, has_symptom headache, has_symptom vomiting, has_symptom altered mental status, has_symptom papilledema." DSA05221,GSE199468,GPL18573,1000,Increased Intracranial Pressure,C0151740,,GEO,RNA-Seq,Homo sapiens,4|3,"DO:A brain disease that is characterized by high pressure inside the skull, the brain tissue and cerebrospinal fluid, has_symptom headache, has_symptom vomiting, has_symptom altered mental status, has_symptom papilledema." DSA05222,GSE199468,GPL18573,4,Increased Intracranial Pressure,C0151740,Whole blood,GEO,RNA-Seq,Homo sapiens,3|4,"DO:A brain disease that is characterized by high pressure inside the skull, the brain tissue and cerebrospinal fluid, has_symptom headache, has_symptom vomiting, has_symptom altered mental status, has_symptom papilledema." DSA05223,GSE199536,GPL16686,0,Major Depression,C0041696,Habenula,GEO,Microarray,Homo sapiens,10|10,DO:A major depressive disorder characterized by near-complete absence of pleasure. DSA05224,GSE199711,GPL24676,1000,Chronic Kidney Disease,C1561643,Kidney cortex,GEO,snRNA-Seq,Homo sapiens,2|3,DO:A kidney failure that is characterized by the gradual loss of kidney function. DSA05225,GSE199715,GPL16791,860,Multiple System Atrophy,C0393571,Cerebellum,GEO,RNA-Seq,Homo sapiens,47|47,"MONDO:Multiple system atrophy (MSA) is a neurodegenerative disorder characterized by autonomic failure (cardiovascular and/or urinary), parkinsonism, cerebellar impairment and corticospinal signs with a median survival of 6-9 years." DSA05226,GSE199724,GPL16791,0,Multiple System Atrophy,C0393571,Cerebellum,GEO,RNA-Seq,Homo sapiens,6|5,"MONDO:Multiple system atrophy (MSA) is a neurodegenerative disorder characterized by autonomic failure (cardiovascular and/or urinary), parkinsonism, cerebellar impairment and corticospinal signs with a median survival of 6-9 years." DSA05227,GSE199837,GPL24247,2,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,9|9,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05228,GSE199837,GPL24247,12,Huntington's Disease,C0020179,Brain,GEO,RNA-Seq,Mus musculus,9|9,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05229,GSE199837,GPL24247,10,Huntington's Disease,C0020179,Brain,GEO,RNA-Seq,Mus musculus,9|8,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05230,GSE199837,GPL24247,11,Huntington's Disease,C0020179,Brain,GEO,RNA-Seq,Mus musculus,9|7,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05231,GSE199837,GPL24247,1000,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,9|10,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05232,GSE199867,GPL28457,3,Alzheimer's Disease,C0002395,Retina,GEO,RNA-Seq,Mus musculus,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05233,GSE199868,GPL20301,214,Primary Sjogren Syndrome,C0151449,Peripheral blood,GEO,RNA-Seq,Homo sapiens,13|11,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA05234,GSE199868,GPL20301,1000,Primary Sjogren Syndrome,C0151449,Peripheral blood,GEO,RNA-Seq,Homo sapiens,13|14,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA05235,GSE199994,GPL24676,1000,Melanoma,C0025202,,GEO,scRNA-Seq,Homo sapiens,2|4,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA05236,GSE199994,GPL24676,1000,Melanoma,C0025202,,GEO,scRNA-Seq,Homo sapiens,2|4,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA05237,GSE200020,GPL18573|GPL20301,12,Primary Sjogren Syndrome,C0151449,Peripheral blood,GEO,RNA-Seq,Homo sapiens,8|9,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA05238,GSE200020,GPL18573|GPL20301,470,Primary Sjogren Syndrome,C0151449,Peripheral blood,GEO,RNA-Seq,Homo sapiens,8|14,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA05239,GSE200069,GPL20301,1000,Congenital Pseudoarthrosis of The Limbs,C0332881,,GEO,RNA-Seq,Homo sapiens,5|5, DSA05240,GSE200306,GPL21847,229,Lupus Nephritis,C0024143,Glomerulus,GEO,Microarray,Homo sapiens,19|34,DO:A glomerulonephritis that is characterized by inflammation of the kidneys resulting from systemic lupus erythematosus. DSA05241,GSE200306,GPL21847,263,Lupus Nephritis,C0024143,Tubulointerstitium,GEO,Microarray,Homo sapiens,19|45,DO:A glomerulonephritis that is characterized by inflammation of the kidneys resulting from systemic lupus erythematosus. DSA05242,GSE200306,GPL21847,193,Lupus Nephritis,C0024143,Glomerulus,GEO,Microarray,Homo sapiens,19|36,DO:A glomerulonephritis that is characterized by inflammation of the kidneys resulting from systemic lupus erythematosus. DSA05243,GSE200306,GPL21847,267,Lupus Nephritis,C0024143,Tubulointerstitium,GEO,Microarray,Homo sapiens,19|47,DO:A glomerulonephritis that is characterized by inflammation of the kidneys resulting from systemic lupus erythematosus. DSA05244,GSE200322,GPL24247,1000,Diabetes,C0011847,Kidney cortex,GEO,RNA-Seq,Mus musculus,6|6,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA05245,E-MTAB-1791,A-MEXP-2271,1000,Cystic Tumor,C1333190,Pancreas,ArrayExpress,Microarray,Homo sapiens,41|24,"MONDO:A benign or malignant neoplasm that contains a single or multiple cystic spaces. Examples include cystadenoma, mucinous cystadenocarcinoma, and serous cystadenocarcinoma." DSA05246,E-MTAB-1791,A-MEXP-2271,1000,Endocrine Tumor,C0014132,Pancreas,ArrayExpress,Microarray,Homo sapiens,41|18,DO:An organ system cancer located_in endocrine system that is characterized by uncontrolled cellular proliferation of the hormone producing glands of the endocrine system. DSA05247,GSE200639,GPL24247,1000,Tuberculosis,C0041296,Lung,GEO,scRNA-Seq,Mus musculus,2|3,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05248,GSE200639,GPL24247,1000,Tuberculosis,C0041296,Lung,GEO,scRNA-Seq,Mus musculus,2|3,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05249,GSE200680,GPL24676,1000,Klinefelter Syndrome,C0022735,Testis,GEO,RNA-Seq,Homo sapiens,5|5,DO:A chromosomal duplication syndrome that is characterized by infertility and that has_material_basis_in an extra X chromosome in cells in men. DSA05250,GSE200680,GPL24676,1000,Atrophy of testis,C0156312,Testis,GEO,RNA-Seq,Homo sapiens,5|5,HPO:Wasting (atrophy) of the testicle (the male gonad) manifested by a decrease in size and potentially by a loss of fertility. DSA05251,GSE200836,GPL20795,1000,Generalized Pustular Psoriasis,C0343055,Blood,GEO,RNA-Seq,Homo sapiens,3|4,"DO:A psoriasis characterized by sudden, repeated episodes of high-grade fever, generalized rash, and disseminated pustules, with hyperleukocytosis and elevated serum levels of C-reactive protein that has_material_basis_in homozygous or compound heterozygous mutation in the IL36RN gene on chromosome 2q14." DSA05252,GSE200836,GPL20795,1000,Generalized Pustular Psoriasis,C0343055,Blood,GEO,RNA-Seq,Homo sapiens,3|4,"DO:A psoriasis characterized by sudden, repeated episodes of high-grade fever, generalized rash, and disseminated pustules, with hyperleukocytosis and elevated serum levels of C-reactive protein that has_material_basis_in homozygous or compound heterozygous mutation in the IL36RN gene on chromosome 2q14." DSA05253,E-MTAB-1791,A-MEXP-2271,1000,Neoplasm,C0027651,Pancreas,ArrayExpress,Microarray,Homo sapiens,41|195,"DO:A disease of cellular proliferation that is malignant and primary, characterized by uncontrolled cellular proliferation, local cell invasion and metastasis." DSA05254,E-MTAB-1791,A-MEXP-2271,1000,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,ArrayExpress,Microarray,Homo sapiens,41|68,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA05255,GSE200856,GPL24247,385,Peripheral Nerve Damage,C0031117,Brain,GEO,RNA-Seq,Mus musculus,5|4,DO:A nervous system disease that affects the peripheral nervous system. DSA05256,GSE200856,GPL24247,61,Peripheral Nerve Damage,C0031117,Brain,GEO,RNA-Seq,Mus musculus,5|5,DO:A nervous system disease that affects the peripheral nervous system. DSA05257,GSE200856,GPL24247,1000,Peripheral Nerve Damage,C0031117,Brain,GEO,RNA-Seq,Mus musculus,5|5,DO:A nervous system disease that affects the peripheral nervous system. DSA05258,GSE200856,GPL24247,1000,Peripheral Nerve Damage,C0031117,Brain,GEO,RNA-Seq,Mus musculus,5|4,DO:A nervous system disease that affects the peripheral nervous system. DSA05259,GSE200923,GPL19057,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,6|6,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA05260,GSE200923,GPL19057,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,6|6,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA05261,GSE200923,GPL19057,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,6|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA05262,GSE200923,GPL19057,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,6|4,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA05263,GSE200923,GPL19057,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,6|4,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA05264,GSE200923,GPL19057,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,6|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA05265,GSE200977,GPL20795,1000,Generalized Pustular Psoriasis,C0343055,Blood,GEO,RNA-Seq,Homo sapiens,8|8,"DO:A psoriasis characterized by sudden, repeated episodes of high-grade fever, generalized rash, and disseminated pustules, with hyperleukocytosis and elevated serum levels of C-reactive protein that has_material_basis_in homozygous or compound heterozygous mutation in the IL36RN gene on chromosome 2q14." DSA05266,GSE200977,GPL20795,150,Psoriasis Vulgaris,C0263361,Blood,GEO,RNA-Seq,Homo sapiens,8|8, DSA05267,GSE200987,GPL21103,224,Multiple Myeloma,C0026764,Osteocytes,GEO,RNA-Seq,Mus musculus,5|5,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA05268,E-MTAB-1791,A-MEXP-2271,1000,Pancreatitis,C0030305,Pancreas,ArrayExpress,Microarray,Homo sapiens,41|31,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA05269,E-MTAB-3970,A-AFFY-45,1000,Prostatic Hyperplasia,C2937421,Prostate,ArrayExpress,Microarray,Mus musculus,3|3,DO:A male reproductive organ benign neoplasm that derives_from glandular epithelial cells and that is located_in the prostate. DSA05270,GSE201091,GPL24676,1000,Aortic Aneurysm,C0003486,Aortic arch,GEO,scRNA-Seq,Homo sapiens,1|1,DO:An aortic disease that is characterized by an enlargement (dilation) of the aorta to greater than 1.5 times normal size. DSA05271,GSE201153,GPL16791,1000,Eosinophilic Esophagitis,C0341106,Esophagus,GEO,scRNA-Seq,Homo sapiens,2|5,DO:An esophagitis characterized by inflammation involving eosinophils located_in esophagus. DSA05272,GSE201153,GPL16791,1000,Eosinophilic Esophagitis,C0341106,Esophagus,GEO,scRNA-Seq,Homo sapiens,2|3,DO:An esophagitis characterized by inflammation involving eosinophils located_in esophagus. DSA05273,E-MTAB-3970,A-AFFY-45,1000,Prostate Tumor,C0600139,Prostate,ArrayExpress,Microarray,Mus musculus,3|13,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05274,GSE201348,GPL24676,1000,Colorectal Carcinoma,C0009402,Colon,GEO,snRNA-Seq,Homo sapiens,8|5,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA05275,E-MTAB-3338,A-MEXP-2039,1000,Liver Cirrhosis,C0023890,Liver,ArrayExpress,Microarray,Homo sapiens,8|30,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA05276,GSE201465,GPL16791,1000,Chronic Obstructive Pulmonary Disease,C0024117,Nasopharynx,GEO,RNA-Seq,Homo sapiens,6|6,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA05277,GSE201530,GPL24676,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,8|47,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05278,GSE20159,GPL6947,0,Parkinson's Disease,C0030567,Substantia nigra,GEO,Microarray,Homo sapiens,17|16,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05279,GSE20163,GPL96,2,Parkinson's Disease,C0030567,Substantia nigra,GEO,Microarray,Homo sapiens,9|8,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05280,GSE201699,GPL20301,1000,Achalasia,C1321756,Esophagus,GEO,RNA-Seq,Homo sapiens,16|28,DO:An esophageal disease that is characterized by an inability of the esophagus to move food toward the stomach resulting from the lower esophogeal sphincter not fully relaxing during swallowing. DSA05281,GSE201753,GPL16791,199,Giant Cell Arteritis,C0039483,Whole blood,GEO,RNA-Seq,Homo sapiens,29|20,"DO:A central nervous system vasculitis that is characterized by inflammation of the lining of arteries, often arteries in the head." DSA05282,GSE201753,GPL16791,0,Giant Cell Arteritis,C0039483,Whole blood,GEO,RNA-Seq,Homo sapiens,29|29,"DO:A central nervous system vasculitis that is characterized by inflammation of the lining of arteries, often arteries in the head." DSA05283,GSE201753,GPL16791,1000,Giant Cell Arteritis,C0039483,Whole blood,GEO,RNA-Seq,Homo sapiens,29|33,"DO:A central nervous system vasculitis that is characterized by inflammation of the lining of arteries, often arteries in the head." DSA05284,GSE201891,GPL24676,1000,Myotonic Dystrophy 1,C3250443,Cortical Organoid,GEO,scRNA-Seq,Homo sapiens,1|2,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA05285,GSE201891,GPL24676,1000,Rett Syndrome,C0035372,Cortical Organoid,GEO,scRNA-Seq,Homo sapiens,1|2,"DO:A pervasive developmental disease that is characterized by normal early growth and development followed by a slowing of development, loss of purposeful use of the hands, distinctive hand movements, slowed brain and head growth, problems with walking, seizures, and intellectual disability." DSA05286,GSE201950,GPL24247,1000,Obesity,C0028754,Liver,GEO,RNA-Seq,Mus musculus,3|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA05287,GSE201951,GPL24248,1000,Obesity,C0028754,Liver,GEO,RNA-Seq,Mus musculus,3|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA05288,E-MTAB-3260,A-MEXP-2102,1000,Active Tuberculosis,C0151332,Whole blood,ArrayExpress,Microarray,Homo sapiens,11|9,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05289,E-MTAB-3260,A-MEXP-2102,243,Active Tuberculosis,C0151332,Whole blood,ArrayExpress,Microarray,Homo sapiens,11|3,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05290,E-MTAB-3260,A-MEXP-2102,1000,Active Tuberculosis,C0151332,Whole blood,ArrayExpress,Microarray,Homo sapiens,11|13,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05291,E-MTAB-3260,A-MEXP-2102,1000,Active Tuberculosis,C0151332,Whole blood,ArrayExpress,Microarray,Homo sapiens,11|16,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05292,GSE202151,GPL20795,1000,Diabetic Vascular Disorder,C0011875,,GEO,RNA-Seq,Homo sapiens,6|6,DO:A peripheral vascular disease that is characterized by narrowing of the arteries as a complication arising from chronic diabetes. DSA05293,GSE202282,GPL23126,156,Environmental Enteric Dysfunction,,Duodenum,GEO,Microarray,Homo sapiens,3|3, DSA05294,GSE202282,GPL23126,879,Environmental Enteric Dysfunction,,Duodenum,GEO,Microarray,Homo sapiens,3|3, DSA05295,GSE202295,GPL16791,1,Type 2 Diabetes,C0011860,Vastus lateralis,GEO,RNA-Seq,Homo sapiens,17|21,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA05296,GSE202295,GPL16791,1,Type 2 Diabetes,C0011860,Vastus lateralis,GEO,RNA-Seq,Homo sapiens,16|20,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA05297,GSE202295,GPL16791,725,Type 2 Diabetes,C0011860,Vastus lateralis,GEO,RNA-Seq,Homo sapiens,17|20,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA05298,GSE202424,GPL24676,1000,Aldh18A1 Mutations,,,GEO,RNA-Seq,Homo sapiens,3|3, DSA05299,GSE202485,GPL24676,1000,POR-deficient,C0268465,,GEO,RNA-Seq,Homo sapiens,11|12,"MONDO:Dihydropteridine reductase (DHPR) deficiency is a severe form of hyperphenylalaninemia (HPA) due to impaired regeneration of tetrahydrobiopterin (BH4), leading to decreased levels of neurotransmitters (dopamine, serotonin) and folate in cerebrospinal fluid, and causing neurological symptoms such as psychomotor delay, hypotonia, seizures, abnormal movements, hypersalivation, and swallowing difficulties." DSA05300,GSE202485,GPL24676,1000,POR-Mutations,,,GEO,RNA-Seq,Homo sapiens,11|12, DSA05301,GSE202649,GPL16791,1000,Scleroderma,C0011644,Skin,GEO,RNA-Seq,Homo sapiens,1|1,"DO:A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies." DSA05302,GSE202657,GPL23159,1000,Meniere Disease,C0025281,Peripheral blood,GEO,Microarray,Homo sapiens,9|9,"DO:A vestibular disease characterized by vertigo, low-pitched tinnitus and hearing loss." DSA05303,GSE20266,GPL570,128,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,10|10,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05304,GSE202676,GPL24247,1000,Primary Biliary Cholangitis,C0008312,,GEO,RNA-Seq,Mus musculus,3|3,DO:A liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts. DSA05305,GSE202676,GPL24247,1000,Primary Biliary Cholangitis,C0008312,,GEO,RNA-Seq,Mus musculus,3|3,DO:A liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts. DSA05306,GSE202676,GPL24247,1000,Primary Biliary Cholangitis,C0008312,,GEO,RNA-Seq,Mus musculus,3|3,DO:A liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts. DSA05307,GSE202676,GPL24247,1000,Primary Biliary Cholangitis,C0008312,,GEO,RNA-Seq,Mus musculus,3|3,DO:A liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts. DSA05308,GSE202745,GPL24676,331,Limb-Girdle Muscular Dystrophy,C0026850,Rectus femoris,GEO,RNA-Seq,Homo sapiens,15|14,"DO:A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted." DSA05309,GSE202745,GPL24676,1000,Limb-Girdle Muscular Dystrophy,C0026850,Semimembranosus muscle,GEO,RNA-Seq,Homo sapiens,14|13,"DO:A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted." DSA05310,GSE202745,GPL24676,1000,Limb-Girdle Muscular Dystrophy,C0026850,Vastus lateralis,GEO,RNA-Seq,Homo sapiens,14|14,"DO:A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted." DSA05311,E-MTAB-3658,A-MEXP-2320,218,Facioscapulohumeral Dystrophy,C0238288,,ArrayExpress,Microarray,Homo sapiens,4|4,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA05312,GSE202937,GPL17303,1000,Acute Coronary Syndrome,C0948089,Whole blood,GEO,RNA-Seq,Homo sapiens,1|10,EFO:Signs and symptoms related to acute ischemia of the myocardium secondary to coronary artery disease. The clinical presentation covers a spectrum of heart diseases from unstable angina to myocardial infarction. DSA05313,GSE202947,GPL20301,1000,Pneumonia,C0032285,,GEO,RNA-Seq,Homo sapiens,12|8,"DO:A lung disease that involves lung parenchyma or alveolar inflammation and abnormal alveolar filling with fluid (consolidation and exudation). It results from a variety of causes including infection with bacteria, viruses, fungi or parasites, and chemical or physical injury to the lungs. It is accompanied by fever, chills, cough, and difficulty in breathing." DSA05314,GSE202947,GPL20301,1000,Bronchitis,C0006277,,GEO,RNA-Seq,Homo sapiens,12|9,"DO:A bronchial disease that is an inflammation of the bronchial tubes. It is caused by bacteria and viruses. The disease has_symptom cough with mucus, has_symptom shortness of breath, has_symptom low fever and has_symptom chest tightness." DSA05315,GSE203160,GPL18573,1000,Ischemic Heart Disease,C0151744,Heart,GEO,RNA-Seq,Homo sapiens,7|8,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA05316,GSE203196,GPL17692,0,Allergy,C1527304,Peripheral blood,GEO,Microarray,Homo sapiens,3|3,"DO:An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods." DSA05317,GSE203196,GPL17692,0,Allergy,C1527304,Peripheral blood,GEO,Microarray,Homo sapiens,3|4,"DO:An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods." DSA05318,GSE203196,GPL17692,1,Allergy,C1527304,Peripheral blood,GEO,Microarray,Homo sapiens,3|3,"DO:An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods." DSA05319,GSE203196,GPL17692,0,Allergy,C1527304,Peripheral blood,GEO,Microarray,Homo sapiens,3|4,"DO:An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods." DSA05320,GSE203196,GPL17692,0,Allergy,C1527304,Peripheral blood,GEO,Microarray,Homo sapiens,3|3,"DO:An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods." DSA05321,GSE203196,GPL17692,0,Allergy,C1527304,Peripheral blood,GEO,Microarray,Homo sapiens,3|4,"DO:An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods." DSA05322,GSE203206,GPL20301,1000,Alzheimer's Disease,C0002395,Occipital lobe,GEO,RNA-Seq,Homo sapiens,8|19,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05323,GSE203206,GPL20301,0,Alzheimer's Disease,C0002395,Occipital lobe,GEO,RNA-Seq,Homo sapiens,8|20,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05324,GSE203257,GPL16791,311,Down Syndrome,C0013080,,GEO,RNA-Seq,Homo sapiens,2|2,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA05325,GSE203340,GPL24247,1000,Endotoxic Shock,C0036981,Lung,GEO,RNA-Seq,Mus musculus,3|3,MSH:Sepsis associated with HYPOTENSION or hypoperfusion despite adequate fluid resuscitation. Perfusion abnormalities may include but are not limited to LACTIC ACIDOSIS; OLIGURIA; or acute alteration in mental status. DSA05326,GSE203346,GPL24676,1,Gestational Diabetes Mellitus,C0085207,Placenta,GEO,RNA-Seq,Homo sapiens,22|21,DO:A diabetes mellitus that manifests during pregnancy. DSA05327,GSE203346,GPL24676,0,Gestational Diabetes Mellitus,C0085207,Umbilical cord blood,GEO,RNA-Seq,Homo sapiens,21|20,DO:A diabetes mellitus that manifests during pregnancy. DSA05328,GSE20407,GPL6885,0,Colon Tumor,C0009375,Colon,GEO,Microarray,Mus musculus,2|2,DO:A colorectal cancer that is located_in the colon. DSA05329,GSE20407,GPL6885,909,Colon Tumor,C0009375,Colon,GEO,Microarray,Mus musculus,2|2,DO:A colorectal cancer that is located_in the colon. DSA05330,GSE203408,GPL18573,67,Alzheimer's Disease,C0002395,Blood,GEO,RNA-Seq,Homo sapiens,3|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05331,GSE203408,GPL18573,86,Alzheimer's Disease,C0002395,Blood,GEO,RNA-Seq,Homo sapiens,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05332,GSE203408,GPL18573,27,Alzheimer's Disease,C0002395,Blood,GEO,RNA-Seq,Homo sapiens,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05333,E-MTAB-2976,A-AGIL-28,1000,Type 1 Diabetes,C0011854,,ArrayExpress,Microarray,Homo sapiens,4|4,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA05334,E-MTAB-910,A-MEXP-2246,0,Erythema Nodosum,C0014743,Skin,ArrayExpress,Microarray,Homo sapiens,2|2,"HPO:An erythematous eruption commonly associated with drug reactions or infection and characterized by inflammatory nodules that are usually tender, multiple, and bilateral." DSA05335,E-MTAB-910,A-MEXP-2246,1000,Panniculitis,C0030326,Skin,ArrayExpress,Microarray,Homo sapiens,2|4,DO:A skin disease that is characterized by inflammation of subcutaneous adipose tissue. DSA05336,E-MTAB-1516,A-MEXP-1173,0,Head And Neck Squamous Cell Carcinoma,C1168401,Plasma,ArrayExpress,Microarray,Homo sapiens,20|16,"DO:A head and neck carcinoma that has_material_basis_in squamous cells that line the moist, mucosal surfaces inside the head and neck." DSA05337,GSE203499,GPL16791,1000,Age Related Macular Degeneration,C0242383,Choroid,GEO,scRNA-Seq,Homo sapiens,8|8,DO:A degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision. DSA05338,GSE203499,GPL16791,1000,Age Related Macular Degeneration,C0242383,Choroid,GEO,scRNA-Seq,Homo sapiens,8|1,DO:A degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision. DSA05339,E-MTAB-1132,A-MEXP-2223,1000,Non-Small Cell Lung Cancer,C0007131,Lung,ArrayExpress,Microarray,Homo sapiens,123|13,DO:A respiratory system cancer that is located_in the lung. DSA05340,E-MTAB-1132,A-MEXP-2223,1000,Non-Small Cell Lung Cancer,C0007131,Lung,ArrayExpress,Microarray,Homo sapiens,123|57,DO:A respiratory system cancer that is located_in the lung. DSA05341,E-MTAB-1132,A-MEXP-2223,1000,Non-Small Cell Lung Cancer,C0007131,Lung,ArrayExpress,Microarray,Homo sapiens,123|50,DO:A respiratory system cancer that is located_in the lung. DSA05342,GSE20430,GPL201,1000,Trachoma,C0040592,Tarsal conjunctiva,GEO,Microarray,Homo sapiens,12|17,"DO:A commensal bacterial infectious disease that results_in infection located_in eye, has_material_basis_in Chlamydia trachomatis (A, B, Ba and C serovars), which is transmitted_by contact with eye discharge from the infected person and transmitted_by congenital method. The infection causes eyelid to turn inward which makes eyelashes to scratch the cornea." DSA05343,GSE20436,GPL570,1000,Trachoma,C0040592,Tarsal conjunctiva,GEO,Microarray,Homo sapiens,20|40,"DO:A commensal bacterial infectious disease that results_in infection located_in eye, has_material_basis_in Chlamydia trachomatis (A, B, Ba and C serovars), which is transmitted_by contact with eye discharge from the infected person and transmitted_by congenital method. The infection causes eyelid to turn inward which makes eyelashes to scratch the cornea." DSA05344,GSE20437,GPL96,1000,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,18|24,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05345,GSE204688,GPL20795,1000,Transfusion Dependent Thalassemia,,Blood,GEO,scRNA-Seq,Homo sapiens,2|1, DSA05346,GSE204775,GPL21185,2,Sotos Syndrome,C4551477,Skin,GEO,Microarray,Homo sapiens,5|14,DO:A syndrome that occurs rarely and is characterized by excessive physical growth during the first 2 to 3 years of life. DSA05347,GSE204791,GPL21185,332,Keratopathy,C0235270,Corneal epithelium,GEO,Microarray,Homo sapiens,8|8,MONDO:Any disorder of the cornea. DSA05348,GSE204791,GPL21185,1000,Keratopathy,C0235270,Corneal stroma,GEO,Microarray,Homo sapiens,7|8,MONDO:Any disorder of the cornea. DSA05349,GSE204804,GPL16791,1000,Emery-Dreifuss Muscular Dystrophy,C0410189,Myotube,GEO,RNA-Seq,Homo sapiens,6|30,DO:A muscular dystrophy that chiefly affects muscles used for movement (skeletal) and heart (cardiac) muscle. DSA05350,GSE204835,GPL30173,772,Hypertensive Pregnancies,,Placenta,GEO,RNA-Seq,Homo sapiens,12|13, DSA05351,GSE204835,GPL30173,10,Hypertensive Pregnancies,,Placenta,GEO,RNA-Seq,Homo sapiens,12|16, DSA05352,GSE204835,GPL30173,169,Hypertensive Pregnancies,,Placenta,GEO,RNA-Seq,Homo sapiens,12|7, DSA05353,E-MTAB-2073,A-MEXP-132,319,Primary Sjogren Syndrome,C0151449,,ArrayExpress,Microarray,Homo sapiens,10|10,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA05354,GSE204882,GPL16791,24,Systemic Capillary Leak Syndrome,C0343084,,GEO,RNA-Seq,Homo sapiens,6|5,"DO:A capillary disease characterized by hypotension, hypoalbuminemia, and hemoconcentration resulting from fluid and protein leakage out of capillaries into surrounding tissues." DSA05355,GSE204935,GPL26963,0,Ventricular Septal Defects,C0018818,,GEO,Microarray,Homo sapiens,5|5,"DO:A heart septal defect characterized by an opening in the interventricular septum, causing a shunt between ventricles." DSA05356,GSE205095,GPL18573,1000,Juvenile Idiopathic Arthritis,C3890205,Peripheral blood,GEO,scRNA-Seq,Homo sapiens,4|12,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA05357,E-MTAB-611,A-AGIL-11,0,Recurrent Epithelial Ovarian Cancer,C0677886,,ArrayExpress,Microarray,Homo sapiens,36|23,DO:A female reproductive organ cancer that is located_in the ovary. DSA05358,GSE205129,GPL23126,0,Attention Deficit Hyperactivity Disorder,C1263846,,GEO,Microarray,Homo sapiens,3|3,"DO:A specific developmental disorder that is characterized by co-existence of attentional problems and hyperactivity, with each behavior occurring infrequently alone and symptoms starting before seven years of age." DSA05359,E-MEXP-3077,A-AFFY-44,0,Brittle Cornea Syndrome,C3280011,Skin,ArrayExpress,Microarray,Homo sapiens,2|2,"DO:An Ehlers-Danlos syndrome that is characterized by blue sclerae, corneal rupture after minor trauma, keratoconus or keratoglobus, hyperelasticity of the skin, and hypermobility of the joints and has_material_basis_in homozygous mutation in the ZNF469 gene on chromosome 16q24." DSA05360,GSE205494,GPL16791,2,Endometriosis,C0014175,,GEO,RNA-Seq,Homo sapiens,6|6,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA05361,GSE205525,GPL24676,1000,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,RNA-Seq,Homo sapiens,27|9,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA05362,GSE205645,GPL23126,0,Non-Alcoholic Fatty Liver Disease,C0400966,Kidney,GEO,Microarray,Homo sapiens,7|6,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA05363,GSE205645,GPL23126,0,Non-Alcoholic Steatohepatitis,C3241937,Kidney,GEO,Microarray,Homo sapiens,7|5,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA05364,GSE205645,GPL23126,0,Adrenoleukodystrophy,C0162309,Kidney,GEO,Microarray,Homo sapiens,7|6,"DO:A leukodystrophy that disrupts the breakdown of very-long-chain fatty acids resulting in progressive brain damage, failure of the adrenal glands and eventually death." DSA05365,GSE205645,GPL23126,0,Hepatitis C,C0019196,Kidney,GEO,Microarray,Homo sapiens,7|6,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA05366,GSE205645,GPL23126,0,Hepatitis C;Adrenoleukodystrophy,,Kidney,GEO,Microarray,Homo sapiens,7|6, DSA05367,GSE20571,GPL6244,0,Gastrointestinal Cancer,C0017185,Adipose tissue,GEO,Microarray,Homo sapiens,14|13,DO:An organ system cancer located_in gastrointestinal tract that is manifested in organs of the gastrointestinal system. DSA05368,GSE205787,GPL11154,1000,Colorectal Carcinoma,C0009402,,GEO,RNA-Seq,Homo sapiens,3|50,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA05369,GSE205812,GPL24676,360,Ankylosing Spondylitis,C0038013,,GEO,RNA-Seq,Homo sapiens,3|2,"DO:A bone inflammation disease that results_in inflammation in the joints of the spine and pelvis. The disease has_symptom pain, has_symptom stiffness in the spine, has_symptom stiffness in the neck, has_symptom stiffness in the hips, has_symptom stiffness in the jaw and has_symptom stiffness in the rib cage." DSA05370,GSE205867,GPL24676,1000,Behcet's Disease,C0004943,Peripheral blood,GEO,RNA-Seq,Homo sapiens,10|10,"DO:A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis." DSA05371,GSE205962,GPL16043,1000,Rheumatoid Arthritis,C0003873,Whole blood,GEO,Microarray,Homo sapiens,4|3,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA05372,GSE205962,GPL16043,1000,Rheumatoid Arthritis,C0003873,Whole blood,GEO,Microarray,Homo sapiens,4|4,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA05373,GSE205962,GPL16043,1000,Rheumatoid Arthritis,C0003873,Whole blood,GEO,Microarray,Homo sapiens,4|3,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA05374,GSE205962,GPL16043,1000,Rheumatoid Arthritis,C0003873,Whole blood,GEO,Microarray,Homo sapiens,4|3,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA05375,GSE205962,GPL16043,1000,Rheumatoid Arthritis,C0003873,Whole blood,GEO,Microarray,Homo sapiens,4|3,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA05376,GSE205974,GPL24247,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,3|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA05377,GSE206202,GPL24247,3,Alzheimer's Disease,C0002395,Cerebrum,GEO,RNA-Seq,Homo sapiens,2|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05378,GSE206250,GPL20301,71,Tracheal Stenosis,C0040583,Blood,GEO,RNA-Seq,Homo sapiens,5|6,MONDO:Narrowing of the lumen of the trachea. DSA05379,GSE206263,GPL24676,410,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|13,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05380,GSE206263,GPL24676,49,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|18,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05381,GSE206263,GPL24676,70,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|14,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05382,GSE206285,GPL13158,1000,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,18|550,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA05383,GSE206311,GPL13607,85,Psoriasis,C0033860,,GEO,Microarray,Homo sapiens,8|9,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA05384,GSE206311,GPL13607,0,Psoriasis,C0033860,,GEO,Microarray,Homo sapiens,8|7,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA05385,GSE206448,GPL24676,142,Giant Cell Tumor,C0017525,Bone,GEO,RNA-Seq,Homo sapiens,4|5,"MONDO:A benign, intermediate, or malignant tumor that arises from the bone or soft tissue. It is characterized by the presence of multinucleated osteoclast-like giant cells." DSA05386,E-MEXP-3291,A-AFFY-183,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,ArrayExpress,Microarray,Homo sapiens,19|9,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA05387,E-MEXP-3291,A-AFFY-183,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,ArrayExpress,Microarray,Homo sapiens,19|7,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA05388,GSE206629,GPL21103,0,Alzheimer's Disease,C0002395,Brain,GEO,RNA-Seq,Mus musculus,5|5,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05389,GSE206635,GPL18573,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,1|4,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05390,E-MEXP-3291,A-AFFY-183,0,Steatosis,C2711227,Liver,ArrayExpress,Microarray,Homo sapiens,19|10,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA05391,E-MEXP-3097,A-AFFY-44,0,Hutchinson-Gilford Progeria Syndrome,C0033300,,ArrayExpress,Microarray,Homo sapiens,3|2,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA05392,GSE206680,GPL16791,6,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,10|11,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA05393,GSE206680,GPL16791,0,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,10|11,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA05394,GSE206680,GPL16791,3,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,10|10,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA05395,GSE206680,GPL16791,6,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,10|11,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA05396,GSE206680,GPL16791,9,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,10|10,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA05397,GSE206680,GPL16791,1,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,10|10,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA05398,GSE206788,GPL32385,384,COVID-19,D8888888,Lung,GEO,Microarray,Homo sapiens,7|12,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05399,GSE206788,GPL32385,17,Idiopathic Myelofibrosis,C0001815,Lung,GEO,Microarray,Homo sapiens,7|4,DO:A myeloid neoplasm that is located in the bone marrow which results in bone marrow being replaced by fibrous (scar) tissue. DSA05400,GSE11906,GPL570,116,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,44|20,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA05401,GSE18090,GPL570,4,Dengue Disease,C0011311,,GEO,Microarray,Homo sapiens,8|8,"DO:A viral infectious disease that results in infection, has_material_basis_in Dengue virus" DSA05402,GSE18090,GPL570,351,Dengue Hemorrhagic Fever,C0019100,,GEO,Microarray,Homo sapiens,8|10,"DO:A dengue disease that occurs when a person experiences a second infection with a heterologous Dengue virus serotype, which is transmitted_by Aedes mosquito bite. The infection has_symptom hemorrhagic lesions of the skin, has_symptom thrombocytopenia, has_symptom reduction in the fluid part of the blood, and has_symptom high fever." DSA05403,GSE206848,GPL570,1000,Osteoarthritis,C0157946,Knee synovium,GEO,Microarray,Homo sapiens,7|7,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA05404,GSE206848,GPL570,2,Rheumatoid Arthritis,C0003873,Knee synovium,GEO,Microarray,Homo sapiens,7|2,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA05405,GSE207006,GPL20301,1000,Prostate Cancer,C0600139,Peripheral blood,GEO,scRNA-Seq,Homo sapiens,1|1,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05406,GSE207243,GPL18573,1000,Duodenitis,C0013298,Duodenum,GEO,RNA-Seq,Homo sapiens,5|4,MONDO:Acute or chronic inflammation of the duodenum. Causes include bacterial and viral infections and gastroesophageal reflux disease. Symptoms include vomiting and abdominal pain. DSA05407,GSE207243,GPL18573,137,Duodenitis,C0013298,Duodenum,GEO,RNA-Seq,Homo sapiens,5|12,MONDO:Acute or chronic inflammation of the duodenum. Causes include bacterial and viral infections and gastroesophageal reflux disease. Symptoms include vomiting and abdominal pain. DSA05408,GSE207313,GPL24247,0,Obesity,C0028754,Placenta,GEO,RNA-Seq,Homo sapiens,8|8,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA05409,GSE207398,GPL24676,125,Familial Adenomatous Polyposis,C2674616,Colon,GEO,RNA-Seq,Homo sapiens,7|6,DO:A familial adenomatous polyposis that has_material_basis_in heterozygous mutation in the APC gene on chromosome 5q22. DSA05410,GSE207713,GPL11154,1000,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,4|6,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05411,GSE207751,GPL18573,20,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,14|19,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA05412,GSE207751,GPL18573,9,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,14|23,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA05413,GSE19439,GPL6947,410,Tuberculosis,C0041296,Whole Blood,GEO,Microarray,Homo sapiens,12|13,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05414,GSE207872,GPL24676,28,Arthritis,C0003864,Blood,GEO,RNA-Seq,Homo sapiens,3|3,DO:A bone disease that is located_in the joint. DSA05415,GSE207872,GPL24676,65,Arthritis,C0003864,Blood,GEO,RNA-Seq,Homo sapiens,3|3,DO:A bone disease that is located_in the joint. DSA05416,GSE207881,GPL21290,1000,Osteoarthritis,C0157946,Cartilage,GEO,RNA-Seq,Homo sapiens,6|63,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA05417,GSE14297,GPL6370,1000,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,7|18,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA05418,GSE208173,GPL32025,7,Anal Melanoma,C0349538,Vagina,GEO,Microarray,Homo sapiens,3|3,"EFO:A melanoma arising from the anus. Clinical presentation includes rectal bleeding, tenesmus, pain, and change in bowel habit. The prognosis is usually poor." DSA05419,GSE208303,GPL16791,1000,Crohn's Disease,C0010346,Mucosa,GEO,RNA-Seq,Homo sapiens,9|13,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA05420,GSE208303,GPL16791,1000,Crohn's Disease,C0010346,Mucosa,GEO,RNA-Seq,Homo sapiens,9|13,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA05421,GSE208338,GPL5188,0,Bipolar Disorder,C0005586,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,62|15,DO:A mood disorder that involves alternating periods of mania and depression. DSA05422,GSE208338,GPL5188,0,Major Depressive Disorder,C1269683,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,62|24,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA05423,GSE208338,GPL5188,0,Schizophrenia,C0036341,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,62|68,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA05424,GSE208347,GPL18460,1,Parkinson's Disease,C0030567,Blood,GEO,RNA-Seq,Homo sapiens,8|8,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05425,GSE208384,GPL17586,0,Pterygium,C0033999,Conjunctiva,GEO,Microarray,Homo sapiens,2|2,DO:A corneal disease that is characterized by a triangular tissue growth located_in cornea of the eye that is the result of collagen degeneration and fibrovascular proliferation. DSA05426,GSE18911,GPL9193,0,Myelodysplastic Syndromes,C3463824,,GEO,Microarray,Homo sapiens,4|4,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA05427,GSE208781,GPL18573,1000,Parkinson's Disease,C0030567,Midbrain,GEO,RNA-Seq,Homo sapiens,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05428,GSE208783,GPL18573,1000,Parkinson's Disease,C0030567,Midbrain,GEO,RNA-Seq,Homo sapiens,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05429,GSE20881,GPL1708,741,Crohn's Disease,C0010346,Ascending colon,GEO,Microarray,Homo sapiens,17|20,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA05430,GSE20881,GPL1708,11,Crohn's Disease,C0010346,Descending colon,GEO,Microarray,Homo sapiens,23|29,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA05431,GSE20881,GPL1708,68,Crohn's Disease,C0010346,Sigmoid colon,GEO,Microarray,Homo sapiens,27|33,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA05432,GSE20881,GPL1708,21,Crohn's Disease,C0010346,Terminal ileum,GEO,Microarray,Homo sapiens,6|17,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA05433,GSE209591,GPL20795,169,Rheumatic Heart Disease,C0035439,Whole blood,GEO,RNA-Seq,Homo sapiens,2|5,"MONDO:An autoinflammatory condition following an infection with Group A Beta Hemolytic Streptococcus (GABHS), in which the heart is attacked by antibodies formed in reaction to a recent GABHS infection. Chief anatomic changes of the valve include leaflet thickening, commissural fusion, and shortening and thickening of the tendinous cords, all of which can result in valvular dysfunction." DSA05434,GSE209591,GPL20795,126,Acute Rheumatic Fever,C0035436,Whole blood,GEO,RNA-Seq,Homo sapiens,2|5,"DO:A connective tissue disease that develops from an antecedent Group A Streptococcal pharyngeal infection and has_symptom carditis, has_symptom polyarthritis, has_symptom chorea, has_symptom erythema marginatum, has_symptom subcutaneous nodules, has_symptom arthralgia, has_symptom prolonged PR interval, and/or has_symptom fever." DSA05435,GSE209673,GPL17021,1000,Major Depressive Disorder,C1269683,Blood,GEO,RNA-Seq,Mus musculus,6|7,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA05436,GSE18911,GPL9193,0,Myelodysplastic Syndromes,C3463824,,GEO,Microarray,Homo sapiens,4|3,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA05437,GSE13507,GPL6102,1000,Bladder Cancer,C0699885,Bladder mucosae,GEO,Microarray,Homo sapiens,10|165,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05438,GSE13507,GPL6102,1000,Recurrent Non-Muscle Invasive Tumor,,Bladder mucosae,GEO,Microarray,Homo sapiens,10|23, DSA05439,GSE16011,GPL8542,1000,Glioma,C0017638,Brain,GEO,Microarray,Homo sapiens,8|276,DO:A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine. DSA05440,GSE20966,GPL1352,54,Type 2 Diabetes,C0011860,Pancreas,GEO,Microarray,Homo sapiens,10|10,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA05441,GSE14895,GPL571,0,Clinically Isolated Syndrome,C2921627,,GEO,Microarray,Homo sapiens,4|13, DSA05442,GSE210022,GPL21273,1000,Dengue Disease,C0011311,Liver,GEO,RNA-Seq,Mus musculus,5|5,"DO:A viral infectious disease that results in infection, has_material_basis_in Dengue virus" DSA05443,GSE210248,GPL20301,1000,Pulmonary Arterial Hypertension,C2973725,Pulmonary artery,GEO,scRNA-Seq,Homo sapiens,3|3,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA05444,GSE210337,GPL21697,1000,Fibrolamellar Hepatocellular Carcinoma,C0334287,Peripheral blood,GEO,scRNA-Seq,Homo sapiens,2|1,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA05445,GSE210611,GPL21810,0,Diabetes,C0011847,Myocardium,GEO,Microarray,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA05446,GSE210611,GPL21810,2,Diabetes,C0011847,Myocardium,GEO,Microarray,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA05447,GSE14975,GPL570,4,Atrial Fibrillation,C0004238,Left atrial appendage,GEO,Microarray,Homo sapiens,5|5,"DO:A heart conduction disease that is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular and has symptoms palpitations, weakness, fatigue, lightheadedness, dizziness, confusion, shortness of breath and chest pain." DSA05448,GSE210707,GPL18573,0,Heart Failure,C0018801,Adipose tissue,GEO,RNA-Seq,Homo sapiens,5|5,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA05449,GSE210797,GPL24676,1000,Sepsis,C0243026,,GEO,RNA-Seq,Homo sapiens,6|6,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA05450,GSE210820,GPL24247,1000,Stress Induced Cardiomyopathy,C1719472,Heart,GEO,RNA-Seq,Mus musculus,3|4, DSA05451,GSE210820,GPL24247,108,Stress Induced Cardiomyopathy,C1719472,Heart,GEO,RNA-Seq,Mus musculus,3|4, DSA05452,GSE210829,GPL6244,1000,Prurigo Nodularis,C0263353,Skin,GEO,Microarray,Homo sapiens,5|5,"MONDO:Prurigonodularis (PN) is a skin disease in which hard crusty lumps are formed on the skin that itches intensely. Repetitive rubbing, scratching, and touching results in more lesions in the skin. The itching is so intense that people scratch themselves to the point of bleeding or pain. The lumps formed in the skin are hard, and have about a half inch across, with a dry and rough top that is often scratched open. They tend to be located in the areas most easily reached and are worse on the outer sides: arms, shoulders and legs. The trunk, face and even palms can also be affected. The exact cause is unknown but some factors triggering PN include liver and kidneys problems, nervous and mental conditions and other skin diseases. Prurigo nodulares, in some cases, can be seen in other diseases such as lymphoma, chronic autoimmune cholestatic hepatitis, HIV infection, severe anemia,or a chronic kidney disease-related itching known as uremic pruritus. Treatment is very difficult, and may include corticoids, antihistaminic and other medication such as thalidomide and similar (Lenalidomide). In some cases, cryotherapy, photochemotherapy and habit reversal therapy for the itch-scratch cycle has improved the symptoms. PN can last for many years, and the itching is so intense that may affect all the everyday activities." DSA05453,GSE210829,GPL6244,0,Prurigo Nodularis,C0263353,Skin,GEO,Microarray,Homo sapiens,5|5,"MONDO:Prurigonodularis (PN) is a skin disease in which hard crusty lumps are formed on the skin that itches intensely. Repetitive rubbing, scratching, and touching results in more lesions in the skin. The itching is so intense that people scratch themselves to the point of bleeding or pain. The lumps formed in the skin are hard, and have about a half inch across, with a dry and rough top that is often scratched open. They tend to be located in the areas most easily reached and are worse on the outer sides: arms, shoulders and legs. The trunk, face and even palms can also be affected. The exact cause is unknown but some factors triggering PN include liver and kidneys problems, nervous and mental conditions and other skin diseases. Prurigo nodulares, in some cases, can be seen in other diseases such as lymphoma, chronic autoimmune cholestatic hepatitis, HIV infection, severe anemia,or a chronic kidney disease-related itching known as uremic pruritus. Treatment is very difficult, and may include corticoids, antihistaminic and other medication such as thalidomide and similar (Lenalidomide). In some cases, cryotherapy, photochemotherapy and habit reversal therapy for the itch-scratch cycle has improved the symptoms. PN can last for many years, and the itching is so intense that may affect all the everyday activities." DSA05454,GSE211154,GPL24676,6,Autism Spectrum Disorder,C1510586,Brain,GEO,RNA-Seq,Homo sapiens,19|20,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA05455,GSE211210,GPL24676,476,Unspecified Septicemia,C0036690,Blood,GEO,RNA-Seq,Homo sapiens,5|5,HPO:Systemic inflammatory response to infection. DSA05456,GSE211358,GPL20301,145,Multiple Sclerosis,C0026769,Blood,GEO,RNA-Seq,Homo sapiens,4|5,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA05457,GSE211359,GPL29988,7,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Mus musculus,3|3,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA05458,GSE211378,GPL32571,243,COVID-19,D8888888,Whole blood,GEO,Microarray,Homo sapiens,40|264,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05459,GSE211739,GPL24676,473,Multiple Sclerosis,C0026769,,GEO,RNA-Seq,Homo sapiens,6|4,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA05460,GSE211979,GPL16791,1000,COVID-19,D8888888,Blood,GEO,RNA-Seq,Homo sapiens,5|8,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05461,GSE211979,GPL16791,1000,COVID-19,D8888888,Blood,GEO,RNA-Seq,Homo sapiens,5|8,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05462,GSE212041,GPL18573,104,COVID-19,D8888888,Blood,GEO,RNA-Seq,Homo sapiens,3|13,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05463,GSE212096,GPL16791,0,Phelan-Mcdermid Syndrome,C1853490,Peripheral blood,GEO,RNA-Seq,Homo sapiens,24|33,"DO:A chromosomal deletion syndrome that has_material_basis_in a deletion, translocation, ring chromosome formation or other structural change of the terminal end of chromosome 22 in the 22q13 region or a disease-causing mutation of the SHANK3 gene and that is characterized by neonatal hypotonia, absent to severely delayed speech, global developmental delay, and minor dysmorphic facial features. Most cases of 22q13.3 deletion syndrome are not inherited with 20% of cases (autosomal dominant) inherited from a parent. The deletion occurs most often as a random event during the formation of reproductive cells (eggs or sperm) or in early fetal development." DSA05464,GSE212096,GPL16791,405,Phelan-Mcdermid Syndrome,C1853490,Peripheral blood,GEO,RNA-Seq,Homo sapiens,24|35,"DO:A chromosomal deletion syndrome that has_material_basis_in a deletion, translocation, ring chromosome formation or other structural change of the terminal end of chromosome 22 in the 22q13 region or a disease-causing mutation of the SHANK3 gene and that is characterized by neonatal hypotonia, absent to severely delayed speech, global developmental delay, and minor dysmorphic facial features. Most cases of 22q13.3 deletion syndrome are not inherited with 20% of cases (autosomal dominant) inherited from a parent. The deletion occurs most often as a random event during the formation of reproductive cells (eggs or sperm) or in early fetal development." DSA05465,GSE212100,GPL20301,34,Systemic Sclerosis [Scleroderma],C2364016,,GEO,RNA-Seq,Homo sapiens,4|10, DSA05466,GSE212100,GPL20301,13,Systemic Sclerosis [Scleroderma],C2364016,,GEO,RNA-Seq,Homo sapiens,4|10, DSA05467,GSE212109,GPL24676,1000,Systemic Sclerosis-Associated Interstitial Lung Disease,,Lung,GEO,scRNA-Seq,Homo sapiens,6|5, DSA05468,GSE18838,GPL5175,0,Parkinson's Disease,C0030567,Peripheral blood,GEO,Microarray,Homo sapiens,11|17,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05469,GSE16759,GPL570,0,Alzheimer's Disease,C0002395,Parietal lobe,GEO,Microarray,Homo sapiens,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05470,GSE212126,GPL24247,533,Psoriasis,C0033860,Skin,GEO,RNA-Seq,Homo sapiens,3|3,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA05471,GSE212255,GPL30173,1000,"Dysautonomia, Familial",C0013364,,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A hereditary sensory neuropathy that is characterized by gastrointestinal dysfunction, gastroesophageal reflux, vomiting crises, recurrent pneumonia, seizures, gait abnormalities with loss of ambulation, kyphoscoliosis, postural hypotension, hypertension crises, absence of fungiform papillae on the tongue, decreased deep tendon reflexes, defective lacrimation, and impaired pain and temperature perception and has_material_basis_in homozygous or compound heterozygous mutation in the IKBKAP gene (ELP1) on chromosome 9q31." DSA05472,GSE212384,GPL24676,259,Lung Disease,C0024115,Blood,GEO,RNA-Seq,Homo sapiens,17|17,"DO:A lower respiratory tract disease in which the function of the lungs is adversely affected by narrowing or blockage of the airways resulting in poor air flow, a loss of elasticity in the lungs that produces a decrease in the total volume of air that the lungs are able to hold, and clotting, scarring, or inflammation of the blood vessels that affect the ability of the lungs to take up oxygen and to release carbon dioxide." DSA05473,GSE212384,GPL24676,169,Lung Disease,C0024115,Blood,GEO,RNA-Seq,Homo sapiens,17|16,"DO:A lower respiratory tract disease in which the function of the lungs is adversely affected by narrowing or blockage of the airways resulting in poor air flow, a loss of elasticity in the lungs that produces a decrease in the total volume of air that the lungs are able to hold, and clotting, scarring, or inflammation of the blood vessels that affect the ability of the lungs to take up oxygen and to release carbon dioxide." DSA05474,GSE212512,GPL16791,1000,Globoid Cell Leukodystrophy,C0023521,Skin,GEO,RNA-Seq,Homo sapiens,3|3,"MONDO:A lysosomal disorder that affects the white matter of the central and peripheral nervous systems. It includes infantile, late-infantile/juvenile and adult forms." DSA05475,GSE212512,GPL16791,1000,Globoid Cell Leukodystrophy,C0023521,Skin,GEO,RNA-Seq,Homo sapiens,3|3,"MONDO:A lysosomal disorder that affects the white matter of the central and peripheral nervous systems. It includes infantile, late-infantile/juvenile and adult forms." DSA05476,GSE212610,GPL16791,1000,Focal Segmental Glomerulosclerosis,C0017668,Whole blood,GEO,RNA-Seq,Homo sapiens,3|3,"EFO:A renal disorder characterized by sclerotic lesions in the glomeruli. Causes include drugs, viruses, and malignancies (lymphomas), or it may be idiopathic. It presents with asymptomatic proteinuria or nephritic syndrome and it may lead to renal failure." DSA05477,GSE212610,GPL16791,30,Focal Segmental Glomerulosclerosis,C0017668,Whole blood,GEO,RNA-Seq,Homo sapiens,3|3,"EFO:A renal disorder characterized by sclerotic lesions in the glomeruli. Causes include drugs, viruses, and malignancies (lymphomas), or it may be idiopathic. It presents with asymptomatic proteinuria or nephritic syndrome and it may lead to renal failure." DSA05478,GSE212613,GPL21290,713,Ankylosing Spondylitis,C0038013,Bone marrow,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A bone inflammation disease that results_in inflammation in the joints of the spine and pelvis. The disease has_symptom pain, has_symptom stiffness in the spine, has_symptom stiffness in the neck, has_symptom stiffness in the hips, has_symptom stiffness in the jaw and has_symptom stiffness in the rib cage." DSA05479,GSE212802,GPL18573,1,Panic Disorder,C0030319,Peripheral blood,GEO,RNA-Seq,Homo sapiens,10|14,"DO:An anxiety disorder that is characterized by unexpected and repeated episodes of intense fear accompanied by physical symptoms that may include chest pain, heart palpitations, shortness of breath, dizziness, or abdominal distress." DSA05480,GSE17549,GPL570,0,Choroideremia,C0008525,,GEO,Microarray,Homo sapiens,4|6,"MONDO:Choroideremia (CHM) is an X-linked chorioretinal dystrophy characterized by progressive degeneration of the choroid, retinal pigment epithelium (RPE) and retina." DSA05481,GSE17549,GPL570,0,Choroideremia,C0008525,,GEO,Microarray,Homo sapiens,1|4,"MONDO:Choroideremia (CHM) is an X-linked chorioretinal dystrophy characterized by progressive degeneration of the choroid, retinal pigment epithelium (RPE) and retina." DSA05482,GSE15197,GPL6480,1000,Pulmonary Arterial Hypertension,C2973725,Lung,GEO,Microarray,Homo sapiens,13|18,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA05483,GSE212939,GPL21273,252,Colitis,C0009319,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA05484,GSE213017,GPL24676,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,scRNA-Seq,Homo sapiens,1|2,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA05485,GSE213096,GPL24676,1000,Pancreatic Cancer,C0235974,Blood,GEO,scRNA-Seq,Homo sapiens,3|3,DO:An endocrine gland cancer located_in the pancreas. DSA05486,GSE16443,GPL2986,10,Breast Cancer,C0678222,Peripheral blood,GEO,Microarray,Homo sapiens,54|67,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05487,GSE213232,GPL24676,16,Schizophrenia,C0036341,,GEO,RNA-Seq,Homo sapiens,6|6,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA05488,GSE213364,GPL24676,1000,Rasmussen Encephalitis,C2930868,Brain,GEO,snRNA-Seq,Homo sapiens,2|2,"MONDO:A rare, progressive chronic inflammation of a single cerebral hemisphere that usually affects children. It is characterized by severe seizures, loss of motor skills and speech, hemiparesis, and dementia." DSA05489,GSE213364,GPL24676,1000,Focal Cortical Dysplasia Type I,C1846385,Brain,GEO,snRNA-Seq,Homo sapiens,2|2,HPO:A type of focal cortical dysplasia that is characterized by disrupted cortical lamination and specific cytological abnormalities. DSA05490,GSE21340,GPL80,0,Type 2 Diabetes Mellitus,C0011847,Skeletal muscle,GEO,Microarray,Homo sapiens,10|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA05491,GSE213500,GPL21103,1000,Down Syndrome,C0013080,Entorhinal cortex,GEO,RNA-Seq,Mus musculus,6|6,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA05492,GSE213500,GPL21103,527,Down Syndrome,C0013080,Hippocampus,GEO,RNA-Seq,Mus musculus,6|6,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA05493,GSE213502,GPL21103,96,Down Syndrome,C0013080,Entorhinal cortex,GEO,RNA-Seq,Mus musculus,5|6,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA05494,GSE213502,GPL21103,337,Down Syndrome,C0013080,Hippocampus,GEO,RNA-Seq,Mus musculus,5|6,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA05495,GSE213707,GPL24247,1000,Dilated Cardiomyopathy,C0007193,Left ventricle,GEO,RNA-Seq,Mus musculus,4|4,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA05496,GSE14580,GPL570,1000,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,6|24,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA05497,GSE213925,GPL24247,1000,Duchenne Muscular Dystrophy,C0013264,Gastrocnemius muscle,GEO,scRNA-Seq,Mus musculus,2|2,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA05498,GSE213925,GPL24247,1000,Duchenne Muscular Dystrophy,C0013264,Gastrocnemius muscle,GEO,scRNA-Seq,Mus musculus,2|2,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA05499,GSE11675,GPL8300,1,Chronic Myelogenous Leukemia,C0023473,Peripheral blood (PB),GEO,Microarray,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA05500,GSE214088,GPL16791,1000,Scleroderma,C0011644,Skin,GEO,scRNA-Seq,Homo sapiens,7|5,"DO:A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies." DSA05501,GSE214108,GPL18573,1000,Huntington's Disease,C0020179,,GEO,RNA-Seq,Homo sapiens,12|12,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05502,GSE214108,GPL18573,1000,Huntington's Disease,C0020179,,GEO,RNA-Seq,Homo sapiens,12|12,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05503,GSE214207,GPL18573,1000,Severe Aplastic Anemia,C1883018,Peripheral blood,GEO,scRNA-Seq,Homo sapiens,2|4,NCI:Life-threatening anemia associated with a high risk of infection or bleeding. DSA05504,GSE214207,GPL18573,1000,Severe Aplastic Anemia,C1883018,Bone marrow,GEO,scRNA-Seq,Homo sapiens,4|2,NCI:Life-threatening anemia associated with a high risk of infection or bleeding. DSA05505,GSE19610,GPL96,985,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,6|6,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA05506,GSE214267,GPL24676,1,Cocaine Related Disorders,C0236736,Brain,GEO,RNA-Seq,Homo sapiens,20|25,DO:A substance abuse that involves the recurring use of cocaine despite negative consequences. DSA05507,GSE214267,GPL24676,0,Cocaine Related Disorders,C0236736,Brain,GEO,RNA-Seq,Homo sapiens,19|25,DO:A substance abuse that involves the recurring use of cocaine despite negative consequences. DSA05508,GSE214334,GPL24676,18,Multiple Sclerosis,C0026769,Brain white matter,GEO,RNA-Seq,Homo sapiens,7|3,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA05509,GSE214334,GPL24676,1000,Multiple Sclerosis,C0026769,Brain white matter,GEO,RNA-Seq,Homo sapiens,7|4,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA05510,GSE214334,GPL24676,1000,Multiple Sclerosis,C0026769,Brain white matter,GEO,RNA-Seq,Homo sapiens,7|4,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA05511,GSE19610,GPL96,139,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,4|4,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA05512,GSE15072,GPL96,0,Chronic Kidney Disease,C1561643,,GEO,Microarray,Homo sapiens,8|9,DO:A kidney failure that is characterized by the gradual loss of kidney function. DSA05513,GSE21440,GPL5188,26,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,Microarray,Homo sapiens,1|9,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA05514,GSE160488,GPL21810,1000,Lupus Nephritis,C0024143,Kidney,GEO,Microarray,Mus musculus,3|3,DO:A glomerulonephritis that is characterized by inflammation of the kidneys resulting from systemic lupus erythematosus. DSA05515,GSE148841,GPL15887,5,Abdominal Aortic Aneurysm,C0162871,Abdominal aorta,GEO,Microarray,Mus musculus,3|3,DO:An aortic aneurysm that is located_in the abdominal aorta. DSA05516,GSE214666,GPL30172,1000,Pancreatitis,C0030305,Pancreas,GEO,RNA-Seq,Mus musculus,4|4,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA05517,GSE214666,GPL30172,1000,Pancreatitis,C0030305,Pancreas,GEO,RNA-Seq,Mus musculus,4|4,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA05518,GSE214914,GPL24676,1000,Secondary Acute Myeloid Leukemia,C0280449,Peripheral blood,GEO,scRNA-Seq,Homo sapiens,1|1,"MONDO:An acute myeloid leukemia secondary to a myelodysplastic syndrome or therapy-related. (WHO, 2001)" DSA05519,GSE214914,GPL24676,1000,Chronic Myeloproliferative Neoplasm,C1292778,Peripheral blood,GEO,scRNA-Seq,Homo sapiens,1|1,"DO:A myeloid neoplasm that is characterized by a group of slow growing blood cancers in which large numbers of abnormal red blood cells, white blood cells, or platelets grow and spread in the bone marrow and the peripheral blood." DSA05520,GSE214914,GPL24676,1000,Chronic Myeloproliferative Neoplasm,C1292778,Peripheral blood,GEO,scRNA-Seq,Homo sapiens,1|1,"DO:A myeloid neoplasm that is characterized by a group of slow growing blood cancers in which large numbers of abnormal red blood cells, white blood cells, or platelets grow and spread in the bone marrow and the peripheral blood." DSA05521,GSE214954,GPL21103,0,"Arthritis, Collagen-Induced",C0971858,Spleen,GEO,RNA-Seq,Mus musculus,1|1,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA05522,GSE215137,GPL13112,1000,Nematode Infections,C0027583,Small intestine,GEO,RNA-Seq,Mus musculus,5|5,DO:A parasitic helminthiasis infectious disease that involves infection of the intestine of humans and birds with nematodes of the genus Ascaridia. DSA05523,GSE215137,GPL13112,1000,Nematode Infections,C0027583,Small intestine,GEO,RNA-Seq,Mus musculus,5|4,DO:A parasitic helminthiasis infectious disease that involves infection of the intestine of humans and birds with nematodes of the genus Ascaridia. DSA05524,GSE215183,GPL20301,190,Schizophrenia,C0036341,,GEO,RNA-Seq,Homo sapiens,6|6,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA05525,GSE215410,GPL21103,46,Cognitive Dysfunction,C1270972,Hippocampus,GEO,RNA-Seq,Mus musculus,2|2,"EFO:mild neurocognitive disorder (MND) is a mild form of HIV-associated neurocognitive disorder (HAND), defined as mild neuropsychological impairment in two or more domains with at least mildly decreased everyday functioning" DSA05526,GSE215865,GPL24676,1000,COVID-19,D8888888,Whole blood,GEO,RNA-Seq,Homo sapiens,148|651,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05527,GSE215876,GPL21697,1000,B-Cell Non-Hodgkin's Lymphoma,C0079731,Blood,GEO,RNA-Seq,Homo sapiens,6|6,DO:A non-Hodgkin lymphoma that has_material_basis_in B cells. DSA05528,GSE215876,GPL21697,1000,Chronic Active Ebv Infection,C4289792,Blood,GEO,RNA-Seq,Homo sapiens,6|9,"NCI:An on-going Epstein-Barr virus (EBV) infection characterized by repeated infectious mononucleosis-like symptoms, a very high titer of anti-EBV antibodies, and high levels of Epstein-Barr virus nucleic acids. Patients with CAEBV often develop progressive cellular and humoral immunodeficiency with pancytopenia and hypogammaglobulinemia." DSA05529,GSE215876,GPL21697,1000,B-Cell Non-Hodgkin Lymphoma,C0079731,Blood,GEO,RNA-Seq,Homo sapiens,6|6,DO:A non-Hodgkin lymphoma that has_material_basis_in B cells. DSA05530,GSE21592,GPL571,0,Narcolepsy,C0027404,Blood,GEO,Microarray,Homo sapiens,10|10,"DO:A sleep disorder that involves an excessive urge to sleep at inappropriate times, such as while at work." DSA05531,GSE215985,GPL570,0,Schizophrenia,C0036341,,GEO,Microarray,Homo sapiens,6|5,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA05532,GSE216020,GPL24676,1000,COVID-19,D8888888,Blood,GEO,scRNA-Seq,Homo sapiens,5|6,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05533,GSE100163,GPL6884,1000,Systemic Lupus Erythematosus,C0024141,Whole blood,GEO,Microarray,Homo sapiens,14|55,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA05534,GSE216026,GPL24676,206,Alzheimer's Disease,C0002395,Blood,GEO,RNA-Seq,Homo sapiens,12|8,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05535,GSE216026,GPL24676,1000,Frontotemporal Dementia,C0338451,Blood,GEO,RNA-Seq,Homo sapiens,12|4,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA05536,GSE216026,GPL24676,322,Major Depressive Disorder,C1269683,Blood,GEO,RNA-Seq,Homo sapiens,12|4,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA05537,GSE216026,GPL24676,297,Multiple Sclerosis,C0026769,Blood,GEO,RNA-Seq,Homo sapiens,12|4,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA05538,GSE216026,GPL24676,103,Multiple System Atrophy,C0393571,Blood,GEO,RNA-Seq,Homo sapiens,12|4,"MONDO:Multiple system atrophy (MSA) is a neurodegenerative disorder characterized by autonomic failure (cardiovascular and/or urinary), parkinsonism, cerebellar impairment and corticospinal signs with a median survival of 6-9 years." DSA05539,GSE216026,GPL24676,353,Parkinson's Disease,C0030567,Blood,GEO,RNA-Seq,Homo sapiens,12|8,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05540,GSE216026,GPL24676,1000,Alzheimer's Disease,C0002395,Grey matter,GEO,RNA-Seq,Homo sapiens,2|2,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05541,GSE216026,GPL24676,1000,Parkinson's Disease,C0030567,Grey matter,GEO,RNA-Seq,Homo sapiens,2|2,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05542,GSE216026,GPL24676,479,Alzheimer's Disease,C0002395,White matter,GEO,RNA-Seq,Homo sapiens,6|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05543,GSE216026,GPL24676,1000,Frontotemporal Dementia,C0338451,White matter,GEO,RNA-Seq,Homo sapiens,6|2,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA05544,GSE216026,GPL24676,545,Major Depressive Disorder,C1269683,White matter,GEO,RNA-Seq,Homo sapiens,6|2,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA05545,GSE216026,GPL24676,63,Multiple Sclerosis,C0026769,White matter,GEO,RNA-Seq,Homo sapiens,6|2,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA05546,GSE216026,GPL24676,116,Multiple System Atrophy,C0393571,White matter,GEO,RNA-Seq,Homo sapiens,6|2,"MONDO:Multiple system atrophy (MSA) is a neurodegenerative disorder characterized by autonomic failure (cardiovascular and/or urinary), parkinsonism, cerebellar impairment and corticospinal signs with a median survival of 6-9 years." DSA05547,GSE216026,GPL24676,83,Parkinson's Disease,C0030567,White matter,GEO,RNA-Seq,Homo sapiens,6|4,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05548,GSE216125,GPL24676,75,Rapid-Onset Obesity With Hypothalamic Dysfunction; Hypoventilation; And Autonomic Dysregulation,C4053506,,GEO,RNA-Seq,Homo sapiens,3|3,"MONDO:A very rare disorder that appears after the first year and a half of life in previously healthy children. It is characterized by rapid-onset weight gain, hypothalamic dysfunction, breathing abnormalities, and autonomic system dysregulation. The hypothalamic dysfunction manifestations include inability to maintain normal water balance, high prolactin levels, low thyroid, low cortisol, and early or late puberty. The breathing abnormalities include sleep apnea and alveolar hypoventilation, requiring ventilation support. The autonomic system dysregulation includes eye abnormalities, intestinal abnormalities, temperature dysregulation, and low heart rhythm. This disorder requires early recognition because it may lead to cardiorespiratory arrest. Up to 40% of the patients develop tumors of neural crest origin." DSA05549,GSE216125,GPL24676,121,Congenital Central Hypoventilation Syndrome,C1275808,,GEO,RNA-Seq,Homo sapiens,3|2,"DO:An autonomic nervous system disease characterized by reduced responsiveness of the respiratory center to carbon dioxide, diminished pupillary light responses, and other symptoms related to defects in the autonomic nervous system and that has_material_basis_in most commonly heterozygous mutation in the PHOX2B gene on chromosome 4p13 and less frequently mutations in the RET, GDNF, EDN3, BDNF, or ASCL1 genes." DSA05550,GSE216281,GPL24676,3,Parkinson's Disease,C0030567,Frontal cortex,GEO,RNA-Seq,Homo sapiens,23|6,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05551,GSE216281,GPL24676,4,Parkinson's Disease,C0030567,Frontal cortex,GEO,RNA-Seq,Homo sapiens,23|2,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05552,GSE216281,GPL24676,14,Parkinson's Disease,C0030567,Frontal cortex,GEO,RNA-Seq,Homo sapiens,23|4,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05553,GSE216281,GPL24676,1,Parkinson's Disease,C0030567,Frontal cortex,GEO,RNA-Seq,Homo sapiens,23|7,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05554,GSE216281,GPL24676,65,Parkinson's Disease,C0030567,Frontal cortex,GEO,RNA-Seq,Homo sapiens,23|19,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05555,GSE216281,GPL24676,17,Parkinson's Disease,C0030567,Frontal cortex,GEO,RNA-Seq,Homo sapiens,23|23,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05556,GSE216442,GPL23038,0,Obesity,C0028754,Anterior cortex,GEO,Microarray,Mus musculus,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA05557,GSE216442,GPL23038,0,Obesity,C0028754,Anterior cortex,GEO,Microarray,Mus musculus,5|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA05558,GSE216442,GPL23038,5,Obesity,C0028754,Anterior cortex,GEO,Microarray,Mus musculus,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA05559,GSE216442,GPL23038,0,Obesity,C0028754,Anterior cortex,GEO,Microarray,Mus musculus,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA05560,GSE216442,GPL23038,0,Obesity,C0028754,Cerebellum,GEO,Microarray,Mus musculus,4|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA05561,GSE216442,GPL23038,0,Obesity,C0028754,Cerebellum,GEO,Microarray,Mus musculus,4|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA05562,GSE216442,GPL23038,0,Obesity,C0028754,Cerebellum,GEO,Microarray,Mus musculus,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA05563,GSE216442,GPL23038,0,Obesity,C0028754,Cerebellum,GEO,Microarray,Mus musculus,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA05564,GSE216613,GPL24676,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA05565,GSE216638,GPL18573,1000,Cutaneous Leishmaniasis,C0023283,Skin,GEO,RNA-Seq,Homo sapiens,6|9,"DO:A leishmaniasis that involves skin infection caused by Leishmania species, resulting in one or more cutaneous lesions." DSA05566,GSE216638,GPL18573,1000,Cutaneous Leishmaniasis,C0023283,Skin,GEO,RNA-Seq,Homo sapiens,6|7,"DO:A leishmaniasis that involves skin infection caused by Leishmania species, resulting in one or more cutaneous lesions." DSA05567,GSE216644,GPL24247,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Mus musculus,4|4,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05568,GSE100153,GPL6884,0,Chronic Obstructive Pulmonary Disease,C0024117,Whole blood,GEO,Microarray,Homo sapiens,24|19,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA05569,GSE93596,GPL4134,0,Cardiac Failure,C0018801,Heart,GEO,Microarray,Mus musculus,2|2,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA05570,GSE216875,GPL23126,73,Fragile X Syndrome,C0016667,,GEO,Microarray,Homo sapiens,9|9,"DO:A syndrome that is characterized by moderate to severe mental retardation, macroorchidism, and distinct facial features, including long face, large ears, and prominent jaw, and has_material_basis_in X-linked inheritance and a loss of FMR1 function." DSA05571,GSE217140,GPL11154,0,X-Linked Adrenoleukodystrophy,C0162309,Blood,GEO,RNA-Seq,Homo sapiens,8|9,"DO:A leukodystrophy that disrupts the breakdown of very-long-chain fatty acids resulting in progressive brain damage, failure of the adrenal glands and eventually death." DSA05572,GSE217320,GPL16791,0,Post-Traumatic Stress Disorder,C0038436,Blood,GEO,RNA-Seq,Homo sapiens,18|20,DO:An anxiety disorder which results from a traumatic experience that results in psychological trauma. DSA05573,GSE217320,GPL16791,42,Post-Traumatic Stress Disorder,C0038436,Blood,GEO,RNA-Seq,Homo sapiens,18|20,DO:An anxiety disorder which results from a traumatic experience that results in psychological trauma. DSA05574,GSE217320,GPL16791,119,Post-Traumatic Stress Disorder,C0038436,Blood,GEO,RNA-Seq,Homo sapiens,18|20,DO:An anxiety disorder which results from a traumatic experience that results in psychological trauma. DSA05575,GSE217320,GPL16791,0,Post-Traumatic Stress Disorder,C0038436,Blood,GEO,RNA-Seq,Homo sapiens,18|20,DO:An anxiety disorder which results from a traumatic experience that results in psychological trauma. DSA05576,GSE217320,GPL16791,0,Post-Traumatic Stress Disorder,C0038436,,GEO,RNA-Seq,Homo sapiens,20|19,DO:An anxiety disorder which results from a traumatic experience that results in psychological trauma. DSA05577,GSE217320,GPL16791,0,Post-Traumatic Stress Disorder,C0038436,,GEO,RNA-Seq,Homo sapiens,20|19,DO:An anxiety disorder which results from a traumatic experience that results in psychological trauma. DSA05578,GSE217320,GPL16791,6,Post-Traumatic Stress Disorder,C0038436,,GEO,RNA-Seq,Homo sapiens,19|17,DO:An anxiety disorder which results from a traumatic experience that results in psychological trauma. DSA05579,GSE217370,GPL18573,1,COVID-19,D8888888,Whole blood,GEO,RNA-Seq,Homo sapiens,12|19,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05580,GSE217370,GPL18573,312,Neonatal-Onset Multisystem Inflammatory Disease,C0409818,Whole blood,GEO,RNA-Seq,Homo sapiens,12|17,"DO:An autoimmune disease characterized by neonatal onset of cutaneous symptoms, chronic meningitis, and joint manifestations with recurrent fever and inflammation that has_material_basis_in heterozygous mutation in the NLRP3 gene on chromosome 1q." DSA05581,GSE217504,GPL24676,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05582,GSE217504,GPL24676,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05583,GSE217504,GPL24676,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA05584,GSE217700,GPL16791,1000,Sepsis,C0243026,Whole blood,GEO,RNA-Seq,Homo sapiens,4|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA05585,GSE217811,GPL26963,1000,Major Depressive Disorder,C1269683,,GEO,Microarray,Homo sapiens,10|10,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA05586,GSE91000,GPL18460,89,Colon Cancer,C0699790,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05587,GSE9801,GPL96,103,Type C Niemann-Pick Disease,C0220756,Blood,GEO,Microarray,Homo sapiens,4|4,DO:A Niemann-Pick disease that has_material_basis_in an autosomal recessive mutation of NPC1 on chromosome 18q11.2. DSA05588,GSE218012,GPL23934,1000,Hypermobile Ehlers-Danlos Syndrome,C0268337,Skin,GEO,RNA-Seq,Homo sapiens,100|50,DO:An Ehlers-Danlos syndrome that is characterized by joint hyperextensibility without skeletal deformity. DSA05589,GSE218012,GPL23934,1000,Hypermobility Spectrum Disorders,,Skin,GEO,RNA-Seq,Homo sapiens,100|50, DSA05590,GSE11784,GPL570,1000,Chronic Obstructive Pulmonary Disease,C0024117,Epithele,GEO,Microarray,Homo sapiens,63|22,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA05591,GSE218494,GPL24676,1000,Pneumonia,C0032285,Plasma,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A lung disease that involves lung parenchyma or alveolar inflammation and abnormal alveolar filling with fluid (consolidation and exudation). It results from a variety of causes including infection with bacteria, viruses, fungi or parasites, and chemical or physical injury to the lungs. It is accompanied by fever, chills, cough, and difficulty in breathing." DSA05592,GSE218494,GPL24676,1000,Pneumonia,C0032285,Plasma,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A lung disease that involves lung parenchyma or alveolar inflammation and abnormal alveolar filling with fluid (consolidation and exudation). It results from a variety of causes including infection with bacteria, viruses, fungi or parasites, and chemical or physical injury to the lungs. It is accompanied by fever, chills, cough, and difficulty in breathing." DSA05593,GSE218810,GPL23227,1000,Rash,C0015230,Skin,GEO,RNA-Seq,Homo sapiens,28|28,"DO:A skin disease that is characterized by a rash that results from a variety of causes including bacteria, viruses, toxins, drugs and autoimmune disorders." DSA05594,GSE218810,GPL23227,1000,Rash,C0015230,Skin,GEO,RNA-Seq,Homo sapiens,28|28,"DO:A skin disease that is characterized by a rash that results from a variety of causes including bacteria, viruses, toxins, drugs and autoimmune disorders." DSA05595,GSE218810,GPL23227,1000,Rash,C0015230,Skin,GEO,RNA-Seq,Homo sapiens,28|26,"DO:A skin disease that is characterized by a rash that results from a variety of causes including bacteria, viruses, toxins, drugs and autoimmune disorders." DSA05596,GSE21899,GPL571,381,Gaucher Disease,C0017205,,GEO,Microarray,Homo sapiens,4|5,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA05597,GSE21899,GPL571,532,Gaucher Disease,C0017205,,GEO,Microarray,Homo sapiens,4|5,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA05598,GSE219154,GPL20301,1000,Non steroidal Anti-Inflammatory Drug,,,GEO,RNA-Seq,Homo sapiens,10|10, DSA05599,GSE219154,GPL20301,1000,Non steroidal Anti-Inflammatory Drug,,,GEO,RNA-Seq,Homo sapiens,10|10, DSA05600,GSE219165,GPL24676,1000,Schizophrenia,C0036341,Middle turbinate,GEO,scRNA-Seq,Homo sapiens,1|1,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA05601,GSE19738,GPL6848,0,Major Depressive Disorder,C1269683,Blood,GEO,Microarray,Homo sapiens,10|9,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA05602,GSE19738,GPL6848,0,Major Depressive Disorder,C1269683,Blood,GEO,Microarray,Homo sapiens,11|9,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA05603,GSE220286,GPL24247,1000,Schistosoma Japonicum Infection,C0036329,Liver,GEO,scRNA-Seq,Mus musculus,1|1,"DO:A schistosomiasis that involves parasitic infection of the intestine caused by Schistosoma mansoni, Schistosoma intercalatum or Schistosomiasis japonicum. The symptoms include fever, cough, abdominal pain, diarrhea, hepatosplenomegaly, colonic polyposis with bloody diarrhea and eosinophilia." DSA05604,GSE19738,GPL6848,0,Major Depressive Disorder,C1269683,Blood,GEO,Microarray,Homo sapiens,9|9,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA05605,GSE19738,GPL6848,0,Major Depressive Disorder,C1269683,Blood,GEO,Microarray,Homo sapiens,9|9,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA05606,GSE22098,GPL6947,1000,Systemic Lupus Erythematosus,C0024141,Whole blood,GEO,Microarray,Homo sapiens,17|28,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA05607,GSE22098,GPL6947,986,Systemic Lupus Erythematosus,C0024141,Whole blood,GEO,Microarray,Homo sapiens,19|82,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA05608,GSE22098,GPL6947,1000,Still's Disease,C0087031,Whole blood,GEO,Microarray,Homo sapiens,22|31,"MONDO:Systemic-onset juvenile idiopathic arthritis is marked by the severity of the extra-articular manifestations (fever, cutaneous eruptions) and by an equal sex ratio." DSA05609,GSE22098,GPL6947,1000,Staphylococcus Infection,,Whole blood,GEO,Microarray,Homo sapiens,23|40, DSA05610,GSE22098,GPL6947,343,Strep Infection,,Whole blood,GEO,Microarray,Homo sapiens,23|12, DSA05611,GSE221091,GPL18573,394,Juvenile Dermatomyositis,C0263666,Blood,GEO,RNA-Seq,Homo sapiens,4|12,EFO:Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness. DSA05612,GSE221091,GPL18573,1000,Juvenile Dermatomyositis,C0263666,Blood,GEO,RNA-Seq,Homo sapiens,4|10,EFO:Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness. DSA05613,GSE221091,GPL18573,13,Juvenile Dermatomyositis,C0263666,Blood,GEO,RNA-Seq,Homo sapiens,4|9,EFO:Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness. DSA05614,GSE221091,GPL18573,445,Juvenile Dermatomyositis,C0263666,Blood,GEO,RNA-Seq,Homo sapiens,4|9,EFO:Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness. DSA05615,GSE221091,GPL18573,63,Juvenile Dermatomyositis,C0263666,Blood,GEO,RNA-Seq,Homo sapiens,6|11,EFO:Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness. DSA05616,GSE221091,GPL18573,799,Juvenile Dermatomyositis,C0263666,Blood,GEO,RNA-Seq,Homo sapiens,6|10,EFO:Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness. DSA05617,GSE221091,GPL18573,13,Juvenile Dermatomyositis,C0263666,Blood,GEO,RNA-Seq,Homo sapiens,3|12,EFO:Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness. DSA05618,GSE221091,GPL18573,651,Juvenile Dermatomyositis,C0263666,Blood,GEO,RNA-Seq,Homo sapiens,3|7,EFO:Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness. DSA05619,GSE221091,GPL18573,1000,Juvenile Dermatomyositis,C0263666,Blood,GEO,RNA-Seq,Homo sapiens,1|3,EFO:Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness. DSA05620,GSE221091,GPL18573,1000,Juvenile Dermatomyositis,C0263666,Blood,GEO,RNA-Seq,Homo sapiens,1|5,EFO:Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness. DSA05621,GSE19738,GPL6848,0,Major Depressive Disorder,C1269683,Blood,GEO,Microarray,Homo sapiens,13|15,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA05622,GSE221261,GPL16791,0,Crohn's Disease,C0010346,Ileum,GEO,RNA-Seq,Homo sapiens,3|5,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA05623,GSE221786,GPL24676,12,Ankylosing Spondylitis,C0038013,Peripheral blood,GEO,RNA-Seq,Homo sapiens,8|20,"DO:A bone inflammation disease that results_in inflammation in the joints of the spine and pelvis. The disease has_symptom pain, has_symptom stiffness in the spine, has_symptom stiffness in the neck, has_symptom stiffness in the hips, has_symptom stiffness in the jaw and has_symptom stiffness in the rib cage." DSA05624,GSE221925,GPL18573,78,Colon Cancer,C0699790,,GEO,RNA-Seq,Homo sapiens,19|18,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05625,GSE221925,GPL18573,7,Rectal Cancer,C0007113,,GEO,RNA-Seq,Homo sapiens,19|25,DO:A colorectal cancer that is located_in the rectum. DSA05626,GSE22196,GPL6246,0,Obesity,C0028754,,GEO,Microarray,Mus musculus,2|2,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA05627,GSE22225,GPL570,0,Juvenile Neuronal Ceroid Lipofuscinosis,C0751383,,GEO,Microarray,Homo sapiens,7|4,"DO:A neuronal ceroid lipofuscinosis that is characterized by autosomal dominant inhetitance, onset of symptoms (psychiatric manifestations, seizures, cerebellar ataxia, and cognitive decline) in adulthood and has_material_basis_in heterozygous mutation in the DNAJC5 gene (611203) on chromosome 20q13." DSA05628,GSE22225,GPL570,1,Juvenile Neuronal Ceroid Lipofuscinosis,C0751383,,GEO,Microarray,Homo sapiens,7|2,"DO:A neuronal ceroid lipofuscinosis that is characterized by autosomal dominant inhetitance, onset of symptoms (psychiatric manifestations, seizures, cerebellar ataxia, and cognitive decline) in adulthood and has_material_basis_in heterozygous mutation in the DNAJC5 gene (611203) on chromosome 20q13." DSA05629,GSE22225,GPL570,1,Juvenile Neuronal Ceroid Lipofuscinosis,C0751383,,GEO,Microarray,Homo sapiens,7|2,"DO:A neuronal ceroid lipofuscinosis that is characterized by autosomal dominant inhetitance, onset of symptoms (psychiatric manifestations, seizures, cerebellar ataxia, and cognitive decline) in adulthood and has_material_basis_in heterozygous mutation in the DNAJC5 gene (611203) on chromosome 20q13." DSA05630,GSE22491,GPL6480,1000,Parkinson's Disease,C0030567,,GEO,Microarray,Homo sapiens,10|8,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05631,GSE22529,GPL96,1000,Chronic Lymphocytic Leukemia,C0023434,Peripheral blood,GEO,Microarray,Homo sapiens,11|41,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA05632,GSE22529,GPL97,832,Chronic Lymphocytic Leukemia,C0023434,Peripheral blood,GEO,Microarray,Homo sapiens,11|41,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA05633,GSE22544,GPL570,1000,Infiltrating Ductal Carcinoma,C1134719,Breast,GEO,Microarray,Homo sapiens,4|14,DO:A breast ductal carcinoma that is characterized by infiltration into the fibrous or fatty tissue of the breast outside of the duct where it originated. DSA05634,GSE22598,GPL570,1000,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,17|17,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA05635,GSE22780,GPL570,0,Pancreatic Cancer,C0235974,Pancreas,GEO,Microarray,Homo sapiens,8|8,DO:An endocrine gland cancer located_in the pancreas. DSA05636,GSE22855,GPL6884,1000,Ollier Enchondroma,,Cartilage,GEO,Microarray,Homo sapiens,4|7, DSA05637,GSE22866,GPL4133,1000,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,6|40,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA05638,GSE22889,GPL1172,2,Crohn's Disease,C0010346,Colon mucosa,GEO,Microarray,Homo sapiens,4|20,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA05639,GSE22889,GPL1172,6,Ulcerative Colitis,C0009324,Colon mucosa,GEO,Microarray,Homo sapiens,4|20,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA05640,GSE22932,GPL9186,1000,Cutaneous Melanoma,C0151779,Lymph node,GEO,RNA-Seq,Homo sapiens,1|3,DO:A skin cancer that has_material_basis_in melanocytes. DSA05641,GSE22932,GPL9186,1000,Cutaneous Melanoma,C0151779,Skin,GEO,RNA-Seq,Homo sapiens,1|3,DO:A skin cancer that has_material_basis_in melanocytes. DSA05642,GSE22932,GPL9186,1000,Cutaneous Melanoma,C0151779,Visceral tissue,GEO,RNA-Seq,Homo sapiens,1|1,DO:A skin cancer that has_material_basis_in melanocytes. DSA05643,GSE22998,GPL570,2,Seborrheic Keratosis,C0022603,Skin,GEO,Microarray,Homo sapiens,4|4,"DO:A dermatitis that is an inflammatory skin condition resulting in flaky, white to yellowish scales on oily areas such as the scalp or inside the ear, which is caused due to a combination of an over production of skin oil and irritation from a yeast Malassezia furfur. The symptoms include itching, skin lesions and scales, redness, plaques and hair loss." DSA05644,GSE23074,GPL4133,2,Tuberculous Meningitis,C0041318,Cortex,GEO,Microarray,Homo sapiens,4|5,EFO:A bacterial infection of the membranes covering the brain and the spinal cord caused by Mycobacterium tuberculosis. DSA05645,GSE23075,GPL5175,87,Sanfilippo Syndrome Type B,C0086648,,GEO,Microarray,Homo sapiens,2|3,"DO:A mucopolysaccharidosis III characterized by neurodegeneration, behavioral problems, mild skeletal changes, and shortened life span that has_material_basis_in homozygous or compound heterozygous mutation in NAGLU on chromosome 17q21.2." DSA05646,GSE23086,GPL6246,751,Gaucher Disease Type 1,C1961835,Liver,GEO,Microarray,Mus musculus,1|1,DO:A Gaucher's disease characterized by absence of primary central nervous system involvement that has_material_basis_in a mutation of GBA on chromosome 1q22. DSA05647,GSE23086,GPL6246,1000,Gaucher Disease Type 1,C1961835,Liver,GEO,Microarray,Mus musculus,1|1,DO:A Gaucher's disease characterized by absence of primary central nervous system involvement that has_material_basis_in a mutation of GBA on chromosome 1q22. DSA05648,GSE23086,GPL6246,701,Gaucher Disease Type 1,C1961835,Spleen,GEO,Microarray,Mus musculus,1|1,DO:A Gaucher's disease characterized by absence of primary central nervous system involvement that has_material_basis_in a mutation of GBA on chromosome 1q22. DSA05649,GSE23086,GPL6246,1000,Gaucher Disease Type 1,C1961835,Spleen,GEO,Microarray,Mus musculus,1|1,DO:A Gaucher's disease characterized by absence of primary central nervous system involvement that has_material_basis_in a mutation of GBA on chromosome 1q22. DSA05650,GSE23086,GPL6246,1000,Gaucher Disease Type 1,C1961835,Spleen,GEO,Microarray,Mus musculus,1|1,DO:A Gaucher's disease characterized by absence of primary central nervous system involvement that has_material_basis_in a mutation of GBA on chromosome 1q22. DSA05651,GSE23105,GPL6887,0,Fetal Alcohol Syndrome,C0015923,Kidney,GEO,Microarray,Mus musculus,6|6,"MONDO:Fetal alcohol syndrome (FAS) is a rare malformation syndrome caused by excessive maternal consumption of alcohol during pregnancy. It is characterized by prenatal and/or postnatal growth deficiency (weight and/or height <10th percentile), a unique cluster of minor facial anomalies (short palpebral fissures, flat and smooth philtrum, and thin upper lip) and severe central nervous system (CNS) abnormalities including microcephaly, and cognitive and behavioral impairment (intellectual disability, deficit in general cognition, learning and language, executive function, visual-spatial processing, memory, and attention)." DSA05652,GSE23106,GPL6887,0,Fetal Alcohol Syndrome,C0015923,Liver,GEO,Microarray,Mus musculus,4|3,"MONDO:Fetal alcohol syndrome (FAS) is a rare malformation syndrome caused by excessive maternal consumption of alcohol during pregnancy. It is characterized by prenatal and/or postnatal growth deficiency (weight and/or height <10th percentile), a unique cluster of minor facial anomalies (short palpebral fissures, flat and smooth philtrum, and thin upper lip) and severe central nervous system (CNS) abnormalities including microcephaly, and cognitive and behavioral impairment (intellectual disability, deficit in general cognition, learning and language, executive function, visual-spatial processing, memory, and attention)." DSA05653,GSE23140,GPL6254,0,Acute Otitis Media,C0271429,Blood,GEO,Microarray,Homo sapiens,4|4,DO:A otitis which involves inflammation of the middle ear. DSA05654,GSE23203,GPL11670,1000,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,6|6,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA05655,GSE23203,GPL11670,1000,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,6|6,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA05656,GSE23290,GPL5175,1000,Parkinson's Disease,C0030567,Putamen,GEO,Microarray,Homo sapiens,5|5,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05657,GSE23290,GPL5175,0,Parkinson's Disease,C0030567,Putamen,GEO,Microarray,Homo sapiens,5|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05658,GSE23293,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,Peripheral blood,GEO,Microarray,Homo sapiens,16|7,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA05659,GSE23293,GPL570,475,Follicular Lymphoma,C0024301,Peripheral blood,GEO,Microarray,Homo sapiens,16|8,DO:A B-cell lymphoma that is characterized as an indolent non-Hodgkin's lymphoma and has_material_basis_in follicle center B-cells (centrocytes and centroblasts). DSA05660,GSE23293,GPL570,69,Malt Lymphoma,C1850900,Peripheral blood,GEO,Microarray,Homo sapiens,16|5,DO:A marginal zone B-cell lymphoma that has_material_basis_in mucosal tissue involved in antibody production. DSA05661,GSE23293,GPL570,0,Monoclonal Gammopathy of Undetermined Significance,C0026470,Peripheral blood,GEO,Microarray,Homo sapiens,16|5,DO:A blood protein disease that is characterized by the presence of an abnormal protein called monoclonal protein in the blood. DSA05662,GSE23350,GPL6884,11,Metachromatic Leukodystrophy,C0023522,Lung,GEO,Microarray,Homo sapiens,24|24,"DO:A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system." DSA05663,GSE23361,GPL5188,532,Lung Cancer,C0684249,Ovary,GEO,Microarray,Homo sapiens,7|5,DO:A respiratory system cancer that is located_in the lung. DSA05664,GSE23391,GPL570,1000,Ovarian Cancer,C1140680,Mucosa,GEO,Microarray,Homo sapiens,5|3,DO:A female reproductive organ cancer that is located_in the ovary. DSA05665,GSE23552,GPL5175,0,Allergic Rhinitis,C2607914,Mucosa,GEO,Microarray,Homo sapiens,13|4,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA05666,GSE23552,GPL5175,1000,Chronic Rhinosinusitis,C0149516,,GEO,Microarray,Homo sapiens,13|11,EFO:An acute or chronic inflammatory process affecting the mucous membranes of any sinus cavity. DSA05667,GSE23558,GPL6480,1000,Oral Squamous Cell Carcinoma,C0585362,Oral cavity,GEO,Microarray,Homo sapiens,5|27,"EFO:A squamous cell carcinoma arising from the oral cavity. It affects predominantly adults in their fifth and sixth decades of life and is associated with alcohol and tobacco use. Human papillomavirus is present in approximately half of the cases. It is characterized by a tendency to metastasize early to the lymph nodes. When the tumor is small, patients are often asymptomatic. Physical examination may reveal erythematous or white lesions or plaques. The majority of patients present with signs and symptoms of locally advanced disease including mucosal ulceration, pain, difficulty with speaking, chewing, and swallowing, bleeding, weight loss, and neck swelling. Patients may also present with swollen neck lymph nodes without any symptoms from the oropharyngeal tumor. The most significant prognostic factors are the size of the tumor and the lymph nodes status." DSA05668,GSE23561,GPL10775,1000,Rheumatoid Arthritis,C0003873,Peripheral blood,GEO,Microarray,Homo sapiens,9|6,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA05669,GSE23561,GPL10775,0,Metabolic Syndrome,C0524620,Peripheral blood,GEO,Microarray,Homo sapiens,9|6,"DO:An abdominal obesity-metabolic syndrome characterized by insulin resistance and hyperinsulinemia, dyslipidemia, essential hypertension, abdominal obesity, glucose intolerance or noninsulin-dependent diabetes mellitus and an increased risk of cardiovascular events." DSA05670,GSE23561,GPL10775,1000,Coronary Artery Disease,C1956346,Peripheral blood,GEO,Microarray,Homo sapiens,9|6,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA05671,GSE23561,GPL10775,0,Type 2 Diabetes,C0011860,Peripheral blood,GEO,Microarray,Homo sapiens,9|8,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA05672,GSE23586,GPL570,0,Periodontitis,C0031099,Gingiva,GEO,Microarray,Homo sapiens,3|3,"EFO:Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology)" DSA05673,GSE23590,GPL571,1000,Sepsis,C0243026,Lung,GEO,Microarray,Homo sapiens,3|3,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA05674,GSE23590,GPL571,717,Sepsis,C0243026,Liver,GEO,Microarray,Homo sapiens,2|3,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA05675,GSE19738,GPL6848,0,Major Depressive Disorder,C1269683,Blood,GEO,Microarray,Homo sapiens,14|15,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA05676,GSE23676,GPL5188,0,Parkinson's Disease,C0030567,Blood,GEO,Microarray,Homo sapiens,6|7,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05677,GSE23676,GPL5188,0,Parkinson's Disease,C0030567,Blood,GEO,Microarray,Homo sapiens,6|14,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05678,GSE23705,GPL6884,1000,Trachoma,C0040592,Conjunctiva,GEO,Microarray,Homo sapiens,14|15,"DO:A commensal bacterial infectious disease that results_in infection located_in eye, has_material_basis_in Chlamydia trachomatis (A, B, Ba and C serovars), which is transmitted_by contact with eye discharge from the infected person and transmitted_by congenital method. The infection causes eyelid to turn inward which makes eyelashes to scratch the cornea." DSA05679,GSE23705,GPL6884,1000,Trachoma,C0040592,Conjunctiva,GEO,Microarray,Homo sapiens,14|13,"DO:A commensal bacterial infectious disease that results_in infection located_in eye, has_material_basis_in Chlamydia trachomatis (A, B, Ba and C serovars), which is transmitted_by contact with eye discharge from the infected person and transmitted_by congenital method. The infection causes eyelid to turn inward which makes eyelashes to scratch the cornea." DSA05680,GSE23732,GPL6244,0,Bladder Cancer,C0699885,,GEO,Microarray,Homo sapiens,1|2,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05681,GSE23732,GPL6244,625,Bladder Cancer,C0699885,Cancerous,GEO,Microarray,Homo sapiens,1|5,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05682,GSE23741,GPL570,0,Systemic Sclerosis [Scleroderma],C2364016,,GEO,Microarray,Homo sapiens,3|3, DSA05683,GSE23741,GPL570,0,Systemic Sclerosis [Scleroderma],C2364016,,GEO,Microarray,Homo sapiens,3|3, DSA05684,GSE23746,GPL2700,1000,Atherosclerosis,C0004153,,GEO,Microarray,Homo sapiens,19|76,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA05685,GSE23848,GPL6106,1000,Bipolar Depression,C0005587,Peripheral blood,GEO,Microarray,Homo sapiens,15|20,DO:A mood disorder that involves alternating periods of mania and depression. DSA05686,GSE23924,GPL6480,0,Chronic Graft-Versus-Host Disease,C0867389,Peripheral blood,GEO,Microarray,Homo sapiens,19|23,"MONDO:Chronic graft versus host disease (GVHD) is a complication that can occur after a stem cell or bone marrow transplant in which the newly transplanted donor cells attack the transplant recipient's body. Symptoms may include skin rash, mouth sores, dry eyes, liver inflammation, development of scar tissue in the skin and joints, and damage to the lungs. The exact cause of chronic GVHD is unknown.It likely results from a complex immune-mediated interaction between the donor and recipient cells.Chronic GVHD is treated with prednisone or other similar anti-inflammatory or immunosuppressive medications." DSA05687,GSE23924,GPL6480,0,Chronic Graft-Versus-Host Disease,C0867389,Peripheral blood,GEO,Microarray,Homo sapiens,9|12,"MONDO:Chronic graft versus host disease (GVHD) is a complication that can occur after a stem cell or bone marrow transplant in which the newly transplanted donor cells attack the transplant recipient's body. Symptoms may include skin rash, mouth sores, dry eyes, liver inflammation, development of scar tissue in the skin and joints, and damage to the lungs. The exact cause of chronic GVHD is unknown.It likely results from a complex immune-mediated interaction between the donor and recipient cells.Chronic GVHD is treated with prednisone or other similar anti-inflammatory or immunosuppressive medications." DSA05688,GSE23933,GPL6480,0,Common Variable Immunodeficiency,C0009447,Duodenum,GEO,Microarray,Homo sapiens,3|3,DO:An agammaglobulinemia that is characterized by low Ig levels with phenotypically normal B cells that can proliferate but do not develop into Ig-producing cells and that esults in insufficient production of antibodies needed to respond to exposure of pathogens. DSA05689,GSE23959,GPL5188,218,Hypoplastic Left Heart Syndrome,C0152101,Heart,GEO,Microarray,Homo sapiens,10|6,DO:A congenital heart disease characterized by abnormal development of the left-sided structures of the heart. DSA05690,GSE20189,GPL571,52,Lung Cancer,C0684249,Lung,GEO,Microarray,Homo sapiens,27|28,DO:A respiratory system cancer that is located_in the lung. DSA05691,GSE20189,GPL571,0,Lung Cancer,C0684249,Lung,GEO,Microarray,Homo sapiens,32|31,DO:A respiratory system cancer that is located_in the lung. DSA05692,GSE20189,GPL571,0,Lung Cancer,C0684249,Lung,GEO,Microarray,Homo sapiens,21|22,DO:A respiratory system cancer that is located_in the lung. DSA05693,GSE14485,GPL339,3,Mastitis,C0024894,Mammary gland,GEO,Microarray,Mus musculus,2|2,DO:A breast disease characterized by painful infection of the breast tissue. DSA05694,GSE23996,GPL10887,108,Crohn's Disease,C0010346,Blood,GEO,Microarray,Homo sapiens,29|3,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA05695,GSE23996,GPL10887,47,Crohn's Disease,C0010346,Blood,GEO,Microarray,Homo sapiens,29|3,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA05696,GSE24084,GPL8755,1000,Glioblastoma Multiforme,C1621958,Blood,GEO,Microarray,Homo sapiens,7|9,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA05697,GSE24086,GPL5371,0,Plasmodium,,Brain,GEO,Microarray,Mus musculus,3|3, DSA05698,GSE24088,GPL8938,199,Chronic Chagas' Disease Cardiomyopathy,C0007930,Heart,GEO,Microarray,Mus musculus,4|4,"EFO:a form of cardiomyopathy that develops as a result of Chagas disease, an infection with the protozoan parasite Trypanosoma Cruzi" DSA05699,GSE24100,GPL4133,0,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,3|4,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA05700,GSE24124,GPL887,1000,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,20|70,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05701,GSE24124,GPL887,1000,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,20|29,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05702,GSE24129,GPL6244,0,Fetal Growth Restriction,C0015934,Placenta,GEO,Microarray,Homo sapiens,8|8,EFO:A fetus that does not grow beyond the 10th percentile of conventionally accepted weight for gestational age. DSA05703,GSE24129,GPL6244,13,Pre-Eclampsia,C0032914,Placenta,GEO,Microarray,Homo sapiens,8|8,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA05704,GSE24132,GPL570,0,Respiratory Syncytial Virus (Rsv),C0375023,,GEO,Microarray,Homo sapiens,3|3, DSA05705,GSE24132,GPL570,0,Respiratory Syncytial Virus (Rsv),C0375023,Umbilical cord blood,GEO,Microarray,Homo sapiens,3|3, DSA05706,GSE24147,GPL570,0,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,3|3,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA05707,GSE24147,GPL570,0,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,3|3,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA05708,GSE24147,GPL570,0,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,3|3,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA05709,GSE24147,GPL570,0,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,3|3,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA05710,GSE24147,GPL570,2,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,3|3,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA05711,GSE24147,GPL570,3,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,3|3,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA05712,GSE24147,GPL570,0,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,3|3,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA05713,GSE24171,GPL10931,0,Prostate Cancer,C0600139,Epithelium,GEO,Microarray,Homo sapiens,9|11,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05714,GSE24171,GPL4133,0,Prostate Cancer,C0600139,Epithelium,GEO,Microarray,Homo sapiens,5|4,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05715,GSE24280,GPL10191,23,Leprosy,C0023343,Blood,GEO,Microarray,Homo sapiens,1|6,"DO:A primary bacterial infectious disease that results_in infection located_in superficial peripheral nerves, located_in skin, located_in mucous membranes of the upper respiratory tract, located_in anterior chamber of the eyes, or located_in testes, has_material_basis_in Mycobacterium leprae, which is transmitted_by aerosol spread from infected nasal secretions to exposed nasal and oral mucosa. The infection has_symptom skin lesions, has_symptom sensory loss, has_symptom motor loss and has_symptom eye damage." DSA05716,GSE24280,GPL10191,44,Leprosy,C0023343,Blood,GEO,Microarray,Homo sapiens,1|6,"DO:A primary bacterial infectious disease that results_in infection located_in superficial peripheral nerves, located_in skin, located_in mucous membranes of the upper respiratory tract, located_in anterior chamber of the eyes, or located_in testes, has_material_basis_in Mycobacterium leprae, which is transmitted_by aerosol spread from infected nasal secretions to exposed nasal and oral mucosa. The infection has_symptom skin lesions, has_symptom sensory loss, has_symptom motor loss and has_symptom eye damage." DSA05717,GSE24280,GPL10191,14,Leprosy,C0023343,Skin,GEO,Microarray,Homo sapiens,1|6,"DO:A primary bacterial infectious disease that results_in infection located_in superficial peripheral nerves, located_in skin, located_in mucous membranes of the upper respiratory tract, located_in anterior chamber of the eyes, or located_in testes, has_material_basis_in Mycobacterium leprae, which is transmitted_by aerosol spread from infected nasal secretions to exposed nasal and oral mucosa. The infection has_symptom skin lesions, has_symptom sensory loss, has_symptom motor loss and has_symptom eye damage." DSA05718,GSE24280,GPL10191,53,Leprosy,C0023343,Skin,GEO,Microarray,Homo sapiens,1|6,"DO:A primary bacterial infectious disease that results_in infection located_in superficial peripheral nerves, located_in skin, located_in mucous membranes of the upper respiratory tract, located_in anterior chamber of the eyes, or located_in testes, has_material_basis_in Mycobacterium leprae, which is transmitted_by aerosol spread from infected nasal secretions to exposed nasal and oral mucosa. The infection has_symptom skin lesions, has_symptom sensory loss, has_symptom motor loss and has_symptom eye damage." DSA05719,GSE24287,GPL6480,228,Ulcerative Colitis,C0009324,,GEO,Microarray,Homo sapiens,25|27,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA05720,GSE24287,GPL6480,703,Crohn's Disease,C0010346,,GEO,Microarray,Homo sapiens,25|47,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA05721,GSE24378,GPL1352,1,Parkinson's Disease,C0030567,,GEO,Microarray,Homo sapiens,9|8,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05722,GSE24383,GPL6884,75,Trachoma,C0040592,,GEO,Microarray,Homo sapiens,14|15,"DO:A commensal bacterial infectious disease that results_in infection located_in eye, has_material_basis_in Chlamydia trachomatis (A, B, Ba and C serovars), which is transmitted_by contact with eye discharge from the infected person and transmitted_by congenital method. The infection causes eyelid to turn inward which makes eyelashes to scratch the cornea." DSA05723,GSE24383,GPL6884,1000,Trachoma,C0040592,,GEO,Microarray,Homo sapiens,14|13,"DO:A commensal bacterial infectious disease that results_in infection located_in eye, has_material_basis_in Chlamydia trachomatis (A, B, Ba and C serovars), which is transmitted_by contact with eye discharge from the infected person and transmitted_by congenital method. The infection causes eyelid to turn inward which makes eyelashes to scratch the cornea." DSA05724,GSE24395,GPL6106,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,5|12,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA05725,GSE24519,GPL2895,1000,Myocardial Infarction,C0027051,,GEO,Microarray,Homo sapiens,4|34,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA05726,GSE24667,GPL4719,413,Fibrosis; Liver,C0239946,Liver,GEO,Microarray,Homo sapiens,15|8,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA05727,GSE24667,GPL4719,256,Liver Cirrhosis,C0023890,Liver,GEO,Microarray,Homo sapiens,15|8,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA05728,GSE24673,GPL6244,1000,Umor of Retina,C0240897,Retina,GEO,Microarray,Homo sapiens,2|9,"HPO:Fluid which has escaped from retinal blood vessels with a high concentration of lipid, protein, and cellular debris with a typically bright, reflective, white or cream colored appearance on the surface of the retina." DSA05729,GSE24706,GPL6884,0,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,10|7,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA05730,GSE24706,GPL6884,4,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,7|6,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA05731,GSE24830,GPL6246,951,Parkinson's Disease,C0030567,,GEO,Microarray,Mus musculus,2|2,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05732,GSE24870,GPL571,0,Multiple Myeloma,C0026764,Bone marrow,GEO,Microarray,Homo sapiens,5|6,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA05733,GSE24870,GPL571,0,Multiple Myeloma,C0026764,Bone marrow,GEO,Microarray,Homo sapiens,5|6,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA05734,GSE24870,GPL571,0,Multiple Myeloma,C0026764,Bone marrow,GEO,Microarray,Homo sapiens,5|6,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA05735,GSE24870,GPL571,2,Multiple Myeloma,C0026764,Bone marrow,GEO,Microarray,Homo sapiens,5|5,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA05736,GSE25031,GPL6255,1000,Acth-Independent Macronodular Adrenal Hyperplasia,C1857451,Adrenal gland,GEO,Microarray,Homo sapiens,3|7,EFO:ACTH-independent macronodular adrenal hyperplasia (AIMAH) is a rare cause of Cushing syndrome (CS; see this term) characterized by nodular enlargement of both adrenal glands (multiple nodules above 1 cm in diameter) that produce excess cortisol and features of adrenocorticotropic hormone (ACTH) independent CS (see this term). DSA05737,GSE25097,GPL10687,1000,Cirrhosis,C1623038,Liver,GEO,Microarray,Homo sapiens,6|40,"MSH:Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury." DSA05738,GSE25097,GPL10687,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,243|268,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA05739,GSE25101,GPL6947,337,Ankylosing Spondylitis,C0038013,Whole blood,GEO,Microarray,Homo sapiens,16|16,"DO:A bone inflammation disease that results_in inflammation in the joints of the spine and pelvis. The disease has_symptom pain, has_symptom stiffness in the spine, has_symptom stiffness in the neck, has_symptom stiffness in the hips, has_symptom stiffness in the jaw and has_symptom stiffness in the rib cage." DSA05740,GSE25186,GPL6947,0,Primary Ciliary Dyskinesia,C4551720,Bronchus,GEO,Microarray,Homo sapiens,9|6,DO:A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer dynein arm defect and in about half of patients situs inversus and has_material_basis_in compound heterozygous mutation in the DNAI1 gene on chromosome 9p13. DSA05741,GSE25226,GPL5621,31,Dengue Disease,C0011311,Whole blood,GEO,Microarray,Homo sapiens,4|6,"DO:A viral infectious disease that results in infection, has_material_basis_in Dengue virus" DSA05742,GSE25226,GPL5621,157,Dengue Disease,C0011311,Whole blood,GEO,Microarray,Homo sapiens,4|20,"DO:A viral infectious disease that results in infection, has_material_basis_in Dengue virus" DSA05743,GSE25226,GPL5621,140,Dengue Disease,C0011311,Whole blood,GEO,Microarray,Homo sapiens,4|6,"DO:A viral infectious disease that results in infection, has_material_basis_in Dengue virus" DSA05744,GSE25226,GPL5621,164,Dengue Disease,C0011311,Whole blood,GEO,Microarray,Homo sapiens,4|8,"DO:A viral infectious disease that results in infection, has_material_basis_in Dengue virus" DSA05745,GSE14485,GPL339,0,Mastitis,C0024894,Mammary gland,GEO,Microarray,Mus musculus,2|2,DO:A breast disease characterized by painful infection of the breast tissue. DSA05746,GSE25624,GPL4133,1000,Neuroblastoma,C0027819,Bone marrow,GEO,Microarray,Homo sapiens,8|9,DO:An autonomic nervous system neoplasm that derives_from immature nerve cells. DSA05747,GSE25624,GPL4133,508,Neuroblastoma,C0027819,Bone marrow,GEO,Microarray,Homo sapiens,8|23,DO:An autonomic nervous system neoplasm that derives_from immature nerve cells. DSA05748,GSE25628,GPL571,1000,Endometriosis,C0014175,Endometrium,GEO,Microarray,Homo sapiens,6|9,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA05749,GSE25628,GPL571,1000,Endometriosis,C0014175,Endometrium,GEO,Microarray,Homo sapiens,6|7,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA05750,GSE25634,GPL570,0,Trisomy 18,C4317091,,GEO,Microarray,Homo sapiens,6|5,DO:A chromosomal duplciation syndrome that is characterized by slow growth before birth and a low birth weight and that has_material_basis_in three copies of chromosome 18. DSA05751,GSE25638,GPL570,1000,Lymphoma,C0024299,Blood,GEO,Microarray,Homo sapiens,13|31,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA05752,GSE25638,GPL570,1000,Lymphoma,C0024299,Blood,GEO,Microarray,Homo sapiens,13|26,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA05753,GSE25638,GPL570,1000,Lymphoma,C0024299,Blood,GEO,Microarray,Homo sapiens,13|15,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA05754,GSE25638,GPL570,1000,Lymphoma,C0024299,Blood,GEO,Microarray,Homo sapiens,13|12,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA05755,GSE25906,GPL6102,254,Pre-Eclampsia,C0032914,Placenta,GEO,Microarray,Homo sapiens,8|16,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA05756,GSE25906,GPL6102,0,Pre-Eclampsia,C0032914,Placenta,GEO,Microarray,Homo sapiens,29|7,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA05757,GSE25908,GPL1261,1000,Skeletal Muscle Atrophy,C0541794,Gastrocnemius,GEO,Microarray,Mus musculus,24|24,HPO:The presence of skeletal muscular atrophy (which is also known as amyotrophy). DSA05758,GSE25908,GPL1261,1000,Skeletal Muscle Atrophy,C0541794,Gastrocnemius,GEO,Microarray,Mus musculus,17|17,HPO:The presence of skeletal muscular atrophy (which is also known as amyotrophy). DSA05759,GSE26050,GPL570,1000,Familial Hemophagocytic Lymphohistiocytosis,C4551514,,GEO,Microarray,Homo sapiens,33|11,DO:A hemophagocytic lymphohistiocytosis that has_material_basis_in an autosomal recessive mutation of HPLH1 on chromosome 9q21.3-q22. DSA05760,GSE26061,GPL8238,2,Facioscapulohumeral Muscular Dystrophy,C0238288,Quadriceps,GEO,Microarray,Homo sapiens,6|6,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA05761,GSE26061,GPL8238,29,Facioscapulohumeral Muscular Dystrophy,C0238288,Quadriceps,GEO,Microarray,Homo sapiens,6|4,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA05762,GSE26125,GPL11329,1000,Tetralogy of Fallot,C0039685,Right ventricle,GEO,Microarray,Homo sapiens,5|16,"HPO:A congenital cardiac malformation comprising pulmonary stenosis, overriding aorta, ventricular septum defect, and right ventricular hypertrophy. The diagnosis of TOF is made if at least three of the four above mentioned features are present." DSA05763,GSE26276,GPL6244,20,Amyotrophic Lateral Sclerosis,C0002736,Skeletal muscle,GEO,Microarray,Homo sapiens,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA05764,GSE26276,GPL6244,0,Multifocal Motor Neuropathy,C0393847,Skeletal muscle,GEO,Microarray,Homo sapiens,3|3,"MONDO:Multifocal motor neuropathy (MMN) is a rare acquired immune-mediatedneuropathy characterized clinically by a purely motor deficit with conduction block and asymmetric multifocal weakness, fasciculations, and cramping." DSA05765,GSE26294,GPL571,0,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,Microarray,Homo sapiens,4|4,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA05766,GSE26294,GPL571,0,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,Microarray,Homo sapiens,4|4,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA05767,GSE26296,GPL6884,31,Emphysema,C0034067,,GEO,Microarray,Homo sapiens,3|3,DO:A chronic obstructive pulmonary disease that is characterized by permanent enlargement of air spaces distal to the terminal bronchioles and the destruction of the alveolar walls. DSA05768,GSE26305,GPL6884,0,Crohn's Disease,C0010346,Colon,GEO,Microarray,Homo sapiens,2|2,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA05769,GSE26305,GPL6884,0,Intestinal Tuberculosis,C0275911,Colon,GEO,Microarray,Homo sapiens,2|2,MONDO:A tuberculosis that involves the intestine. DSA05770,GSE26322,GPL4133,0,Surf1 Gene Mutations,C3711368,,GEO,Microarray,Homo sapiens,3|9, DSA05771,GSE26341,GPL5175,321,Herpesviral Infections,C0019372,Dermis,GEO,Microarray,Homo sapiens,2|3,MONDO:Virus diseases caused by the herpesviridae. DSA05772,GSE26378,GPL570,1000,Septic Shock,C0036983,Whole blood,GEO,Microarray,Homo sapiens,21|82,"DO:A commensal bacterial infectious disease that results_in infection, has_material_basis_in Streptococcus pyogenes or has_material_basis_in Staphylococcus aureus , which produce toxins that are absorbed systemically and produce the systemic manifestations. The infection has_symptom fever, has_symptom rash, has_symptom hypotension, has_symptom multiorgan failure, has_symptom desquamation, has_symptom vomiting, has_symptom diarrhea, has_symptom headache, and has_symptom nonfocal neurologic abnormalities." DSA05773,GSE26415,GPL6480,1000,Autism Spectrum Disorder,C1510586,Blood,GEO,Microarray,Homo sapiens,21|21,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA05774,GSE26440,GPL570,1000,Septic Shock,C0036983,Whole blood,GEO,Microarray,Homo sapiens,32|98,"DO:A commensal bacterial infectious disease that results_in infection, has_material_basis_in Streptococcus pyogenes or has_material_basis_in Staphylococcus aureus , which produce toxins that are absorbed systemically and produce the systemic manifestations. The infection has_symptom fever, has_symptom rash, has_symptom hypotension, has_symptom multiorgan failure, has_symptom desquamation, has_symptom vomiting, has_symptom diarrhea, has_symptom headache, and has_symptom nonfocal neurologic abnormalities." DSA05775,GSE26484,GPL570,0,Multiple Sclerosis,C0026769,Peripheral blood,GEO,Microarray,Homo sapiens,4|3,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA05776,GSE26484,GPL570,0,Multiple Sclerosis,C0026769,Peripheral blood,GEO,Microarray,Homo sapiens,4|3,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA05777,GSE26538,GPL1261,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Mus musculus,6|6,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA05778,GSE26554,GPL570,101,Juvenile Idiopathic Arthritis,C3890205,Peripheral blood,GEO,Microarray,Homo sapiens,23|24,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA05779,GSE26712,GPL96,1000,Ovarian Cancer,C1140680,Ovary,GEO,Microarray,Homo sapiens,10|185,DO:A female reproductive organ cancer that is located_in the ovary. DSA05780,GSE26713,GPL570,1000,T-Cell Acute Lymphoblastic Leukemia,C1961099,,GEO,Microarray,Homo sapiens,7|117,DO:An acute lymphoblastic leukemia that is characterized by too many T-cell lymphoblasts found in the bone marrow and blood. DSA05781,GSE26886,GPL570,1000,Barrett's Esophagus,C0004763,,GEO,Microarray,Homo sapiens,19|20,DO:An esophageal disease characterized by a change of normal esophageal squamous epithelium to a columnar and intestinal-type epithelium. DSA05782,GSE26886,GPL570,1000,Esophageal Adenocarcinoma,C0279628,,GEO,Microarray,Homo sapiens,19|21,DO:An esophageal carcinoma that derives_from epithelial cells of glandular origin. DSA05783,GSE26886,GPL570,1000,Esophageal Squamous Cell Carcinoma,C0279626,,GEO,Microarray,Homo sapiens,19|9,DO:An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus. DSA05784,GSE26887,GPL6244,272,Diabetes;Heart Failure,,Left ventricle,GEO,Microarray,Homo sapiens,5|7, DSA05785,GSE26887,GPL6244,1000,Heart Failure,C0018801,Left ventricle,GEO,Microarray,Homo sapiens,5|12,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA05786,GSE26934,GPL6480,621,Eosinophilia Myalgia Syndrome,C0085179,Skin,GEO,Microarray,Homo sapiens,3|3,"DO:A hypereosinophilic syndrome that is characterized by subacute onset of myalgias and peripheral eosinophilia, followed by chronic neuropathy and skin induration." DSA05787,GSE26972,GPL5188,0,Alzheimer's Disease,C0002395,Entorhinal cortex,GEO,Microarray,Homo sapiens,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA05788,GSE26975,GPL11670,0,Lupus,C0409974,Peripheral blood,GEO,Microarray,Homo sapiens,9|10,"DO:An autoimmune disease that is characterized by a constellation of findings that include elevated antibodies to nuclear antigens, antiphospholipids, low complement levels, ulcers, non-scarring alopecia, renal or neurologic damage, and low white blood cell and platelet counts, has_symptom rashes, fatigue, arthritis, hair loss, seizures, and symptoms related to affected organs." DSA05789,GSE26975,GPL11670,352,Lupus,C0409974,Peripheral blood,GEO,Microarray,Homo sapiens,9|10,"DO:An autoimmune disease that is characterized by a constellation of findings that include elevated antibodies to nuclear antigens, antiphospholipids, low complement levels, ulcers, non-scarring alopecia, renal or neurologic damage, and low white blood cell and platelet counts, has_symptom rashes, fatigue, arthritis, hair loss, seizures, and symptoms related to affected organs." DSA05790,GSE27034,GPL570,2,Peripheral Artery Disease,C4025272,Peripheral blood,GEO,Microarray,Homo sapiens,18|19,"HPO:Narrowing of peripheral arteries with reduction of blood flow to the limbs. This feature may be quantified as an ankle-brachial index of less than 0.9, and may be manifested clinically as claudication." DSA05791,GSE27041,GPL570,46,Defective Complex I,,,GEO,Microarray,Homo sapiens,10|10, DSA05792,GSE27057,GPL11094,0,Glaucoma,C0017601,,GEO,Microarray,Homo sapiens,5|5,DO:An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. DSA05793,GSE27058,GPL11094,0,Glaucoma,C0017601,,GEO,Microarray,Homo sapiens,4|5,DO:An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. DSA05794,GSE20257,GPL570,64,Chronic Obstructive Pulmonary Disease,C0024117,Epithelium,GEO,Microarray,Homo sapiens,59|23,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA05795,GSE27199,GPL9115,84,Intellectual Disability,C3714756,,GEO,RNA-Seq,Homo sapiens,2|4,"DO:A specific developmental disorder that involves significant limitations both in mental functioning and in adaptive behavior such as communicating, taking care of him or herself, and social skills." DSA05796,GSE27205,GPL5175,1,Spinal Muscular Atrophy,C0026847,,GEO,Microarray,Homo sapiens,3|3,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA05797,GSE27205,GPL5175,1,Spinal Muscular Atrophy,C0026847,,GEO,Microarray,Homo sapiens,3|3,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA05798,GSE27206,GPL570,1000,Spinal Muscular Atrophy,C0026847,,GEO,Microarray,Homo sapiens,3|2,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA05799,GSE27342,GPL5175,1000,Gastric Cancer,C0699791,Stomach,GEO,Microarray,Homo sapiens,80|80,DO:A gastrointestinal system cancer that is located_in the stomach. DSA05800,GSE27356,GPL11094,0,Schizophrenia,C0036341,Brain,GEO,Microarray,Homo sapiens,16|16,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA05801,GSE2737,GPL91,49,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,1|4,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA05802,GSE2737,GPL91,1,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,1|4,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA05803,GSE2738,GPL2130,76,Rectal Carcinoma,C0007113,Rectum,GEO,Microarray,Homo sapiens,5|16,DO:A colorectal cancer that is located_in the rectum. DSA05804,GSE27427,GPL6106,1000,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,12|21,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA05805,GSE21795,GPL5188,46,Myotonic Dystrophy,C0027126,,GEO,Microarray,Homo sapiens,3|3,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA05806,GSE27489,GPL570,0,Adenocarcinoma,C0001418,,GEO,Microarray,Homo sapiens,10|10,"DO:A carcinoma that has_material_basis_in abnormally proliferating cells, derives_from epithelial cells, which originate in glandular tissue." DSA05807,GSE27489,GPL570,0,Squamous Cell Carcinoma,C0007137,,GEO,Microarray,Homo sapiens,10|10,DO:A carcinoma that derives_from squamous epithelial cells. DSA05808,GSE27536,GPL570,2,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,12|9,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA05809,GSE27536,GPL570,440,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,12|6,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA05810,GSE27536,GPL570,16,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,12|9,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA05811,GSE27536,GPL570,229,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,12|6,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA05812,GSE27543,GPL201,0,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,3|5,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA05813,GSE27543,GPL201,0,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,3|5,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA05814,GSE27562,GPL570,212,Breast Cancer,C0678222,Peripheral blood,GEO,Microarray,Homo sapiens,10|10,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05815,GSE27562,GPL570,18,Breast Cancer,C0678222,Peripheral blood,GEO,Microarray,Homo sapiens,10|10,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05816,GSE27562,GPL570,1000,Breast Cancer,C0678222,Peripheral blood,GEO,Microarray,Homo sapiens,21|41,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05817,GSE27562,GPL570,1000,Breast Cancer,C0678222,Peripheral blood,GEO,Microarray,Homo sapiens,21|27,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05818,GSE27588,GPL11094,0,Huntington's Disease,C0020179,Brain,GEO,Microarray,Mus musculus,3|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05819,GSE27588,GPL11094,0,Huntington's Disease,C0020179,Brain,GEO,Microarray,Mus musculus,3|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05820,GSE27601,GPL11094,0,Schizophrenia,C0036341,Brain,GEO,Microarray,Homo sapiens,13|13,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA05821,GSE27864,GPL6244,1000,Neonatal-Onset Multisystem Inflammatory Disease,C0409818,Skin,GEO,Microarray,Homo sapiens,5|6,"DO:An autoimmune disease characterized by neonatal onset of cutaneous symptoms, chronic meningitis, and joint manifestations with recurrent fever and inflammation that has_material_basis_in heterozygous mutation in the NLRP3 gene on chromosome 1q." DSA05822,GSE27864,GPL6244,1000,Neonatal-Onset Multisystem Inflammatory Disease,C0409818,Skin,GEO,Microarray,Homo sapiens,5|8,"DO:An autoimmune disease characterized by neonatal onset of cutaneous symptoms, chronic meningitis, and joint manifestations with recurrent fever and inflammation that has_material_basis_in heterozygous mutation in the NLRP3 gene on chromosome 1q." DSA05823,GSE27864,GPL6244,252,Neonatal-Onset Multisystem Inflammatory Disease,C0409818,Skin,GEO,Microarray,Homo sapiens,5|4,"DO:An autoimmune disease characterized by neonatal onset of cutaneous symptoms, chronic meningitis, and joint manifestations with recurrent fever and inflammation that has_material_basis_in heterozygous mutation in the NLRP3 gene on chromosome 1q." DSA05824,GSE27882,GPL6480,139,Tuberculosis,C0041296,Peripheral blood,GEO,Microarray,Homo sapiens,1|2,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05825,GSE16972,GPL96,2,Chronic Obstructive Pulmonary Disease,C0024117,Lung,GEO,Microarray,Homo sapiens,5|5,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA05826,GSE27890,GPL570,0,Pancreatic Adenocarcinoma,C0281361,Pancreas,GEO,Microarray,Homo sapiens,2|2,DO:A pancreatic carcinoma that derives_from epithelial cells of glandular origin. DSA05827,GSE27915,GPL4133,0,"Dysautonomia, Familial",C0013364,,GEO,Microarray,Homo sapiens,4|4,"DO:A hereditary sensory neuropathy that is characterized by gastrointestinal dysfunction, gastroesophageal reflux, vomiting crises, recurrent pneumonia, seizures, gait abnormalities with loss of ambulation, kyphoscoliosis, postural hypotension, hypertension crises, absence of fungiform papillae on the tongue, decreased deep tendon reflexes, defective lacrimation, and impaired pain and temperature perception and has_material_basis_in homozygous or compound heterozygous mutation in the IKBKAP gene (ELP1) on chromosome 9q31." DSA05828,GSE27915,GPL4133,0,"Dysautonomia, Familial",C0013364,,GEO,Microarray,Homo sapiens,4|4,"DO:A hereditary sensory neuropathy that is characterized by gastrointestinal dysfunction, gastroesophageal reflux, vomiting crises, recurrent pneumonia, seizures, gait abnormalities with loss of ambulation, kyphoscoliosis, postural hypotension, hypertension crises, absence of fungiform papillae on the tongue, decreased deep tendon reflexes, defective lacrimation, and impaired pain and temperature perception and has_material_basis_in homozygous or compound heterozygous mutation in the IKBKAP gene (ELP1) on chromosome 9q31." DSA05829,GSE27953,GPL5175,0,FRAXE Mutations,,,GEO,Microarray,Homo sapiens,4|8, DSA05830,GSE27976,GPL6244,28,Craniosynostosis,C0010278,Skull,GEO,Microarray,Homo sapiens,50|50,DO:A synostosis that results_in premature fusion located_in skull. DSA05831,GSE27976,GPL6244,2,Craniosynostosis,C0010278,Skull,GEO,Microarray,Homo sapiens,50|49,DO:A synostosis that results_in premature fusion located_in skull. DSA05832,GSE27976,GPL6244,119,Craniosynostosis,C0010278,Skull,GEO,Microarray,Homo sapiens,50|100,DO:A synostosis that results_in premature fusion located_in skull. DSA05833,GSE27984,GPL6848,0,Tuberculosis,C0041296,,GEO,Microarray,Homo sapiens,4|4,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05834,GSE27984,GPL6848,4,Tuberculosis,C0041296,,GEO,Microarray,Homo sapiens,4|4,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05835,GSE27990,GPL13287,0,Acute Otitis Media,C0271429,Blood,GEO,Microarray,Homo sapiens,4|4,DO:A otitis which involves inflammation of the middle ear. DSA05836,GSE27993,GPL6244,0,Periodontitis,C0031099,,GEO,Microarray,Homo sapiens,5|5,"EFO:Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology)" DSA05837,GSE28000,GPL4133,1000,Colon Tumor,C0009375,Colon,GEO,Microarray,Homo sapiens,11|41,DO:A colorectal cancer that is located_in the colon. DSA05838,GSE28000,GPL4133,1000,Colon Tumor,C0009375,Colon,GEO,Microarray,Homo sapiens,23|40,DO:A colorectal cancer that is located_in the colon. DSA05839,GSE28000,GPL1708,0,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,2|2,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA05840,GSE28000,GPL1708,0,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,4|3,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA05841,GSE28042,GPL6480,1000,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,Microarray,Homo sapiens,19|75,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA05842,GSE28107,GPL96,0,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,3|3,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA05843,GSE28107,GPL96,0,Multiple Myeloma,C0026764,,GEO,Microarray,Homo sapiens,3|3,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA05844,GSE28160,GPL570,1000,HIV-Associated Neurocognitive Disorder,C4285693,Brain,GEO,Microarray,Homo sapiens,9|14,"EFO:HIV-associated neurocognitive disorder (HAND) remains a common complication of HIV infection in the combination antiretroviral therapy (ART) era. Although modern ART has substantially improved life expectancy and reduced the incidence of HIVassociated dementia (HAD), milder forms of HAND remain prevalent, including asymptomatic neurocognitive impairment (ANI) and mild neurocognitive disorder (MND). The overall prevalence of HAND is 30�0% among unselected HIV-infected persons." DSA05845,GSE28192,GPL6102,1000,Medulloblastoma,C0025149,Brain,GEO,Microarray,Homo sapiens,6|18,DO:An infratentorial cancer that is located_in the lower part of the brain and is a type of primitive neuroectodermal tumor. DSA05846,GSE28253,GPL4133,11,Amyotrophic Lateral Sclerosis,C0002736,,GEO,Microarray,Homo sapiens,11|11,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA05847,GSE28345,GPL6244,0,Hypertension,C0020538,Renal cortex,GEO,Microarray,Homo sapiens,3|5,DO:An artery disease characterized by chronic elevated blood pressure in the arteries. DSA05848,GSE28360,GPL6244,0,Hypertension,C0020538,Renal medulla,GEO,Microarray,Homo sapiens,5|9,DO:An artery disease characterized by chronic elevated blood pressure in the arteries. DSA05849,GSE28405,GPL2700,1000,Dengue Disease,C0011311,Whole blood,GEO,Microarray,Homo sapiens,26|31,"DO:A viral infectious disease that results in infection, has_material_basis_in Dengue virus" DSA05850,GSE28405,GPL2700,1000,Dengue Disease,C0011311,Whole blood,GEO,Microarray,Homo sapiens,26|31,"DO:A viral infectious disease that results in infection, has_material_basis_in Dengue virus" DSA05851,GSE28405,GPL2700,1000,Dengue Disease,C0011311,Whole blood,GEO,Microarray,Homo sapiens,26|31,"DO:A viral infectious disease that results in infection, has_material_basis_in Dengue virus" DSA05852,GSE28536,GPL9324,146,Nodular Lymphocyte Predominant Hodgkin Lymphoma,C1334968,Blood,GEO,Microarray,Homo sapiens,10|8,EFO:Hodgkin lymphoma (HL) is a heterogeneous group of malignant lymphoid neoplasms of B-cell origin characterized histologically by the presence of Hodgkin and Reed-Sternberg (HRS) cells in the vast majority of cases. There are two distinct subtypes: nodular lymphocyte predominant Hodgkin lymphoma and classical Hodgkin lymphoma. Hodgkin lymphoma involves primarily lymph nodes. DSA05853,GSE28536,GPL9324,0,Nodular Lymphocyte Predominant Hodgkin Lymphoma,C1334968,Blood,GEO,Microarray,Homo sapiens,10|2,EFO:Hodgkin lymphoma (HL) is a heterogeneous group of malignant lymphoid neoplasms of B-cell origin characterized histologically by the presence of Hodgkin and Reed-Sternberg (HRS) cells in the vast majority of cases. There are two distinct subtypes: nodular lymphocyte predominant Hodgkin lymphoma and classical Hodgkin lymphoma. Hodgkin lymphoma involves primarily lymph nodes. DSA05854,GSE14882,GPL96,1,Melas Syndrome,C0162671,Blood,GEO,Microarray,Homo sapiens,6|10,"DO:A mitochondrial encephalomyopathy that is characterized by mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes, has_symptom myalgia, motor weakness, headaches, seizures, and stroke-like episodes with acute hemiparesis and severe headaches, and develops_from mutation in mitochondrial genes including MT-TL1, which encodes tRNA proteins." DSA05855,GSE19724,GPL6480,0,Golabi-Ito-Hall Syndrome,,Lymphoblast,GEO,Microarray,Homo sapiens,2|2, DSA05856,GSE28623,GPL4133,0,Tuberculosis,C0041296,Peripheral blood,GEO,Microarray,Homo sapiens,37|25,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05857,GSE28623,GPL4133,644,Tuberculosis,C0041296,Peripheral blood,GEO,Microarray,Homo sapiens,37|46,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA05858,GSE28660,GPL2895,10,Pelvic Organ Prolapse,C0877015,Uterosacral ligament,GEO,Microarray,Homo sapiens,4|4,"EFO:Abnormal descent of a pelvic organ resulting in the protrusion of the organ beyond its normal anatomical confines. Symptoms often include vaginal discomfort, dyspareunia; urinary stress incontinence; and fecal incontinence." DSA05859,GSE28660,GPL2895,5,Pelvic Organ Prolapse,C0877015,Uterosacral ligament,GEO,Microarray,Homo sapiens,4|4,"EFO:Abnormal descent of a pelvic organ resulting in the protrusion of the organ beyond its normal anatomical confines. Symptoms often include vaginal discomfort, dyspareunia; urinary stress incontinence; and fecal incontinence." DSA05860,GSE28720,GPL6887,1000,Ovarian Tumor,C1140680,Oviduct,GEO,Microarray,Mus musculus,3|3,DO:A female reproductive organ cancer that is located_in the ovary. DSA05861,GSE28863,GPL5188,10,Hutchinson-Gilford Progeria Syndrome,C0033300,,GEO,Microarray,Homo sapiens,6|4,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA05862,GSE28894,GPL6104,0,Parkinson's Disease,C0030567,Brain,GEO,Microarray,Homo sapiens,15|11,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05863,GSE28894,GPL6104,0,Parkinson's Disease,C0030567,Brain,GEO,Microarray,Homo sapiens,14|15,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05864,GSE28894,GPL6104,90,Parkinson's Disease,C0030567,Brain,GEO,Microarray,Homo sapiens,15|15,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05865,GSE28894,GPL6104,0,Parkinson's Disease,C0030567,Brain,GEO,Microarray,Homo sapiens,15|14,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA05866,GSE28941,GPL11095,0,Dry Eyes,C0013238,Conjunctival epithelium,GEO,Microarray,Homo sapiens,3|3,"DO:A dry eye syndrome that is characterized by conjunctival and corneal xerosis, Bitot's spots, keratomalacia, nyctalopia, and retinopathy resulting from vitamin A deficiency." DSA05867,GSE28945,GPL11095,159,Leiomyoma,C0042133,Myometrium,GEO,Microarray,Homo sapiens,10|10,DO:An uterine benign neoplasm derived from the smooth muscle layer of the uterus. DSA05868,GSE10989,GPL1261,1000,Renal Cell Carcinoma,C0007134,Kidney,GEO,Microarray,Mus musculus,3|3,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA05869,GSE29044,GPL570,1000,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,36|73,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05870,GSE29142,GPL13507,8,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,10|9,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA05871,GSE29142,GPL13507,29,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,10|10,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA05872,GSE29156,GPL5188,0,Ovarian Tumor,C1140680,Ovary,GEO,Microarray,Homo sapiens,4|14,DO:A female reproductive organ cancer that is located_in the ovary. DSA05873,GSE29156,GPL5188,4,Ovarian Tumor,C1140680,Ovary,GEO,Microarray,Homo sapiens,4|5,DO:A female reproductive organ cancer that is located_in the ovary. DSA05874,GSE29156,GPL5188,0,Ovarian Tumor,C1140680,Ovary,GEO,Microarray,Homo sapiens,5|14,DO:A female reproductive organ cancer that is located_in the ovary. DSA05875,GSE29156,GPL5188,1,Ovarian Tumor,C1140680,Ovary,GEO,Microarray,Homo sapiens,5|8,DO:A female reproductive organ cancer that is located_in the ovary. DSA05876,GSE29161,GPL6480,1000,Infective Endocarditis,C1541923,Peripheral blood,GEO,Microarray,Homo sapiens,5|5,DO:An endocarditis that is characterized by inflammation of the endocardium caused by infectious agents. DSA05877,GSE29216,GPL6244,1000,Cervical Cancer,C4048328,Exocervix,GEO,Microarray,Homo sapiens,10|3,DO:A female reproductive organ cancer that is located_in the cervix. DSA05878,GSE29216,GPL6244,1000,Cervical Cancer,C4048328,Exocervix,GEO,Microarray,Homo sapiens,10|3,DO:A female reproductive organ cancer that is located_in the cervix. DSA05879,GSE29216,GPL6244,1000,Cervical Cancer,C4048328,Exocervix,GEO,Microarray,Homo sapiens,10|3,DO:A female reproductive organ cancer that is located_in the cervix. DSA05880,GSE29216,GPL6244,1000,Cervical Cancer,C4048328,Exocervix,GEO,Microarray,Homo sapiens,10|3,DO:A female reproductive organ cancer that is located_in the cervix. DSA05881,GSE29220,GPL570,0,Ovarian Cancer,C1140680,Ovary,GEO,Microarray,Homo sapiens,11|11,DO:A female reproductive organ cancer that is located_in the ovary. DSA05882,GSE29265,GPL570,1000,Papillary Thyroid Carcinoma,C0238463,,GEO,Microarray,Homo sapiens,10|10,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA05883,GSE29265,GPL570,819,Papillary Thyroid Carcinoma,C0238463,,GEO,Microarray,Homo sapiens,10|10,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA05884,GSE29304,GPL1476,1000,Melanoma,C0025202,Skin,GEO,Microarray,Mus musculus,4|14,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA05885,GSE29304,GPL1476,422,Melanoma,C0025202,Skin,GEO,Microarray,Mus musculus,4|6,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA05886,GSE29330,GPL570,1000,Head And Neck Cancer,C0018671,Oropharynx,GEO,Microarray,Homo sapiens,5|13,"DO:An organ system cancer that arises in the head or neck region. This region includes the nasal cavity, sinuses, lips, mouth, salivary glands, throat, or larynx." DSA05887,GSE29332,GPL6884,0,Human T-Cell Lymphotrophic Virus; Type I,C0375019,Whole blood,GEO,Microarray,Homo sapiens,8|17, DSA05888,GSE29332,GPL6884,1,Human T-Cell Lymphotrophic Virus; Type I,C0375019,Whole blood,GEO,Microarray,Homo sapiens,8|10, DSA05889,GSE29366,GPL6884,39,Influenza,C0021400,Whole blood,GEO,Microarray,Homo sapiens,12|4,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA05890,GSE29366,GPL6884,439,Influenza,C0021400,Whole blood,GEO,Microarray,Homo sapiens,12|9,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA05891,GSE29366,GPL6884,27,Influenza,C0021400,Whole blood,GEO,Microarray,Homo sapiens,12|2,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA05892,GSE29366,GPL6884,1000,Influenza,C0021400,Whole blood,GEO,Microarray,Homo sapiens,12|4,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA05893,GSE65561,GPL16686,0,Diabetes,C0011847,Blood,GEO,Microarray,Homo sapiens,4|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA05894,GSE21816,GPL10175,1000,Golabi-Ito-Hall Syndrome,,Kidney,GEO,Microarray,Homo sapiens,12|6, DSA05895,GSE18608,GPL570,0,Coronary Artery Disease,C1956346,Blood,GEO,Microarray,Homo sapiens,4|10,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA05896,GSE65634,GPL11154,1000,Complex I Deficiency,,,GEO,RNA-Seq,Homo sapiens,4|2, DSA05897,GSE65634,GPL11154,828,Complex I Deficiency,,,GEO,RNA-Seq,Homo sapiens,4|2, DSA05898,GSE65635,GPL14951,1000,Bladder Cancer,C0699885,Bladder,GEO,Microarray,Homo sapiens,4|8,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA05899,GSE18608,GPL570,0,Coronary Artery Disease,C1956346,Blood,GEO,Microarray,Homo sapiens,4|10,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA05900,GSE65705,GPL11154,1000,Myocardial Infarction,C0027051,Plalelets,GEO,RNA-Seq,Homo sapiens,2|16,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA05901,GSE65705,GPL11154,1000,Myocardial Infarction,C0027051,Plalelets,GEO,RNA-Seq,Homo sapiens,2|14,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA05902,GSE21959,GPL4133,7,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,9|9,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA05903,GSE21959,GPL4133,54,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,9|9,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA05904,GSE58294,GPL570,1000,Cardioembolic Stroke,C1531624,Blood,GEO,Microarray,Homo sapiens,23|23, DSA05905,GSE58294,GPL570,1000,Cardioembolic Stroke,C1531624,Blood,GEO,Microarray,Homo sapiens,23|23, DSA05906,GSE65770,GPL13112,7,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05907,GSE65770,GPL13112,7,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05908,GSE65770,GPL13112,1000,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05909,GSE65770,GPL13112,1000,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05910,GSE65770,GPL13112,50,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05911,GSE65770,GPL13112,0,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05912,GSE65770,GPL13112,0,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05913,GSE65770,GPL13112,4,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05914,GSE65770,GPL13112,1000,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05915,GSE65770,GPL13112,1000,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05916,GSE65770,GPL13112,15,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05917,GSE65770,GPL13112,112,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05918,GSE65770,GPL13112,2,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05919,GSE65770,GPL13112,4,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05920,GSE65770,GPL13112,1000,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05921,GSE65770,GPL13112,1000,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05922,GSE65770,GPL13112,777,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05923,GSE65770,GPL13112,633,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05924,GSE65770,GPL13112,0,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05925,GSE65770,GPL13112,0,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05926,GSE65770,GPL13112,1000,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05927,GSE65770,GPL13112,1000,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05928,GSE65770,GPL13112,5,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05929,GSE65770,GPL13112,0,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05930,GSE65770,GPL13112,0,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05931,GSE65770,GPL13112,0,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|5,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05932,GSE65770,GPL13112,1000,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05933,GSE65770,GPL13112,1000,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05934,GSE65770,GPL13112,20,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05935,GSE65770,GPL13112,127,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05936,GSE65770,GPL13112,2,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05937,GSE65770,GPL13112,1,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05938,GSE65770,GPL13112,1000,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05939,GSE65770,GPL13112,1000,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05940,GSE65770,GPL13112,20,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05941,GSE65770,GPL13112,24,Huntington's Disease,C0020179,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05942,GSE65772,GPL13112,13,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05943,GSE65772,GPL13112,48,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05944,GSE65772,GPL13112,1000,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05945,GSE65772,GPL13112,887,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05946,GSE65772,GPL13112,18,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05947,GSE65772,GPL13112,30,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05948,GSE65772,GPL13112,15,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05949,GSE65772,GPL13112,202,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05950,GSE65772,GPL13112,1000,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05951,GSE65772,GPL13112,986,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05952,GSE65772,GPL13112,35,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05953,GSE65772,GPL13112,2,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05954,GSE65772,GPL13112,267,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05955,GSE65772,GPL13112,403,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05956,GSE65772,GPL13112,1000,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05957,GSE65772,GPL13112,983,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05958,GSE65772,GPL13112,343,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05959,GSE65772,GPL13112,358,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05960,GSE65772,GPL13112,0,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05961,GSE65772,GPL13112,2,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05962,GSE65772,GPL13112,1000,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05963,GSE65772,GPL13112,1000,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05964,GSE65772,GPL13112,2,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05965,GSE65772,GPL13112,0,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05966,GSE65772,GPL13112,25,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05967,GSE65772,GPL13112,5,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|5,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05968,GSE65772,GPL13112,1000,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05969,GSE65772,GPL13112,545,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05970,GSE65772,GPL13112,21,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05971,GSE65772,GPL13112,129,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05972,GSE65772,GPL13112,41,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05973,GSE65772,GPL13112,322,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05974,GSE65772,GPL13112,1000,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05975,GSE65772,GPL13112,656,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05976,GSE65772,GPL13112,635,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05977,GSE65772,GPL13112,79,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05978,GSE65774,GPL13112,161,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05979,GSE65774,GPL13112,205,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05980,GSE65774,GPL13112,733,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,1|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05981,GSE65774,GPL13112,1000,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05982,GSE65774,GPL13112,1000,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05983,GSE65774,GPL13112,1000,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05984,GSE65774,GPL13112,1,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05985,GSE65774,GPL13112,184,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05986,GSE65774,GPL13112,449,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05987,GSE65774,GPL13112,517,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,1|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05988,GSE65774,GPL13112,951,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05989,GSE65774,GPL13112,1000,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05990,GSE65774,GPL13112,2,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05991,GSE65774,GPL13112,0,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05992,GSE65774,GPL13112,7,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05993,GSE65774,GPL13112,2,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05994,GSE65774,GPL13112,2,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|5,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05995,GSE65774,GPL13112,1,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05996,GSE65774,GPL13112,1,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05997,GSE65774,GPL13112,1,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|5,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05998,GSE65774,GPL13112,4,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA05999,GSE65774,GPL13112,20,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06000,GSE65774,GPL13112,3,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06001,GSE65774,GPL13112,1000,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06002,GSE65774,GPL13112,23,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06003,GSE65774,GPL13112,26,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06004,GSE65774,GPL13112,1000,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06005,GSE65774,GPL13112,1000,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06006,GSE65774,GPL13112,1000,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06007,GSE65774,GPL13112,1000,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06008,GSE65774,GPL13112,1,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06009,GSE65774,GPL13112,3,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06010,GSE65774,GPL13112,87,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06011,GSE65774,GPL13112,16,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06012,GSE65774,GPL13112,66,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06013,GSE65774,GPL13112,82,Huntington's Disease,C0020179,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06014,GSE65775,GPL13112,167,Huntington's Disease,C0020179,Brown adipose tissue,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06015,GSE65775,GPL13112,1000,Huntington's Disease,C0020179,Brown adipose tissue,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06016,GSE65775,GPL13112,1000,Huntington's Disease,C0020179,White adipose tissue,GEO,RNA-Seq,Mus musculus,3|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06017,GSE65775,GPL13112,1000,Huntington's Disease,C0020179,White adipose tissue,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06018,GSE65775,GPL13112,4,Huntington's Disease,C0020179,White adipose tissue,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06019,GSE65775,GPL13112,8,Huntington's Disease,C0020179,White adipose tissue,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06020,GSE65775,GPL13112,257,Huntington's Disease,C0020179,Brainstem,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06021,GSE65775,GPL13112,361,Huntington's Disease,C0020179,Brainstem,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06022,GSE65775,GPL13112,1000,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06023,GSE65775,GPL13112,1000,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06024,GSE65775,GPL13112,377,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06025,GSE65775,GPL13112,1000,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06026,GSE65775,GPL13112,95,Huntington's Disease,C0020179,Hypothalamus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06027,GSE65775,GPL13112,389,Huntington's Disease,C0020179,Hypothalamus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06028,GSE65775,GPL13112,140,Huntington's Disease,C0020179,Callosum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06029,GSE65775,GPL13112,6,Huntington's Disease,C0020179,Callosum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06030,GSE65775,GPL13112,14,Huntington's Disease,C0020179,Gastrocnemius,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06031,GSE65775,GPL13112,48,Huntington's Disease,C0020179,Gastrocnemius,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06032,GSE65775,GPL13112,36,Huntington's Disease,C0020179,Heart,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06033,GSE65775,GPL13112,5,Huntington's Disease,C0020179,Heart,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06034,GSE65775,GPL13112,1000,Huntington's Disease,C0020179,Skin,GEO,RNA-Seq,Mus musculus,3|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06035,GSE65775,GPL13112,1000,Huntington's Disease,C0020179,Skin,GEO,RNA-Seq,Mus musculus,3|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06036,GSE65914,GPL570,1000,Erythematotelangiectatic Rosacea,C1449852,Skin,GEO,Microarray,Homo sapiens,20|14,MSH:A variant of rosacea. DSA06037,GSE65914,GPL570,1000,Papulopustular Rosacea,C1449853,Skin,GEO,Microarray,Homo sapiens,20|12,MSH:A variant of rosacea. DSA06038,GSE65914,GPL570,1000,Rosacea,C0035854,Skin,GEO,Microarray,Homo sapiens,20|12,"HPO:Redness of the skin of the face, caused by hyperemia of the capillaries in the lower layers of the skin." DSA06039,GSE66061,GPL6244,0,Spinal Muscular Atrophy,C0026847,,GEO,Microarray,Homo sapiens,2|1,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA06040,GSE66099,GPL570,1000,Septic Shock,C0036983,Whole blood,GEO,Microarray,Homo sapiens,47|182,"DO:A commensal bacterial infectious disease that results_in infection, has_material_basis_in Streptococcus pyogenes or has_material_basis_in Staphylococcus aureus , which produce toxins that are absorbed systemically and produce the systemic manifestations. The infection has_symptom fever, has_symptom rash, has_symptom hypotension, has_symptom multiorgan failure, has_symptom desquamation, has_symptom vomiting, has_symptom diarrhea, has_symptom headache, and has_symptom nonfocal neurologic abnormalities." DSA06041,GSE66099,GPL570,1000,Systemic Inflammatory Response Syndrome,C0242966,Whole blood,GEO,Microarray,Homo sapiens,47|29,"MSH:A systemic inflammatory response to a variety of clinical insults, characterized by two or more of the following conditions: (1) fever >38 degrees C or HYPOTHERMIA <36 degrees C; (2) TACHYCARDIA >90 beat/minute; (3) tachypnea >24 breaths/minute; (4) LEUKOCYTOSIS >12,000 cells/cubic mm or 10% immature forms. While usually related to infection, SIRS can also be associated with noninfectious insults such as TRAUMA; BURNS; or PANCREATITIS. If infection is involved, a patient with SIRS is said to have SEPSIS." DSA06042,GSE66099,GPL570,1000,Sepsis,C0243026,Whole blood,GEO,Microarray,Homo sapiens,47|18,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA06043,GSE66117,GPL11154,1000,Chronic Lymphocytic Leukemia,C0023434,Blood,GEO,RNA-Seq,Homo sapiens,3|47,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA06044,GSE58294,GPL570,1000,Cardioembolic Stroke,C1531624,Blood,GEO,Microarray,Homo sapiens,23|23, DSA06045,GSE66196,GPL570,393,Bipolar Disorder,C0005586,,GEO,Microarray,Homo sapiens,2|2,DO:A mood disorder that involves alternating periods of mania and depression. DSA06046,GSE56787,GPL16791,316,Facioscapulohumeral Dystrophy,C0238288,,GEO,RNA-Seq,Homo sapiens,8|13,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA06047,GSE66196,GPL570,316,Bipolar Disorder,C0005586,,GEO,Microarray,Homo sapiens,2|2,DO:A mood disorder that involves alternating periods of mania and depression. DSA06048,GSE66207,GPL16791,621,Crohn's Disease,C0010346,Colon,GEO,RNA-Seq,Homo sapiens,13|7,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06049,GSE66207,GPL16791,1000,Crohn's Disease,C0010346,Colon,GEO,RNA-Seq,Homo sapiens,13|7,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06050,GSE66207,GPL16791,145,Crohn's Disease,C0010346,Colon,GEO,RNA-Seq,Homo sapiens,13|6,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06051,GSE66238,GPL17303,1000,Cerebral Aneurysm,C0917996,Temporal artery,GEO,RNA-Seq,Homo sapiens,12|6,EFO:Outpouching of BASILAR ARTERY at the base of the skull. The basilar artery is the most important artery in the posterior cerebral circulation. DSA06052,GSE66273,GPL4133,24,Pre-Eclampsia,C0032914,Placenta,GEO,Microarray,Homo sapiens,5|6,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA06053,GSE66273,GPL4133,20,Hellp Syndrome,C0162739,Placenta,GEO,Microarray,Homo sapiens,5|6,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA06054,GSE66387,GPL19832,0,Breast Cancer,C0678222,Ovary,GEO,Microarray,Homo sapiens,3|6,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06055,GSE66387,GPL19832,1,Breast Cancer,C0678222,Fallopian tube,GEO,Microarray,Homo sapiens,3|6,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06056,GSE66407,GPL19833,0,Crohn's Disease,C0010346,Ascendens,GEO,Microarray,Homo sapiens,14|8,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06057,GSE66407,GPL19833,1000,Crohn's Disease,C0010346,Sigmoideum,GEO,Microarray,Homo sapiens,14|19,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06058,GSE66407,GPL19833,4,Crohn's Disease,C0010346,Ileum,GEO,Microarray,Homo sapiens,6|23,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06059,GSE66407,GPL19833,2,Crohn's Disease,C0010346,Rectum,GEO,Microarray,Homo sapiens,16|13,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06060,GSE66407,GPL19833,483,Crohn's Disease,C0010346,Descendens,GEO,Microarray,Homo sapiens,14|15,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06061,GSE66407,GPL19833,509,Crohn's Disease,C0010346,Transversum,GEO,Microarray,Homo sapiens,13|15,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06062,GSE66407,GPL19833,2,Crohn's Disease,C0010346,Cecum,GEO,Microarray,Homo sapiens,9|9,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06063,GSE66407,GPL19833,2,Crohn's Disease,C0010346,Bulbus durodenum,GEO,Microarray,Homo sapiens,13|1,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06064,GSE66407,GPL19833,1,Ulcerative Colitis,C0009324,Ascendens,GEO,Microarray,Homo sapiens,14|11,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA06065,GSE66407,GPL19833,1000,Ulcerative Colitis,C0009324,Sigmoideum,GEO,Microarray,Homo sapiens,14|53,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA06066,GSE66407,GPL19833,0,Ulcerative Colitis,C0009324,Ileum,GEO,Microarray,Homo sapiens,6|10,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA06067,GSE66407,GPL19833,1000,Ulcerative Colitis,C0009324,Rectum,GEO,Microarray,Homo sapiens,16|41,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA06068,GSE66407,GPL19833,3,Ulcerative Colitis,C0009324,,GEO,Microarray,Homo sapiens,14|24,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA06069,GSE66407,GPL19833,417,Ulcerative Colitis,C0009324,Transversum,GEO,Microarray,Homo sapiens,13|13,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA06070,GSE66407,GPL19833,0,Ulcerative Colitis,C0009324,,GEO,Microarray,Homo sapiens,9|5,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA06071,GSE66407,GPL19833,765,Ulcerative Colitis,C0009324,Bulbus durodenum,GEO,Microarray,Homo sapiens,13|1,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA06072,GSE66430,GPL11154,1000,Gallstones,C0008350,Gall bladder,GEO,RNA-Seq,Homo sapiens,3|1,EFO:The presence of calculi in the gallbladder. DSA06073,GSE66446,GPL11154,679,Cushing's Disease,C0221406,Adipose tissue,GEO,RNA-Seq,Homo sapiens,11|5,DO:A functioning pituitary adenoma that characterized by excess cortisol a primary cause of Cushing's syndrome. DSA06074,GSE66465,GPL6244,13,IgG4-Related Disease,C3203653,,GEO,Microarray,Homo sapiens,4|2,"DO:An autoimmune disease that is characterized by tumefactive lesions, a dense lymphoplasmacytic infiltrate rich in IgG4-positive plasma cells, storiform fibrosis, obliterative phlebitis, autoimmune pancreatitis, and sometimes elevated serum IgG4 levels affecting various organs." DSA06075,GSE66476,GPL6480,1,Q Fever,C0034362,,GEO,Microarray,Homo sapiens,4|6,"DO:A primary bacterial infectious disease that is a zoonotic infectious disease affecting multiple organs, has_material_basis_in Coxiella burnetii, which is transmitted_by inhalation of air contaminated by barnyard dust containing dried placental material, birth fluids, or excreta of infected herd animals, transmitted_by ingestion of contaminated milk, transmitted_by tick bites and transmitted_by contact with infected person. The infection has_symptom fever, has_symptom headache, has_symptom cough, has_symptom pleuritic chest pain, has_symptom myalgia and has_symptom arthralgia." DSA06076,GSE66511,GPL16288,1000,Plaque Psoriasis,C0263361,Skin,GEO,RNA-Seq,Homo sapiens,12|12, DSA06077,GSE66511,GPL16288,1000,Plaque Psoriasis,C0263361,Skin,GEO,RNA-Seq,Homo sapiens,12|12, DSA06078,GSE66573,GPL16791,1000,Relapsing-Remitting Multiple Sclerosis,C0751967,Peripheral blood,GEO,RNA-Seq,Homo sapiens,8|6,"DO:A multiple sclerosis that is characterized by relapse (attacks of symptom flare-ups) followed by remission (periods of recovery). Symptoms may vary from mild to severe, and relapses and remissions may last for days or months. More than 80 percent of people who have MS begin with relapsing-remitting cycles." DSA06079,GSE66634,GPL15103,1000,Pulmonary Fibrosis,C0034069,Lung,GEO,RNA-Seq,Mus musculus,3|3,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA06080,GSE66730,GPL1261,0,Progressive Neurodegeneration,C1854838,Midbrain,GEO,Microarray,Mus musculus,3|4, DSA06081,GSE66730,GPL1261,0,Progressive Neurodegeneration,C1854838,Midbrain,GEO,Microarray,Mus musculus,4|3, DSA06082,GSE66763,GPL16791,648,Multiple Sclerosis,C0026769,,GEO,RNA-Seq,Homo sapiens,6|10,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA06083,GSE66849,GPL5188,0,Dyskeratosis Congenita,C0265965,,GEO,Microarray,Homo sapiens,1|2,"DO:A skin disease characterized by cutaneous pigmentation, premature graying, dystrophy of the nails, leukoplakia of the oral mucosa, continuous lacrimation due to atresia of the lacrimal ducts, often thrombocytopenia, anemia, testicular atrophy in the male carriers and predisposition to cancer." DSA06084,GSE66849,GPL5188,0,Dyskeratosis Congenita,C0265965,,GEO,Microarray,Homo sapiens,1|2,"DO:A skin disease characterized by cutaneous pigmentation, premature graying, dystrophy of the nails, leukoplakia of the oral mucosa, continuous lacrimation due to atresia of the lacrimal ducts, often thrombocytopenia, anemia, testicular atrophy in the male carriers and predisposition to cancer." DSA06085,GSE56787,GPL16791,145,Facioscapulohumeral Dystrophy,C0238288,,GEO,RNA-Seq,Homo sapiens,3|9,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA06086,GSE66936,GPL570,183,Uveitis,C0042164,,GEO,Microarray,Homo sapiens,8|5,"DO:An uveitis that is characterized by inflammation of all layers of the uvea (middle layer) of the eye, which includes the iris, ciliary body, and choroid." DSA06087,GSE66988,GPL6244,92,Multiple Sclerosis,C0026769,,GEO,Microarray,Homo sapiens,4|4,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA06088,GSE66988,GPL6244,18,Multiple Sclerosis,C0026769,,GEO,Microarray,Homo sapiens,4|4,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA06089,GSE66988,GPL6244,118,Multiple Sclerosis,C0026769,,GEO,Microarray,Homo sapiens,4|4,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA06090,GSE13782,GPL1261,1000,Spondylitis,C0038012,Spine,GEO,Microarray,Mus musculus,3|5,MONDO:The inflammation of a vertebra. DSA06091,GSE67067,GPL5175,0,Myotonic Dystrophy Type 1,C0027126,Heart,GEO,Microarray,Homo sapiens,3|3,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA06092,GSE67073,GPL11154,1000,"Dysautonomia, Familial",C0013364,,GEO,RNA-Seq,Homo sapiens,1|2,"DO:A hereditary sensory neuropathy that is characterized by gastrointestinal dysfunction, gastroesophageal reflux, vomiting crises, recurrent pneumonia, seizures, gait abnormalities with loss of ambulation, kyphoscoliosis, postural hypotension, hypertension crises, absence of fungiform papillae on the tongue, decreased deep tendon reflexes, defective lacrimation, and impaired pain and temperature perception and has_material_basis_in homozygous or compound heterozygous mutation in the IKBKAP gene (ELP1) on chromosome 9q31." DSA06093,GSE67073,GPL11154,1000,"Dysautonomia, Familial",C0013364,,GEO,RNA-Seq,Homo sapiens,1|2,"DO:A hereditary sensory neuropathy that is characterized by gastrointestinal dysfunction, gastroesophageal reflux, vomiting crises, recurrent pneumonia, seizures, gait abnormalities with loss of ambulation, kyphoscoliosis, postural hypotension, hypertension crises, absence of fungiform papillae on the tongue, decreased deep tendon reflexes, defective lacrimation, and impaired pain and temperature perception and has_material_basis_in homozygous or compound heterozygous mutation in the IKBKAP gene (ELP1) on chromosome 9q31." DSA06094,GSE37927,GPL15555,427,Pituitary Tumor,C0032019,,GEO,Microarray,Mus musculus,9|21,DO:An endocrine gland cancer located_in the pituitary gland located at the base of the brain. DSA06095,GSE30210,GPL6947,45,Type 1 Diabetes,C0011854,Peripheral blood,GEO,Microarray,Homo sapiens,122|125,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA06096,GSE42230,GPL6246,3,Male Infertility,C0021364,Testis,GEO,Microarray,Mus musculus,3|3,EFO:The inability of the male to effect fertilization of an ovum after a specified period of unprotected intercourse. Male sterility is permanent infertility. DSA06097,GSE19674,GPL8321,1000,Spinal Muscular Atrophy,C0026847,Spinal,GEO,Microarray,Mus musculus,4|4,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA06098,GSE67250,GPL11154|GPL16791,524,Crohn's Disease,C0010346,Colon,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06099,GSE67311,GPL11532,6,Fibromyalgia,C0016053,Peripheral blood,GEO,Microarray,Homo sapiens,75|67,"DO:A syndrome that is is characterized by chronic widespread musculoskeletal pain, fatigue, sleep disturbances, cognitive dysfunction and depression." DSA06100,GSE67333,GPL11154,51,Late-Onset Form of Familial Alzheimer Disease,C0002395,Hippocampus,GEO,RNA-Seq,Homo sapiens,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA06101,GSE67472,GPL16311,82,Asthma,C0004096,,GEO,Microarray,Homo sapiens,43|22,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06102,GSE67472,GPL16311,1000,Asthma,C0004096,,GEO,Microarray,Homo sapiens,43|40,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06103,GSE67515,GPL6096,0,Spinal Cord Disorder,C0037928,Spinal cord,GEO,Microarray,Mus musculus,1|4,EFO:A disease involving the spinal cord. DSA06104,GSE67522,GPL10558,1000,Cervical Cancer,C4048328,Cervix,GEO,Microarray,Homo sapiens,11|20,DO:A female reproductive organ cancer that is located_in the cervix. DSA06105,GSE67522,GPL10558,1000,Cervical Cancer,C4048328,Cervix,GEO,Microarray,Homo sapiens,11|20,DO:A female reproductive organ cancer that is located_in the cervix. DSA06106,GSE67527,GPL6244,0,Spoan Syndrome,C0037773,Skin,GEO,Microarray,Homo sapiens,4|4,"DO:A hereditary spastic paraplegia that is characterized by spasticity of the leg muscles, progressive muscle weakness, paraplegia, muscle wasting in the hands and feet (distal amyotrophy), small stature, developmental delay, learning disorders, speech difficulties (dysarthria), and mood swings, and has_material_basis_in a mutation of the SPG20 gene." DSA06107,GSE67528,GPL11154,94,Autism Spectrum Disorder,C1510586,,GEO,RNA-Seq,Homo sapiens,8|17,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA06108,GSE67528,GPL11154,12,Autism Spectrum Disorder,C1510586,,GEO,RNA-Seq,Homo sapiens,9|20,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA06109,GSE67528,GPL11154,27,Autism Spectrum Disorder,C1510586,,GEO,RNA-Seq,Homo sapiens,11|16,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA06110,GSE67640,GPL10558,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,9|15,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA06111,GSE67764,GPL17077,0,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,3|3,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA06112,GSE67764,GPL17077,134,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,3|3,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA06113,GSE67780,GPL1261,2,Hypoglycemia,C0020615,Muscle,GEO,Microarray,Mus musculus,3|3,DO:A glucose metabolism disease that is characterized by abnormally low levels of blood glucose. DSA06114,GSE67784,GPL11532,10,Familial Amyloid Polyneuropathy,C0206245,,GEO,Microarray,Homo sapiens,43|46,EFO:The familial amyloid neuropathies are a rare group of autosomal dominant neuropathies of autonomic and peripheral nerves. DSA06115,GSE67784,GPL11532,0,Familial Amyloid Polyneuropathy,C0206245,,GEO,Microarray,Homo sapiens,37|41,EFO:The familial amyloid neuropathies are a rare group of autosomal dominant neuropathies of autonomic and peripheral nerves. DSA06116,GSE67784,GPL11532,72,Familial Amyloid Polyneuropathy,C0206245,,GEO,Microarray,Homo sapiens,43|50,EFO:The familial amyloid neuropathies are a rare group of autosomal dominant neuropathies of autonomic and peripheral nerves. DSA06117,GSE67784,GPL11532,0,Familial Amyloid Polyneuropathy,C0206245,,GEO,Microarray,Homo sapiens,37|46,EFO:The familial amyloid neuropathies are a rare group of autosomal dominant neuropathies of autonomic and peripheral nerves. DSA06118,GSE67801,GPL6480,439,Acute Hepatitis B,C0276609,,GEO,Microarray,Homo sapiens,5|5,"EFO:INFLAMMATION of the LIVER in humans caused by a member of the ORTHOHEPADNAVIRUS genus, HEPATITIS B VIRUS. It is primarily transmitted by parenteral exposure, such as transfusion of contaminated blood or blood products, but can also be transmitted via sexual or intimate personal contact." DSA06119,GSE67801,GPL6480,3,Hepatitis B,C0019163,,GEO,Microarray,Homo sapiens,5|4,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus, which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice." DSA06120,GSE67801,GPL6480,0,Hepatitis B,C0019163,,GEO,Microarray,Homo sapiens,5|4,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus, which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice." DSA06121,GSE67812,GPL11154,193,Myotonic Dystrophy,C0027126,Left ventricle,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA06122,GSE67939,GPL16288,631,Breast Cancer,C0678222,,GEO,RNA-Seq,Homo sapiens,2|15,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06123,GSE67945,GPL16791,445,Colon Tumor,C0009375,Colon,GEO,RNA-Seq,Homo sapiens,3|3,DO:A colorectal cancer that is located_in the colon. DSA06124,GSE68004,GPL10558,1000,Kawasaki Disease,C0026691,Whole blood,GEO,Microarray,Homo sapiens,37|57,"DO:A lymphadenitis characterized by swelling of cervical lymph nodes in infants and young children and inflammation of medium-sized blood vessels located_in body, has_symptom fever, has_symptom congestion of ocular conjunctivae, has_symptom reddening of lips, has_symptom reddening of oral cavity, has_symptom protuberance of tongue papillae and has_symptom edema of extremities." DSA06125,GSE68004,GPL10558,1000,Group A Streptococcal Infections,C0554628,Whole blood,GEO,Microarray,Homo sapiens,37|14,MSH:Infections with bacteria of the genus STREPTOCOCCUS. DSA06126,GSE68004,GPL10558,1000,Kawasaki Disease,C0026691,Whole blood,GEO,Microarray,Homo sapiens,37|13,"DO:A lymphadenitis characterized by swelling of cervical lymph nodes in infants and young children and inflammation of medium-sized blood vessels located_in body, has_symptom fever, has_symptom congestion of ocular conjunctivae, has_symptom reddening of lips, has_symptom reddening of oral cavity, has_symptom protuberance of tongue papillae and has_symptom edema of extremities." DSA06127,GSE68036,GPL10787,14,Biphasic Inflammatory,,Lung,GEO,Microarray,Mus musculus,5|4, DSA06128,GSE68036,GPL10787,172,Biphasic Inflammatory,,Lung,GEO,Microarray,Mus musculus,5|5, DSA06129,GSE68036,GPL10787,10,Biphasic Inflammatory,,Lung,GEO,Microarray,Mus musculus,5|4, DSA06130,GSE68036,GPL10787,0,Biphasic Inflammatory,,Lung,GEO,Microarray,Mus musculus,5|4, DSA06131,GSE68036,GPL10787,743,Biphasic Inflammatory,,Lung,GEO,Microarray,Mus musculus,5|5, DSA06132,GSE68036,GPL10787,1,Biphasic Inflammatory,,Lung,GEO,Microarray,Mus musculus,5|5, DSA06133,GSE68036,GPL10787,107,Biphasic Inflammatory,,Lung,GEO,Microarray,Mus musculus,4|5, DSA06134,GSE68036,GPL10787,0,Biphasic Inflammatory,,Lung,GEO,Microarray,Mus musculus,5|5, DSA06135,GSE52130,GPL10558,1000,Lichen Planus,C0023646,Oral epithelium,GEO,Microarray,Homo sapiens,7|7,"DO:A lichen disease that is located_in skin, located_in tongue or located_in oral mucosa, which presents itself in the form of papules, lesions or rashes." DSA06136,GSE68133,GPL1261,4,Diabetes,C0011847,Pancreas,GEO,Microarray,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA06137,GSE68183,GPL16686,0,Diabetes,C0011847,Skin,GEO,Microarray,Homo sapiens,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA06138,GSE68309,GPL6883,0,Varicose Vein,C0042345,,GEO,Microarray,Homo sapiens,7|7,"DO:A vein disease that is characterized by swollen, twisted veins visible just under the surface of the skin." DSA06139,GSE68316,GPL20113,1000,Hypertrophic Cardiomyopathy,C0007194,Heart,GEO,Microarray,Homo sapiens,5|7,DO:A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations. DSA06140,GSE68419,GPL9250,1000,Dextran Sodium Sulfate Induced-Colitis,,Colon,GEO,RNA-Seq,Mus musculus,3|3, DSA06141,GSE52130,GPL10558,1000,Lichen Planus,C0023646,,GEO,Microarray,Homo sapiens,4|5,"DO:A lichen disease that is located_in skin, located_in tongue or located_in oral mucosa, which presents itself in the form of papules, lesions or rashes." DSA06142,GSE23598,GPL1261,136,Cardiomyopathy,C0878544,Heart,GEO,Microarray,Mus musculus,2|2,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA06143,GSE68570,GPL10558,879,Crohn's Disease,C0010346,Ileum,GEO,Microarray,Homo sapiens,5|6,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06144,GSE68605,GPL570,5,Amyotrophic Lateral Sclerosis,C0002736,,GEO,Microarray,Homo sapiens,3|8,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA06145,GSE68607,GPL20149,744,Amyotrophic Lateral Sclerosis,C0002736,,GEO,Microarray,Homo sapiens,15|31,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA06146,GSE68607,GPL20149,1000,Amyotrophic Lateral Sclerosis,C0002736,,GEO,Microarray,Homo sapiens,15|23,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA06147,GSE68689,GPL20171,0,Rheumatoid Arthritis,C0003873,Whole blood,GEO,Microarray,Homo sapiens,5|16,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA06148,GSE68741,GPL96,0,Lyme Disease,C0024198,,GEO,Microarray,Homo sapiens,3|2,"DO:A primary bacterial infectious disease that results_in infection, has_material_basis_in Borrelia burgdorferi, which is transmitted_by blacklegged tick (Ixodes scapularis) or transmitted_by western blacklegged tick (Ixodes pacificus). The infection has_symptom fever, has_symptom headache, has_symptom fatigue, and has_symptom skin rash called erythema migrans. If left untreated, infection can spread to joints, the heart, and the nervous system." DSA06149,GSE68741,GPL96,0,Lyme Disease,C0024198,,GEO,Microarray,Homo sapiens,3|2,"DO:A primary bacterial infectious disease that results_in infection, has_material_basis_in Borrelia burgdorferi, which is transmitted_by blacklegged tick (Ixodes scapularis) or transmitted_by western blacklegged tick (Ixodes pacificus). The infection has_symptom fever, has_symptom headache, has_symptom fatigue, and has_symptom skin rash called erythema migrans. If left untreated, infection can spread to joints, the heart, and the nervous system." DSA06150,GSE68741,GPL96,0,Lyme Disease,C0024198,,GEO,Microarray,Homo sapiens,3|3,"DO:A primary bacterial infectious disease that results_in infection, has_material_basis_in Borrelia burgdorferi, which is transmitted_by blacklegged tick (Ixodes scapularis) or transmitted_by western blacklegged tick (Ixodes pacificus). The infection has_symptom fever, has_symptom headache, has_symptom fatigue, and has_symptom skin rash called erythema migrans. If left untreated, infection can spread to joints, the heart, and the nervous system." DSA06151,GSE68799,GPL11154,1000,Nasopharyngeal Carcinoma,C2931822,Nasopharynx,GEO,RNA-Seq,Homo sapiens,4|42,"DO:A pharynx cancer that is located in the nasopharynx, the uppermost region of the pharynx or throat, where the nasal passages and auditory tubes join the remainder of the upper respiratory tract." DSA06152,GSE68801,GPL570,1000,Patchy Type Disease,,Skin,GEO,Microarray,Homo sapiens,36|22, DSA06153,GSE68801,GPL570,0,Patchy Type Disease,,Skin,GEO,Microarray,Homo sapiens,36|20, DSA06154,GSE68801,GPL570,672,Transient Patchy Type Disease,,Skin,GEO,Microarray,Homo sapiens,36|6, DSA06155,GSE68801,GPL570,34,Transient Patchy Type Disease,,Skin,GEO,Microarray,Homo sapiens,36|6, DSA06156,GSE68801,GPL570,1000,Alopecia Totalis,C0263504,Skin,GEO,Microarray,Homo sapiens,36|9,HPO:Loss of all scalp hair. DSA06157,GSE68801,GPL570,1000,Alopecia Universalis,C0263505,Skin,GEO,Microarray,Homo sapiens,36|23,DO:An autoimmune disease resulting in the loss of hair on the scalp and elsewhere on the body initially causing bald spots. DSA06158,GSE68857,GPL8321,1000,Dilated Cardiomyopathy,C0007193,Left ventricle,GEO,Microarray,Mus musculus,10|10,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA06159,GSE68857,GPL8321,1000,Dilated Cardiomyopathy,C0007193,Left ventricle,GEO,Microarray,Mus musculus,12|12,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA06160,GSE68925,GPL11154,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,Blood,GEO,RNA-Seq,Homo sapiens,3|4,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA06161,GSE23598,GPL1261,305,Cardiomyopathy,C0878544,Heart,GEO,Microarray,Mus musculus,2|2,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA06162,GSE69063,GPL19983,327,Anaphylaxis,C0002792,Peripheral blood,GEO,Microarray,Homo sapiens,10|16,HPO:An acute hypersensitivity reaction due to exposure to a previously encountered antigen. DSA06163,GSE69063,GPL19983,1000,Anaphylaxis,C0002792,Peripheral blood,GEO,Microarray,Homo sapiens,10|17,HPO:An acute hypersensitivity reaction due to exposure to a previously encountered antigen. DSA06164,GSE69063,GPL19983,1000,Sepsis,C0243026,Peripheral blood,GEO,Microarray,Homo sapiens,11|30,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA06165,GSE69063,GPL19983,1000,Sepsis,C0243026,Peripheral blood,GEO,Microarray,Homo sapiens,11|27,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA06166,GSE69063,GPL19983,1000,Head Trauma,,Peripheral blood,GEO,Microarray,Homo sapiens,12|17, DSA06167,GSE69063,GPL19983,1000,Head Trauma,,Peripheral blood,GEO,Microarray,Homo sapiens,12|13, DSA06168,GSE69066,GPL571,0,Peroxisome Biogenesis Disorders,C1832200,,GEO,Microarray,Homo sapiens,1|2,"MONDO:Peroxisome biogenesis disorders, Zellweger syndrome spectrum (PBD-ZSS) is a group of autosomal recessive disorders affecting the formation of functional peroxisomes, characterized by sensorineural hearing loss, pigmentary retinal degeneration, multiple organ dysfunction and psychomotor impairment, and is comprised of the phenotypic variants Zellweger syndrome (ZS), neonatal adrenoleukodystrophy (NALD) and infantile Refsum disease (IRD)." DSA06169,GSE69090,GPL10558,1000,Atypical Hemolytic Uremic Syndrome;Common Variable Immune Deficiency,,,GEO,Microarray,Homo sapiens,3|3, DSA06170,GSE69093,GPL10558,0,Chronic Sinusitis,C0149516,,GEO,Microarray,Homo sapiens,11|13,EFO:An acute or chronic inflammatory process affecting the mucous membranes of any sinus cavity. DSA06171,GSE69093,GPL10558,2,Chronic Sinusitis,C0149516,,GEO,Microarray,Homo sapiens,12|12,EFO:An acute or chronic inflammatory process affecting the mucous membranes of any sinus cavity. DSA06172,GSE69175,GPL15520,1000,Spinal Muscular Atrophy,C0026847,,GEO,RNA-Seq,Homo sapiens,2|2,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA06173,GSE69197,GPL11154,960,Renal Cell Carcinoma,C0007134,Kidney,GEO,RNA-Seq,Homo sapiens,3|3,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA06174,GSE69210,GPL13497,63,Down Syndrome,C0013080,Thymus,GEO,Microarray,Homo sapiens,10|10,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA06175,GSE69391,GPL570,1000,Hutchinson-Gilford Progeria Syndrome,C0033300,Skin,GEO,Microarray,Homo sapiens,3|6,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA06176,GSE69391,GPL570,1000,Hutchinson-Gilford Progeria Syndrome,C0033300,Skin,GEO,Microarray,Homo sapiens,3|6,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA06177,GSE69416,GPL17077,0,Pulmonary Arterial Hypertension,C2973725,Lung,GEO,Microarray,Homo sapiens,2|2,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA06178,GSE69416,GPL17077,0,Pulmonary Arterial Hypertension,C2973725,Lung,GEO,Microarray,Homo sapiens,2|2,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA06179,GSE69416,GPL17077,0,Pulmonary Arterial Hypertension,C2973725,Lung,GEO,Microarray,Homo sapiens,2|2,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA06180,GSE69446,GPL10999,440,Crohn's Disease,C0010346,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06181,GSE69446,GPL10999,174,Crohn's Disease,C0010346,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06182,GSE69486,GPL10558,0,Bipolar Disorder,C0005586,Skin,GEO,Microarray,Homo sapiens,2|10,DO:A mood disorder that involves alternating periods of mania and depression. DSA06183,GSE69528,GPL10558,355,Type 2 Diabetes Mellitus,C0011847,Whole blood,GEO,Microarray,Homo sapiens,28|27,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA06184,GSE69549,GPL11154,1000,Coeliac Disease,C0007570,,GEO,RNA-Seq,Homo sapiens,11|15,"DO:An autoimmune disease of gastrointestinal tract that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite." DSA06185,GSE69549,GPL11154,1000,Coeliac Disease,C0007570,,GEO,RNA-Seq,Homo sapiens,11|14,"DO:An autoimmune disease of gastrointestinal tract that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite." DSA06186,GSE69549,GPL11154,357,Coeliac Disease,C0007570,,GEO,RNA-Seq,Homo sapiens,10|13,"DO:An autoimmune disease of gastrointestinal tract that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite." DSA06187,GSE69557,GPL6244,0,HIV Infection,C0019693,,GEO,Microarray,Homo sapiens,2|2,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA06188,GSE69597,GPL16791,1000,Leishmaniasis,C0023281,Whole blood,GEO,RNA-Seq,Homo sapiens,47|17,"DO:A parasitic protozoa infectious disease that involves infection caused by protozoan parasite of the genus Leishmania, which is transmitted by the bite of sand fly (subfamily Phlebotominae)." DSA06189,GSE69597,GPL16791,1000,Brucellosis,C0006309,Whole blood,GEO,RNA-Seq,Homo sapiens,47|76,"DO:A primary bacterial infectious disease that is caused by the bacteria of the genus Brucella, when humans come in contact with contaminated animals or animal products or ingestion of infected food products. The disease has_symptom fever, has_symptom sweat, has_symptom headache, has_symptom back pain, has_symptom physical weakness, has_symptom joint pain and has_symptom fatigue." DSA06190,GSE69597,GPL16791,3,Brucellosis,C0006309,Whole blood,GEO,RNA-Seq,Homo sapiens,47|29,"DO:A primary bacterial infectious disease that is caused by the bacteria of the genus Brucella, when humans come in contact with contaminated animals or animal products or ingestion of infected food products. The disease has_symptom fever, has_symptom sweat, has_symptom headache, has_symptom back pain, has_symptom physical weakness, has_symptom joint pain and has_symptom fatigue." DSA06191,GSE69621,GPL5973,0,Myeloproliferative Disorder,C0027022,,GEO,Microarray,Mus musculus,1|2,"DO:A myeloid neoplasm that is characterized by a group of slow growing blood cancers in which large numbers of abnormal red blood cells, white blood cells, or platelets grow and spread in the bone marrow and the peripheral blood." DSA06192,GSE69683,GPL13158,0,Asthma,C0004096,Blood,GEO,Microarray,Homo sapiens,34|37,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06193,GSE69683,GPL13158,6,Asthma,C0004096,Blood,GEO,Microarray,Homo sapiens,53|40,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06194,GSE69683,GPL13158,8,Asthma,C0004096,Blood,GEO,Microarray,Homo sapiens,34|161,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06195,GSE69683,GPL13158,1000,Asthma,C0004096,Blood,GEO,Microarray,Homo sapiens,53|85,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06196,GSE69683,GPL13158,29,Asthma,C0004096,Blood,GEO,Microarray,Homo sapiens,34|43,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06197,GSE69683,GPL13158,1000,Asthma,C0004096,Blood,GEO,Microarray,Homo sapiens,53|45,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06198,GSE69732,GPL14951,0,Non-Small Cell Lung Cancer,C0007131,Peripheral blood,GEO,Microarray,Homo sapiens,3|3,DO:A respiratory system cancer that is located_in the lung. DSA06199,GSE44711,GPL10558,107,Pre-Eclampsia,C0032914,Placenta,GEO,Microarray,Homo sapiens,8|8,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA06200,GSE21933,GPL6254,1000,Non-Small Cell Lung Cancer,C0007131,Lung,GEO,Microarray,Homo sapiens,21|21,DO:A respiratory system cancer that is located_in the lung. DSA06201,GSE52558,GPL10787,0,Diabetes,C0011847,Small intestine,GEO,Microarray,Mus musculus,5|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA06202,GSE69762,GPL6244,1000,Crohn's Disease,C0010346,,GEO,Microarray,Homo sapiens,14|16,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06203,GSE69988,GPL15207,739,Charcot-Marie-Tooth Disease Type 1A,C0007959,,GEO,Microarray,Homo sapiens,2|4,"DO:A hereditary sensory neuropathy characterized by progressively reduced sensation to pain, temperature, and touch, loss of myelinated and unmyelinated fibers, and hypotonia with onset at birth or in early childhood." DSA06204,GSE70019,GPL10904,5,Schnitzler Syndrome,C0524988,,GEO,Microarray,Homo sapiens,3|3,"DO:A hypersensitivity reaction type IV disease that is characterized by chronic urticarial rash and monoclonal IgM gammopathy, has_symptom rash, intermittent fever, arthralgia, and lymphadenopathy." DSA06205,GSE70031,GPL13112,729,Chronic Myeloid Leukemia,C0023473,Bone marrow,GEO,RNA-Seq,Mus musculus,2|2,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA06206,GSE70031,GPL13112,1000,Chronic Myeloid Leukemia,C0023473,Bone marrow,GEO,RNA-Seq,Mus musculus,1|1,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA06207,GSE70031,GPL13112,1000,Chronic Myeloid Leukemia,C0023473,Bone marrow,GEO,RNA-Seq,Mus musculus,1|1,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA06208,GSE70213,GPL6246,1000,Nemaline Myopathy,C0206157,Quadriceps,GEO,Microarray,Mus musculus,6|6,"DO:A congenital muscular dystrophy characterized by muscle weakness, cognitive impairment and brain abnormalities and has_material_basis_in mutation to the POMT1 gene that encodes O-mannosyltransferase." DSA06209,GSE70213,GPL6246,1000,Nemaline Myopathy,C0206157,Soleus,GEO,Microarray,Mus musculus,6|6,"DO:A congenital muscular dystrophy characterized by muscle weakness, cognitive impairment and brain abnormalities and has_material_basis_in mutation to the POMT1 gene that encodes O-mannosyltransferase." DSA06210,GSE70404,GPL16791,364,Metastatic Prostate Cancer,C0936223,,GEO,RNA-Seq,Homo sapiens,4|4,EFO:A carcinoma that arises from the prostate gland and has spread to other anatomic sites. DSA06211,GSE70468,GPL17077,0,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,7|7,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA06212,GSE70468,GPL17077,1,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,7|7,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA06213,GSE70469,GPL20650,1000,Crohn's Disease,C0010346,Colon,GEO,Microarray,Homo sapiens,4|7,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06214,GSE70469,GPL20650,1000,Crohn's Disease,C0010346,Peripheral blood,GEO,Microarray,Homo sapiens,4|3,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06215,GSE70604,GPL2986,55,Oral Squamous Cell Carcinoma,C0585362,Lymph node,GEO,Microarray,Homo sapiens,1|7,"EFO:A squamous cell carcinoma arising from the oral cavity. It affects predominantly adults in their fifth and sixth decades of life and is associated with alcohol and tobacco use. Human papillomavirus is present in approximately half of the cases. It is characterized by a tendency to metastasize early to the lymph nodes. When the tumor is small, patients are often asymptomatic. Physical examination may reveal erythematous or white lesions or plaques. The majority of patients present with signs and symptoms of locally advanced disease including mucosal ulceration, pain, difficulty with speaking, chewing, and swallowing, bleeding, weight loss, and neck swelling. Patients may also present with swollen neck lymph nodes without any symptoms from the oropharyngeal tumor. The most significant prognostic factors are the size of the tumor and the lymph nodes status." DSA06216,GSE70604,GPL2986,1000,Oral Squamous Cell Carcinoma,C0585362,,GEO,Microarray,Homo sapiens,5|7,"EFO:A squamous cell carcinoma arising from the oral cavity. It affects predominantly adults in their fifth and sixth decades of life and is associated with alcohol and tobacco use. Human papillomavirus is present in approximately half of the cases. It is characterized by a tendency to metastasize early to the lymph nodes. When the tumor is small, patients are often asymptomatic. Physical examination may reveal erythematous or white lesions or plaques. The majority of patients present with signs and symptoms of locally advanced disease including mucosal ulceration, pain, difficulty with speaking, chewing, and swallowing, bleeding, weight loss, and neck swelling. Patients may also present with swollen neck lymph nodes without any symptoms from the oropharyngeal tumor. The most significant prognostic factors are the size of the tumor and the lymph nodes status." DSA06217,GSE70659,GPL6885,0,Age-Related Hearing Loss,,Cochlea,GEO,Microarray,Mus musculus,3|3, DSA06218,GSE70752,GPL10904,271,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,8|8,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA06219,GSE70752,GPL10904,226,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,8|8,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA06220,GSE52558,GPL10787,0,Diabetes,C0011847,Small intestine,GEO,Microarray,Mus musculus,5|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA06221,GSE52557,GPL10787,0,Diabetes,C0011847,Small intestine,GEO,Microarray,Mus musculus,5|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA06222,GSE52557,GPL10787,1,Diabetes,C0011847,Small intestine,GEO,Microarray,Mus musculus,5|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA06223,GSE72005,GPL16570,829,Asthma,C0004096,Lung,GEO,Microarray,Mus musculus,3|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06224,GSE70818,GPL570,292,Xeroderma Pigmentosum,C0043346,Skin,GEO,Microarray,Homo sapiens,5|3,DO:A syndrome that is characterized by a deficiency in the ability to repair ultraviolet damage that has_material_basis_in autosomal recessive inheritance of DNA repair. DSA06225,GSE70818,GPL570,144,Xeroderma Pigmentosum Variant,C1848410,Skin,GEO,Microarray,Homo sapiens,5|3,"DO:A xeroderma pigmentosum characterized by normal DNA excision repair, but defective postreplication repair that has_material_basis_in mutations in the POLH gene on chromosome 6p21.1." DSA06226,GSE70866,GPL14550,569,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,Microarray,Homo sapiens,4|19,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA06227,GSE70866,GPL14550,1000,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,Microarray,Homo sapiens,16|93,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA06228,GSE70955,GPL15207,1000,Duchenne Muscular Dystrophy,C0013264,,GEO,Microarray,Homo sapiens,3|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA06229,GSE71010,GPL5188,105,Juvenile Idiopathic Arthritis,C3890205,,GEO,Microarray,Homo sapiens,43|35,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA06230,GSE71010,GPL5188,1000,Cystic Fibrosis,C0010674,,GEO,Microarray,Homo sapiens,43|15,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA06231,GSE7116,GPL570,1,Multiple Myeloma,C0026764,,GEO,Microarray,Homo sapiens,5|11,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA06232,GSE7116,GPL570,143,Multiple Myeloma,C0026764,,GEO,Microarray,Homo sapiens,5|10,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA06233,GSE70489,GPL1261,0,Glucose Intolerance,C0271650,Skeletal muscle,GEO,Microarray,Mus musculus,3|3,"DO:A glucose metabolism disease that is characterized by blood glucose levels are high, but not high enough to be classified as type 2 diabetes." DSA06234,GSE70489,GPL1261,2,Glucose Intolerance,C0271650,Skeletal muscle,GEO,Microarray,Mus musculus,3|3,"DO:A glucose metabolism disease that is characterized by blood glucose levels are high, but not high enough to be classified as type 2 diabetes." DSA06235,GSE71192,GPL11154,1000,Breast Cancer,C0678222,,GEO,RNA-Seq,Homo sapiens,2|6,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06236,GSE71220,GPL11532,0,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,16|149,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA06237,GSE71220,GPL11532,133,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,28|256,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA06238,GSE71220,GPL11532,0,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,5|39,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA06239,GSE71220,GPL11532,0,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,8|116,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA06240,GSE71226,GPL570,0,Coronary Heart Disease,C0010068,Peripheral blood,GEO,Microarray,Homo sapiens,3|3,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA06241,GSE71233,GPL13112,23,Mecp2 Duplication Syndrome,C1846058,Hippocampus,GEO,RNA-Seq,Mus musculus,3|3,"DO:A syndromic X-linked intellectual disability characterized by moderate to profound intellectual disability, infantile hypotonia, mild dysmorphic features, poor speech development, autistic features, seizures, progressive spasticity, and recurrent infections in males that has_material_basis_in duplication or triplication of the MECP2 gene on chromosome Xq28." DSA06242,GSE71234,GPL13112,14,Mecp2 Duplication Syndrome,C1846058,Hippocampus,GEO,RNA-Seq,Mus musculus,3|3,"DO:A syndromic X-linked intellectual disability characterized by moderate to profound intellectual disability, infantile hypotonia, mild dysmorphic features, poor speech development, autistic features, seizures, progressive spasticity, and recurrent infections in males that has_material_basis_in duplication or triplication of the MECP2 gene on chromosome Xq28." DSA06243,GSE62547,GPL570,1000,Hepatic Steatosis,C2711227,Foreskin,GEO,Microarray,Homo sapiens,3|3,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA06244,GSE71356,GPL2700,0,Obstructive Sleep Apnea,C4237227,,GEO,Microarray,Homo sapiens,4|4,"DO:A sleep apnea that is characterized by repeated collapse and obstruction of the upper airway during sleep, which results in reduced airflow (hypopnea) or complete airflow cessation (apnea), oxygen desaturation, and arousals from sleep." DSA06245,GSE71370,GPL16268,0,Rheumatoid Arthritis,C0003873,Peripheral blood,GEO,Microarray,Homo sapiens,8|9,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA06246,GSE71370,GPL16268,1000,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,8|9,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA06247,GSE71415,GPL19099,0,Morbid Obesity,C0028756,Adipose tissue,GEO,Microarray,Homo sapiens,4|4,"EFO:The condition of weighing two, three, or more times the ideal weight, so called because it is associated with many serious and life-threatening disorders. In the BODY MASS INDEX, morbid obesity is defined as having a BMI greater than 40.0 kg/m2." DSA06248,GSE71426,GPL11202,0,Obliterative Airway Disease,,Lung,GEO,Microarray,Mus musculus,3|3, DSA06249,GSE71426,GPL11202,0,Obliterative Airway Disease,,Lung,GEO,Microarray,Mus musculus,3|3, DSA06250,GSE71426,GPL11202,0,Obliterative Airway Disease,,Lung,GEO,Microarray,Mus musculus,3|3, DSA06251,GSE71426,GPL11202,0,Obliterative Airway Disease,,Lung,GEO,Microarray,Mus musculus,3|3, DSA06252,GSE71449,GPL19197,64,Juvenile Myelomonocytic Leukemia,C0349639,Bone marrow,GEO,Microarray,Homo sapiens,7|16,DO:A myelodysplastic/myeloproliferative neoplasm that is characterized by the uncontrolled growth of monocytes. DSA06253,GSE52752,GPL13915,1000,Hepatitis B,C0019163,Human hepatocyte,GEO,Microarray,Homo sapiens,6|5,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus, which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice." DSA06254,GSE52752,GPL13915,1000,Hepatitis C,C0019196,Human hepatocyte,GEO,Microarray,Homo sapiens,6|5,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA06255,GSE71613,GPL11154,1000,Restrictive Cardiomyopathy,C0007196,Heart,GEO,RNA-Seq,Homo sapiens,4|2,"DO:An intrinsic cardiomyopathy characterized by impaired ventricular filling, with normal or decreased diastolic volume of either or both ventricles typically resulting from increased stiffness of the myocardium." DSA06256,GSE71613,GPL11154,436,Dilated Cardiomyopathy,C0007193,Heart,GEO,RNA-Seq,Homo sapiens,4|2,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA06257,GSE71664,GPL10558,153,Williams Syndrome,C0175702,,GEO,Microarray,Homo sapiens,6|6,"DO:A syndrome that is characterized by mild to moderate intellectual disability, a broad forehead, a short nose with a broad tip, full cheeks, and a wide mouth with full lips and difficulty with visual-spatial tasks and has_material_basis_in hemizygous deletion of 1.5 to 1.8 Mb on chromosome 7q11.23." DSA06258,GSE71664,GPL10558,82,Williams Syndrome,C0175702,,GEO,Microarray,Homo sapiens,6|6,"DO:A syndrome that is characterized by mild to moderate intellectual disability, a broad forehead, a short nose with a broad tip, full cheeks, and a wide mouth with full lips and difficulty with visual-spatial tasks and has_material_basis_in hemizygous deletion of 1.5 to 1.8 Mb on chromosome 7q11.23." DSA06259,GSE71706,GPL6096,678,Esophageal Tumor,C0014859,Spleen,GEO,Microarray,Mus musculus,3|6,DO:A esophageal cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06260,GSE71709,GPL16791,1000,Dyskeratosis Congenita,C0265965,,GEO,RNA-Seq,Homo sapiens,2|1,"DO:A skin disease characterized by cutaneous pigmentation, premature graying, dystrophy of the nails, leukoplakia of the oral mucosa, continuous lacrimation due to atresia of the lacrimal ducts, often thrombocytopenia, anemia, testicular atrophy in the male carriers and predisposition to cancer." DSA06261,GSE71709,GPL16791,11,Dyskeratosis Congenita,C0265965,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A skin disease characterized by cutaneous pigmentation, premature graying, dystrophy of the nails, leukoplakia of the oral mucosa, continuous lacrimation due to atresia of the lacrimal ducts, often thrombocytopenia, anemia, testicular atrophy in the male carriers and predisposition to cancer." DSA06262,GSE71730,GPL570,1000,Crohn's Disease,C0010346,,GEO,Microarray,Homo sapiens,10|22,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06263,GSE71730,GPL570,1000,Ulcerative Colitis,C0009324,,GEO,Microarray,Homo sapiens,10|15,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA06264,GSE71799,GPL570,1000,Cystic Fibrosis,C0010674,,GEO,Microarray,Homo sapiens,31|103,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA06265,GSE71846,GPL6885,0,Blast Traumatic Brain Injury,,Brain,GEO,Microarray,Mus musculus,5|5, DSA06266,GSE71920,GPL6887,845,Inflammatory Bowel Disease,C0021390,Colon,GEO,Microarray,Mus musculus,3|3,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA06267,GSE71935,GPL570,1000,Juvenile Myelomonocytic Leukemia,C0349639,Bone marrow,GEO,Microarray,Homo sapiens,9|17,DO:A myelodysplastic/myeloproliferative neoplasm that is characterized by the uncontrolled growth of monocytes. DSA06268,GSE71956,GPL10558,0,Graves Disease,C0018213,Blood,GEO,Microarray,Homo sapiens,10|15,"DO:An autoimmune disease of endocrine system that involves production of excessive amount of thyroid hormones, located_in thyroid gland." DSA06269,GSE71956,GPL10558,0,Graves Disease,C0018213,Blood,GEO,Microarray,Homo sapiens,8|16,"DO:An autoimmune disease of endocrine system that involves production of excessive amount of thyroid hormones, located_in thyroid gland." DSA06270,GSE72026,GPL17077,1000,Intravascular Large B-Cell Lymphoma,C1292753,,GEO,Microarray,Homo sapiens,4|4,"EFO:Primary effusion lymphoma (PEL) is a large B-cell lymphoma located in the body cavities, characterized by pleural, peritoneal, and pericardial fluid lymphomatous effusions and that is always associated with human herpes virus-8 (HHV-8)." DSA06271,GSE72039,GPL11533,0,Prion Disease,C0162534,Brain,GEO,Microarray,Mus musculus,8|7,"DO:A brain disease that is characterized by brain damage resulting from the abnormal folding, clumping and accumulation of cellular proteins in the brain induced by prion proteins." DSA06272,GSE72073,GPL17586,329,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,3|5,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA06273,GSE72149,GPL1261,1000,Autism,C1510586,,GEO,Microarray,Mus musculus,3|3,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA06274,GSE72149,GPL1261,1000,Autism,C1510586,,GEO,Microarray,Mus musculus,3|3,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA06275,GSE72151,GPL6246,1000,Muscular Dystrophy,C0026850,Calf muscle,GEO,Microarray,Mus musculus,5|5,"DO:A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted." DSA06276,GSE72151,GPL6246,1000,Muscular Dystrophy,C0026850,Calf muscle,GEO,Microarray,Mus musculus,5|5,"DO:A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted." DSA06277,GSE72151,GPL6246,1000,Muscular Dystrophy,C0026850,Calf muscle,GEO,Microarray,Mus musculus,5|5,"DO:A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted." DSA06278,GSE72213,GPL17077,1000,Multiple Myeloma,C0026764,Bone marrow,GEO,Microarray,Homo sapiens,3|19,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA06279,GSE72213,GPL17077,1000,Multiple Myeloma,C0026764,Bone marrow,GEO,Microarray,Homo sapiens,3|7,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA06280,GSE72220,GPL5175,1000,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,45|57,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06281,GSE72220,GPL5175,1000,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,45|57,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06282,GSE72267,GPL571,0,Parkinson's Disease,C0030567,Blood,GEO,Microarray,Homo sapiens,19|40,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA06283,GSE72269,GPL17586,30,Pilocytic Astrocytoma,C0334583,Glia tissue,GEO,Microarray,Homo sapiens,2|3,DO:A childhood low-grade glioma that is characterized by cells that look like fibers when viewed under a microscope and is located_in the brain. DSA06284,GSE72269,GPL17586,0,Glioblastoma Multiforme,C1621958,Glia tissue,GEO,Microarray,Homo sapiens,2|4,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA06285,GSE72304,GPL10332,1000,Renal Cell Carcinoma,C0007134,Kidney,GEO,Microarray,Homo sapiens,4|4,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA06286,GSE72304,GPL10332,994,Renal Cell Carcinoma,C0007134,Kidney,GEO,Microarray,Homo sapiens,4|4,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA06287,GSE72304,GPL10332,1000,Renal Cell Carcinoma,C0007134,Chest wall,GEO,Microarray,Homo sapiens,4|4,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA06288,GSE52752,GPL13915,1000,Hepatitis B,C0019163,Human hepatocyte,GEO,Microarray,Homo sapiens,6|7,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus, which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice." DSA06289,GSE52752,GPL13915,1000,Hepatitis C,C0019196,Human hepatocyte,GEO,Microarray,Homo sapiens,6|5,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA06290,GSE72326,GPL10558,1000,Kidney Disease,C0022658,Whole Blood,GEO,Microarray,Homo sapiens,21|25,DO:A kidney disease that is characterized by an inflammation of the kidneys. DSA06291,GSE72326,GPL10558,1000,Systemic Lupus Erythematosus,C0024141,Whole Blood,GEO,Microarray,Homo sapiens,20|157,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA06292,GSE72377,GPL10558,11,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,20|15,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA06293,GSE72377,GPL10558,0,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,9|6,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA06294,GSE72377,GPL10558,0,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,5|9,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA06295,GSE72377,GPL10558,1,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,11|8,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA06296,GSE72377,GPL10558,0,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,8|8,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA06297,GSE72377,GPL10558,2,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,20|15,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA06298,GSE72377,GPL10558,0,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,19|12,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA06299,GSE72484,GPL11180,1000,Colon Cancer,C0699790,Liver,GEO,Microarray,Mus musculus,4|4,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06300,GSE72484,GPL11180,1000,Colon Cancer,C0699790,Liver,GEO,Microarray,Mus musculus,4|4,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06301,GSE72484,GPL11180,1000,Colon Cancer,C0699790,Liver,GEO,Microarray,Mus musculus,4|4,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06302,GSE72484,GPL11180,1000,Colon Cancer,C0699790,Liver,GEO,Microarray,Mus musculus,4|4,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06303,GSE72509,GPL16791,1000,Systemic Lupus Erythematosus,C0024141,Whole blood,GEO,RNA-Seq,Homo sapiens,18|24,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA06304,GSE72509,GPL16791,1000,Systemic Lupus Erythematosus,C0024141,Whole blood,GEO,RNA-Seq,Homo sapiens,18|23,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA06305,GSE72509,GPL16791,1000,Systemic Lupus Erythematosus,C0024141,Whole blood,GEO,RNA-Seq,Homo sapiens,18|52,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA06306,GSE72540,GPL16699,11,Chronic Spontaneous Urticaria,C0578870,Skin,GEO,Microarray,Homo sapiens,8|13,HPO:Urticaria characterized by spontaneously recurring hives for 6 weeks or longer. DSA06307,GSE72540,GPL16699,1000,Chronic Spontaneous Urticaria,C0578870,,GEO,Microarray,Homo sapiens,8|10,HPO:Urticaria characterized by spontaneously recurring hives for 6 weeks or longer. DSA06308,GSE72541,GPL16699,162,Chronic Spontaneous Urticaria,C0578870,Blood,GEO,Microarray,Homo sapiens,10|20,HPO:Urticaria characterized by spontaneously recurring hives for 6 weeks or longer. DSA06309,GSE72589,GPL16791,822,Pola1 Deficiency,,Skin,GEO,RNA-Seq,Homo sapiens,14|4, DSA06310,GSE72589,GPL16791,383,Pola1 Deficiency,,Skin,GEO,RNA-Seq,Homo sapiens,14|8, DSA06311,GSE72625,GPL10558,1000,Common Variable Immunodeficiency,C0009447,Duodenum,GEO,Microarray,Homo sapiens,17|12,DO:An agammaglobulinemia that is characterized by low Ig levels with phenotypically normal B cells that can proliferate but do not develop into Ig-producing cells and that esults in insufficient production of antibodies needed to respond to exposure of pathogens. DSA06312,GSE72625,GPL10558,136,Common Variable Immunodeficiency,C0009447,Duodenum,GEO,Microarray,Homo sapiens,17|8,DO:An agammaglobulinemia that is characterized by low Ig levels with phenotypically normal B cells that can proliferate but do not develop into Ig-producing cells and that esults in insufficient production of antibodies needed to respond to exposure of pathogens. DSA06313,GSE72625,GPL10558,1000,Coeliac Disease,C0007570,Duodenum,GEO,Microarray,Homo sapiens,17|10,"DO:An autoimmune disease of gastrointestinal tract that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite." DSA06314,GSE72644,GPL6480,0,Tumorigenesis,C0007621,Breast,GEO,Microarray,Homo sapiens,9|9,"MSH:Cell changes manifested by escape from control mechanisms, increased growth potential, alterations in the cell surface, karyotypic abnormalities, morphological and biochemical deviations from the norm, and other attributes conferring the ability to invade, metastasize, and kill." DSA06315,GSE72644,GPL6480,191,Tumorigenesis,C0007621,Breast,GEO,Microarray,Homo sapiens,9|9,"MSH:Cell changes manifested by escape from control mechanisms, increased growth potential, alterations in the cell surface, karyotypic abnormalities, morphological and biochemical deviations from the norm, and other attributes conferring the ability to invade, metastasize, and kill." DSA06316,GSE72644,GPL6480,409,Tumorigenesis,C0007621,Breast,GEO,Microarray,Homo sapiens,9|9,"MSH:Cell changes manifested by escape from control mechanisms, increased growth potential, alterations in the cell surface, karyotypic abnormalities, morphological and biochemical deviations from the norm, and other attributes conferring the ability to invade, metastasize, and kill." DSA06317,GSE72702,GPL13158,1000,Hidradenitis,C0085160,Skin,GEO,Microarray,Homo sapiens,13|17,"DO:A sweat gland disease that is characterized by inflammation of the apocrine sweat glands and has_symptom erythema, edema, papules, plaques, pruritis, and pain." DSA06318,GSE72713,GPL11154,1000,Chronic Rhinosinusitis,C0149516,Sphenoid sinus mucosa,GEO,RNA-Seq,Homo sapiens,3|3,EFO:An acute or chronic inflammatory process affecting the mucous membranes of any sinus cavity. DSA06319,GSE72713,GPL11154,582,Chronic Rhinosinusitis,C0149516,Sphenoid sinus mucosa,GEO,RNA-Seq,Homo sapiens,3|3,EFO:An acute or chronic inflammatory process affecting the mucous membranes of any sinus cavity. DSA06320,GSE72748,GPL10999,33,Guillain-Barre Syndrome,C0018378,Blood,GEO,RNA-Seq,Homo sapiens,3|3,DO:An autoimmune disease of peripheral nervous system that causes body's immune system to attack part of the peripheral nervous system. DSA06321,GSE72780,GPL570,0,Crohn's Disease,C0010346,Ileum,GEO,Microarray,Homo sapiens,4|5,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06322,GSE72920,GPL10558,1000,Prostate Cancer,C0600139,,GEO,Microarray,Homo sapiens,15|15,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06323,GSE72922,GPL14951,0,Clear Cell Renal Cell Carcinoma,C0007134,,GEO,Microarray,Homo sapiens,2|2,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA06324,GSE72922,GPL14951,0,Clear Cell Renal Cell Carcinoma,C0007134,,GEO,Microarray,Homo sapiens,9|10,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA06325,GSE72946,GPL17077,1000,Leptospirosis,C0023364,Whole blood,GEO,Microarray,Homo sapiens,4|16,"DO:A primary bacterial infectious disease that involves systemic infection, has_material_basis_in Leptospira, which is transmitted by contact with water, food, or soil containing urine from the infected animals. The infection has symptom jaundice, has symptom chills, has symptom fever, has symptom muscle pain, and has symptom hepatomegaly." DSA06326,GSE72946,GPL17077,0,Leptospirosis,C0023364,Whole blood,GEO,Microarray,Homo sapiens,4|13,"DO:A primary bacterial infectious disease that involves systemic infection, has_material_basis_in Leptospira, which is transmitted by contact with water, food, or soil containing urine from the infected animals. The infection has symptom jaundice, has symptom chills, has symptom fever, has symptom muscle pain, and has symptom hepatomegaly." DSA06327,GSE72994,GPL11154,74,Lissencephaly,C0266463,Forebrain,GEO,RNA-Seq,Homo sapiens,2|5,DO:A congenital nervous system abnormality characterized by the absence of folds in the cerebral cortex and caused_by defective neuronal migration during the 12th to 24th weeks of gestation. DSA06328,GSE72999,GPL13497,18,Sickle Cell Disease,C0002895,Whole blood,GEO,Microarray,Homo sapiens,3|2,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA06329,GSE72999,GPL13497,0,Sickle Cell Disease,C0002895,Whole blood,GEO,Microarray,Homo sapiens,3|5,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA06330,GSE72999,GPL13497,8,Sickle Cell Disease,C0002895,Whole blood,GEO,Microarray,Homo sapiens,3|3,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA06331,GSE72999,GPL13497,387,Sickle Cell Disease,C0002895,Whole blood,GEO,Microarray,Homo sapiens,3|4,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA06332,GSE73018,GPL17021,80,Behavioral Sensitization,,Brain,GEO,RNA-Seq,Mus musculus,4|3, DSA06333,GSE73018,GPL17021,11,Behavioral Sensitization,,Brain,GEO,RNA-Seq,Mus musculus,4|4, DSA06334,GSE73018,GPL17021,158,Behavioral Sensitization,,Brain,GEO,RNA-Seq,Mus musculus,4|4, DSA06335,GSE73018,GPL17021,1000,Behavioral Sensitization,,Brain,GEO,RNA-Seq,Mus musculus,4|4, DSA06336,GSE73040,GPL6244,18,Amyloidosis,C0002726,Bone marrow,GEO,Microarray,Homo sapiens,5|9,"DO:A disease of metabolsism that is characterized by extracellular tissue deposition of mis-folded amyloid fibrils built up by twisted protofilaments, deposited in the spaces between the cells of vital organs, causing disruption of organ tissue structure and function. These deposits may result in a wide range of clinical manifestations depending upon their type, location, and the amount of deposition." DSA06337,GSE73078,GPL17077,0,Obesity,C0028754,Vastus lateralis,GEO,Microarray,Homo sapiens,7|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA06338,GSE73078,GPL17077,0,Obesity,C0028754,Vastus lateralis,GEO,Microarray,Homo sapiens,3|6,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA06339,GSE73129,GPL570,0,Schizophrenia,C0036341,,GEO,Microarray,Homo sapiens,21|16,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA06340,GSE73129,GPL570,1000,Schizophrenia,C0036341,,GEO,Microarray,Homo sapiens,19|19,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA06341,GSE73129,GPL570,6,Schizophrenia,C0036341,,GEO,Microarray,Homo sapiens,20|20,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA06342,GSE73295,GPL7202,1000,Liver Cancer,C2239176,,GEO,Microarray,Mus musculus,4|4,DO:A hepatobiliary system cancer that is located_in the liver. DSA06343,GSE73295,GPL7202,1000,Liver Cancer,C2239176,,GEO,Microarray,Mus musculus,4|4,DO:A hepatobiliary system cancer that is located_in the liver. DSA06344,GSE52752,GPL13915,1000,Hepatitis B,C0019163,Human hepatocyte,GEO,Microarray,Homo sapiens,6|4,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus, which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice." DSA06345,GSE52752,GPL13915,168,Hepatitis C,C0019196,Human hepatocyte,GEO,Microarray,Homo sapiens,6|3,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA06346,GSE73336,GPL15103,1000,Ulcer,C0041582,Stomach,GEO,RNA-Seq,Mus musculus,4|4,"MONDO:A lesion on the surface of the skin or a mucous surface, produced by the sloughing of inflammatory necrotic tissue." DSA06347,GSE73378,GPL10558,0,Subarachnoid Hemorrhage,C0038525,Whole blood,GEO,Microarray,Homo sapiens,43|68,EFO:Intracranial hemorrhage into the subarachnoid space. DSA06348,GSE73378,GPL10558,0,Perinatal Subarachnoid Hemorrhage,C0270192,Whole blood,GEO,Microarray,Homo sapiens,64|35,"MSH:Bleeding into the intracranial or spinal SUBARACHNOID SPACE, most resulting from INTRACRANIAL ANEURYSM rupture. It can occur after traumatic injuries (SUBARACHNOID HEMORRHAGE, TRAUMATIC). Clinical features include HEADACHE; NAUSEA; VOMITING, nuchal rigidity, variable neurological deficits and reduced mental status." DSA06349,GSE73394,GPL10739,1000,Sarcoidosis,C0036202,,GEO,Microarray,Homo sapiens,8|9,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA06350,GSE73394,GPL10739,1000,Sarcoidosis,C0036202,,GEO,Microarray,Homo sapiens,12|17,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA06351,GSE73395,GPL570,491,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,28|29,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA06352,GSE73451,GPL6887,1000,Lewis Lung Carcinoma,,Spleen,GEO,Microarray,Mus musculus,10|9, DSA06353,GSE73451,GPL6887,1000,Lewis Lung Carcinoma,,Spleen,GEO,Microarray,Mus musculus,10|7, DSA06354,GSE73451,GPL6887,1000,Lewis Lung Carcinoma,,Spleen,GEO,Microarray,Mus musculus,10|6, DSA06355,GSE73451,GPL6887,1000,Lewis Lung Carcinoma,,Spleen,GEO,Microarray,Mus musculus,10|10, DSA06356,GSE73457,GPL13112,1000,Leukemia,C0023418,,GEO,RNA-Seq,Mus musculus,2|2,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA06357,GSE73457,GPL13112,1000,Leukemia,C0023418,,GEO,RNA-Seq,Mus musculus,2|2,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA06358,GSE73457,GPL13112,1000,Leukemia,C0023418,,GEO,RNA-Seq,Mus musculus,2|2,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA06359,GSE73457,GPL13112,1000,Leukemia,C0023418,,GEO,RNA-Seq,Mus musculus,2|2,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA06360,GSE73457,GPL13112,1000,Leukemia,C0023418,,GEO,RNA-Seq,Mus musculus,2|2,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA06361,GSE73461,GPL10558,1000,Henoch-Schoenlein Purpura,C0034152,Whole Blood,GEO,Microarray,Homo sapiens,26|9,"DO:A hypersensitivity vasculitis that is characterized by purpura (purplish plaques), arthralgia, gastrointestinal upset, and/or glomerulonephritis, and may be related to increased immune response following an infection." DSA06362,GSE73461,GPL10558,21,Henoch-Schoenlein Purpura,C0034152,Whole Blood,GEO,Microarray,Homo sapiens,29|9,"DO:A hypersensitivity vasculitis that is characterized by purpura (purplish plaques), arthralgia, gastrointestinal upset, and/or glomerulonephritis, and may be related to increased immune response following an infection." DSA06363,GSE73461,GPL10558,1000,Juvenile Idiopathic Arthritis,C3890205,Whole Blood,GEO,Microarray,Homo sapiens,26|41,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA06364,GSE73461,GPL10558,1000,Juvenile Idiopathic Arthritis,C3890205,Whole Blood,GEO,Microarray,Homo sapiens,29|25,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA06365,GSE73461,GPL10558,1000,Kawasaki Disease,C0026691,Whole Blood,GEO,Microarray,Homo sapiens,26|35,"DO:A lymphadenitis characterized by swelling of cervical lymph nodes in infants and young children and inflammation of medium-sized blood vessels located_in body, has_symptom fever, has_symptom congestion of ocular conjunctivae, has_symptom reddening of lips, has_symptom reddening of oral cavity, has_symptom protuberance of tongue papillae and has_symptom edema of extremities." DSA06366,GSE73461,GPL10558,1000,Kawasaki Disease,C0026691,Whole Blood,GEO,Microarray,Homo sapiens,29|42,"DO:A lymphadenitis characterized by swelling of cervical lymph nodes in infants and young children and inflammation of medium-sized blood vessels located_in body, has_symptom fever, has_symptom congestion of ocular conjunctivae, has_symptom reddening of lips, has_symptom reddening of oral cavity, has_symptom protuberance of tongue papillae and has_symptom edema of extremities." DSA06367,GSE73462,GPL6947,179,Kawasaki Disease,C0026691,Whole Blood,GEO,Microarray,Homo sapiens,10|1,"DO:A lymphadenitis characterized by swelling of cervical lymph nodes in infants and young children and inflammation of medium-sized blood vessels located_in body, has_symptom fever, has_symptom congestion of ocular conjunctivae, has_symptom reddening of lips, has_symptom reddening of oral cavity, has_symptom protuberance of tongue papillae and has_symptom edema of extremities." DSA06368,GSE73468,GPL13112,10,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06369,GSE73468,GPL13112,2,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06370,GSE73468,GPL13112,5,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06371,GSE73468,GPL13112,3,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06372,GSE73468,GPL13112,869,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06373,GSE73468,GPL13112,127,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06374,GSE73468,GPL13112,54,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06375,GSE73468,GPL13112,257,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06376,GSE73468,GPL13112,1,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06377,GSE73468,GPL13112,2,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06378,GSE73468,GPL13112,633,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06379,GSE73468,GPL13112,52,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06380,GSE73468,GPL13112,891,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06381,GSE73468,GPL13112,1000,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06382,GSE73468,GPL13112,0,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06383,GSE73468,GPL13112,5,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06384,GSE73468,GPL13112,1000,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06385,GSE73468,GPL13112,1000,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06386,GSE73468,GPL13112,12,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|5,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06387,GSE73468,GPL13112,1,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06388,GSE73468,GPL13112,5,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06389,GSE73468,GPL13112,2,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06390,GSE73468,GPL13112,93,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06391,GSE73468,GPL13112,92,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06392,GSE73468,GPL13112,1,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06393,GSE73468,GPL13112,98,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06394,GSE73468,GPL13112,3,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06395,GSE73468,GPL13112,2,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|5,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06396,GSE73468,GPL13112,149,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06397,GSE73468,GPL13112,123,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06398,GSE73468,GPL13112,14,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06399,GSE73468,GPL13112,4,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06400,GSE73468,GPL13112,0,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06401,GSE73468,GPL13112,2,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06402,GSE73468,GPL13112,1000,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06403,GSE73468,GPL13112,14,Huntington's Disease,C0020179,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06404,GSE73503,GPL13112,34,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06405,GSE73503,GPL13112,4,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06406,GSE73503,GPL13112,0,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06407,GSE73503,GPL13112,5,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06408,GSE73503,GPL13112,18,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06409,GSE73503,GPL13112,728,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06410,GSE73503,GPL13112,339,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06411,GSE73503,GPL13112,48,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06412,GSE73503,GPL13112,1,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06413,GSE73503,GPL13112,6,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06414,GSE73503,GPL13112,1000,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06415,GSE73503,GPL13112,987,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06416,GSE73503,GPL13112,1000,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06417,GSE73503,GPL13112,301,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06418,GSE73503,GPL13112,24,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06419,GSE73503,GPL13112,2,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06420,GSE73503,GPL13112,595,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06421,GSE73503,GPL13112,1000,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06422,GSE73503,GPL13112,602,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06423,GSE73503,GPL13112,1,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06424,GSE73503,GPL13112,0,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06425,GSE73503,GPL13112,0,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06426,GSE73503,GPL13112,1000,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06427,GSE73503,GPL13112,491,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06428,GSE73503,GPL13112,68,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06429,GSE73503,GPL13112,193,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06430,GSE73503,GPL13112,4,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|3,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06431,GSE73503,GPL13112,3,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|5,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06432,GSE73503,GPL13112,1000,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06433,GSE73503,GPL13112,88,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06434,GSE73503,GPL13112,75,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06435,GSE73503,GPL13112,113,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06436,GSE73503,GPL13112,3,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06437,GSE73503,GPL13112,0,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06438,GSE73503,GPL13112,608,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06439,GSE73503,GPL13112,184,Huntington's Disease,C0020179,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06440,GSE73512,GPL15207,1000,Ichthyosis Hystrix of Curth-Macklin,C0432307,Skin,GEO,Microarray,Homo sapiens,3|1,MONDO:Ichthyosis hystrix of Curth-Macklin (IHCM) is a rare type of keratinopathic ichthyosis that is characterized by the presence of severe hyperkeratotic lesions and palmoplantar keratoderma (PPK). DSA06441,GSE73579,GPL16791,34,Polycystic Liver Disease,C0158683,,GEO,RNA-Seq,Homo sapiens,4|8,MONDO:An autosomal dominant inherited condition characterized by many cysts of various sizes scattered throughout the liver. DSA06442,GSE73592,GPL1261,1000,Neutrophilic Dermatosis,C1142272,Bone marrow,GEO,Microarray,Mus musculus,5|5, DSA06443,GSE73622,GPL6244,0,Endometriosis,C0014175,,GEO,Microarray,Homo sapiens,5|5,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA06444,GSE73622,GPL6244,0,Endometriosis,C0014175,Endometrium,GEO,Microarray,Homo sapiens,4|5,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA06445,GSE73622,GPL6244,2,Endometriosis,C0014175,Endometrium,GEO,Microarray,Homo sapiens,5|3,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA06446,GSE73622,GPL6244,3,Endometriosis,C0014175,Endometrium,GEO,Microarray,Homo sapiens,4|3,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA06447,GSE73622,GPL6244,0,Endometriosis,C0014175,Endometrium,GEO,Microarray,Homo sapiens,5|3,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA06448,GSE73622,GPL6244,0,Endometriosis,C0014175,,GEO,Microarray,Homo sapiens,5|3,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA06449,GSE73655,GPL6244,1,Huntington's Disease,C0020179,Subcutaneous adipose tissue,GEO,Microarray,Homo sapiens,7|8,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06450,GSE73655,GPL6244,0,Huntington's Disease,C0020179,Subcutaneous adipose tissue,GEO,Microarray,Homo sapiens,7|5,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06451,GSE73674,GPL20982,0,Systemic Sclerosis [Scleroderma],C2364016,,GEO,Microarray,Homo sapiens,9|6, DSA06452,GSE73674,GPL20982,0,Systemic Sclerosis [Scleroderma],C2364016,,GEO,Microarray,Homo sapiens,9|6, DSA06453,GSE73674,GPL20982,0,Systemic Sclerosis [Scleroderma],C2364016,,GEO,Microarray,Homo sapiens,9|20, DSA06454,GSE73674,GPL20982,0,Systemic Sclerosis [Scleroderma],C2364016,,GEO,Microarray,Homo sapiens,9|20, DSA06455,GSE73680,GPL17077,0,Randall's Plaque,,,GEO,Microarray,Homo sapiens,9|9, DSA06456,GSE73680,GPL17077,0,Randall's Plaque,,,GEO,Microarray,Homo sapiens,18|20, DSA06457,GSE73680,GPL17077,0,Randall's Plaque,,,GEO,Microarray,Homo sapiens,4|9, DSA06458,GSE73680,GPL17077,1,Randall's Plaque,,,GEO,Microarray,Homo sapiens,2|20, DSA06459,GSE73754,GPL10558,0,Ankylosing Spondylitis,C0038013,Whole blood,GEO,Microarray,Homo sapiens,10|6,"DO:A bone inflammation disease that results_in inflammation in the joints of the spine and pelvis. The disease has_symptom pain, has_symptom stiffness in the spine, has_symptom stiffness in the neck, has_symptom stiffness in the hips, has_symptom stiffness in the jaw and has_symptom stiffness in the rib cage." DSA06460,GSE73754,GPL10558,24,Ankylosing Spondylitis,C0038013,Whole blood,GEO,Microarray,Homo sapiens,10|19,"DO:A bone inflammation disease that results_in inflammation in the joints of the spine and pelvis. The disease has_symptom pain, has_symptom stiffness in the spine, has_symptom stiffness in the neck, has_symptom stiffness in the hips, has_symptom stiffness in the jaw and has_symptom stiffness in the rib cage." DSA06461,GSE73754,GPL10558,637,Ankylosing Spondylitis,C0038013,Whole blood,GEO,Microarray,Homo sapiens,10|7,"DO:A bone inflammation disease that results_in inflammation in the joints of the spine and pelvis. The disease has_symptom pain, has_symptom stiffness in the spine, has_symptom stiffness in the neck, has_symptom stiffness in the hips, has_symptom stiffness in the jaw and has_symptom stiffness in the rib cage." DSA06462,GSE73754,GPL10558,485,Ankylosing Spondylitis,C0038013,Whole blood,GEO,Microarray,Homo sapiens,10|20,"DO:A bone inflammation disease that results_in inflammation in the joints of the spine and pelvis. The disease has_symptom pain, has_symptom stiffness in the spine, has_symptom stiffness in the neck, has_symptom stiffness in the hips, has_symptom stiffness in the jaw and has_symptom stiffness in the rib cage." DSA06463,GSE73809,GPL17586,0,Graft Versus Host Disease,C0018133,,GEO,Microarray,Homo sapiens,13|11,MONDO:An immune system disorder that occurs after allogeneic hematopoietic stem cell transplant and is a reaction of donor immune cells against host tissues. Activated donor T cells damage host epithelial cells after an inflammatory cascade that begins with the preparative regimen. DSA06464,GSE73882,GPL17400,0,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Mus musculus,2|5,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA06465,GSE73882,GPL17400,0,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Mus musculus,4|5,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA06466,GSE73882,GPL17400,16,Crohn's Disease,C0010346,Colon,GEO,Microarray,Mus musculus,2|5,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06467,GSE73882,GPL17400,1,Crohn's Disease,C0010346,Colon,GEO,Microarray,Mus musculus,4|5,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06468,GSE73953,GPL4133,1000,IgA Nephropathy,C0017661,,GEO,Microarray,Homo sapiens,2|15,DO:A glomerulonephritis characterized by build up of IgA antibody in the glomerulus. DSA06469,GSE73953,GPL4133,1000,Membranous Nephropathy,C0017665,,GEO,Microarray,Homo sapiens,2|8,"EFO:A type of glomerulonephritis that is characterized by the accumulation of immune deposits ( COMPLEMENT MEMBRANE ATTACK COMPLEX) on the outer aspect of the GLOMERULAR BASEMENT MEMBRANE. It progresses from subepithelial dense deposits, to basement membrane reaction and eventual thickening of the basement membrane." DSA06470,GSE73968,GPL6244,381,Acquired Immunodeficiency Syndrome,C0001175,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA06471,GSE73968,GPL6244,229,Acquired Immunodeficiency Syndrome,C0001175,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA06472,GSE74000,GPL570,1000,Liver Failure,C0085605,Liver,GEO,Microarray,Homo sapiens,2|3,"MSH:Severe inability of the LIVER to perform its normal metabolic functions, as evidenced by severe JAUNDICE and abnormal serum levels of AMMONIA; BILIRUBIN; ALKALINE PHOSPHATASE; ASPARTATE AMINOTRANSFERASE; LACTATE DEHYDROGENASES; and albumin/globulin ratio. (Blakiston's Gould Medical Dictionary, 4th ed)" DSA06473,GSE74048,GPL20115,0,Gallbladder Cancer,C0235782,Gallbladder,GEO,Microarray,Homo sapiens,3|3,DO:A biliary tract cancer that is located_in the gallbladder. DSA06474,GSE74068,GPL17077,0,X-Linked Dystonia Disorders-Parkinsonism,C1839130,Whole blood,GEO,Microarray,Homo sapiens,13|9,DO:A focal dystonia that is characterized by parkinsonism that is frequently accompanied by focal dystonia and progresses to generalized dystonia that has_material_basis_in X-linked recessive inheritance of SVA retrotransposon insertion in the intron of the TATA-box binding protein associated factor 1 gene (TAF1) on chromosome Xq13.1. DSA06475,GSE74068,GPL17077,24,X-Linked Dystonia Disorders-Parkinsonism,C1839130,,GEO,Microarray,Homo sapiens,10|15,DO:A focal dystonia that is characterized by parkinsonism that is frequently accompanied by focal dystonia and progresses to generalized dystonia that has_material_basis_in X-linked recessive inheritance of SVA retrotransposon insertion in the intron of the TATA-box binding protein associated factor 1 gene (TAF1) on chromosome Xq13.1. DSA06476,GSE74075,GPL6883,529,Asthma,C0004096,Sputum,GEO,Microarray,Homo sapiens,6|10,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06477,GSE74089,GPL13497,1000,Avascular Necrosis of Femoral Head,C0410480,,GEO,Microarray,Homo sapiens,4|4,"MONDO:Avascular necrosis of femoral head (ANFH) is a severely disabling disease characterised by progressive groin pain, a limping gait, leg length discrepancy, collapse of the subchondral bone, limitation of hip function and eventual degeneration of the hip joint requiring total hip arthroplasty." DSA06478,GSE74123,GPL6244,1000,Fuchs Endothelial Corneal Dystrophy,C0016781,Corneal endothelium,GEO,Microarray,Homo sapiens,4|4,"DO:A corneal dystrophy that is characterized by corneal edema, iris atrophy, and secondary angle-closure glaucoma caused by an inflammatory or infectious insult that causes the endothelium to fail to pump aqueous humor from the cornea, leading to fluid accumulation, microcystic edema, and angle-closure glaucoma." DSA06479,GSE74144,GPL13497,0,Hypertension,C0020538,,GEO,Microarray,Homo sapiens,8|14,DO:An artery disease characterized by chronic elevated blood pressure in the arteries. DSA06480,GSE74144,GPL13497,181,Hypertension,C0020538,,GEO,Microarray,Homo sapiens,8|14,DO:An artery disease characterized by chronic elevated blood pressure in the arteries. DSA06481,GSE74163,GPL10558,964,Bronchiolitis Obliterans,C0006272,Lung,GEO,Microarray,Homo sapiens,3|3,DO:A obstructive lung disease involving obstruction of the bronchioles due to inflammation and fibrosis which occurs as a complication of various lung conditions or physiological insults. DSA06482,GSE74263,GPL11154,1000,X-Linked Syndromic Intellectual Disability,C0796250,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A syndrome characterized by intellectual disability, focal dystonia of the hands and dysarthria." DSA06483,GSE74358,GPL570,0,Bipolar Disorder,C0005586,,GEO,Microarray,Homo sapiens,2|2,DO:A mood disorder that involves alternating periods of mania and depression. DSA06484,GSE74358,GPL570,2,Bipolar Disorder,C0005586,,GEO,Microarray,Homo sapiens,4|4,DO:A mood disorder that involves alternating periods of mania and depression. DSA06485,GSE74358,GPL570,0,Bipolar Disorder,C0005586,,GEO,Microarray,Homo sapiens,4|4,DO:A mood disorder that involves alternating periods of mania and depression. DSA06486,GSE74358,GPL570,0,Bipolar Disorder,C0005586,,GEO,Microarray,Homo sapiens,4|4,DO:A mood disorder that involves alternating periods of mania and depression. DSA06487,GSE74369,GPL16791,820,Colorectal Carcinoma,C0009402,Colon,GEO,RNA-Seq,Homo sapiens,7|10,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA06488,GSE74369,GPL16791,3,Colorectal Carcinoma,C0009402,Colon,GEO,RNA-Seq,Homo sapiens,7|8,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA06489,GSE74437,GPL6885,146,Alzheimer's Disease,C0002395,Hippocampus,GEO,Microarray,Mus musculus,11|8,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA06490,GSE74437,GPL6885,499,Alzheimer's Disease,C0002395,Frontal cortex,GEO,Microarray,Mus musculus,11|8,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA06491,GSE74438,GPL6885,1000,Alzheimer's Disease,C0002395,Frontal cortex,GEO,Microarray,Mus musculus,12|9,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA06492,GSE74438,GPL6885,263,Alzheimer's Disease,C0002395,Hippocampus,GEO,Microarray,Mus musculus,12|9,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA06493,GSE74451,GPL17077,0,Autosomal Dominant Polycystic Kidney Disease,C0085413,,GEO,Microarray,Homo sapiens,2|4,DO:A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3. DSA06494,GSE74451,GPL17077,1000,Autosomal Dominant Polycystic Kidney Disease,C0085413,,GEO,Microarray,Homo sapiens,5|3,DO:A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3. DSA06495,GSE74451,GPL17077,1000,Autosomal Dominant Polycystic Kidney Disease,C0085413,,GEO,Microarray,Homo sapiens,6|4,DO:A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3. DSA06496,GSE74451,GPL17077,142,Autosomal Dominant Polycystic Kidney Disease,C0085413,,GEO,Microarray,Homo sapiens,4|3,DO:A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3. DSA06497,GSE74614,GPL10333,0,Alzheimer's Disease,C0002395,Brain,GEO,Microarray,Mus musculus,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA06498,GSE74614,GPL10333,1000,Alzheimer's Disease,C0002395,Brain,GEO,Microarray,Mus musculus,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA06499,GSE74615,GPL10333,1000,Alzheimer's Disease,C0002395,Brain,GEO,Microarray,Mus musculus,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA06500,GSE74615,GPL10333,1000,Alzheimer's Disease,C0002395,Brain,GEO,Microarray,Mus musculus,7|7,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA06501,GSE74629,GPL10558,422,Pancreatic Ductal Adenocarcinoma,C1335302,Peripheral blood,GEO,Microarray,Homo sapiens,7|12,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA06502,GSE74629,GPL10558,848,Pancreatic Ductal Adenocarcinoma,C1335302,Peripheral blood,GEO,Microarray,Homo sapiens,7|24,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA06503,GSE74697,GPL16791,1000,Psoriasis,C0033860,Skin,GEO,RNA-Seq,Homo sapiens,16|18,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA06504,GSE74737,GPL11154,18,Meth-Dependency Without Psychosis,,Blood,GEO,RNA-Seq,Homo sapiens,10|10, DSA06505,GSE74737,GPL11154,1,Methamphetamine Dependence,C0236733,Blood,GEO,RNA-Seq,Homo sapiens,10|10,DO:A substance abuse that involves the recurring use of amphetamines despite negative consequences. DSA06506,GSE74761,GPL570,1,Alopecia Areata,C0002171,Scalp skin,GEO,Microarray,Homo sapiens,3|3,DO:An autoimmune disease resulting in the loss of hair on the scalp and elsewhere on the body initially causing bald spots. DSA06507,GSE74761,GPL570,2,Alopecia Areata,C0002171,Scalp skin,GEO,Microarray,Homo sapiens,3|2,DO:An autoimmune disease resulting in the loss of hair on the scalp and elsewhere on the body initially causing bald spots. DSA06508,GSE74893,GPL13112,1000,Tuberous Sclerosis Complex,C0041341,Optic nerve,GEO,RNA-Seq,Mus musculus,1|1,DO:A tuberous sclerosis that is characterized by hamartomas in multiple organ systems and has_material_basis_in heterozygous mutation in the TSC1 gene on chromosome 9q34. DSA06509,GSE74986,GPL6480,1000,Asthma,C0004096,Lung,GEO,Microarray,Homo sapiens,12|28,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06510,GSE74986,GPL6480,1000,Asthma,C0004096,Lung,GEO,Microarray,Homo sapiens,12|46,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06511,GSE75011,GPL16791,162,Allergic Rhinitis,C2607914,Blood,GEO,RNA-Seq,Homo sapiens,15|25,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA06512,GSE75011,GPL16791,744,Allergic Rhinitis,C2607914,Blood,GEO,RNA-Seq,Homo sapiens,15|40,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA06513,GSE75023,GPL571,1000,Sarcoidosis,C0036202,,GEO,Microarray,Homo sapiens,12|15,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA06514,GSE75061,GPL11154,1000,Schimke Immuno-Osseous Dysplasia,C0877024,Kidney,GEO,RNA-Seq,Homo sapiens,1|1,"DO:A spondyloepiphyseal dysplasia characterized by short stature with hyperpigmented macules, unusual facies, proteinuria with progressive renal failure, lymphopenia with recurrent infections, and cerebral ischaemia. It has_material_basis_in mutations in the SMARCAL1 gene." DSA06515,GSE61373,GPL1261,180,Congenital Insensitivity To Pain,C1855739,Dorsal root ganglion,GEO,Microarray,Mus musculus,3|3,DO:A hereditary sensory neuropathy characterized by impaired pain and thermal perception in the extremities and selective reduction in small myelinated fibers that has_material_basis_in homozygous mutation in the NGF gene on chromosome 1p13. DSA06516,GSE61373,GPL1261,1,Congenital Insensitivity To Pain,C1855739,Dorsal root ganglion,GEO,Microarray,Mus musculus,3|3,DO:A hereditary sensory neuropathy characterized by impaired pain and thermal perception in the extremities and selective reduction in small myelinated fibers that has_material_basis_in homozygous mutation in the NGF gene on chromosome 1p13. DSA06517,GSE75152,GPL6884,0,Dupuytren's Disease,C4082974,,GEO,Microarray,Homo sapiens,3|4,EFO:A fibromatosis of the palmar fascia characterized by thickening and contracture of the fibrous bands on the palmar surfaces of the hand and fingers. It arises most commonly in men between the ages of 30 and 50. DSA06518,GSE75152,GPL6884,1000,Dupuytren's Disease,C4082974,,GEO,Microarray,Homo sapiens,6|8,EFO:A fibromatosis of the palmar fascia characterized by thickening and contracture of the fibrous bands on the palmar surfaces of the hand and fingers. It arises most commonly in men between the ages of 30 and 50. DSA06519,GSE75152,GPL6884,0,Dupuytren's Disease,C4082974,Connective tissue,GEO,Microarray,Homo sapiens,1|4,EFO:A fibromatosis of the palmar fascia characterized by thickening and contracture of the fibrous bands on the palmar surfaces of the hand and fingers. It arises most commonly in men between the ages of 30 and 50. DSA06520,GSE75152,GPL6884,1000,Dupuytren's Disease,C4082974,Connective tissue,GEO,Microarray,Homo sapiens,2|8,EFO:A fibromatosis of the palmar fascia characterized by thickening and contracture of the fibrous bands on the palmar surfaces of the hand and fingers. It arises most commonly in men between the ages of 30 and 50. DSA06521,GSE75214,GPL6244,1000,Crohn's Disease,C0010346,Colon,GEO,Microarray,Homo sapiens,11|8,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06522,GSE75214,GPL6244,1000,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,11|74,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA06523,GSE75214,GPL6244,1000,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,11|23,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA06524,GSE75214,GPL6244,1000,Crohn's Disease,C0010346,Ileum,GEO,Microarray,Homo sapiens,11|51,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06525,GSE75214,GPL6244,1000,Crohn's Disease,C0010346,Ileum,GEO,Microarray,Homo sapiens,11|16,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA06526,GSE75303,GPL10558,0,Rett Syndrome,C0035372,Brain,GEO,Microarray,Homo sapiens,3|3,"DO:A pervasive developmental disease that is characterized by normal early growth and development followed by a slowing of development, loss of purposeful use of the hands, distinctive hand movements, slowed brain and head growth, problems with walking, seizures, and intellectual disability." DSA06527,GSE75303,GPL10558,0,Rett Syndrome,C0035372,Brain,GEO,Microarray,Homo sapiens,3|3,"DO:A pervasive developmental disease that is characterized by normal early growth and development followed by a slowing of development, loss of purposeful use of the hands, distinctive hand movements, slowed brain and head growth, problems with walking, seizures, and intellectual disability." DSA06528,GSE75343,GPL571,46,Psoriasis,C0033860,Scalp skin,GEO,Microarray,Homo sapiens,10|22,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA06529,GSE75343,GPL571,12,Psoriasis,C0033860,Scalp skin,GEO,Microarray,Homo sapiens,10|13,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA06530,GSE75344,GPL570,0,Graft Versus Host Disease,C0018133,,GEO,Microarray,Homo sapiens,7|4,MONDO:An immune system disorder that occurs after allogeneic hematopoietic stem cell transplant and is a reaction of donor immune cells against host tissues. Activated donor T cells damage host epithelial cells after an inflammatory cascade that begins with the preparative regimen. DSA06531,GSE75344,GPL570,0,Graft Versus Host Disease,C0018133,,GEO,Microarray,Homo sapiens,7|4,MONDO:An immune system disorder that occurs after allogeneic hematopoietic stem cell transplant and is a reaction of donor immune cells against host tissues. Activated donor T cells damage host epithelial cells after an inflammatory cascade that begins with the preparative regimen. DSA06532,GSE75344,GPL570,0,Graft Versus Host Disease,C0018133,,GEO,Microarray,Homo sapiens,7|2,MONDO:An immune system disorder that occurs after allogeneic hematopoietic stem cell transplant and is a reaction of donor immune cells against host tissues. Activated donor T cells damage host epithelial cells after an inflammatory cascade that begins with the preparative regimen. DSA06533,GSE75344,GPL570,0,Graft Versus Host Disease,C0018133,,GEO,Microarray,Homo sapiens,7|2,MONDO:An immune system disorder that occurs after allogeneic hematopoietic stem cell transplant and is a reaction of donor immune cells against host tissues. Activated donor T cells damage host epithelial cells after an inflammatory cascade that begins with the preparative regimen. DSA06534,GSE75344,GPL570,0,Graft Versus Host Disease,C0018133,,GEO,Microarray,Homo sapiens,7|4,MONDO:An immune system disorder that occurs after allogeneic hematopoietic stem cell transplant and is a reaction of donor immune cells against host tissues. Activated donor T cells damage host epithelial cells after an inflammatory cascade that begins with the preparative regimen. DSA06535,GSE75344,GPL570,0,Graft Versus Host Disease,C0018133,,GEO,Microarray,Homo sapiens,7|4,MONDO:An immune system disorder that occurs after allogeneic hematopoietic stem cell transplant and is a reaction of donor immune cells against host tissues. Activated donor T cells damage host epithelial cells after an inflammatory cascade that begins with the preparative regimen. DSA06536,GSE75344,GPL570,0,Graft Versus Host Disease,C0018133,,GEO,Microarray,Homo sapiens,7|1,MONDO:An immune system disorder that occurs after allogeneic hematopoietic stem cell transplant and is a reaction of donor immune cells against host tissues. Activated donor T cells damage host epithelial cells after an inflammatory cascade that begins with the preparative regimen. DSA06537,GSE75344,GPL570,0,Graft Versus Host Disease,C0018133,,GEO,Microarray,Homo sapiens,7|1,MONDO:An immune system disorder that occurs after allogeneic hematopoietic stem cell transplant and is a reaction of donor immune cells against host tissues. Activated donor T cells damage host epithelial cells after an inflammatory cascade that begins with the preparative regimen. DSA06538,GSE75436,GPL570,1000,Intracranial Aneurysm,C0007766,,GEO,Microarray,Homo sapiens,15|15,EFO:Outpouching of BASILAR ARTERY at the base of the skull. The basilar artery is the most important artery in the posterior cerebral circulation. DSA06539,GSE61373,GPL1261,7,Congenital Insensitivity To Pain,C1855739,Dorsal root ganglion,GEO,Microarray,Mus musculus,3|3,DO:A hereditary sensory neuropathy characterized by impaired pain and thermal perception in the extremities and selective reduction in small myelinated fibers that has_material_basis_in homozygous mutation in the NGF gene on chromosome 1p13. DSA06540,GSE75538,GPL18281,33,Tongue Squamous Cell Carcinoma,C0349566,,GEO,Microarray,Homo sapiens,6|6,DO:A head and neck squamous cell carcinoma that is located_in the tongue. DSA06541,GSE75538,GPL18281,135,Tongue Squamous Cell Carcinoma,C0349566,,GEO,Microarray,Homo sapiens,8|8,DO:A head and neck squamous cell carcinoma that is located_in the tongue. DSA06542,GSE75539,GPL10904,355,Tongue Squamous Cell Carcinoma,C0349566,,GEO,Microarray,Homo sapiens,8|7,DO:A head and neck squamous cell carcinoma that is located_in the tongue. DSA06543,GSE75545,GPL13607,272,Hypercholesterolemia,C0020443,,GEO,Microarray,Homo sapiens,2|2,HPO:An increased concentration of cholesterol in the blood. DSA06544,GSE75545,GPL13607,1,Hypercholesterolemia,C0020443,,GEO,Microarray,Homo sapiens,3|3,HPO:An increased concentration of cholesterol in the blood. DSA06545,GSE43497,GPL6244,0,Allergic Rhinitis,C2607914,,GEO,Microarray,Homo sapiens,12|12,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA06546,GSE75672,GPL10558,0,Hypertension,C0020538,,GEO,Microarray,Homo sapiens,11|10,DO:An artery disease characterized by chronic elevated blood pressure in the arteries. DSA06547,GSE43497,GPL6244,0,Allergic Rhinitis,C2607914,,GEO,Microarray,Homo sapiens,11|12,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA06548,GSE43497,GPL6244,0,Allergic Rhinitis,C2607914,,GEO,Microarray,Homo sapiens,11|12,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA06549,GSE43497,GPL6244,0,Allergic Rhinitis,C2607914,,GEO,Microarray,Homo sapiens,12|12,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA06550,GSE43497,GPL6244,0,Allergic Rhinitis,C2607914,Blood,GEO,Microarray,Homo sapiens,12|12,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA06551,GSE75852,GPL16791,1000,Ataxia Telangiectasia,C0004135,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An autosomal recessive cerebellar ataxia that is characterized by cerebellar ataxia, telangiectases, immune defects, and a predisposition to malignancy and that has_material_basis_in homozygous or compound heterozygous mutation in the ATM gene on chromosome 11q22." DSA06552,GSE75852,GPL16791,1000,Ataxia Telangiectasia,C0004135,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An autosomal recessive cerebellar ataxia that is characterized by cerebellar ataxia, telangiectases, immune defects, and a predisposition to malignancy and that has_material_basis_in homozygous or compound heterozygous mutation in the ATM gene on chromosome 11q22." DSA06553,GSE7586,GPL570,425,Malaria,C0024530,Placenta,GEO,Microarray,Homo sapiens,10|7,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA06554,GSE75890,GPL17692,228,Atopic Dermatitis,C0011615,Skin,GEO,Microarray,Homo sapiens,8|5,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA06555,GSE75890,GPL17692,1000,Atopic Dermatitis,C0011615,Skin,GEO,Microarray,Homo sapiens,8|9,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA06556,GSE75890,GPL17692,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,8|9,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA06557,GSE75916,GPL20650,0,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,11|8,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA06558,GSE75916,GPL20650,0,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,10|7,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA06559,GSE76070,GPL21251,1000,Glioblastoma,C0017636,,GEO,Microarray,Homo sapiens,3|3,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA06560,GSE76211,GPL17586,0,Bladder Cancer,C0699885,Bladder,GEO,Microarray,Homo sapiens,3|3,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06561,GSE76220,GPL9115,1000,Sporadic Amyotrophic Lateral Sclerosis,C1862941,,GEO,RNA-Seq,Homo sapiens,8|13,DO:An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SOD1 gene on chromosome 21. The most common type of familial ALS. DSA06562,GSE76237,GPL6244,0,Age Related Macular Degeneration,C0242383,,GEO,Microarray,Homo sapiens,15|14,DO:A degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision. DSA06563,GSE76262,GPL13158,0,Asthma,C0004096,Sputum,GEO,Microarray,Homo sapiens,6|13,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06564,GSE76262,GPL13158,0,Asthma,C0004096,Sputum,GEO,Microarray,Homo sapiens,15|12,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06565,GSE76262,GPL13158,0,Asthma,C0004096,Sputum,GEO,Microarray,Homo sapiens,6|31,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06566,GSE76262,GPL13158,8,Asthma,C0004096,Sputum,GEO,Microarray,Homo sapiens,15|18,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06567,GSE76293,GPL570,1000,Acute Respiratory Distress Syndrome,C0035222,,GEO,Microarray,Homo sapiens,12|12,"DO:A respiratory failure that results from diffuse injury to the endothelium of the lung (as in sepsis, chest trauma, massive blood transfusion, aspiration of the gastric contents, or pneumonia) and is characterized by pulmonary edema with an abnormally high amount of protein in the edematous fluid and by difficult rapid breathing and hypoxemia." DSA06568,GSE76349,GPL10558,1000,B-Acute Lymphoblastic Leukemia,C0279593,,GEO,Microarray,Homo sapiens,8|57,DO:An adult acute lymphoblastic leukemia occurring in adults and that has_material_basis_in B lymphocytes. DSA06569,GSE76349,GPL10558,1000,B-Acute Lymphoblastic Leukemia,C0279593,,GEO,Microarray,Homo sapiens,8|9,DO:An adult acute lymphoblastic leukemia occurring in adults and that has_material_basis_in B lymphocytes. DSA06570,GSE76349,GPL10558,1000,B-Acute Lymphoblastic Leukemia,C0279593,,GEO,Microarray,Homo sapiens,8|18,DO:An adult acute lymphoblastic leukemia occurring in adults and that has_material_basis_in B lymphocytes. DSA06571,GSE76351,GPL11532,1000,Renal Cell Carcinoma,C0007134,Kidney,GEO,Microarray,Homo sapiens,12|12,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA06572,GSE76427,GPL10558,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,52|115,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA06573,GSE76469,GPL13912,1000,Acute Pyelonephritis,C0520575,Kidney,GEO,Microarray,Mus musculus,4|4,MONDO:Sudden onset pyelonephritis. DSA06574,GSE76490,GPL11154,1000,Fragile X Syndrome,C0016667,,GEO,RNA-Seq,Homo sapiens,1|1,"DO:A syndrome that is characterized by moderate to severe mental retardation, macroorchidism, and distinct facial features, including long face, large ears, and prominent jaw, and has_material_basis_in X-linked inheritance and a loss of FMR1 function." DSA06575,GSE76490,GPL11154,1000,Fragile X Syndrome,C0016667,,GEO,RNA-Seq,Homo sapiens,1|1,"DO:A syndrome that is characterized by moderate to severe mental retardation, macroorchidism, and distinct facial features, including long face, large ears, and prominent jaw, and has_material_basis_in X-linked inheritance and a loss of FMR1 function." DSA06576,GSE76490,GPL11154,1000,Fragile X Syndrome,C0016667,,GEO,RNA-Seq,Homo sapiens,1|1,"DO:A syndrome that is characterized by moderate to severe mental retardation, macroorchidism, and distinct facial features, including long face, large ears, and prominent jaw, and has_material_basis_in X-linked inheritance and a loss of FMR1 function." DSA06577,GSE76490,GPL11154,1000,Fragile X Syndrome,C0016667,,GEO,RNA-Seq,Homo sapiens,1|1,"DO:A syndrome that is characterized by moderate to severe mental retardation, macroorchidism, and distinct facial features, including long face, large ears, and prominent jaw, and has_material_basis_in X-linked inheritance and a loss of FMR1 function." DSA06578,GSE76593,GPL6885,0,Myocardial Fibrosis,C0151654,Heart,GEO,Microarray,Mus musculus,4|4,DO:An extrinsic cardiomyopathy that is characterized as an inflammation of the heart muscle. DSA06579,GSE43497,GPL6244,0,Allergic Rhinitis,C2607914,Blood,GEO,Microarray,Homo sapiens,12|12,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA06580,GSE76643,GPL14951,47,Juvenile Neuronal Ceroid Lipofuscinosis,C0751383,,GEO,Microarray,Homo sapiens,3|3,"DO:A neuronal ceroid lipofuscinosis that is characterized by autosomal dominant inhetitance, onset of symptoms (psychiatric manifestations, seizures, cerebellar ataxia, and cognitive decline) in adulthood and has_material_basis_in heterozygous mutation in the DNAJC5 gene (611203) on chromosome 20q13." DSA06581,GSE76643,GPL14951,27,Juvenile Neuronal Ceroid Lipofuscinosis,C0751383,,GEO,Microarray,Homo sapiens,3|3,"DO:A neuronal ceroid lipofuscinosis that is characterized by autosomal dominant inhetitance, onset of symptoms (psychiatric manifestations, seizures, cerebellar ataxia, and cognitive decline) in adulthood and has_material_basis_in heterozygous mutation in the DNAJC5 gene (611203) on chromosome 20q13." DSA06582,GSE76698,GPL5175,12,"Amyotrophic Lateral Sclerosis, Familial",C4551993,,GEO,Microarray,Homo sapiens,3|6, DSA06583,GSE76752,GPL13112,108,Huntington's Disease,C0020179,White adipose tissue,GEO,RNA-Seq,Mus musculus,3|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06584,GSE76752,GPL13112,254,Huntington's Disease,C0020179,White adipose tissue,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06585,GSE76752,GPL13112,63,Huntington's Disease,C0020179,White adipose tissue,GEO,RNA-Seq,Mus musculus,3|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06586,GSE76752,GPL13112,44,Huntington's Disease,C0020179,White adipose tissue,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06587,GSE76752,GPL13112,1000,Huntington's Disease,C0020179,White adipose tissue,GEO,RNA-Seq,Mus musculus,3|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06588,GSE76752,GPL13112,1000,Huntington's Disease,C0020179,White adipose tissue,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06589,GSE76752,GPL13112,5,Huntington's Disease,C0020179,White adipose tissue,GEO,RNA-Seq,Mus musculus,3|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06590,GSE76752,GPL13112,148,Huntington's Disease,C0020179,White adipose tissue,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06591,GSE76752,GPL13112,408,Huntington's Disease,C0020179,White adipose tissue,GEO,RNA-Seq,Mus musculus,3|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06592,GSE76752,GPL13112,302,Huntington's Disease,C0020179,White adipose tissue,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06593,GSE76752,GPL13112,101,Huntington's Disease,C0020179,White adipose tissue,GEO,RNA-Seq,Mus musculus,3|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06594,GSE76752,GPL13112,1000,Huntington's Disease,C0020179,White adipose tissue,GEO,RNA-Seq,Mus musculus,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06595,GSE76807,GPL6480,0,Systemic Sclerosis [Scleroderma],C2364016,Skin,GEO,Microarray,Homo sapiens,5|10, DSA06596,GSE76808,GPL571,1000,Interstitial Lung Disease,C0206062,Lung,GEO,Microarray,Homo sapiens,4|14,"DO:A lung disease that is characterized by inflammation and altered lung interstitium compromising pulmonary function and often has_symptom shortness of breath, dyspnea, and/or cough." DSA06597,GSE76818,GPL13684,1000,Hepatocellular Carcinoma,C0334287,,GEO,Microarray,Mus musculus,3|3,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA06598,GSE76826,GPL17077,0,Major Depressive Disorder,C1269683,,GEO,Microarray,Homo sapiens,7|6,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA06599,GSE76826,GPL17077,0,Major Depressive Disorder,C1269683,,GEO,Microarray,Homo sapiens,5|4,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA06600,GSE76826,GPL17077,0,Major Depressive Disorder,C1269683,,GEO,Microarray,Homo sapiens,7|5,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA06601,GSE76826,GPL17077,0,Major Depressive Disorder,C1269683,,GEO,Microarray,Homo sapiens,5|5,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA06602,GSE43497,GPL6244,0,Allergic Rhinitis,C2607914,Blood,GEO,Microarray,Homo sapiens,12|12,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA06603,GSE76862,GPL17586,0,Miscarriage,C4552766,Placental villi,GEO,Microarray,Homo sapiens,3|3,MSH:A loss of PREGNANCY from natural causes before the 20th week of pregnancy. (2017/18 ICD-10-CM) DSA06604,GSE76878,GPL11154,1000,Neurodevelopmental Disorder,C1535926,,GEO,RNA-Seq,Homo sapiens,2|2,"MSH:These are a group of conditions with onset in the developmental period. The disorders typically manifest early in development, often before the child enters grade school, and are characterized by developmental deficits that produce impairments of personal, social, academic, or occupational functioning. (From DSM-5)." DSA06605,GSE76885,GPL6480,596,Systemic Sclerosis [Scleroderma],C2364016,Skin,GEO,Microarray,Homo sapiens,18|59, DSA06606,GSE76922,GPL11154,1000,22Q11 Deletion Syndrome,C2936346,,GEO,RNA-Seq,Homo sapiens,8|5,"MONDO:22q11.2 deletion syndrome (DS) is a chromosomal anomaly which causes a congenital malformation disorder whose common features include cardiac defects, palatal anomalies, facial dysmorphism, developmental delay and immune deficiency." DSA06607,GSE76923,GPL16686,81,Age Related Macular Degeneration,C0242383,,GEO,Microarray,Homo sapiens,1|2,DO:A degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision. DSA06608,GSE76923,GPL16686,5,Age Related Macular Degeneration,C0242383,,GEO,Microarray,Homo sapiens,1|2,DO:A degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision. DSA06609,GSE76925,GPL10558,1000,Chronic Obstructive Pulmonary Disease,C0024117,Lung,GEO,Microarray,Homo sapiens,25|59,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA06610,GSE76925,GPL10558,92,Chronic Obstructive Pulmonary Disease,C0024117,Lung,GEO,Microarray,Homo sapiens,15|52,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA06611,GSE76940,GPL16570,0,Leukemia,C0023418,Bone marrow,GEO,Microarray,Mus musculus,2|4,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA06612,GSE76987,GPL11154,1000,Colon Serrated Polyposis,C3272797,Colon,GEO,RNA-Seq,Homo sapiens,20|12,"NCI:The presence of multiple serrated polyps in the colon. The polyps are predominantly sessile serrated adenomas/polyps. A minority of the polyps are microvesicular variants of hyperplastic polyps. According to some authors, the polyps are proximal to the sigmoid colon. According to others, the polyps are distributed throughout the entire colon." DSA06613,GSE76987,GPL11154,1000,Colon Serrated Polyposis,C3272797,Colon,GEO,RNA-Seq,Homo sapiens,6|12,"NCI:The presence of multiple serrated polyps in the colon. The polyps are predominantly sessile serrated adenomas/polyps. A minority of the polyps are microvesicular variants of hyperplastic polyps. According to some authors, the polyps are proximal to the sigmoid colon. According to others, the polyps are distributed throughout the entire colon." DSA06614,GSE76987,GPL11154,1000,Sessile Serrated Adenoma/Polyp,C2732618,Colon,GEO,RNA-Seq,Homo sapiens,20|9,"EFO:A sessile serrated polyp is a serrated polyp that demonstrates abnormal cellular proliferation characterized by a proximally displaced proliferative zone, epithelial serrations, and characteristic distorted basilar crypt architecture with crypt dilation, branching, and lateral growth along the muscularis mucosa." DSA06615,GSE76987,GPL11154,1000,Sessile Serrated Adenoma/Polyp,C2732618,Colon,GEO,RNA-Seq,Homo sapiens,15|9,"EFO:A sessile serrated polyp is a serrated polyp that demonstrates abnormal cellular proliferation characterized by a proximally displaced proliferative zone, epithelial serrations, and characteristic distorted basilar crypt architecture with crypt dilation, branching, and lateral growth along the muscularis mucosa." DSA06616,GSE76987,GPL11154,1000,Hyperplastic Polyp,C0333983,Colon,GEO,RNA-Seq,Homo sapiens,20|10,"EFO:A polyp found mainly in the stomach and colon. Microscopically, it is characterized by elongated, serrated crypts lined by proliferative epithelium. Hyperplastic polyps are traditionally considered non-neoplastic, but ras mutation is common, clonality has been demonstrated and biochemical abnormalities and epidemiological associations that occur in colorectal adenomas and carcinomas have been found (WHO Tumors of the Digestive System, 2000)." DSA06617,GSE76987,GPL11154,1000,Hyperplastic Polyp,C0333983,Colon,GEO,RNA-Seq,Homo sapiens,15|10,"EFO:A polyp found mainly in the stomach and colon. Microscopically, it is characterized by elongated, serrated crypts lined by proliferative epithelium. Hyperplastic polyps are traditionally considered non-neoplastic, but ras mutation is common, clonality has been demonstrated and biochemical abnormalities and epidemiological associations that occur in colorectal adenomas and carcinomas have been found (WHO Tumors of the Digestive System, 2000)." DSA06618,GSE76987,GPL11154,1000,Adenomatous Polyps,C0206677,Colon,GEO,RNA-Seq,Homo sapiens,20|10,"MSH:Benign neoplasms derived from glandular epithelium. (From Stedman, 25th ed)" DSA06619,GSE76987,GPL11154,2,Adenomatous Polyps,C0206677,Colon,GEO,RNA-Seq,Homo sapiens,15|10,"MSH:Benign neoplasms derived from glandular epithelium. (From Stedman, 25th ed)" DSA06620,GSE76987,GPL11154,1000,Colon Cancer,C0699790,Colon,GEO,RNA-Seq,Homo sapiens,20|4,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06621,GSE76987,GPL11154,1000,Colon Cancer,C0699790,Colon,GEO,RNA-Seq,Homo sapiens,15|4,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06622,GSE77018,GPL17077,47,Allergy,C1527304,,GEO,Microarray,Homo sapiens,5|6,"DO:An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods." DSA06623,GSE77018,GPL17077,0,Allergy,C1527304,,GEO,Microarray,Homo sapiens,5|6,"DO:An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods." DSA06624,GSE77018,GPL17077,1,Allergy,C1527304,,GEO,Microarray,Homo sapiens,6|4,"DO:An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods." DSA06625,GSE77018,GPL17077,4,Allergy,C1527304,,GEO,Microarray,Homo sapiens,6|4,"DO:An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods." DSA06626,GSE77043,GPL13693,1000,Glioblastoma,C0017636,,GEO,Microarray,Homo sapiens,4|4,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA06627,GSE77088,GPL18573,1000,Acquired Immunodeficiency Syndrome,C0001175,Peripheral blood,GEO,RNA-Seq,Homo sapiens,18|12,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA06628,GSE77102,GPL6887,0,Listeriosis,C0023860,Blood,GEO,Microarray,Mus musculus,4|3,"DO:A primary bacterial infectious disease that results_in infection, has_material_basis_in Listeria monocytogenes, which is transmitted_by ingestion of contaminated food or raw milk or transmitted_by congenital method. Ingestion of Listeria by pregnant women has_symptom nausea, has_symptom vomiting, has_symptom diarrhea, has_symptom fever, has_symptom malaise, has_symptom back pain, and has_symptom headache. Maternal infection with Listeria can result in chorioamnionitis, premature labor, spontaneous abortion, or stillbirth." DSA06629,GSE77102,GPL6887,1000,Listeriosis,C0023860,Blood,GEO,Microarray,Mus musculus,15|19,"DO:A primary bacterial infectious disease that results_in infection, has_material_basis_in Listeria monocytogenes, which is transmitted_by ingestion of contaminated food or raw milk or transmitted_by congenital method. Ingestion of Listeria by pregnant women has_symptom nausea, has_symptom vomiting, has_symptom diarrhea, has_symptom fever, has_symptom malaise, has_symptom back pain, and has_symptom headache. Maternal infection with Listeria can result in chorioamnionitis, premature labor, spontaneous abortion, or stillbirth." DSA06630,GSE77102,GPL6887,5,Listeriosis,C0023860,Liver,GEO,Microarray,Mus musculus,4|4,"DO:A primary bacterial infectious disease that results_in infection, has_material_basis_in Listeria monocytogenes, which is transmitted_by ingestion of contaminated food or raw milk or transmitted_by congenital method. Ingestion of Listeria by pregnant women has_symptom nausea, has_symptom vomiting, has_symptom diarrhea, has_symptom fever, has_symptom malaise, has_symptom back pain, and has_symptom headache. Maternal infection with Listeria can result in chorioamnionitis, premature labor, spontaneous abortion, or stillbirth." DSA06631,GSE77102,GPL6887,1000,Listeriosis,C0023860,Liver,GEO,Microarray,Mus musculus,5|9,"DO:A primary bacterial infectious disease that results_in infection, has_material_basis_in Listeria monocytogenes, which is transmitted_by ingestion of contaminated food or raw milk or transmitted_by congenital method. Ingestion of Listeria by pregnant women has_symptom nausea, has_symptom vomiting, has_symptom diarrhea, has_symptom fever, has_symptom malaise, has_symptom back pain, and has_symptom headache. Maternal infection with Listeria can result in chorioamnionitis, premature labor, spontaneous abortion, or stillbirth." DSA06632,GSE77102,GPL6887,28,Listeriosis,C0023860,Spleen,GEO,Microarray,Mus musculus,4|4,"DO:A primary bacterial infectious disease that results_in infection, has_material_basis_in Listeria monocytogenes, which is transmitted_by ingestion of contaminated food or raw milk or transmitted_by congenital method. Ingestion of Listeria by pregnant women has_symptom nausea, has_symptom vomiting, has_symptom diarrhea, has_symptom fever, has_symptom malaise, has_symptom back pain, and has_symptom headache. Maternal infection with Listeria can result in chorioamnionitis, premature labor, spontaneous abortion, or stillbirth." DSA06633,GSE77102,GPL6887,1000,Listeriosis,C0023860,Spleen,GEO,Microarray,Mus musculus,14|20,"DO:A primary bacterial infectious disease that results_in infection, has_material_basis_in Listeria monocytogenes, which is transmitted_by ingestion of contaminated food or raw milk or transmitted_by congenital method. Ingestion of Listeria by pregnant women has_symptom nausea, has_symptom vomiting, has_symptom diarrhea, has_symptom fever, has_symptom malaise, has_symptom back pain, and has_symptom headache. Maternal infection with Listeria can result in chorioamnionitis, premature labor, spontaneous abortion, or stillbirth." DSA06634,GSE77102,GPL6887,1000,Listeriosis,C0023860,Blood,GEO,Microarray,Mus musculus,3|4,"DO:A primary bacterial infectious disease that results_in infection, has_material_basis_in Listeria monocytogenes, which is transmitted_by ingestion of contaminated food or raw milk or transmitted_by congenital method. Ingestion of Listeria by pregnant women has_symptom nausea, has_symptom vomiting, has_symptom diarrhea, has_symptom fever, has_symptom malaise, has_symptom back pain, and has_symptom headache. Maternal infection with Listeria can result in chorioamnionitis, premature labor, spontaneous abortion, or stillbirth." DSA06635,GSE77102,GPL6887,722,Listeriosis,C0023860,Blood,GEO,Microarray,Mus musculus,5|8,"DO:A primary bacterial infectious disease that results_in infection, has_material_basis_in Listeria monocytogenes, which is transmitted_by ingestion of contaminated food or raw milk or transmitted_by congenital method. Ingestion of Listeria by pregnant women has_symptom nausea, has_symptom vomiting, has_symptom diarrhea, has_symptom fever, has_symptom malaise, has_symptom back pain, and has_symptom headache. Maternal infection with Listeria can result in chorioamnionitis, premature labor, spontaneous abortion, or stillbirth." DSA06636,GSE77102,GPL6887,449,Listeriosis,C0023860,Liver,GEO,Microarray,Mus musculus,4|4,"DO:A primary bacterial infectious disease that results_in infection, has_material_basis_in Listeria monocytogenes, which is transmitted_by ingestion of contaminated food or raw milk or transmitted_by congenital method. Ingestion of Listeria by pregnant women has_symptom nausea, has_symptom vomiting, has_symptom diarrhea, has_symptom fever, has_symptom malaise, has_symptom back pain, and has_symptom headache. Maternal infection with Listeria can result in chorioamnionitis, premature labor, spontaneous abortion, or stillbirth." DSA06637,GSE77102,GPL6887,1000,Listeriosis,C0023860,Liver,GEO,Microarray,Mus musculus,5|9,"DO:A primary bacterial infectious disease that results_in infection, has_material_basis_in Listeria monocytogenes, which is transmitted_by ingestion of contaminated food or raw milk or transmitted_by congenital method. Ingestion of Listeria by pregnant women has_symptom nausea, has_symptom vomiting, has_symptom diarrhea, has_symptom fever, has_symptom malaise, has_symptom back pain, and has_symptom headache. Maternal infection with Listeria can result in chorioamnionitis, premature labor, spontaneous abortion, or stillbirth." DSA06638,GSE77102,GPL6887,172,Listeriosis,C0023860,Spleen,GEO,Microarray,Mus musculus,4|4,"DO:A primary bacterial infectious disease that results_in infection, has_material_basis_in Listeria monocytogenes, which is transmitted_by ingestion of contaminated food or raw milk or transmitted_by congenital method. Ingestion of Listeria by pregnant women has_symptom nausea, has_symptom vomiting, has_symptom diarrhea, has_symptom fever, has_symptom malaise, has_symptom back pain, and has_symptom headache. Maternal infection with Listeria can result in chorioamnionitis, premature labor, spontaneous abortion, or stillbirth." DSA06639,GSE77102,GPL6887,1000,Listeriosis,C0023860,Spleen,GEO,Microarray,Mus musculus,5|9,"DO:A primary bacterial infectious disease that results_in infection, has_material_basis_in Listeria monocytogenes, which is transmitted_by ingestion of contaminated food or raw milk or transmitted_by congenital method. Ingestion of Listeria by pregnant women has_symptom nausea, has_symptom vomiting, has_symptom diarrhea, has_symptom fever, has_symptom malaise, has_symptom back pain, and has_symptom headache. Maternal infection with Listeria can result in chorioamnionitis, premature labor, spontaneous abortion, or stillbirth." DSA06640,GSE77126,GPL6246,1000,Duchenne Muscular Dystrophy,C0013264,Calf muscle,GEO,Microarray,Mus musculus,8|14,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA06641,GSE77191,GPL17586,1000,Chronic Myeloid Leukemia,C0023473,Blood,GEO,Microarray,Homo sapiens,4|1,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA06642,GSE77199,GPL14550,7,Colorectal Carcinoma,C0009402,Endothelium,GEO,Microarray,Homo sapiens,4|4,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA06643,GSE77199,GPL14550,2,Colon Carcinoma Metastatic To The Liver,C1333085,Endothelium,GEO,Microarray,Homo sapiens,4|4,NCI:A carcinoma that originates from the colonic wall and has spread to the liver. DSA06644,GSE77199,GPL14550,0,Renal Cell Carcinoma,C0007134,Endothelium,GEO,Microarray,Homo sapiens,4|4,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA06645,GSE77298,GPL570,531,Rheumatoid Arthritis,C0003873,Synovium,GEO,Microarray,Homo sapiens,7|16,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA06646,GSE77307,GPL11154,1000,Glioblastoma,C0017636,Brain,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA06647,GSE77307,GPL11154,1000,Glioblastoma,C0017636,Brain,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA06648,GSE77312,GPL17301,26,Early Proximal Colon Preneoplasia,,Colon,GEO,RNA-Seq,Homo sapiens,10|12, DSA06649,GSE77312,GPL17301,0,Early Proximal Colon Preneoplasia,,Colon,GEO,RNA-Seq,Homo sapiens,10|12, DSA06650,GSE77321,GPL11180,1000,Progeria,C0033300,,GEO,Microarray,Mus musculus,5|5,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA06651,GSE77321,GPL11180,1000,Progeria,C0033300,,GEO,Microarray,Mus musculus,5|5,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA06652,GSE77361,GPL10558,0,Pemphigoid,C0030805,Conjunctiva,GEO,Microarray,Homo sapiens,6|6,DO:A pemphigoid that is characterized by large blisters. DSA06653,GSE77361,GPL10558,0,Pemphigoid,C0030805,Conjunctiva,GEO,Microarray,Homo sapiens,6|3,DO:A pemphigoid that is characterized by large blisters. DSA06654,GSE77361,GPL10558,0,Pemphigoid,C0030805,Conjunctiva,GEO,Microarray,Homo sapiens,6|3,DO:A pemphigoid that is characterized by large blisters. DSA06655,GSE77361,GPL10558,0,Pemphigoid,C0030805,Conjunctiva,GEO,Microarray,Homo sapiens,2|2,DO:A pemphigoid that is characterized by large blisters. DSA06656,GSE77361,GPL10558,0,Pemphigoid,C0030805,Conjunctiva,GEO,Microarray,Homo sapiens,2|2,DO:A pemphigoid that is characterized by large blisters. DSA06657,GSE43497,GPL6244,0,Allergic Rhinitis,C2607914,Blood,GEO,Microarray,Homo sapiens,12|12,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA06658,GSE77513,GPL16791,1000,"Dysautonomia, Familial",C0013364,,GEO,RNA-Seq,Homo sapiens,3|2,"DO:A hereditary sensory neuropathy that is characterized by gastrointestinal dysfunction, gastroesophageal reflux, vomiting crises, recurrent pneumonia, seizures, gait abnormalities with loss of ambulation, kyphoscoliosis, postural hypotension, hypertension crises, absence of fungiform papillae on the tongue, decreased deep tendon reflexes, defective lacrimation, and impaired pain and temperature perception and has_material_basis_in homozygous or compound heterozygous mutation in the IKBKAP gene (ELP1) on chromosome 9q31." DSA06659,GSE77513,GPL16791,1000,"Dysautonomia, Familial",C0013364,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A hereditary sensory neuropathy that is characterized by gastrointestinal dysfunction, gastroesophageal reflux, vomiting crises, recurrent pneumonia, seizures, gait abnormalities with loss of ambulation, kyphoscoliosis, postural hypotension, hypertension crises, absence of fungiform papillae on the tongue, decreased deep tendon reflexes, defective lacrimation, and impaired pain and temperature perception and has_material_basis_in homozygous or compound heterozygous mutation in the IKBKAP gene (ELP1) on chromosome 9q31." DSA06660,GSE77528,GPL10558,292,Visceral Leishmaniasis,C0023290,Peripheral blood,GEO,Microarray,Homo sapiens,7|1,"DO:A leishmaniasis that is the most severe form of the disease caused by protozoan parasites of the Leishmania genus, resulting in the infection of the internal organs such as liver, spleen and bone marrow. The symptoms include fever, weight loss, and an enlarged spleen and liver." DSA06661,GSE77528,GPL10558,486,Visceral Leishmaniasis,C0023290,Peripheral blood,GEO,Microarray,Homo sapiens,6|1,"DO:A leishmaniasis that is the most severe form of the disease caused by protozoan parasites of the Leishmania genus, resulting in the infection of the internal organs such as liver, spleen and bone marrow. The symptoms include fever, weight loss, and an enlarged spleen and liver." DSA06662,GSE77528,GPL10558,1000,Visceral Leishmaniasis,C0023290,Peripheral blood,GEO,Microarray,Homo sapiens,8|7,"DO:A leishmaniasis that is the most severe form of the disease caused by protozoan parasites of the Leishmania genus, resulting in the infection of the internal organs such as liver, spleen and bone marrow. The symptoms include fever, weight loss, and an enlarged spleen and liver." DSA06663,GSE77528,GPL10558,1000,Visceral Leishmaniasis,C0023290,Peripheral blood,GEO,Microarray,Homo sapiens,8|7,"DO:A leishmaniasis that is the most severe form of the disease caused by protozoan parasites of the Leishmania genus, resulting in the infection of the internal organs such as liver, spleen and bone marrow. The symptoms include fever, weight loss, and an enlarged spleen and liver." DSA06664,GSE77558,GPL10558,1000,Huntington's Disease,C0020179,Striatum,GEO,Microarray,Homo sapiens,2|2,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06665,GSE77558,GPL10558,288,Huntington's Disease,C0020179,Striatum,GEO,Microarray,Homo sapiens,4|4,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA06666,GSE77563,GPL17692,1000,Barrett's Esophagus,C0004763,Esophagus,GEO,Microarray,Homo sapiens,24|16,DO:An esophageal disease characterized by a change of normal esophageal squamous epithelium to a columnar and intestinal-type epithelium. DSA06667,GSE77578,GPL6885,1000,Epilepsy,C0014544,Hippocampus,GEO,Microarray,Mus musculus,6|17,"DO:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions." DSA06668,GSE77598,GPL11154,164,Multiple Sclerosis,C0026769,,GEO,RNA-Seq,Homo sapiens,3|5,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA06669,GSE41342,GPL1261,0,Osteoarthritis Arthritis,C0029410,Joint,GEO,Microarray,Mus musculus,3|2,"EFO:A progressive, degenerative joint disease, the most common form of arthritis, especially in older persons. The disease is thought to result not from the aging process but from biochemical changes and biomechanical stresses affecting articular cartilage. In the foreign literature it is often called osteoarthrosis deformans." DSA06670,GSE41342,GPL1261,1000,Osteoarthritis Arthritis,C0029410,Joint,GEO,Microarray,Mus musculus,3|3,"EFO:A progressive, degenerative joint disease, the most common form of arthritis, especially in older persons. The disease is thought to result not from the aging process but from biochemical changes and biomechanical stresses affecting articular cartilage. In the foreign literature it is often called osteoarthrosis deformans." DSA06671,GSE41342,GPL1261,0,Osteoarthritis Arthritis,C0029410,Joint,GEO,Microarray,Mus musculus,3|3,"EFO:A progressive, degenerative joint disease, the most common form of arthritis, especially in older persons. The disease is thought to result not from the aging process but from biochemical changes and biomechanical stresses affecting articular cartilage. In the foreign literature it is often called osteoarthrosis deformans." DSA06672,GSE41342,GPL1261,8,Osteoarthritis Arthritis,C0029410,Joint,GEO,Microarray,Mus musculus,3|3,"EFO:A progressive, degenerative joint disease, the most common form of arthritis, especially in older persons. The disease is thought to result not from the aging process but from biochemical changes and biomechanical stresses affecting articular cartilage. In the foreign literature it is often called osteoarthrosis deformans." DSA06673,GSE41414,GPL201,507,Amyotrophic Lateral Sclerosis,C0002736,Deltoid,GEO,Microarray,Homo sapiens,7|4,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA06674,GSE41418,GPL1261,1000,Chronic Pancreatitis,C0149521,Pancreas,GEO,Microarray,Mus musculus,3|3,"EFO:INFLAMMATION of the PANCREAS that is characterized by recurring or persistent ABDOMINAL PAIN with or without STEATORRHEA or DIABETES MELLITUS. It is characterized by the irregular destruction of the pancreatic parenchyma which may be focal, segmental, or diffuse." DSA06675,GSE41418,GPL1261,1000,Chronic Pancreatitis,C0149521,Pancreas,GEO,Microarray,Mus musculus,3|3,"EFO:INFLAMMATION of the PANCREAS that is characterized by recurring or persistent ABDOMINAL PAIN with or without STEATORRHEA or DIABETES MELLITUS. It is characterized by the irregular destruction of the pancreatic parenchyma which may be focal, segmental, or diffuse." DSA06676,GSE41524,GPL5175,1000,Dupuytren's Disease,C4082974,Skin,GEO,Microarray,Homo sapiens,6|4,EFO:A fibromatosis of the palmar fascia characterized by thickening and contracture of the fibrous bands on the palmar surfaces of the hand and fingers. It arises most commonly in men between the ages of 30 and 50. DSA06677,GSE31475,GPL570,358,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA06678,GSE41599,GPL96,0,Diamond-Blackfan Anemia,C1260899,Bone marrow,GEO,Microarray,Homo sapiens,6|3,DO:A congenital hypoplastic anemia that is characterized by anemia (low red blood cell counts) with decreased erythroid progenitors in the bone marrow and has_material_basis_insufficient levels of red blood cells due to bone marrow dysfunction. DSA06679,GSE41599,GPL96,2,Diamond-Blackfan Anemia,C1260899,Bone marrow,GEO,Microarray,Homo sapiens,6|3,DO:A congenital hypoplastic anemia that is characterized by anemia (low red blood cell counts) with decreased erythroid progenitors in the bone marrow and has_material_basis_insufficient levels of red blood cells due to bone marrow dysfunction. DSA06680,GSE41621,GPL10558,1000,T-Cell Acute Lymphoblastic Leukemia,C1961099,Bone marrow,GEO,Microarray,Homo sapiens,2|18,DO:An acute lymphoblastic leukemia that is characterized by too many T-cell lymphoblasts found in the bone marrow and blood. DSA06681,GSE41681,GPL14550,0,Pre-Eclampsia,C0032914,,GEO,Microarray,Homo sapiens,2|2,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA06682,GSE41687,GPL9115,388,Eosinophilic Esophagitis,C0341106,Esophagus,GEO,RNA-Seq,Homo sapiens,3|3,DO:An esophagitis characterized by inflammation involving eosinophils located_in esophagus. DSA06683,GSE41687,GPL9115,5,Gastroesophageal Reflux Disease,C0017168,Esophagus,GEO,RNA-Seq,Homo sapiens,3|3,"EFO:A malignant tumor with glandular differentiation arising predominantly from Barrett mucosa in the lower third of the esophagus. Rare examples of esophageal adenocarcinoma deriving from ectopic gastric mucosa in the upper esophagus have also been reported. Grossly, esophageal adenocarcinomas are similar to esophageal squamous cell carcinomas. Microscopically, adenocarcinomas arising in the setting of Barrett esophagus are typically papillary and/or tubular. The prognosis is poor." DSA06684,GSE41687,GPL9115,932,Eosinophilic Esophagitis,C0341106,Esophagus,GEO,RNA-Seq,Homo sapiens,3|3,DO:An esophagitis characterized by inflammation involving eosinophils located_in esophagus. DSA06685,GSE41687,GPL9115,25,Gastroesophageal Reflux Disease,C0017168,Esophagus,GEO,RNA-Seq,Homo sapiens,3|3,"EFO:A malignant tumor with glandular differentiation arising predominantly from Barrett mucosa in the lower third of the esophagus. Rare examples of esophageal adenocarcinoma deriving from ectopic gastric mucosa in the upper esophagus have also been reported. Grossly, esophageal adenocarcinomas are similar to esophageal squamous cell carcinomas. Microscopically, adenocarcinomas arising in the setting of Barrett esophagus are typically papillary and/or tubular. The prognosis is poor." DSA06686,GSE41751,GPL570,1000,Hutchinson-Gilford Progeria Syndrome,C0033300,Skin,GEO,Microarray,Homo sapiens,2|2,"DO:A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22." DSA06687,GSE41759,GPL1261,6,Prader-Willi Syndrome,C0032897,Brain,GEO,Microarray,Mus musculus,4|3,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA06688,GSE41759,GPL1261,10,Prader-Willi Syndrome,C0032897,Skeletal muscle,GEO,Microarray,Mus musculus,4|3,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA06689,GSE41817,GPL16212,5,Diamond-Blackfan Anemia,C1260899,Bone marrow,GEO,Microarray,Homo sapiens,6|3,DO:A congenital hypoplastic anemia that is characterized by anemia (low red blood cell counts) with decreased erythroid progenitors in the bone marrow and has_material_basis_insufficient levels of red blood cells due to bone marrow dysfunction. DSA06690,GSE4182,GPL570,6,Spina Bifida,C0080178,Amniotic fluid,GEO,Microarray,Homo sapiens,5|4,"DO:A spina bifida characterized by protrusion of the spinal cord through an opening, covered by meningeal membranes." DSA06691,GSE41848,GPL16209,1000,Multiple Sclerosis,C0026769,Blood,GEO,Microarray,Homo sapiens,79|133,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA06692,GSE41849,GPL16209,730,Multiple Sclerosis,C0026769,Blood,GEO,Microarray,Homo sapiens,46|56,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA06693,GSE41861,GPL570,585,Asthma,C0004096,Upper airway,GEO,Microarray,Homo sapiens,17|19,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06694,GSE41861,GPL570,1000,Asthma,C0004096,Lower airway,GEO,Microarray,Homo sapiens,30|25,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06695,GSE41861,GPL570,44,Asthma,C0004096,Upper airway,GEO,Microarray,Homo sapiens,17|16,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06696,GSE41861,GPL570,1000,Asthma,C0004096,Lower airway,GEO,Microarray,Homo sapiens,30|21,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06697,GSE41861,GPL570,0,Asthma,C0004096,Upper airway,GEO,Microarray,Homo sapiens,17|5,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06698,GSE41861,GPL570,233,Asthma,C0004096,Lower airway,GEO,Microarray,Homo sapiens,30|5,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06699,GSE41862,GPL570,0,Asthma,C0004096,Nasal scrape,GEO,Microarray,Homo sapiens,21|95,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06700,GSE41863,GPL570,0,Asthma,C0004096,Sputum,GEO,Microarray,Homo sapiens,9|47,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06701,GSE41890,GPL6244,0,Multiple Sclerosis,C0026769,Peripheral blood,GEO,Microarray,Homo sapiens,24|22,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA06702,GSE41890,GPL6244,0,Multiple Sclerosis,C0026769,Peripheral blood,GEO,Microarray,Homo sapiens,24|22,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA06703,GSE41919,GPL14550,10,Chronic Hepatic Encephalopathy,C4024937,Brain,GEO,Microarray,Homo sapiens,8|8, DSA06704,GSE41919,GPL14550,0,Cirrhosis,C1623038,Brain,GEO,Microarray,Homo sapiens,8|3,"MSH:Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury." DSA06705,GSE42002,GPL6947,0,Trauma,,Blood,GEO,Microarray,Homo sapiens,60|40, DSA06706,GSE42002,GPL6947,0,Trauma,,Blood,GEO,Microarray,Homo sapiens,14|15, DSA06707,GSE42057,GPL570,51,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,42|94,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA06708,GSE42133,GPL10558,716,Autism Spectrum Disorder,C1510586,Blood,GEO,Microarray,Homo sapiens,56|91,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA06709,GSE42148,GPL13607,1,Coronary Artery Disease,C1956346,Peripheral blood,GEO,Microarray,Homo sapiens,11|13,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA06710,GSE4226,GPL1211,0,Alzheimer's Disease,C0002395,Peripheral blood,GEO,Microarray,Homo sapiens,7|7,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA06711,GSE4226,GPL1211,0,Alzheimer's Disease,C0002395,Peripheral blood,GEO,Microarray,Homo sapiens,7|7,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA06712,GSE42301,GPL2894,228,Inflammatory Mfh,C1334180,Lung,GEO,Microarray,Mus musculus,3|3,EFO:An undifferentiated pleomorphic sarcoma characterized by the presence of numerous inflammatory cells. DSA06713,GSE42301,GPL2894,158,Pulmonary Fibrosis,C0034069,Lung,GEO,Microarray,Mus musculus,3|3,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA06714,GSE42301,GPL2894,232,Pulmonary Fibrosis,C0034069,Lung,GEO,Microarray,Mus musculus,3|3,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA06715,GSE42331,GPL6244,59,Klinefelter Syndrome,C0022735,Blood,GEO,Microarray,Homo sapiens,30|35,DO:A chromosomal duplication syndrome that is characterized by infertility and that has_material_basis_in an extra X chromosome in cells in men. DSA06716,GSE42406,GPL571,0,Spinocerebellar Ataxia Type 28,C1853249,,GEO,Microarray,Homo sapiens,6|4,"DO:An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria, hyperreflexia, ophthalmoparesis, nystagmus and ptosis, and has_material_basis_in mutation in the AFG3L2 gene." DSA06717,GSE42492,GPL6883,0,Alzheimer's Disease,C0002395,Skin,GEO,Microarray,Homo sapiens,2|1,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA06718,GSE42492,GPL6883,1000,Alzheimer's Disease,C0002395,,GEO,Microarray,Homo sapiens,4|2,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA06719,GSE42546,GPL13393,1,Bipolar Disorder,C0005586,Hippocampus,GEO,RNA-Seq,Homo sapiens,29|16,DO:A mood disorder that involves alternating periods of mania and depression. DSA06720,GSE42546,GPL13393,74,Depression,C0011581,Hippocampus,GEO,RNA-Seq,Homo sapiens,29|17,DO:A mood disorder that involves the presence of a low mood almost daily over a span of at least two years. DSA06721,GSE42546,GPL13393,24,Schizophrenia,C0036341,Hippocampus,GEO,RNA-Seq,Homo sapiens,29|17,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA06722,GSE42572,GPL13376,0,Osteosarcoma,C0029463,,GEO,Microarray,Homo sapiens,5|7,DO:A bone sarcoma that is located_in bone that has_material_basis_in cells of mesenchymal origin. DSA06723,GSE31474,GPL570,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA06724,GSE31471,GPL570,1,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA06725,GSE31471,GPL570,0,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA06726,GSE42632,GPL13497,425,Psoriasis,C0033860,,GEO,Microarray,Homo sapiens,6|6,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA06727,GSE42677,GPL571,1000,Actinic Keratosis,C0022602,Epidermis,GEO,Microarray,Homo sapiens,10|5,"EFO:An actinic keratosis (ak-TIN-ik ker-uh-TOE-sis) is a rough, scaly patch on your skin that develops from years of exposure to the sun. It's most commonly found on your face, lips, ears, back of your hands, forearms, scalp or neck. Also known as solar keratosis, an actinic keratosis enlarges slowly and usually causes no signs or symptoms other than a patch or small spot on your skin. These lesions take years to develop, usually first appearing in older adults. A small percentage of actinic keratosis lesions can eventually become skin cancer. You can reduce your risk of actinic keratosis by minimizing your sun exposure and protecting your skin from ultraviolet (UV) rays." DSA06728,GSE42677,GPL571,1000,Squamous Cell Carcinoma In Situ,C0334245,Epidermis,GEO,Microarray,Homo sapiens,10|5,DO:An uterus carcinoma in situ that is located_in the uterine cervix. DSA06729,GSE42677,GPL571,1000,Microinvasive Squamous Cell Carcinoma,C0334252,Epidermis,GEO,Microarray,Homo sapiens,10|5,NCI:A squamous cell carcinoma with minimal stromal invasion. DSA06730,GSE42733,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,5|10,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA06731,GSE42764,GPL16356,241,Squamous Cell Carcinoma,C0007137,Cervix,GEO,Microarray,Homo sapiens,2|12,DO:A carcinoma that derives_from squamous epithelial cells. DSA06732,GSE42764,GPL16356,166,Squamous Cell Carcinoma,C0007137,Cervix,GEO,Microarray,Homo sapiens,2|12,DO:A carcinoma that derives_from squamous epithelial cells. DSA06733,GSE42768,GPL6246,1000,Colitis,C0009319,Colon,GEO,Microarray,Mus musculus,5|5,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA06734,GSE42768,GPL6246,1000,Colitis,C0009319,Colon,GEO,Microarray,Mus musculus,5|5,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA06735,GSE42768,GPL6246,1000,Colitis,C0009319,Colon,GEO,Microarray,Mus musculus,5|5,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA06736,GSE42768,GPL6246,1000,Colitis,C0009319,Colon,GEO,Microarray,Mus musculus,5|5,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA06737,GSE42768,GPL6246,1000,Colitis,C0009319,Colon,GEO,Microarray,Mus musculus,5|5,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA06738,GSE42813,GPL1261,655,Atherosclerosis,C0004153,Aorta,GEO,Microarray,Mus musculus,2|2,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA06739,GSE42826,GPL10558,1000,Sarcoidosis,C0036202,Blood,GEO,Microarray,Homo sapiens,52|16,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA06740,GSE42826,GPL10558,1000,Lung Cancer,C0684249,Blood,GEO,Microarray,Homo sapiens,52|8,DO:A respiratory system cancer that is located_in the lung. DSA06741,GSE42826,GPL10558,292,Sarcoidosis,C0036202,Blood,GEO,Microarray,Homo sapiens,52|9,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA06742,GSE42826,GPL10558,1000,Pneumonia,C0032285,Blood,GEO,Microarray,Homo sapiens,52|6,"DO:A lung disease that involves lung parenchyma or alveolar inflammation and abnormal alveolar filling with fluid (consolidation and exudation). It results from a variety of causes including infection with bacteria, viruses, fungi or parasites, and chemical or physical injury to the lungs. It is accompanied by fever, chills, cough, and difficulty in breathing." DSA06743,GSE42826,GPL10558,1000,Tuberculosis,C0041296,Blood,GEO,Microarray,Homo sapiens,52|11,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA06744,GSE42830,GPL10558,1000,Sarcoidosis,C0036202,Blood,GEO,Microarray,Homo sapiens,38|17,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA06745,GSE42830,GPL10558,1000,Lung Cancer,C0684249,Blood,GEO,Microarray,Homo sapiens,38|8,DO:A respiratory system cancer that is located_in the lung. DSA06746,GSE42830,GPL10558,19,Sarcoidosis,C0036202,Blood,GEO,Microarray,Homo sapiens,38|8,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA06747,GSE42830,GPL10558,1000,Tuberculosis,C0041296,Blood,GEO,Microarray,Homo sapiens,38|16,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA06748,GSE42832,GPL10558,3,Sarcoidosis,C0036202,,GEO,Microarray,Homo sapiens,5|5,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA06749,GSE42832,GPL10558,101,Sarcoidosis,C0036202,,GEO,Microarray,Homo sapiens,5|5,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA06750,GSE42832,GPL10558,6,Sarcoidosis,C0036202,,GEO,Microarray,Homo sapiens,5|5,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA06751,GSE42832,GPL10558,0,Sarcoidosis,C0036202,,GEO,Microarray,Homo sapiens,5|5,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA06752,GSE42832,GPL10558,1000,Sarcoidosis,C0036202,,GEO,Microarray,Homo sapiens,5|5,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA06753,GSE42832,GPL10558,38,Sarcoidosis,C0036202,Blood,GEO,Microarray,Homo sapiens,5|5,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA06754,GSE42832,GPL10558,117,Tuberculosis,C0041296,,GEO,Microarray,Homo sapiens,5|5,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA06755,GSE42832,GPL10558,344,Tuberculosis,C0041296,,GEO,Microarray,Homo sapiens,5|5,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA06756,GSE42832,GPL10558,11,Tuberculosis,C0041296,,GEO,Microarray,Homo sapiens,5|5,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA06757,GSE42832,GPL10558,1,Tuberculosis,C0041296,,GEO,Microarray,Homo sapiens,5|5,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA06758,GSE42832,GPL10558,1000,Tuberculosis,C0041296,,GEO,Microarray,Homo sapiens,5|5,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA06759,GSE42832,GPL10558,572,Tuberculosis,C0041296,Blood,GEO,Microarray,Homo sapiens,5|5,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA06760,GSE42966,GPL4133,0,Parkinson's Disease,C0030567,Brain,GEO,Microarray,Homo sapiens,6|9,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA06761,GSE42986,GPL16240,0,Primary Mitochondrial Respiratory Chain Disease,,Skeletal muscle,GEO,Microarray,Homo sapiens,10|13, DSA06762,GSE42986,GPL16240,67,Primary Mitochondrial Respiratory Chain Disease,,,GEO,Microarray,Homo sapiens,8|12, DSA06763,GSE43017,GPL570,1000,T-Cell Leukemia,C0023492,Peripheral blood,GEO,Microarray,Homo sapiens,5|7,"EFO:A malignant disease of the T-lymphocytes in the bone marrow, thymus, and/or blood." DSA06764,GSE43106,GPL6246,49,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,Microarray,Mus musculus,8|7,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA06765,GSE43106,GPL6246,100,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,Microarray,Mus musculus,8|7,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA06766,GSE43106,GPL6246,211,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,Microarray,Mus musculus,8|8,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA06767,GSE43106,GPL6246,101,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,Microarray,Mus musculus,18|8,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA06768,GSE43177,GPL570,0,Immune Thrombocytopenia,C0242584,Peripheral blood,GEO,Microarray,Homo sapiens,10|9,DO:A primary thrombocytopenia that involves relatively few platelets in blood as a result of autoantibodies. DSA06769,GSE43187,GPL10192,1000,Type 2 Diabetes,C0011860,Pancreatic islet,GEO,Microarray,Mus musculus,6|6,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA06770,GSE43264,GPL15362,0,Polycystic Ovary Syndrome,C0032460,Subcutaneous adipose tissue,GEO,Microarray,Homo sapiens,7|8,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA06771,GSE43326,GPL6244,2,Alzheimer's Disease,C0002395,,GEO,Microarray,Homo sapiens,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA06772,GSE43366,GPL13112,886,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,RNA-Seq,Mus musculus,3|5,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA06773,GSE43366,GPL13112,1000,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,RNA-Seq,Mus musculus,3|7,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA06774,GSE43366,GPL13112,1000,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,RNA-Seq,Mus musculus,4|9,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA06775,GSE43366,GPL13112,21,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,RNA-Seq,Mus musculus,3|2,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA06776,GSE43366,GPL13112,59,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,RNA-Seq,Mus musculus,4|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA06777,GSE43399,GPL15401,964,Myelodysplastic Syndrome,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,4|26,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA06778,GSE43484,GPL571,0,Uremia,C0041948,Peripheral blood,GEO,Microarray,Homo sapiens,3|3,DO:A kidney disease characterized by the failure of the kidneys to adequately filter waste products from the blood. DSA06779,GSE43488,GPL13667,700,Type 1 Diabetes,C0011854,Peripheral blood,GEO,Microarray,Homo sapiens,205|151,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA06780,GSE43523,GPL6883,0,Seasonal Allergic Rhinitis,C0018621,,GEO,Microarray,Homo sapiens,5|7,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA06781,GSE43525,GPL10558,0,Periodontitis,C0031099,Blood,GEO,Microarray,Homo sapiens,4|4,"EFO:Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology)" DSA06782,GSE43525,GPL10558,0,Periodontitis,C0031099,Saliva,GEO,Microarray,Homo sapiens,3|4,"EFO:Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology)" DSA06783,GSE43525,GPL10558,0,Periodontitis,C0031099,Blood,GEO,Microarray,Homo sapiens,4|5,"EFO:Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology)" DSA06784,GSE43525,GPL10558,0,Periodontitis,C0031099,Saliva,GEO,Microarray,Homo sapiens,3|3,"EFO:Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology)" DSA06785,GSE43575,GPL13112,54,Prader-Willi Syndrome,C0032897,Cortex,GEO,RNA-Seq,Mus musculus,3|2,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA06786,GSE43575,GPL13112,2,Prader-Willi Syndrome,C0032897,Cortex,GEO,RNA-Seq,Mus musculus,2|2,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA06787,GSE43591,GPL570,1000,Multiple Sclerosis,C0026769,Peripheral blood,GEO,Microarray,Homo sapiens,10|10,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA06788,GSE43603,GPL11154,1000,Refractory Anemia With Ring Sideroblasts,C1264195,Bone marrow,GEO,RNA-Seq,Homo sapiens,1|2,"EFO:Acquired idiopathic sideroblastic anaemia is one of a group of disorders known as the myelodysplastic syndromes (MDS) characterised by ineffective haemopoiesis affecting one or more blood cell lineages (myeloid, erythroid or megakaryocytic) leading to peripheral blood cytopenias and an increased risk of developing leukaemia. Acquired idiopathic sideroblastic anaemia is now more commonly referred to as refractory anaemia with ringed sideroblasts or the acronym RARS." DSA06789,GSE43698,GPL13607,25,Congenital Muscular Dystrophy (Disorder),C0699743,Skeletal muscle,GEO,Microarray,Homo sapiens,4|3,"DO:A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted." DSA06790,GSE43698,GPL13607,0,Duchenne Muscular Dystrophy,C0013264,Skeletal muscle,GEO,Microarray,Homo sapiens,4|3,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA06791,GSE43698,GPL13607,0,Mitochondrial Myopathy,C0162670,Skeletal muscle,GEO,Microarray,Homo sapiens,4|2,DO:A myopathy that is characterized by mitochondrial dysfunction. DSA06792,GSE43698,GPL13607,0,Mitochondrial Myopathy,C0162670,Skeletal muscle,GEO,Microarray,Homo sapiens,4|9,DO:A myopathy that is characterized by mitochondrial dysfunction. DSA06793,GSE43698,GPL13607,0,Congenital Muscular Dystrophy (Disorder),C0699743,Skeletal muscle,GEO,Microarray,Homo sapiens,4|8,"DO:A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted." DSA06794,GSE31471,GPL570,0,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA06795,GSE43754,GPL5188,4,Chronic Myeloid Leukemia,C0023473,Bone marrow,GEO,Microarray,Homo sapiens,5|5,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA06796,GSE43754,GPL5188,1,Chronic Myeloid Leukemia,C0023473,Bone marrow,GEO,Microarray,Homo sapiens,5|5,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA06797,GSE43760,GPL6244,0,Metabolic Syndrome,C0524620,Vastus lateralis,GEO,Microarray,Homo sapiens,6|6,"DO:An abdominal obesity-metabolic syndrome characterized by insulin resistance and hyperinsulinemia, dyslipidemia, essential hypertension, abdominal obesity, glucose intolerance or noninsulin-dependent diabetes mellitus and an increased risk of cardiovascular events." DSA06798,GSE43760,GPL6244,0,Metabolic Syndrome,C0524620,Vastus lateralis muscle,GEO,Microarray,Homo sapiens,6|6,"DO:An abdominal obesity-metabolic syndrome characterized by insulin resistance and hyperinsulinemia, dyslipidemia, essential hypertension, abdominal obesity, glucose intolerance or noninsulin-dependent diabetes mellitus and an increased risk of cardiovascular events." DSA06799,GSE31471,GPL570,24,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA06800,GSE43771,GPL10558,0,Dystonia Disorders,C0013421,Blood,GEO,Microarray,Homo sapiens,4|4,DO:A movement disease that is characterized by involuntary muscle contractions causing repetitive or twisting movements. DSA06801,GSE43825,GPL1261,1000,Basal-Like Breast Cancer,C3642347,Breast,GEO,Microarray,Mus musculus,4|11,"EFO:A biologic subset of breast carcinoma defined by high expression of genes characteristic of basal epithelial cells, including KRT5 and KRT17, annexin 8, CX3CL1, and TRIM29, and usually by lack of expression of the estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2). It is the most common subtype of breast cancer associated with BRCA1 mutations, and is associated with a poor prognosis." DSA06802,GSE43825,GPL1261,1000,Breast Hypoplasia,C0266013,Breast,GEO,Microarray,Mus musculus,4|5,HPO:Underdevelopment of the breast. DSA06803,GSE43825,GPL1261,1000,Breast Hypoplasia,C0266013,Breast,GEO,Microarray,Mus musculus,4|5,HPO:Underdevelopment of the breast. DSA06804,GSE43861,GPL15207,1000,Fibrogensis Imperfecta Ossium,,Trans iliac bone,GEO,Microarray,Homo sapiens,2|2, DSA06805,GSE43924,GPL5175,17,Leber Congenital Amaurosis,C0339527,,GEO,Microarray,Homo sapiens,9|9,"DO:A retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness." DSA06806,GSE43926,GPL5175,0,Leber Congenital Amaurosis,C0339527,,GEO,Microarray,Homo sapiens,4|9,"DO:A retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness." DSA06807,GSE43994,GPL6885,1000,Medulloblastoma,C0025149,Cerebellum,GEO,Microarray,Mus musculus,6|6,DO:An infratentorial cancer that is located_in the lower part of the brain and is a type of primitive neuroectodermal tumor. DSA06808,GSE43994,GPL6885,1000,Medulloblastoma,C0025149,Cerebellum,GEO,Microarray,Mus musculus,6|6,DO:An infratentorial cancer that is located_in the lower part of the brain and is a type of primitive neuroectodermal tumor. DSA06809,GSE43994,GPL6885,1000,Medulloblastoma,C0025149,Cerebellum,GEO,Microarray,Mus musculus,6|30,DO:An infratentorial cancer that is located_in the lower part of the brain and is a type of primitive neuroectodermal tumor. DSA06810,GSE43996,GPL571,0,Zellweger Spectrum Disorder,C4687396,,GEO,Microarray,Homo sapiens,3|6,"MONDO:Peroxisome biogenesis disorders, Zellweger syndrome spectrum (PBD-ZSS) is a group of autosomal recessive disorders affecting the formation of functional peroxisomes, characterized by sensorineural hearing loss, pigmentary retinal degeneration, multiple organ dysfunction and psychomotor impairment, and is comprised of the phenotypic variants Zellweger syndrome (ZS), neonatal adrenoleukodystrophy (NALD) and infantile Refsum disease (IRD)." DSA06811,GSE43996,GPL571,10,Zellweger Spectrum Disorder,C4687396,,GEO,Microarray,Homo sapiens,12|14,"MONDO:Peroxisome biogenesis disorders, Zellweger syndrome spectrum (PBD-ZSS) is a group of autosomal recessive disorders affecting the formation of functional peroxisomes, characterized by sensorineural hearing loss, pigmentary retinal degeneration, multiple organ dysfunction and psychomotor impairment, and is comprised of the phenotypic variants Zellweger syndrome (ZS), neonatal adrenoleukodystrophy (NALD) and infantile Refsum disease (IRD)." DSA06812,GSE44037,GPL13158,0,Asthma,C0004096,Bronchial epithelium,GEO,Microarray,Homo sapiens,6|6,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06813,GSE44037,GPL13158,0,Asthma,C0004096,Nasal epithelium,GEO,Microarray,Homo sapiens,6|6,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06814,GSE44037,GPL13158,0,Rhinitis,C0035455,Bronchial epithelium,GEO,Microarray,Homo sapiens,6|5,"DO:A upper respiratory infectious disease which involves irritation and inflammation of the mucous membrane of the nose due to viruses, bacteria or irritants. The inflammation results in generation of excessive amounts of mucus leading to runny nose, as well as nasal congestion and post-nasal drip." DSA06815,GSE44037,GPL13158,0,Rhinitis,C0035455,Nasal epithelium,GEO,Microarray,Homo sapiens,6|5,"DO:A upper respiratory infectious disease which involves irritation and inflammation of the mucous membrane of the nose due to viruses, bacteria or irritants. The inflammation results in generation of excessive amounts of mucus leading to runny nose, as well as nasal congestion and post-nasal drip." DSA06816,GSE44076,GPL13667,1000,Colon Adenocarcinoma,C0699790,Colon,GEO,Microarray,Homo sapiens,23|60,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06817,GSE44076,GPL13667,1000,Colon Adenocarcinoma,C0699790,Colon,GEO,Microarray,Homo sapiens,27|38,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06818,GSE44076,GPL13667,1000,Colon Adenocarcinoma,C0699790,Colon,GEO,Microarray,Homo sapiens,60|60,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06819,GSE44076,GPL13667,1000,Colon Adenocarcinoma,C0699790,Colon,GEO,Microarray,Homo sapiens,38|38,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06820,GSE44101,GPL1261,1000,Xerophthalmia,C0043349,Conjunctiva,GEO,Microarray,Mus musculus,3|3,"DO:A dry eye syndrome that is characterized by conjunctival and corneal xerosis, Bitot's spots, keratomalacia, nyctalopia, and retinopathy resulting from vitamin A deficiency." DSA06821,GSE44314,GPL6480,0,Type 1 Diabetes,C0011854,Blood,GEO,Microarray,Homo sapiens,6|5,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA06822,GSE44314,GPL6480,0,Type 1 Diabetes,C0011854,Blood,GEO,Microarray,Homo sapiens,6|5,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA06823,GSE44426,GPL4133,32,Primary Myelofibrosis,C0001815,Bone marrow,GEO,Microarray,Homo sapiens,6|6,DO:A myeloid neoplasm that is located in the bone marrow which results in bone marrow being replaced by fibrous (scar) tissue. DSA06824,GSE44593,GPL570,0,Major Depressive Disorder,C1269683,Brain,GEO,Microarray,Homo sapiens,14|14,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA06825,GSE44605,GPL6887,0,Peripheral Neuropathy,C0031117,Sciatic nerve,GEO,Microarray,Mus musculus,2|2,DO:A nervous system disease that affects the peripheral nervous system. DSA06826,GSE44625,GPL6885,0,Traumatic Brain Injury,,Hippocampus,GEO,Microarray,Mus musculus,5|4, DSA06827,GSE44625,GPL6885,40,Traumatic Brain Injury,,Hippocampus,GEO,Microarray,Mus musculus,5|7, DSA06828,GSE44647,GPL6246,19,Gaucher Disease,C0017205,Liver,GEO,Microarray,Mus musculus,4|4,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA06829,GSE44647,GPL6246,177,Gaucher Disease,C0017205,Lung,GEO,Microarray,Mus musculus,4|4,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA06830,GSE44647,GPL6246,14,Gaucher Disease,C0017205,Spleen,GEO,Microarray,Mus musculus,8|7,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA06831,GSE44660,GPL5175,1000,Melanoma,C0025202,,GEO,Microarray,Homo sapiens,3|12,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA06832,GSE44660,GPL5175,1000,Melanoma,C0025202,,GEO,Microarray,Homo sapiens,3|7,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA06833,GSE44674,GPL13112,1000,Gaucher Disease,C0017205,Liver,GEO,RNA-Seq,Mus musculus,4|4,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA06834,GSE44674,GPL13112,1000,Gaucher Disease,C0017205,Lung,GEO,RNA-Seq,Mus musculus,4|4,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA06835,GSE44674,GPL13112,1000,Gaucher Disease,C0017205,Spleen,GEO,RNA-Seq,Mus musculus,8|7,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA06836,GSE44705,GPL6246,0,Central Nervous System Neurodegenerative Disorder,C0270715,Retina,GEO,Microarray,Mus musculus,2|2,DO:A central nervous system disease that results in the progressive deterioration of function or structure of neurons. DSA06837,GSE44705,GPL6246,64,Central Nervous System Neurodegenerative Disorder,C0270715,Retina,GEO,Microarray,Mus musculus,2|2,DO:A central nervous system disease that results in the progressive deterioration of function or structure of neurons. DSA06838,GSE44705,GPL6246,25,Central Nervous System Neurodegenerative Disorder,C0270715,Retina,GEO,Microarray,Mus musculus,2|2,DO:A central nervous system disease that results in the progressive deterioration of function or structure of neurons. DSA06839,GSE44705,GPL6246,0,Central Nervous System Neurodegenerative Disorder,C0270715,Retina,GEO,Microarray,Mus musculus,2|2,DO:A central nervous system disease that results in the progressive deterioration of function or structure of neurons. DSA06840,GSE44705,GPL6246,8,Central Nervous System Neurodegenerative Disorder,C0270715,Retina,GEO,Microarray,Mus musculus,2|2,DO:A central nervous system disease that results in the progressive deterioration of function or structure of neurons. DSA06841,GSE44707,GPL6246,0,Central Nervous System Neurodegenerative Disorder,C0270715,Retina,GEO,Microarray,Mus musculus,2|2,DO:A central nervous system disease that results in the progressive deterioration of function or structure of neurons. DSA06842,GSE44707,GPL6246,1,Central Nervous System Neurodegenerative Disorder,C0270715,Retina,GEO,Microarray,Mus musculus,2|2,DO:A central nervous system disease that results in the progressive deterioration of function or structure of neurons. DSA06843,GSE44707,GPL6246,10,Central Nervous System Neurodegenerative Disorder,C0270715,Retina,GEO,Microarray,Mus musculus,2|2,DO:A central nervous system disease that results in the progressive deterioration of function or structure of neurons. DSA06844,GSE44707,GPL6246,6,Central Nervous System Neurodegenerative Disorder,C0270715,Retina,GEO,Microarray,Mus musculus,2|2,DO:A central nervous system disease that results in the progressive deterioration of function or structure of neurons. DSA06845,GSE44707,GPL6246,1,Central Nervous System Neurodegenerative Disorder,C0270715,Retina,GEO,Microarray,Mus musculus,2|2,DO:A central nervous system disease that results in the progressive deterioration of function or structure of neurons. DSA06846,GSE44874,GPL5188,0,Dysferlinopathy,C2931687,Vastus lateralis,GEO,Microarray,Homo sapiens,7|4, DSA06847,GSE44874,GPL5188,8,Caveolinopathy 3,,Vastus lateralis,GEO,Microarray,Homo sapiens,7|4, DSA06848,GSE44874,GPL5188,0,Facioscapulohumeral Dystrophy,C0238288,Vastus lateralis,GEO,Microarray,Homo sapiens,7|4,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA06849,GSE44874,GPL5188,2,Four And A Half Lim Domains Protein 1 Deficiency,,Vastus lateralis,GEO,Microarray,Homo sapiens,7|3, DSA06850,GSE44925,GPL6246,1000,Rhabdomyolysis;Acute Kidney Injury,,Kidney,GEO,Microarray,Mus musculus,3|5, DSA06851,GSE44925,GPL6246,1000,Rhabdomyolysis;Acute Kidney Injury,,Kidney,GEO,Microarray,Mus musculus,3|5, DSA06852,GSE44960,GPL14552,0,Seasonal Allergic Rhinitis,C0018621,Blood,GEO,Microarray,Homo sapiens,10|10,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA06853,GSE44960,GPL14552,0,Seasonal Allergic Rhinitis,C0018621,Blood,GEO,Microarray,Homo sapiens,10|10,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA06854,GSE44969,GPL6947,63,Chronic Granulomatous Disease,C0018203,Blood,GEO,Microarray,Homo sapiens,13|7,"DO:A phagocyte bactericidal dysfunction characterized by an inability to resist repeated infectious diseases and a tendency to develop chronic inflammation. Life-threatening recurrent fungal and bacterial infections affecting the skin, lungs, liver, lymph nodes, and bones may occur along with swollen areas of inflamed tissues known as granulomas that can be widely distributed." DSA06855,GSE44973,GPL16766,2,Melanoma,C0025202,,GEO,Microarray,Homo sapiens,3|1,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA06856,GSE44989,GPL81,1000,Experimental Autoimmune Encephalomyelitis,C0014072,Spinal cord,GEO,Microarray,Mus musculus,3|5,"EFO:An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)" DSA06857,GSE45016,GPL570,7,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,1|10,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA06858,GSE45050,GPL6244,6,Cirrhosis,C1623038,Liver,GEO,Microarray,Homo sapiens,3|5,"MSH:Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury." DSA06859,GSE45050,GPL6244,155,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,3|6,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA06860,GSE45188,GPL6244,1,Leiomyoma,C0042133,Myometrium,GEO,Microarray,Homo sapiens,3|3,DO:An uterine benign neoplasm derived from the smooth muscle layer of the uterus. DSA06861,GSE45188,GPL6244,845,Leiomyoma,C0042133,Myometrium,GEO,Microarray,Homo sapiens,3|3,DO:An uterine benign neoplasm derived from the smooth muscle layer of the uterus. DSA06862,GSE45291,GPL13158,1000,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,20|292,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA06863,GSE45291,GPL13158,1000,Rheumatoid Arthritis,C0003873,Blood,GEO,Microarray,Homo sapiens,20|115,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA06864,GSE45291,GPL13158,1000,Rheumatoid Arthritis,C0003873,Blood,GEO,Microarray,Homo sapiens,20|378,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA06865,GSE45331,GPL6102,460,Myotonic Dystrophy Type 2,C2931689,Vastus lateralis,GEO,Microarray,Homo sapiens,4|6,"DO:A myotonic disease that is characterized by myotonia and progressive, proximal muscle wasting and weakness affecting the skeletal and smooth muscles of the neck, shoulders, elbows and hips and has_material_basis_in the autosomal dominant inheritance of the CNBP (ZNF9) gene containing an expansion of a CCTG repeat in intron one." DSA06866,GSE45376,GPL13112,1000,Spinal Cord Disorder,C0037928,Spinal cord,GEO,RNA-Seq,Mus musculus,2|3,EFO:A disease involving the spinal cord. DSA06867,GSE45376,GPL13112,1000,Spinal Cord Disorder,C0037928,Spinal cord,GEO,RNA-Seq,Mus musculus,2|2,EFO:A disease involving the spinal cord. DSA06868,GSE45512,GPL570,1,Alopecia Areata,C0002171,Scalp skin,GEO,Microarray,Homo sapiens,5|5,DO:An autoimmune disease resulting in the loss of hair on the scalp and elsewhere on the body initially causing bald spots. DSA06869,GSE45536,GPL570,1000,Scleroderma,C0011644,Blood,GEO,Microarray,Homo sapiens,24|16,"DO:A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies." DSA06870,GSE45603,GPL10558,0,Depression,C0011581,Blood,GEO,Microarray,Homo sapiens,13|56,DO:A mood disorder that involves the presence of a low mood almost daily over a span of at least two years. DSA06871,GSE45603,GPL10558,1000,Postpartum Depression,C0221074,Blood,GEO,Microarray,Homo sapiens,13|53,"DO:An endogenous depression that involves intense, sustained and sometimes disabling depression experienced by women after giving birth." DSA06872,GSE45686,GPL10558,0,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,5|5,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA06873,GSE45686,GPL10558,0,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,5|5,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA06874,GSE45686,GPL10558,0,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,5|5,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA06875,GSE45686,GPL10558,0,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,5|5,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA06876,GSE45709,GPL6244,0,Uremia,C0041948,Plasma,GEO,Microarray,Homo sapiens,5|5,DO:A kidney disease characterized by the failure of the kidneys to adequately filter waste products from the blood. DSA06877,GSE45709,GPL6244,0,Uremia,C0041948,Plasma,GEO,Microarray,Homo sapiens,5|5,DO:A kidney disease characterized by the failure of the kidneys to adequately filter waste products from the blood. DSA06878,GSE45717,GPL9793,1000,Mantle Cell Lymphoma,C4721414,Peripheral blood,GEO,Microarray,Homo sapiens,8|5,MONDO:Mantle cell lymphoma is a rare form of malignant non-Hodgkin lymphoma affecting B lymphocytes in the lymph nodes in a region called the ``mantle zone''. DSA06879,GSE45818,GPL11533,3,Heart Ischemia,,Left ventricle,GEO,Microarray,Mus musculus,3|3, DSA06880,GSE45818,GPL11533,12,Ischemia Reperfusion Injury,C0035126,Left ventricle,GEO,Microarray,Mus musculus,3|3,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA06881,GSE45818,GPL11533,4,Ischemia Reperfusion Injury,C0035126,Left ventricle,GEO,Microarray,Mus musculus,3|3,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA06882,GSE45818,GPL11533,1,Heart Ischemia,,Left ventricle,GEO,Microarray,Mus musculus,3|3, DSA06883,GSE45818,GPL11533,27,Ischemia Reperfusion Injury,C0035126,Left ventricle,GEO,Microarray,Mus musculus,3|3,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA06884,GSE45818,GPL11533,1,Ischemia Reperfusion Injury,C0035126,Left ventricle,GEO,Microarray,Mus musculus,3|3,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA06885,GSE45885,GPL6244,135,Non-Obstructive Azoospermia,C4021107,Testis,GEO,Microarray,Homo sapiens,4|11,"HPO:Absence of any measurable level of sperm in his semen, resulting from a defect in the production of spermatozoa in the testes. This can be differentiated from obstructive azoospermia on the basis of testicular biopsy." DSA06886,GSE45885,GPL6244,126,Non-Obstructive Azoospermia,C4021107,Testis,GEO,Microarray,Homo sapiens,4|7,"HPO:Absence of any measurable level of sperm in his semen, resulting from a defect in the production of spermatozoa in the testes. This can be differentiated from obstructive azoospermia on the basis of testicular biopsy." DSA06887,GSE45885,GPL6244,1000,Non-Obstructive Azoospermia,C4021107,Testis,GEO,Microarray,Homo sapiens,4|2,"HPO:Absence of any measurable level of sperm in his semen, resulting from a defect in the production of spermatozoa in the testes. This can be differentiated from obstructive azoospermia on the basis of testicular biopsy." DSA06888,GSE45885,GPL6244,1000,Non-Obstructive Azoospermia,C4021107,Testis,GEO,Microarray,Homo sapiens,4|7,"HPO:Absence of any measurable level of sperm in his semen, resulting from a defect in the production of spermatozoa in the testes. This can be differentiated from obstructive azoospermia on the basis of testicular biopsy." DSA06889,GSE45887,GPL6244,3,Non-Obstructive Azoospermia,C4021107,Testis,GEO,Microarray,Homo sapiens,4|7,"HPO:Absence of any measurable level of sperm in his semen, resulting from a defect in the production of spermatozoa in the testes. This can be differentiated from obstructive azoospermia on the basis of testicular biopsy." DSA06890,GSE45887,GPL6244,4,Non-Obstructive Azoospermia,C4021107,Testis,GEO,Microarray,Homo sapiens,4|4,"HPO:Absence of any measurable level of sperm in his semen, resulting from a defect in the production of spermatozoa in the testes. This can be differentiated from obstructive azoospermia on the basis of testicular biopsy." DSA06891,GSE45887,GPL6244,1000,Non-Obstructive Azoospermia,C4021107,Testis,GEO,Microarray,Homo sapiens,4|5,"HPO:Absence of any measurable level of sperm in his semen, resulting from a defect in the production of spermatozoa in the testes. This can be differentiated from obstructive azoospermia on the basis of testicular biopsy." DSA06892,GSE45897,GPL7202,1000,Non-Obese Diabetes,,Pancreatic islet,GEO,Microarray,Mus musculus,6|6, DSA06893,GSE45918,GPL6883,319,Monocytosis,C0085702,Peripheral blood,GEO,Microarray,Homo sapiens,8|8,HPO:An increased number of circulating monocytes. DSA06894,GSE45919,GPL10558,1000,Monocytosis,C0085702,Peripheral blood,GEO,Microarray,Homo sapiens,9|3,HPO:An increased number of circulating monocytes. DSA06895,GSE45919,GPL10558,1000,Monocytosis,C0085702,Peripheral blood,GEO,Microarray,Homo sapiens,9|12,HPO:An increased number of circulating monocytes. DSA06896,GSE45923,GPL11670,1000,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,5|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA06897,GSE45923,GPL11670,926,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,5|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA06898,GSE46021,GPL4133,27,Primary Myelofibrosis,C0001815,Bone marrow,GEO,Microarray,Homo sapiens,6|4,DO:A myeloid neoplasm that is located in the bone marrow which results in bone marrow being replaced by fibrous (scar) tissue. DSA06899,GSE46021,GPL4133,2,Primary Myelofibrosis,C0001815,Bone marrow,GEO,Microarray,Homo sapiens,6|4,DO:A myeloid neoplasm that is located in the bone marrow which results in bone marrow being replaced by fibrous (scar) tissue. DSA06900,GSE4603,GPL891,370,Chronic Cholangitis,C0267918,Liver,GEO,Microarray,Mus musculus,3|3,MONDO:Cholangitis that is persistent and long-standing. DSA06901,GSE4603,GPL891,1000,Chronic Cholangitis,C0267918,Liver,GEO,Microarray,Mus musculus,3|3,MONDO:Cholangitis that is persistent and long-standing. DSA06902,GSE4603,GPL891,1000,Chronic Cholangitis,C0267918,Liver,GEO,Microarray,Mus musculus,3|3,MONDO:Cholangitis that is persistent and long-standing. DSA06903,GSE4603,GPL891,1000,Chronic Cholangitis,C0267918,Liver,GEO,Microarray,Mus musculus,3|3,MONDO:Cholangitis that is persistent and long-standing. DSA06904,GSE46053,GPL16100,29,Multiple Myeloma,C0026764,Bone marrow,GEO,Microarray,Homo sapiens,8|12,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA06905,GSE46053,GPL16100,11,Multiple Myeloma,C0026764,Bone marrow,GEO,Microarray,Homo sapiens,8|9,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA06906,GSE4607,GPL570,1000,Septic Shock,C0036983,Blood,GEO,Microarray,Homo sapiens,15|42,"DO:A commensal bacterial infectious disease that results_in infection, has_material_basis_in Streptococcus pyogenes or has_material_basis_in Staphylococcus aureus , which produce toxins that are absorbed systemically and produce the systemic manifestations. The infection has_symptom fever, has_symptom rash, has_symptom hypotension, has_symptom multiorgan failure, has_symptom desquamation, has_symptom vomiting, has_symptom diarrhea, has_symptom headache, and has_symptom nonfocal neurologic abnormalities." DSA06907,GSE4607,GPL570,1000,Septic Shock,C0036983,Blood,GEO,Microarray,Homo sapiens,15|27,"DO:A commensal bacterial infectious disease that results_in infection, has_material_basis_in Streptococcus pyogenes or has_material_basis_in Staphylococcus aureus , which produce toxins that are absorbed systemically and produce the systemic manifestations. The infection has_symptom fever, has_symptom rash, has_symptom hypotension, has_symptom multiorgan failure, has_symptom desquamation, has_symptom vomiting, has_symptom diarrhea, has_symptom headache, and has_symptom nonfocal neurologic abnormalities." DSA06908,GSE4607,GPL570,1000,Systemic Inflammatory Response Syndrome,C0242966,Blood,GEO,Microarray,Homo sapiens,15|19,"MSH:A systemic inflammatory response to a variety of clinical insults, characterized by two or more of the following conditions: (1) fever >38 degrees C or HYPOTHERMIA <36 degrees C; (2) TACHYCARDIA >90 beat/minute; (3) tachypnea >24 breaths/minute; (4) LEUKOCYTOSIS >12,000 cells/cubic mm or 10% immature forms. While usually related to infection, SIRS can also be associated with noninfectious insults such as TRAUMA; BURNS; or PANCREATITIS. If infection is involved, a patient with SIRS is said to have SEPSIS." DSA06909,GSE4607,GPL570,1000,Systemic Inflammatory Response Syndrome,C0242966,Blood,GEO,Microarray,Homo sapiens,15|20,"MSH:A systemic inflammatory response to a variety of clinical insults, characterized by two or more of the following conditions: (1) fever >38 degrees C or HYPOTHERMIA <36 degrees C; (2) TACHYCARDIA >90 beat/minute; (3) tachypnea >24 breaths/minute; (4) LEUKOCYTOSIS >12,000 cells/cubic mm or 10% immature forms. While usually related to infection, SIRS can also be associated with noninfectious insults such as TRAUMA; BURNS; or PANCREATITIS. If infection is involved, a patient with SIRS is said to have SEPSIS." DSA06910,GSE46097,GPL571,744,Cardiovascular Disease,C0007222,Blood,GEO,Microarray,Homo sapiens,159|159,"DO:A disease of anatomical entity which occurs in the blood, heart, blood vessels or the lymphatic system that passes nutrients (such as amino acids and electrolytes), gases, hormones, blood cells or lymph to and from cells in the body to help fight diseases and help stabilize body temperature and pH to maintain homeostasis." DSA06911,GSE46097,GPL571,175,Cardiovascular Disease,C0007222,Blood,GEO,Microarray,Homo sapiens,30|30,"DO:A disease of anatomical entity which occurs in the blood, heart, blood vessels or the lymphatic system that passes nutrients (such as amino acids and electrolytes), gases, hormones, blood cells or lymph to and from cells in the body to help fight diseases and help stabilize body temperature and pH to maintain homeostasis." DSA06912,GSE46157,GPL10332,1000,Intrahepatic Cholestasis of Pregnancy,C3489728,Placenta,GEO,Microarray,Homo sapiens,2|2, DSA06913,GSE46157,GPL10332,1000,Intrahepatic Cholestasis of Pregnancy,C3489728,Placenta,GEO,Microarray,Homo sapiens,2|2, DSA06914,GSE46171,GPL16981,1,Allergic Rhinitis,C2607914,Nasal mucosa,GEO,Microarray,Homo sapiens,14|5,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA06915,GSE46171,GPL16981,227,Asthma,C0004096,Nasal mucosa,GEO,Microarray,Homo sapiens,14|19,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06916,GSE46171,GPL16981,11,Asthma,C0004096,Nasal mucosa,GEO,Microarray,Homo sapiens,14|6,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06917,GSE46171,GPL6480,28,Allergic Rhinitis,C2607914,Nasal mucosa,GEO,Microarray,Homo sapiens,3|6,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA06918,GSE46171,GPL6480,1,Asthma,C0004096,Nasal mucosa,GEO,Microarray,Homo sapiens,3|11,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06919,GSE46171,GPL6480,22,Asthma,C0004096,Nasal mucosa,GEO,Microarray,Homo sapiens,3|27,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA06920,GSE46234,GPL570,0,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,Microarray,Homo sapiens,4|2,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA06921,GSE46234,GPL570,0,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,Microarray,Homo sapiens,4|2,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA06922,GSE46239,GPL570,871,Dermatomyositis,C0011633,Skin,GEO,Microarray,Homo sapiens,4|48,DO:A myositis that results_in inflammation located_in muscle or located_in skin where a skin rash is often seen prior to the onset of muscle weakness. The disease may result from either a viral infection or an autoimmune reaction. DSA06923,GSE46416,GPL11028,1000,Bipolar Disorder,C0005586,Blood,GEO,Microarray,Homo sapiens,10|11,DO:A mood disorder that involves alternating periods of mania and depression. DSA06924,GSE46416,GPL11028,108,Bipolar Disorder,C0005586,Blood,GEO,Microarray,Homo sapiens,10|11,DO:A mood disorder that involves alternating periods of mania and depression. DSA06925,GSE31471,GPL570,101,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA06926,GSE46562,GPL11154,64,Schizophrenia,C0036341,,GEO,RNA-Seq,Homo sapiens,3|6,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA06927,GSE46562,GPL11154,1000,Schizophrenia,C0036341,,GEO,RNA-Seq,Homo sapiens,4|6,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA06928,GSE46600,GPL1261,344,Non-Obese Diabetes,,Spleen,GEO,Microarray,Mus musculus,5|4, DSA06929,GSE46600,GPL1261,1000,Non-Obese Diabetes,,Spleen,GEO,Microarray,Mus musculus,5|5, DSA06930,GSE46600,GPL1261,639,Non-Obese Diabetes,,Spleen,GEO,Microarray,Mus musculus,5|5, DSA06931,GSE46831,GPL13393,1000,Intellectual Disability,C3714756,,GEO,RNA-Seq,Homo sapiens,8|3,"DO:A specific developmental disorder that involves significant limitations both in mental functioning and in adaptive behavior such as communicating, taking care of him or herself, and social skills." DSA06932,GSE46846,GPL11154,1000,Mantle Cell Lymphoma,C4721414,,GEO,RNA-Seq,Homo sapiens,3|4,MONDO:Mantle cell lymphoma is a rare form of malignant non-Hodgkin lymphoma affecting B lymphocytes in the lymph nodes in a region called the ``mantle zone''. DSA06933,GSE46897,GPL6884,0,Diabetes,C0011847,,GEO,Microarray,Homo sapiens,2|2,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA06934,GSE46897,GPL6884,0,Diabetic Kidney Disease,C0011881,,GEO,Microarray,Homo sapiens,2|2,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA06935,GSE46899,GPL10558,0,Diabetes,C0011847,,GEO,Microarray,Homo sapiens,2|2,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA06936,GSE46899,GPL10558,0,Diabetic Kidney Disease,C0011881,,GEO,Microarray,Homo sapiens,2|2,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA06937,GSE46907,GPL96,146,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,5|5,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA06938,GSE46907,GPL97,38,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,5|5,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA06939,GSE46955,GPL6104,1000,Sepsis,C0243026,,GEO,Microarray,Homo sapiens,6|8,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA06940,GSE46955,GPL6104,1000,Sepsis,C0243026,,GEO,Microarray,Homo sapiens,6|8,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA06941,GSE46960,GPL6244,1000,Intrahepatic Cholestasis,C0008372,Liver,GEO,Microarray,Homo sapiens,7|14,DO:A cholestasis characterized by impairment of the bile flow caused by obstruction located_in liver. DSA06942,GSE46960,GPL6244,1000,Biliary Atresia,C0005411,Liver,GEO,Microarray,Homo sapiens,7|64,DO:A cholestasis characterized by blockage of the ducts that carry bile from the liver to the gallbladder. DSA06943,GSE47018,GPL96,271,Polycythemia Vera,C0032463,Peripheral blood,GEO,Microarray,Homo sapiens,7|11,"DO:A myeloproliferative neoplasm characterized by erythroid hyperplasia, myeloid leukocytosis, thrombocytosis, and splenomegaly." DSA06944,GSE47172,GPL96,24,Invasive Pneumococcal Disease; Recurrent Isolated,C1835828,Peripheral blood,GEO,Microarray,Homo sapiens,3|3, DSA06945,GSE47172,GPL96,402,Invasive Pneumococcal Disease; Recurrent Isolated,C1835828,Peripheral blood,GEO,Microarray,Homo sapiens,3|3, DSA06946,GSE47172,GPL96,139,Invasive Pneumococcal Disease; Recurrent Isolated,C1835828,Peripheral blood,GEO,Microarray,Homo sapiens,3|3, DSA06947,GSE47172,GPL96,308,Invasive Pneumococcal Disease; Recurrent Isolated,C1835828,Peripheral blood,GEO,Microarray,Homo sapiens,3|3, DSA06948,GSE47197,GPL16699,1000,Liver Tumor,C0345904,Liver,GEO,Microarray,Homo sapiens,63|61,DO:A hepatobiliary system cancer that is located_in the liver. DSA06949,GSE47360,GPL6244,0,Endometriosis,C0014175,,GEO,Microarray,Homo sapiens,3|3,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA06950,GSE47392,GPL570,5,Twin-Twin Transfusion Syndrome,,,GEO,Microarray,Homo sapiens,8|8, DSA06951,GSE47460,GPL14550,1000,Chronic Obstructive Pulmonary Disease,C0024117,Lung,GEO,Microarray,Homo sapiens,91|145,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA06952,GSE47460,GPL14550,1000,Interstitial Lung Disease,C0206062,Lung,GEO,Microarray,Homo sapiens,91|193,"DO:A lung disease that is characterized by inflammation and altered lung interstitium compromising pulmonary function and often has_symptom shortness of breath, dyspnea, and/or cough." DSA06953,GSE47460,GPL6480,113,Chronic Obstructive Pulmonary Disease,C0024117,Lung,GEO,Microarray,Homo sapiens,17|75,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA06954,GSE47460,GPL6480,1000,Interstitial Lung Disease,C0206062,Lung,GEO,Microarray,Homo sapiens,17|61,"DO:A lung disease that is characterized by inflammation and altered lung interstitium compromising pulmonary function and often has_symptom shortness of breath, dyspnea, and/or cough." DSA06955,GSE47584,GPL14550,15,Klinefelter Syndrome,C0022735,Peripheral blood,GEO,Microarray,Homo sapiens,5|5,DO:A chromosomal duplication syndrome that is characterized by infertility and that has_material_basis_in an extra X chromosome in cells in men. DSA06956,GSE47598,GPL10558,0,Psoriasis,C0033860,,GEO,Microarray,Homo sapiens,7|17,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA06957,GSE47603,GPL10558,1000,Complex Regional Pain Syndrome,C0458219,Blood,GEO,Microarray,Homo sapiens,5|4,"MONDO:Complex regional pain syndrome (CRPS) is a rare neurologic disease painful progressive condition that corresponds to a group of disorders characterized by a disproportionate spontaneous or stimulus-induced pain, accompanied by a variably mixed myriad of autonomic and motor disorders including symptoms such as swelling, allodynia, skin blood supply and trophic disturbances. CRPS most often affects one of the arms, legs, hands, or feet and usually occurs after an injury or trauma to that limb." DSA06958,GSE47642,GPL7363,0,Kindler Syndrome,C0406557,Skin,GEO,Microarray,Homo sapiens,3|3,"DO:A skin disease characterized by congenital blistering, skin atrophy, photosensitivity, skin fragility, and scaling." DSA06959,GSE47756,GPL10558,1000,Colorectal Carcinoma,C0009402,Peripheral blood,GEO,Microarray,Homo sapiens,38|27,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA06960,GSE47756,GPL10558,1000,Colorectal Carcinoma,C0009402,Peripheral blood,GEO,Microarray,Homo sapiens,38|28,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA06961,GSE47756,GPL10558,0,Metastatic Colorectal Carcinoma,C0009402,Peripheral blood,GEO,Microarray,Homo sapiens,27|28,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA06962,GSE47811,GPL1261,2,Pancreatic Tumor,C0030297,Saliva,GEO,Microarray,Mus musculus,6|6,DO:An endocrine gland cancer located_in the pancreas. DSA06963,GSE47900,GPL1261,391,Experimental Autoimmune Encephalomyelitis,C0014072,Brain,GEO,Microarray,Mus musculus,4|6,"EFO:An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)" DSA06964,GSE47900,GPL1261,342,Experimental Autoimmune Encephalomyelitis,C0014072,Brain,GEO,Microarray,Mus musculus,4|6,"EFO:An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)" DSA06965,GSE47908,GPL570,1000,Colitis,C0009319,Colon,GEO,Microarray,Homo sapiens,15|20,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA06966,GSE47908,GPL570,1000,Colitis,C0009319,Colon,GEO,Microarray,Homo sapiens,15|19,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA06967,GSE47908,GPL570,1000,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,15|6,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA06968,GSE47944,GPL11154,1000,Psoriasis,C0033860,Skin,GEO,RNA-Seq,Homo sapiens,5|7,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA06969,GSE47944,GPL11154,1000,Psoriasis,C0033860,Skin,GEO,RNA-Seq,Homo sapiens,5|8,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA06970,GSE47944,GPL11154,1000,Psoriasis,C0033860,Skin,GEO,RNA-Seq,Homo sapiens,5|8,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA06971,GSE47944,GPL11154,1000,Psoriasis,C0033860,Skin,GEO,RNA-Seq,Homo sapiens,5|8,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA06972,GSE47944,GPL11154,1000,Psoriasis,C0033860,Skin,GEO,RNA-Seq,Homo sapiens,8|7,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA06973,GSE47944,GPL11154,1000,Psoriasis,C0033860,Skin,GEO,RNA-Seq,Homo sapiens,8|8,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA06974,GSE47944,GPL11154,1000,Psoriasis,C0033860,Skin,GEO,RNA-Seq,Homo sapiens,8|8,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA06975,GSE47944,GPL11154,1000,Psoriasis,C0033860,Skin,GEO,RNA-Seq,Homo sapiens,8|8,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA06976,GSE47968,GPL5188,100,Myotonic Dystrophy,C0027126,Quadriceps,GEO,Microarray,Homo sapiens,8|2,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA06977,GSE47968,GPL5188,87,Myotonic Dystrophy,C0027126,Quadriceps,GEO,Microarray,Homo sapiens,8|7,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA06978,GSE47968,GPL5188,0,Facioscapulohumeral Dystrophy,C0238288,Quadriceps,GEO,Microarray,Homo sapiens,8|8,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA06979,GSE48041,GPL10787,1000,Hydronephrosis,C0020295,Kidney,GEO,Microarray,Mus musculus,6|7,"EFO:Collection of urine in the renal pelvis that results in dilatation of the renal pelvis and calyces. It is caused by obstruction of urine flow, nephrolithiasis, or vesicoureteral reflux. Signs and symptoms include flank pain, nausea, vomiting, fever, and dysuria." DSA06980,GSE48041,GPL10787,305,Hydronephrosis,C0020295,Kidney,GEO,Microarray,Mus musculus,6|5,"EFO:Collection of urine in the renal pelvis that results in dilatation of the renal pelvis and calyces. It is caused by obstruction of urine flow, nephrolithiasis, or vesicoureteral reflux. Signs and symptoms include flank pain, nausea, vomiting, fever, and dysuria." DSA06981,GSE48041,GPL10787,1000,Hydronephrosis,C0020295,Kidney,GEO,Microarray,Mus musculus,6|6,"EFO:Collection of urine in the renal pelvis that results in dilatation of the renal pelvis and calyces. It is caused by obstruction of urine flow, nephrolithiasis, or vesicoureteral reflux. Signs and symptoms include flank pain, nausea, vomiting, fever, and dysuria." DSA06982,GSE48120,GPL570,0,Osteoma Cutis,C0334041,Skin,GEO,Microarray,Homo sapiens,5|5,"HPO:The term osteoma refers to the anomalous presence of ossification (bone formation) in the interior of the dermis or epidermis. The dermal or subcutaneous bone formation presents as stony hard nodules. The osteomata appear as irregular, hardened small nodules that are well circumscribed and generally of the same color as the skin." DSA06983,GSE48129,GPL570,0,Osteoma Cutis,C0334041,Skin,GEO,Microarray,Homo sapiens,5|5,"HPO:The term osteoma refers to the anomalous presence of ossification (bone formation) in the interior of the dermis or epidermis. The dermal or subcutaneous bone formation presents as stony hard nodules. The osteomata appear as irregular, hardened small nodules that are well circumscribed and generally of the same color as the skin." DSA06984,GSE48166,GPL9115|GPL9442,17,Ischemic Cardiomyopathy,C0349782,Heart,GEO,RNA-Seq,Homo sapiens,15|14,EFO:Ischemic cardiomyopathy is a cardiomyopathy in which a weakness in the muscle of the heart due to inadequate oxygen delivery to the myocardium with coronary artery disease being the most common cause. DSA06985,GSE48350,GPL570,179,Alzheimer's Disease,C0002395,Entorhinal cortex,GEO,Microarray,Homo sapiens,39|15,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA06986,GSE48350,GPL570,1000,Alzheimer's Disease,C0002395,Hippocampus,GEO,Microarray,Homo sapiens,43|19,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA06987,GSE48350,GPL570,161,Alzheimer's Disease,C0002395,Brain,GEO,Microarray,Homo sapiens,43|25,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA06988,GSE48350,GPL570,1000,Alzheimer's Disease,C0002395,Superior frontal gyrus,GEO,Microarray,Homo sapiens,48|21,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA06989,GSE48378,GPL5175,1000,Sjogren's Syndrome,C1527336,,GEO,Microarray,Homo sapiens,16|11,DO:An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. DSA06990,GSE48424,GPL6480,1000,Pre-Eclampsia,C0032914,Blood,GEO,Microarray,Homo sapiens,18|5,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA06991,GSE48424,GPL6480,25,Pre-Eclampsia,C0032914,Blood,GEO,Microarray,Homo sapiens,18|13,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA06992,GSE48452,GPL11532,0,Obesity,C0028754,Liver,GEO,Microarray,Homo sapiens,12|16,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA06993,GSE48452,GPL11532,14,Steatosis,C2711227,Liver,GEO,Microarray,Homo sapiens,12|9,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA06994,GSE48452,GPL11532,11,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Homo sapiens,12|17,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA06995,GSE48556,GPL6947,1000,Osteoarthritis,C0157946,Blood,GEO,Microarray,Homo sapiens,33|106,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA06996,GSE48828,GPL5175,1000,Becker Muscular Dystrophy,C0917713,Skeletal muscle,GEO,Microarray,Homo sapiens,4|3,"DO:A muscular dystrophy that involves slowly worsening muscle weakness of the legs and pelvis, and has_material_basis_in X-linked recessive inheritance of mutation in the dystrophin gene on chromosome Xp21." DSA06997,GSE48828,GPL5175,1000,Myotonic Dystrophy Type 1,C0027126,Skeletal muscle,GEO,Microarray,Homo sapiens,4|8,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA06998,GSE48828,GPL5175,1000,Myotonic Dystrophy Type 2,C2931689,Skeletal muscle,GEO,Microarray,Homo sapiens,4|10,"DO:A myotonic disease that is characterized by myotonia and progressive, proximal muscle wasting and weakness affecting the skeletal and smooth muscles of the neck, shoulders, elbows and hips and has_material_basis_in the autosomal dominant inheritance of the CNBP (ZNF9) gene containing an expansion of a CCTG repeat in intron one." DSA06999,GSE48828,GPL5175,269,Tibial Muscular Dystrophy,C1450052,Skeletal muscle,GEO,Microarray,Homo sapiens,4|2,DO:A distal muscular dystrophy characterized by autosomal dominant inheritance of late-onset muscular dystrophy beginning in the anterior comparment of the legs that has_material_basis_in heterozygous mutation in the TTN gene on chromosome 2q31. DSA07000,GSE48828,GPL5188,527,Myotonic Dystrophy Type 1,C0027126,Skeletal muscle,GEO,Microarray,Homo sapiens,4|8,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA07001,GSE48828,GPL5188,902,Myotonic Dystrophy Type 2,C2931689,Skeletal muscle,GEO,Microarray,Homo sapiens,4|10,"DO:A myotonic disease that is characterized by myotonia and progressive, proximal muscle wasting and weakness affecting the skeletal and smooth muscles of the neck, shoulders, elbows and hips and has_material_basis_in the autosomal dominant inheritance of the CNBP (ZNF9) gene containing an expansion of a CCTG repeat in intron one." DSA07002,GSE48828,GPL5188,424,Becker Muscular Dystrophy,C0917713,Skeletal muscle,GEO,Microarray,Homo sapiens,4|3,"DO:A muscular dystrophy that involves slowly worsening muscle weakness of the legs and pelvis, and has_material_basis_in X-linked recessive inheritance of mutation in the dystrophin gene on chromosome Xp21." DSA07003,GSE48828,GPL5188,140,Tibial Muscular Dystrophy,C1450052,Skeletal muscle,GEO,Microarray,Homo sapiens,4|2,DO:A distal muscular dystrophy characterized by autosomal dominant inheritance of late-onset muscular dystrophy beginning in the anterior comparment of the legs that has_material_basis_in heterozygous mutation in the TTN gene on chromosome 2q31. DSA07004,GSE48936,GPL6246,1000,Pulmonary Hypertension,C0020542,Lung,GEO,Microarray,Mus musculus,3|3,"DO:A hypertension characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein or pulmonary capillaries." DSA07005,GSE48958,GPL6244,1000,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,8|7,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA07006,GSE48958,GPL6244,1000,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,8|6,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA07007,GSE49072,GPL96,433,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,Microarray,Homo sapiens,61|8,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA07008,GSE49072,GPL96,1000,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,Microarray,Homo sapiens,61|15,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA07009,GSE49105,GPL5188,0,Ausitm Spectrum Disorder,C1510586,Blood,GEO,Microarray,Homo sapiens,20|10,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA07010,GSE49105,GPL5188,0,Ausitm Spectrum Disorder,C1510586,Blood,GEO,Microarray,Homo sapiens,20|20,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA07011,GSE49114,GPL13112,1000,Pulmonary Hypertension,C0020542,Lung,GEO,RNA-Seq,Mus musculus,5|5,"DO:A hypertension characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein or pulmonary capillaries." DSA07012,GSE49114,GPL13112,1000,Pulmonary Hypertension,C0020542,Lung,GEO,RNA-Seq,Mus musculus,3|3,"DO:A hypertension characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein or pulmonary capillaries." DSA07013,GSE49126,GPL4133,0,Parkinson's Disease,C0030567,,GEO,Microarray,Homo sapiens,20|30,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA07014,GSE49292,GPL5175,1000,Barrett's Esophagus,C0004763,,GEO,Microarray,Homo sapiens,3|6,DO:An esophageal disease characterized by a change of normal esophageal squamous epithelium to a columnar and intestinal-type epithelium. DSA07015,GSE49376,GPL10904,0,Alcohol Use Disorder,C0001956,Prefrontal cortex,GEO,Microarray,Homo sapiens,25|14,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA07016,GSE49376,GPL10904,0,Alcohol Use Disorder,C0001956,Prefrontal cortex,GEO,Microarray,Homo sapiens,25|9,"MSH:A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4)" DSA07017,GSE49454,GPL10558,1000,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,20|157,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA07018,GSE49522,GPL339,10,Presbycusis,C0033074,Inferior colliculus,GEO,Microarray,Mus musculus,17|9,"MONDO:Bilateral hearing loss caused by progressive degeneration of cochlear structures and central auditory pathways, typically associated with the aging process." DSA07019,GSE49522,GPL339,43,Presbycusis,C0033074,Inferior colliculus,GEO,Microarray,Mus musculus,17|5,"MONDO:Bilateral hearing loss caused by progressive degeneration of cochlear structures and central auditory pathways, typically associated with the aging process." DSA07020,GSE49543,GPL339,19,Presbycusis,C0033074,Cochlea,GEO,Microarray,Mus musculus,17|9,"MONDO:Bilateral hearing loss caused by progressive degeneration of cochlear structures and central auditory pathways, typically associated with the aging process." DSA07021,GSE49543,GPL339,76,Presbycusis,C0033074,Cochlea,GEO,Microarray,Mus musculus,17|6,"MONDO:Bilateral hearing loss caused by progressive degeneration of cochlear structures and central auditory pathways, typically associated with the aging process." DSA07022,GSE49566,GPL8300,16,Lipodystrophy,C0023787,,GEO,Microarray,Homo sapiens,6|3,DO:A congenital generalized lipodystrophy that has_material_basis_in an autosomal recessive mutation of AGPAT2 on chromosome 9q34.3. DSA07023,GSE49641,GPL6244,451,Pancreatic Ductal Adenocarcinoma,C1335302,,GEO,Microarray,Homo sapiens,18|18,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA07024,GSE49753,GPL10558,16,Sepsis,C0243026,Plasma,GEO,Microarray,Homo sapiens,12|22,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07025,GSE49754,GPL10558,682,Sepsis,C0243026,Plasma,GEO,Microarray,Homo sapiens,16|22,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07026,GSE49755,GPL10558,1000,Sepsis,C0243026,Plasma,GEO,Microarray,Homo sapiens,16|22,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07027,GSE49756,GPL10558,1000,Sepsis,C0243026,Plasma,GEO,Microarray,Homo sapiens,18|17,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07028,GSE49756,GPL10558,817,Sepsis,C0243026,Plasma,GEO,Microarray,Homo sapiens,18|12,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07029,GSE49757,GPL10558,1000,Sepsis,C0243026,Plasma,GEO,Microarray,Homo sapiens,21|20,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07030,GSE49757,GPL10558,507,Sepsis,C0243026,Plasma,GEO,Microarray,Homo sapiens,21|15,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07031,GSE31470,GPL570,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA07032,GSE31469,GPL570,0,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA07033,GSE50006,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,Blood,GEO,Microarray,Homo sapiens,32|188,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA07034,GSE50101,GPL10558,0,Allergic Rhinitis,C2607914,,GEO,Microarray,Homo sapiens,10|9,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA07035,GSE50101,GPL10558,0,Allergic Rhinitis,C2607914,,GEO,Microarray,Homo sapiens,10|9,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA07036,GSE50223,GPL6884,711,Allergic Rhinitis,C2607914,,GEO,Microarray,Homo sapiens,21|21,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA07037,GSE50223,GPL6884,324,Allergic Rhinitis,C2607914,,GEO,Microarray,Homo sapiens,21|21,"DO:A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites." DSA07038,GSE50395,GPL4133,2,Antiphospholipid Syndrome,C0085278,,GEO,Microarray,Homo sapiens,3|3,DO:An autoimmune disease that is characterized by recurrent venous or arterial thrombosis and/or fetal losses associated with characteristic elevated levels of antibodies directed against membrane anionic phospholipids (anticardiolipin). DSA07039,GSE50395,GPL4133,0,Lupus With Antiphospholipid Syndrome,,,GEO,Microarray,Homo sapiens,3|3, DSA07040,GSE50395,GPL4133,0,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,3|3,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA07041,GSE50484,GPL570,0,Obesity,C0028754,Skeletal muscle,GEO,Microarray,Homo sapiens,7|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07042,GSE50484,GPL570,0,Obesity,C0028754,Skeletal muscle,GEO,Microarray,Homo sapiens,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07043,GSE50579,GPL14550,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,10|24,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07044,GSE50579,GPL14550,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,10|10,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07045,GSE50579,GPL14550,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,10|11,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07046,GSE50579,GPL14550,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,10|8,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07047,GSE50579,GPL14550,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,10|9,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07048,GSE51034,GPL6246,0,Coffin-Lowry Syndrome,C0265252,Mandibular molar,GEO,Microarray,Mus musculus,8|8,"DO:A syndrome that is characterized by skeletal malformations, growth retardation, hearing deficit, paroxysmal movement disorders, and cognitive impairment in affected males and some carrier females, and has_material_basis_in mutation in the RSK2 gene on chromosome Xp22." DSA07049,GSE51041,GPL16791,373,Facioscapulohumeral Muscular Dystrophy,C0238288,,GEO,RNA-Seq,Homo sapiens,3|2,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA07050,GSE51092,GPL6884,1000,Sjogren's Syndrome,C1527336,Peripheral blood,GEO,Microarray,Homo sapiens,32|190,DO:An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. DSA07051,GSE51257,GPL6244,0,Colon Tumor,C0009375,Colon mucosa,GEO,Microarray,Homo sapiens,2|4,DO:A colorectal cancer that is located_in the colon. DSA07052,GSE31469,GPL570,0,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA07053,GSE51404,GPL10558,9,Common Variable Immunodeficiency,C0009447,Blood,GEO,Microarray,Homo sapiens,21|14,DO:An agammaglobulinemia that is characterized by low Ig levels with phenotypically normal B cells that can proliferate but do not develop into Ig-producing cells and that esults in insufficient production of antibodies needed to respond to exposure of pathogens. DSA07054,GSE51404,GPL10558,366,Common Variable Immunodeficiency,C0009447,Blood,GEO,Microarray,Homo sapiens,21|18,DO:An agammaglobulinemia that is characterized by low Ig levels with phenotypically normal B cells that can proliferate but do not develop into Ig-producing cells and that esults in insufficient production of antibodies needed to respond to exposure of pathogens. DSA07055,GSE51405,GPL6947,1000,Common Variable Immunodeficiency,C0009447,Blood,GEO,Microarray,Homo sapiens,24|30,DO:An agammaglobulinemia that is characterized by low Ig levels with phenotypically normal B cells that can proliferate but do not develop into Ig-producing cells and that esults in insufficient production of antibodies needed to respond to exposure of pathogens. DSA07056,GSE51405,GPL6947,1000,Common Variable Immunodeficiency,C0009447,Blood,GEO,Microarray,Homo sapiens,24|29,DO:An agammaglobulinemia that is characterized by low Ig levels with phenotypically normal B cells that can proliferate but do not develop into Ig-producing cells and that esults in insufficient production of antibodies needed to respond to exposure of pathogens. DSA07057,GSE51490,GPL15640,1000,Renal Cell Carcinoma,C0007134,,GEO,Microarray,Homo sapiens,9|9,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA07058,GSE51546,GPL10558,16,Diabetes,C0011847,Umbilical cord,GEO,Microarray,Homo sapiens,6|6,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA07059,GSE51575,GPL13607,1000,Gastric Cancer,C0699791,,GEO,Microarray,Homo sapiens,26|14,DO:A gastrointestinal system cancer that is located_in the stomach. DSA07060,GSE51575,GPL13607,1000,Gastric Cancer,C0699791,,GEO,Microarray,Homo sapiens,26|12,DO:A gastrointestinal system cancer that is located_in the stomach. DSA07061,GSE51675,GPL6480,0,Chronic Antibody-Mediated Rejection,,,GEO,Microarray,Homo sapiens,8|10, DSA07062,GSE51684,GPL11154,1000,"Amyotrophic Lateral Sclerosis, Familial",C4551993,,GEO,RNA-Seq,Homo sapiens,8|6, DSA07063,GSE51684,GPL11154,896,"Amyotrophic Lateral Sclerosis, Familial",C4551993,,GEO,RNA-Seq,Homo sapiens,8|3, DSA07064,GSE51684,GPL11154,68,Sporadic Amyotrophic Lateral Sclerosis,C1862941,,GEO,RNA-Seq,Homo sapiens,8|4,DO:An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SOD1 gene on chromosome 21. The most common type of familial ALS. DSA07065,GSE51684,GPL11154,384,Sporadic Amyotrophic Lateral Sclerosis,C1862941,,GEO,RNA-Seq,Homo sapiens,8|3,DO:An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SOD1 gene on chromosome 21. The most common type of familial ALS. DSA07066,GSE51757,GPL14550,1000,Myelodysplastic Syndrome,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,4|4,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA07067,GSE51799,GPL10999|GPL11154,7,Huntington's Disease,C0020179,Blood,GEO,RNA-Seq,Homo sapiens,27|71,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA07068,GSE51843,GPL10558,0,Bladder Cancer,C0699885,Urine,GEO,Microarray,Homo sapiens,6|5,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07069,GSE51922,GPL5175,63,Parkinson's Disease,C0030567,,GEO,Microarray,Homo sapiens,4|6,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA07070,GSE51922,GPL5175,87,Parkinson's Disease,C0030567,,GEO,Microarray,Homo sapiens,4|4,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA07071,GSE51997,GPL570,330,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,4|6,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA07072,GSE51997,GPL570,1000,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,4|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA07073,GSE51997,GPL570,107,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,3|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA07074,GSE52011,GPL6885,438,Ovarian Cancer,C1140680,Fallopian tube,GEO,Microarray,Mus musculus,2|2,DO:A female reproductive organ cancer that is located_in the ovary. DSA07075,GSE52011,GPL6885,1000,Ovarian Cancer,C1140680,Fallopian tube,GEO,Microarray,Mus musculus,2|2,DO:A female reproductive organ cancer that is located_in the ovary. DSA07076,GSE52011,GPL6885,1000,Ovarian Cancer,C1140680,Fallopian tube,GEO,Microarray,Mus musculus,2|2,DO:A female reproductive organ cancer that is located_in the ovary. DSA07077,GSE52042,GPL17882,1,Osteoarthritis,C0157946,,GEO,Microarray,Homo sapiens,4|4,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA07078,GSE52093,GPL10558,792,Type A Aortic Dissection,C0578575,Ascending aorta,GEO,Microarray,Homo sapiens,5|7,HPO:A separation of the layers within the wall of the ascending aorta. Tears in the intimal layer result in the propagation of dissection (proximally or distally) secondary to blood entering the intima-media space. DSA07079,GSE52202,GPL11154,0,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA07080,GSE52249,GPL11154,1000,Down Syndrome,C0013080,,GEO,RNA-Seq,Homo sapiens,4|3,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA07081,GSE5243,GPL339,1,X-Linked Hypophosphatemia;Low Renal Retention,,Kidney,GEO,Microarray,Mus musculus,3|3, DSA07082,GSE5243,GPL339,0,X-Linked Hypophosphatemia;Low Renal Retention,,Kidney,GEO,Microarray,Mus musculus,3|3, DSA07083,GSE5243,GPL339,0,X-Linked Hypophosphatemia;Low Renal Retention,,Kidney,GEO,Microarray,Mus musculus,3|3, DSA07084,GSE5243,GPL339,2,X-Linked Hypophosphatemia;Low Renal Retention,,Kidney,GEO,Microarray,Mus musculus,3|3, DSA07085,GSE52463,GPL11154,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,RNA-Seq,Homo sapiens,7|8,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA07086,GSE52506,GPL1261,93,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Mus musculus,3|3,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA07087,GSE52506,GPL1261,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Mus musculus,3|3,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA07088,GSE52519,GPL6884,52,Bladder Cancer,C0699885,Bladder,GEO,Microarray,Homo sapiens,3|9,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07089,GSE52742,GPL11154,0,Allergic Asthma,C0155877,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA07090,GSE52746,GPL17996,1000,Crohn's Disease,C0010346,Colon,GEO,Microarray,Homo sapiens,17|10,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA07091,GSE52748,GPL17997,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Mus musculus,4|4,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA07092,GSE52766,GPL6885,1000,Duchenne Muscular Dystrophy,C0013264,Gastrocnemius muscle,GEO,Microarray,Mus musculus,4|5,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA07093,GSE52790,GPL17976,1000,Major Depressive Disorder,C1269683,Peripheral blood,GEO,Microarray,Homo sapiens,12|10,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA07094,GSE52871,GPL13912,2,Post-Traumatic Stress Disorder,C0038436,Heart,GEO,Microarray,Mus musculus,4|4,DO:An anxiety disorder which results from a traumatic experience that results in psychological trauma. DSA07095,GSE52871,GPL13912,1000,Post-Traumatic Stress Disorder,C0038436,Heart,GEO,Microarray,Mus musculus,4|4,DO:An anxiety disorder which results from a traumatic experience that results in psychological trauma. DSA07096,GSE52871,GPL13912,2,Post-Traumatic Stress Disorder,C0038436,Heart,GEO,Microarray,Mus musculus,4|4,DO:An anxiety disorder which results from a traumatic experience that results in psychological trauma. DSA07097,GSE52903,GPL6244,1000,Cervical Cancer,C4048328,Exocervix,GEO,Microarray,Homo sapiens,17|55,DO:A female reproductive organ cancer that is located_in the cervix. DSA07098,GSE52946,GPL11154,149,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,RNA-Seq,Homo sapiens,10|2,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA07099,GSE52946,GPL11154,80,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,RNA-Seq,Homo sapiens,10|8,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA07100,GSE31469,GPL570,7,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA07101,GSE40649,GPL13185,2,Amyotrophic Lateral Sclerosis,C0002736,Brain striatum,GEO,Microarray,Mus musculus,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA07102,GSE53146,GPL14951,0,Vitiligo,C0042900,Skin,GEO,Microarray,Homo sapiens,5|5,DO:An autoimmune disease that causes depigmentation of patches of skin resulting from loss of function or death of melanoctyes. DSA07103,GSE53239,GPL9115|GPL15433,1000,Bipolar Disorder,C0005586,Prefrontal cortex,GEO,RNA-Seq,Homo sapiens,6|3,DO:A mood disorder that involves alternating periods of mania and depression. DSA07104,GSE53257,GPL18056,2,Diabetes,C0011847,Neural retina,GEO,Microarray,Homo sapiens,5|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA07105,GSE53257,GPL18056,35,Diabetic Retinopathy,C0011884,Neural retina,GEO,Microarray,Homo sapiens,5|6,"EFO:Disease of the RETINA as a complication of DIABETES MELLITUS. It is characterized by the progressive microvascular complications, such as ANEURYSM, interretinal EDEMA, and intraocular PATHOLOGIC NEOVASCULARIZATION." DSA07106,GSE53306,GPL14951,1000,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,12|16,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA07107,GSE53306,GPL14951,1000,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,12|12,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA07108,GSE53381,GPL7202,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Mus musculus,4|4,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA07109,GSE53408,GPL6244,1000,Pulmonary Arterial Hypertension,C2973725,Lung,GEO,Microarray,Homo sapiens,11|12,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA07110,GSE53419,GPL9442,84,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,8|9,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA07111,GSE53607,GPL6246,72,Viral Myocarditis,C0276138,Heart,GEO,Microarray,Mus musculus,5|5,MONDO:Myocarditis that is caused by an infection with a viral agent. DSA07112,GSE53607,GPL6246,641,Viral Myocarditis,C0276138,Heart,GEO,Microarray,Mus musculus,5|5,MONDO:Myocarditis that is caused by an infection with a viral agent. DSA07113,GSE53607,GPL6246,1000,Viral Myocarditis,C0276138,Heart,GEO,Microarray,Mus musculus,5|5,MONDO:Myocarditis that is caused by an infection with a viral agent. DSA07114,GSE53613,GPL17077,0,Focal Palmoplantar Keratoderma,C2931923,Skin,GEO,Microarray,Homo sapiens,2|2,"DO:A palmoplantar keratosis characterized by a well-demarcated, symmetric keratoderma located_in palms and located_in soles." DSA07115,GSE53697,GPL16791,0,Alzheimer's Disease,C0002395,Brain,GEO,RNA-Seq,Homo sapiens,8|9,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA07116,GSE53702,GPL5188,3,Critical Illness Myopathy,C1135188,Skeletal muscle,GEO,Microarray,Homo sapiens,6|3,NCI:Acute muscle weakness and paralysis that develops in critically ill patients who have been treated with multiple drugs during their intensive care unit stay. It is associated with delayed weaning from mechanical ventilation and prolonged rehabilitation. DSA07117,GSE53702,GPL5188,86,Myopathy,C0026848,Skeletal muscle,GEO,Microarray,Homo sapiens,6|4,DO:A muscular disease in which the muscle fibers do not function resulting in muscular weakness. DSA07118,GSE53795,GPL570,1000,Acne,C0702166,Skin,GEO,Microarray,Homo sapiens,12|12,"DO:A sebaceous gland disease characterized by areas of blackheads, whiteheads, pimples, greasy skin, and possibly scarring." DSA07119,GSE53808,GPL13667,0,Hepatic Encephalopathy,C0019151,Frontal cortex,GEO,Microarray,Homo sapiens,5|4,"DO:A brain disease that is characterized by loss of brain function, the occurrence of confusion, altered level of consciousness, and coma that results when the liver is unable to remove toxins from the blood." DSA07120,GSE53808,GPL13667,0,Hepatic Encephalopathy,C0019151,Motor cortex,GEO,Microarray,Homo sapiens,4|4,"DO:A brain disease that is characterized by loss of brain function, the occurrence of confusion, altered level of consciousness, and coma that results when the liver is unable to remove toxins from the blood." DSA07121,GSE53819,GPL6480,1000,Nasopharyngeal Carcinoma,C2931822,,GEO,Microarray,Homo sapiens,18|18,"DO:A pharynx cancer that is located in the nasopharynx, the uppermost region of the pharynx or throat, where the nasal passages and auditory tubes join the remainder of the upper respiratory tract." DSA07122,GSE53873,GPL15496,2,Pemphigus Foliaceus,C0263313,Peripheral blood,GEO,Microarray,Homo sapiens,5|10,"EFO:Pemphigus foliaceus is an autoimmune blistering disease of the skin with characteristic lesions that are scaly, crusted erosions, often on an erythematous base." DSA07123,GSE53873,GPL15496,17,Pemphigus Vulgaris,C0030809,Peripheral blood,GEO,Microarray,Homo sapiens,5|2,DO:A pemphigus characterized by autosomal dominant blisters and erosions on the skin and mucous membranes erosions cause by autoantibodies to intercellular cement substance. DSA07124,GSE53987,GPL570,0,Bipolar Disorder,C0005586,Striatum,GEO,Microarray,Homo sapiens,18|17,DO:A mood disorder that involves alternating periods of mania and depression. DSA07125,GSE53987,GPL570,0,Major Depressive Disorder,C1269683,Striatum,GEO,Microarray,Homo sapiens,18|16,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA07126,GSE53987,GPL570,2,Schizophrenia,C0036341,Striatum,GEO,Microarray,Homo sapiens,18|18,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA07127,GSE53987,GPL570,0,Bipolar Disorder,C0005586,Hippocampus,GEO,Microarray,Homo sapiens,18|18,DO:A mood disorder that involves alternating periods of mania and depression. DSA07128,GSE53987,GPL570,0,Major Depressive Disorder,C1269683,Hippocampus,GEO,Microarray,Homo sapiens,18|17,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA07129,GSE53987,GPL570,1000,Schizophrenia,C0036341,Hippocampus,GEO,Microarray,Homo sapiens,18|15,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA07130,GSE53987,GPL570,5,Bipolar Disorder,C0005586,Prefrontal cortex,GEO,Microarray,Homo sapiens,19|17,DO:A mood disorder that involves alternating periods of mania and depression. DSA07131,GSE53987,GPL570,0,Major Depressive Disorder,C1269683,Prefrontal cortex,GEO,Microarray,Homo sapiens,19|17,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA07132,GSE53987,GPL570,46,Schizophrenia,C0036341,Prefrontal cortex,GEO,Microarray,Homo sapiens,19|15,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA07133,GSE54002,GPL570,1000,Breast Cancer,C0678222,,GEO,Microarray,Homo sapiens,16|417,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07134,GSE54043,GPL570,0,Eosinophilic Gastritis,C0267154,Gastric antrum,GEO,Microarray,Homo sapiens,5|5,"HPO:Infiltration of eosinophils in the stomach mucosa, that is diagnosed by an upper endoscopy and microscopy that shows more than 20 eosinophils per high-power field in association with peripheral eosinophilia and the absence of secondary cause of eosinophilia." DSA07135,GSE54248,GPL10558,0,Polycystic Ovary Syndrome,C0032460,Peripheral blood,GEO,Microarray,Homo sapiens,4|4,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA07136,GSE54387,GPL1261,0,Obesity,C0028754,,GEO,Microarray,Mus musculus,2|2,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07137,GSE54388,GPL570,1000,Ovarian Cancer,C1140680,Ovary,GEO,Microarray,Homo sapiens,6|16,DO:A female reproductive organ cancer that is located_in the ovary. DSA07138,GSE54400,GPL10558,1000,Pre-Eclampsia,C0032914,Umbilical cord,GEO,Microarray,Homo sapiens,9|38,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA07139,GSE54456,GPL9052,1000,Psoriasis,C0033860,Skin,GEO,RNA-Seq,Homo sapiens,80|89,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA07140,GSE16238,GPL570,1,Acute Myeloid Leukemia,C0023467,,GEO,Microarray,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA07141,GSE124728,GPL21103,1000,Sensory Neuropathy,C0151313,,GEO,RNA-Seq,Mus musculus,15|12,DO:A neuropathy that involves damage to nerves of the peripheral nervous system. DSA07142,GSE32154,GPL5175,0,Mucopolysaccharidosis Type Iiib,C0086648,,GEO,Microarray,Homo sapiens,2|2,"DO:A mucopolysaccharidosis III characterized by neurodegeneration, behavioral problems, mild skeletal changes, and shortened life span that has_material_basis_in homozygous or compound heterozygous mutation in NAGLU on chromosome 17q21.2." DSA07143,GSE21125,GPL1456,0,Heart Failure,C0018801,,GEO,Microarray,Homo sapiens,9|9,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA07144,GSE124927,GPL23038,0,Obesity,C0028754,Utero placental tissue,GEO,Microarray,Mus musculus,10|6,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07145,GSE124927,GPL23038,0,Obesity,C0028754,Utero placental tissue,GEO,Microarray,Mus musculus,10|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07146,GSE124993,GPL16791,865,Colorectal Carcinoma,C0009402,Colon,GEO,RNA-Seq,Homo sapiens,3|3,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA07147,GSE125260,GPL17400,1000,Colon Adenocarcinoma,C0699790,Colon,GEO,Microarray,Mus musculus,3|12,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07148,GSE125261,GPL17400,1000,Colon Tumor,C0009375,Colon,GEO,Microarray,Mus musculus,4|8,DO:A colorectal cancer that is located_in the colon. DSA07149,GSE125537,GPL11533,18,Pulmonary Arterial Hypertension,C2973725,Right ventricle,GEO,Microarray,Mus musculus,3|3,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA07150,GSE125537,GPL11533,11,Pulmonary Arterial Hypertension,C2973725,Right ventricle,GEO,Microarray,Mus musculus,3|3,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA07151,GSE126033,GPL6887,1000,Lymphoma,C0024299,,GEO,Microarray,Mus musculus,3|3,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA07152,GSE126033,GPL6887,99,Lymphoma,C0024299,,GEO,Microarray,Mus musculus,3|3,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA07153,GSE126033,GPL6887,1,Lymphoma,C0024299,,GEO,Microarray,Mus musculus,3|3,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA07154,GSE126033,GPL6887,71,Lymphoma,C0024299,,GEO,Microarray,Mus musculus,3|3,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA07155,GSE126033,GPL6887,1000,Lymphoma,C0024299,,GEO,Microarray,Mus musculus,3|3,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA07156,GSE126033,GPL6887,69,Lymphoma,C0024299,,GEO,Microarray,Mus musculus,3|3,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA07157,GSE126033,GPL6887,0,Lymphoma,C0024299,,GEO,Microarray,Mus musculus,3|3,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA07158,GSE126033,GPL6887,44,Lymphoma,C0024299,,GEO,Microarray,Mus musculus,3|3,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA07159,GSE126217,GPL13112,1000,Proteinuria;Glomerulosclerosis;Progressive Renal Failure,,Glomerulus,GEO,RNA-Seq,Mus musculus,5|3, DSA07160,GSE126648,GPL16570,1000,Bone Fracture,,Tibia bone,GEO,Microarray,Mus musculus,3|3, DSA07161,GSE126648,GPL16570,1000,Bone Fracture,,Tibia bone,GEO,Microarray,Mus musculus,3|3, DSA07162,GSE127526,GPL23479,1000,Colitis,C0009319,Colon,GEO,RNA-Seq,Mus musculus,3|5,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA07163,GSE127526,GPL23479,1000,Colitis,C0009319,Colon,GEO,RNA-Seq,Mus musculus,3|5,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA07164,GSE127891,GPL6246,38,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,Microarray,Mus musculus,5|8,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA07165,GSE21125,GPL1456,71,Heart Failure,C0018801,,GEO,Microarray,Homo sapiens,9|9,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA07166,GSE35574,GPL6102,1000,Pre-Eclampsia,C0032914,Placenta,GEO,Microarray,Homo sapiens,40|19,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA07167,GSE128012,GPL21493,1000,Brain Tumor,C0006118,Brain,GEO,RNA-Seq,Mus musculus,3|3,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA07168,GSE128012,GPL21493,1000,Brain Tumor,C0006118,Brain,GEO,RNA-Seq,Mus musculus,3|3,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA07169,GSE128207,GPL21103,854,Brain Tumor,C0006118,,GEO,RNA-Seq,Mus musculus,3|3,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA07170,GSE128207,GPL21103,522,Brain Tumor,C0006118,,GEO,RNA-Seq,Mus musculus,3|3,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA07171,GSE128423,GPL19057,1000,Leukemia,C0023418,Bone marrow,GEO,scRNA-Seq,Mus musculus,5|4,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA07172,GSE128543,GPL20775,1000,Traumatic Brain Injury,,Brain,GEO,Microarray,Mus musculus,7|7, DSA07173,GSE128543,GPL20775,1000,Traumatic Brain Injury,,Brain,GEO,Microarray,Mus musculus,7|7, DSA07174,GSE128610,GPL570,1000,Breast Cancer,C0678222,,GEO,Microarray,Homo sapiens,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07175,GSE128925,GPL18635,570,Sepsis,C0243026,Hippocampus,GEO,RNA-Seq,Mus musculus,3|3,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07176,GSE128925,GPL18635,122,Sepsis,C0243026,Hippocampus,GEO,RNA-Seq,Mus musculus,3|3,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07177,GSE128925,GPL18635,917,Sepsis,C0243026,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07178,GSE128925,GPL18635,1000,Sepsis,C0243026,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07179,GSE128925,GPL18635,684,Sepsis,C0243026,Hippocampus,GEO,RNA-Seq,Mus musculus,2|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07180,GSE128925,GPL18635,68,Sepsis,C0243026,Hippocampus,GEO,RNA-Seq,Mus musculus,2|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07181,GSE128925,GPL18635,1000,Sepsis,C0243026,Hippocampus,GEO,RNA-Seq,Mus musculus,3|3,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07182,GSE128925,GPL18635,270,Sepsis,C0243026,Hippocampus,GEO,RNA-Seq,Mus musculus,3|1,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07183,GSE128999,GPL17021,2,Metastatic Lung Tumor,C0242379,Lung,GEO,RNA-Seq,Mus musculus,4|3,DO:A lung cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells and is located_in the lungs and has_symptom cough and has_symptom chest discomfort or pain and has_symptom weight loss and has_symptom hemoptysis. DSA07184,GSE128999,GPL17021,760,Metastatic Lung Tumor,C0242379,Lung,GEO,RNA-Seq,Mus musculus,4|4,DO:A lung cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells and is located_in the lungs and has_symptom cough and has_symptom chest discomfort or pain and has_symptom weight loss and has_symptom hemoptysis. DSA07185,GSE20129,GPL10558,0,Atherosclerosis,C0004153,Blood,GEO,Microarray,Homo sapiens,15|1,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA07186,GSE20129,GPL6104,0,Atherosclerosis,C0004153,Blood,GEO,Microarray,Homo sapiens,41|26,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA07187,GSE129511,GPL17021,104,"Arthritis, Collagen-Induced",C0971858,Bone marrow,GEO,RNA-Seq,Mus musculus,3|3,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA07188,GSE20129,GPL6104,0,Atherosclerosis,C0004153,Blood,GEO,Microarray,Homo sapiens,3|3,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA07189,GSE130003,GPL17021,1000,Gastric Squamous Cell Carcinoma,C1333789,,GEO,RNA-Seq,Mus musculus,3|5,DO:A squamous cell carcinoma that is located_in the stomach. DSA07190,GSE130062,GPL17021,1000,Myocardial Infarction,C0027051,Heart,GEO,RNA-Seq,Mus musculus,1|1,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07191,GSE130062,GPL17021,1000,Myocardial Infarction,C0027051,Heart,GEO,RNA-Seq,Mus musculus,1|1,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07192,GSE130183,GPL21103,1000,Skin Injury,,Skin,GEO,RNA-Seq,Mus musculus,4|3, DSA07193,GSE130447,GPL17021,1000,Rotator Cuff Tear,C0263912,Muscle,GEO,RNA-Seq,Mus musculus,4|4,"MONDO:Tear of one or more of the tendons of the four rotator cuff muscles of the shoulder. A rotator cuff 'injury' can include any type of irritation or overuse of those muscles or tendons, and is among the most common conditions affecting the shoulder." DSA07194,GSE130447,GPL17021,1000,Rotator Cuff Tear,C0263912,Muscle,GEO,RNA-Seq,Mus musculus,4|4,"MONDO:Tear of one or more of the tendons of the four rotator cuff muscles of the shoulder. A rotator cuff 'injury' can include any type of irritation or overuse of those muscles or tendons, and is among the most common conditions affecting the shoulder." DSA07195,GSE20129,GPL6104,0,Atherosclerosis,C0004153,Blood,GEO,Microarray,Homo sapiens,17|13,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA07196,GSE130697,GPL17021,1000,Melanoma,C0025202,,GEO,RNA-Seq,Mus musculus,2|2,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA07197,GSE130704,GPL21103,1000,Lung Adenocarcinoma,C0152013,Heart,GEO,RNA-Seq,Mus musculus,4|4,DO:A respiratory system cancer that is located_in the lung. DSA07198,GSE77627,GPL14951,1000,Idiopathic Non-Cirrhotic Portal Hypertension,C4476912,Liver,GEO,Microarray,Homo sapiens,14|18,"HPO:Sclerosis of the intrahepatic portal veins of the liver and generally accompanied by non-cirrhotic portal hypertension, features of which may include splenomegaly and varices." DSA07199,GSE77627,GPL14951,1000,Liver Cirrhosis,C0023890,Liver,GEO,Microarray,Homo sapiens,14|22,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA07200,GSE77664,GPL10558,0,Parkinson's Disease,C0030567,Dermis,GEO,Microarray,Homo sapiens,1|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA07201,GSE77666,GPL21436,0,Parkinson's Disease,C0030567,Prefrontal cortex,GEO,Microarray,Homo sapiens,12|12,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA07202,GSE77693,GPL17021,49,Aicardi Goutieres Syndrome,C0393591,,GEO,RNA-Seq,Mus musculus,3|3,"DO:A syndrome that is a genetically heterogeneous encephalopathy characterized in its most severe form by cerebral atrophy, leukodystrophy, intracranial calcifications, chronic cerebrospinal fluid lymphocytosis, increased CSF alpha-interferon, and negative serologic investigations for common prenatal infections." DSA07203,GSE77742,GPL11154,1000,Pitt-Hopkins Syndrome,C1970431,Skin,GEO,RNA-Seq,Homo sapiens,2|1,"DO:A syndrome characterized by intellectual disability and developmental delay, breathing problems, recurrent seizures, and distinctive facial features and that has_material_basis_in heterozygous de novo mutations in the TCF4 gene in chromosome 18q21." DSA07204,GSE77758,GPL6244,0,"Ehlers-Danlos Syndrome, Hypermobility Type",C0268337,,GEO,Microarray,Homo sapiens,6|5,DO:An Ehlers-Danlos syndrome that is characterized by joint hyperextensibility without skeletal deformity. DSA07205,GSE77784,GPL17021,434,Hypertrophic Cardiomyopathy,C0007194,,GEO,RNA-Seq,Homo sapiens,5|3,DO:A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations. DSA07206,GSE77798,GPL13112,201,Hypoplastic Left Heart Syndrome,C0152101,Heart ventricle,GEO,RNA-Seq,Mus musculus,5|3,DO:A congenital heart disease characterized by abnormal development of the left-sided structures of the heart. DSA07207,GSE77798,GPL13112,155,Hypoplastic Left Heart Syndrome,C0152101,Heart ventricle,GEO,RNA-Seq,Mus musculus,5|3,DO:A congenital heart disease characterized by abnormal development of the left-sided structures of the heart. DSA07208,GSE77861,GPL570,1000,Esophageal Squamous Cell Carcinoma,C0279626,Esophagus,GEO,Microarray,Homo sapiens,7|7,DO:An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus. DSA07209,GSE78000,GPL21464,1000,Invasive Aspergillosis,C0238013,Blood,GEO,Microarray,Homo sapiens,9|23,"MONDO:An aspergillosis that is a serious fungal infection of the lung with pneumonia caused by Aspergillus, which spreads to other parts of the body through bloodstream in patients with acute leukemia and recipients of tissue transplants. Clinical symptoms include pulmonary nodules and hemorrhage." DSA07210,GSE78081,GPL16791,3,Fibrodysplasia Ossificans Progressiva,C0016037,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A connective tissue disease that is characterized by progressive ossification of skeletal muscle, fascia, tendons, and ligaments and has_material_basis_in heterozygous mutation in the ACVR1 gene." DSA07211,GSE78104,GPL19612,27,Obsessive-Compulsive Disorder,C0028768,Blood,GEO,Microarray,Homo sapiens,30|30,"DO:An anxiety disorder that involves unwanted and repeated thoughts, feelings, ideas, sensations (obsessions), or behaviors that make them feel driven to do something (compulsions)." DSA07212,GSE78152,GPL10558,11,Parkinson's Disease,C0030567,Skin,GEO,Microarray,Homo sapiens,1|7,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA07213,GSE78244,GPL17077,1,Multiple Sclerosis,C0026769,,GEO,Microarray,Homo sapiens,14|14,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA07214,GSE78244,GPL17077,0,Multiple Sclerosis,C0026769,,GEO,Microarray,Homo sapiens,14|14,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA07215,GSE78246,GPL5175,0,Bipolar Disorder,C0005586,Anterioir cingulate cortex,GEO,Microarray,Homo sapiens,11|9,DO:A mood disorder that involves alternating periods of mania and depression. DSA07216,GSE7846,GPL570,4,Endometriosis,C0014175,,GEO,Microarray,Homo sapiens,5|5,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA07217,GSE7862,GPL201,4,Malignant Buccal Mucosa Tumor,C0153373,,GEO,Microarray,Homo sapiens,2|2,MONDO:A malignant neoplasm involving the buccal mucosa. DSA07218,GSE78757,GPL16570,4,Gaucher Disease,C0017205,Cortex,GEO,Microarray,Mus musculus,3|3,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA07219,GSE78757,GPL16570,59,Gaucher Disease,C0017205,Cortex,GEO,Microarray,Mus musculus,3|3,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA07220,GSE78757,GPL16570,96,Gaucher Disease,C0017205,Cortex,GEO,Microarray,Mus musculus,3|3,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA07221,GSE78757,GPL16570,0,Gaucher Disease,C0017205,Cortex,GEO,Microarray,Mus musculus,3|3,"DO:A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver." DSA07222,GSE78809,GPL17021,1000,Experimental Autoimmune Encephalomyelitis,C0014072,,GEO,RNA-Seq,Mus musculus,3|6,"EFO:An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)" DSA07223,GSE78891,GPL15207,1,Insulin Receptor Mutations,,,GEO,Microarray,Homo sapiens,5|6, DSA07224,GSE78891,GPL15207,0,Insulin Receptor Mutations,,,GEO,Microarray,Homo sapiens,3|3, DSA07225,GSE20129,GPL6104,0,Atherosclerosis,C0004153,Blood,GEO,Microarray,Homo sapiens,10|6,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA07226,GSE78929,GPL10558,0,Intensive Care Unit Acquired Weakness,,Vastus lateralis,GEO,Microarray,Homo sapiens,8|10, DSA07227,GSE78929,GPL10558,0,Intensive Care Unit Acquired Weakness,,Vastus lateralis,GEO,Microarray,Homo sapiens,8|10, DSA07228,GSE78933,GPL17586,0,Melanosis,C0025209,Colon,GEO,Microarray,Homo sapiens,5|5,EFO:Disorders of increased melanin pigmentation that develop without preceding inflammatory disease. DSA07229,GSE78936,GPL11154,555,Bipolar Disorder,C0005586,Brain,GEO,RNA-Seq,Homo sapiens,12|16,DO:A mood disorder that involves alternating periods of mania and depression. DSA07230,GSE78936,GPL11154,0,Schizophrenia,C0036341,Brain,GEO,RNA-Seq,Homo sapiens,12|16,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA07231,GSE78936,GPL11154,0,Bipolar Disorder,C0005586,Brain,GEO,RNA-Seq,Homo sapiens,6|7,DO:A mood disorder that involves alternating periods of mania and depression. DSA07232,GSE78936,GPL11154,15,Schizophrenia,C0036341,Brain,GEO,RNA-Seq,Homo sapiens,6|6,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA07233,GSE78936,GPL11154,3,Bipolar Disorder,C0005586,Brain,GEO,RNA-Seq,Homo sapiens,6|7,DO:A mood disorder that involves alternating periods of mania and depression. DSA07234,GSE78936,GPL11154,1000,Schizophrenia,C0036341,Brain,GEO,RNA-Seq,Homo sapiens,6|6,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA07235,GSE78996,GPL19057,1000,Experimental Autoimmune Encephalomyelitis,C0014072,Spinal cord,GEO,RNA-Seq,Mus musculus,3|3,"EFO:An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)" DSA07236,GSE79021,GPL19370,1000,Prostate Tumor,C0600139,Prostate,GEO,Microarray,Homo sapiens,49|153,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07237,GSE79150,GPL13158,0,Hidradenitis,C0085160,Whole blood,GEO,Microarray,Homo sapiens,10|16,"DO:A sweat gland disease that is characterized by inflammation of the apocrine sweat glands and has_symptom erythema, edema, papules, plaques, pruritis, and pain." DSA07238,GSE19339,GPL570,295,Acute Coronary Syndrome,C0948089,Blood vessel,GEO,Microarray,Homo sapiens,4|4,EFO:Signs and symptoms related to acute ischemia of the myocardium secondary to coronary artery disease. The clinical presentation covers a spectrum of heart diseases from unstable angina to myocardial infarction. DSA07239,GSE79263,GPL10558,1000,Duchenne Muscular Dystrophy,C0013264,,GEO,Microarray,Homo sapiens,8|11,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA07240,GSE79263,GPL10558,1000,Duchenne Muscular Dystrophy,C0013264,,GEO,Microarray,Homo sapiens,8|11,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA07241,GSE79263,GPL10558,1000,Duchenne Muscular Dystrophy,C0013264,Myotube,GEO,Microarray,Homo sapiens,10|14,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA07242,GSE79263,GPL10558,1000,Duchenne Muscular Dystrophy,C0013264,Myotube,GEO,Microarray,Homo sapiens,10|14,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA07243,GSE79338,GPL11154,1000,Glioma,C0017638,Brain,GEO,RNA-Seq,Homo sapiens,3|3,DO:A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine. DSA07244,GSE79338,GPL11154,1000,Glioma,C0017638,Brain,GEO,RNA-Seq,Homo sapiens,3|8,DO:A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine. DSA07245,GSE79362,GPL11154,1000,Tuberculosis,C0041296,Blood,GEO,RNA-Seq,Homo sapiens,245|110,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA07246,GSE79462,GPL13158,309,Tubular Adenoma,C0334292,Colon,GEO,Microarray,Homo sapiens,2|5,MONDO:A usually polypoid neoplasm arising from the glandular epithelium. It is characterized by a tubular architectural pattern. The neoplastic glandular cells have dysplastic features. Representative examples include the tubular adenomas of the colon and rectum. DSA07247,GSE79462,GPL13158,560,Tubular Adenoma,C0334292,Colon,GEO,Microarray,Homo sapiens,2|6,MONDO:A usually polypoid neoplasm arising from the glandular epithelium. It is characterized by a tubular architectural pattern. The neoplastic glandular cells have dysplastic features. Representative examples include the tubular adenomas of the colon and rectum. DSA07248,GSE79533,GPL570,617,B-Cell Acute Lymphoblastic Leukemia,C0862030,,GEO,Microarray,Homo sapiens,3|17,DO:A precursor lymphoblastic lymphoma/leukemia that is characterized by the presence of too many B-cell lymphoblasts in the blood and bone marrow. DSA07249,GSE79533,GPL570,48,B-Cell Acute Lymphoblastic Leukemia,C0862030,,GEO,Microarray,Homo sapiens,3|2,DO:A precursor lymphoblastic lymphoma/leukemia that is characterized by the presence of too many B-cell lymphoblasts in the blood and bone marrow. DSA07250,GSE79533,GPL570,5,B-Cell Acute Lymphoblastic Leukemia,C0862030,,GEO,Microarray,Homo sapiens,3|5,DO:A precursor lymphoblastic lymphoma/leukemia that is characterized by the presence of too many B-cell lymphoblasts in the blood and bone marrow. DSA07251,GSE79533,GPL570,1000,B-Cell Acute Lymphoblastic Leukemia,C0862030,,GEO,Microarray,Homo sapiens,3|70,DO:A precursor lymphoblastic lymphoma/leukemia that is characterized by the presence of too many B-cell lymphoblasts in the blood and bone marrow. DSA07252,GSE79533,GPL570,913,B-Cell Acute Lymphoblastic Leukemia,C0862030,,GEO,Microarray,Homo sapiens,3|90,DO:A precursor lymphoblastic lymphoma/leukemia that is characterized by the presence of too many B-cell lymphoblasts in the blood and bone marrow. DSA07253,GSE79533,GPL570,1000,B-Cell Acute Lymphoblastic Leukemia,C0862030,,GEO,Microarray,Homo sapiens,3|13,DO:A precursor lymphoblastic lymphoma/leukemia that is characterized by the presence of too many B-cell lymphoblasts in the blood and bone marrow. DSA07254,GSE79533,GPL570,917,B-Cell Acute Lymphoblastic Leukemia,C0862030,,GEO,Microarray,Homo sapiens,3|19,DO:A precursor lymphoblastic lymphoma/leukemia that is characterized by the presence of too many B-cell lymphoblasts in the blood and bone marrow. DSA07255,GSE79533,GPL570,428,B-Cell Acute Lymphoblastic Leukemia,C0862030,,GEO,Microarray,Homo sapiens,3|10,DO:A precursor lymphoblastic lymphoma/leukemia that is characterized by the presence of too many B-cell lymphoblasts in the blood and bone marrow. DSA07256,GSE79544,GPL18573,11,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,RNA-Seq,Homo sapiens,7|16,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA07257,GSE79605,GPL6480,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,2|2,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA07258,GSE79613,GPL11154,3,Familial Pulmonary Arterial Hypertension,C1701939,,GEO,RNA-Seq,Homo sapiens,3|5,"MONDO:Heritable pulmonary arterial hypertension (HPAH) is a form of pulmonary arterial hypertension (PAH), occurring due to mutations in PAH predisposing genes or in a familial context. HPAH is characterized by elevated pulmonary arterial resistance leading to right heart failure. HPAH is progressive and potentially fatal." DSA07259,GSE79623,GPL1261,1,Diabetes,C0011847,Aorta,GEO,Microarray,Mus musculus,4|4,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA07260,GSE79623,GPL1261,6,Diabetes,C0011847,Aorta,GEO,Microarray,Mus musculus,4|4,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA07261,GSE79666,GPL11154,649,Huntington's Disease,C0020179,Brain,GEO,RNA-Seq,Homo sapiens,7|7,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA07262,GSE79704,GPL19983,1000,Chronic Small Plaque Psoriasis,C0406317,Skin,GEO,Microarray,Homo sapiens,20|12, DSA07263,GSE79704,GPL19983,1000,Generalized Pustular Psoriasis,C0343055,Skin,GEO,Microarray,Homo sapiens,20|32,"DO:A psoriasis characterized by sudden, repeated episodes of high-grade fever, generalized rash, and disseminated pustules, with hyperleukocytosis and elevated serum levels of C-reactive protein that has_material_basis_in homozygous or compound heterozygous mutation in the IL36RN gene on chromosome 2q14." DSA07264,GSE79705,GPL18734,0,Generalized Periodontitis,C4023560,Gingiva,GEO,Microarray,Homo sapiens,4|4,HPO:A generalized form of periodontitis. DSA07265,GSE79705,GPL18734,0,Generalized Chronic Periodontitis,C1719498,Gingiva,GEO,Microarray,Homo sapiens,4|4, DSA07266,GSE79711,GPL16570,0,Huntington's Disease,C0020179,White adipose tissue,GEO,Microarray,Mus musculus,6|6,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA07267,GSE79786,GPL10904,0,Pulmonary Arterial Hypertension,C2973725,Lung,GEO,Microarray,Homo sapiens,3|3,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA07268,GSE79850,GPL19965,260,Primary Biliary Cholangitis,C0008312,Liver,GEO,Microarray,Homo sapiens,8|7,DO:A liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts. DSA07269,GSE79850,GPL19965,292,Primary Biliary Cholangitis,C0008312,Liver,GEO,Microarray,Homo sapiens,8|9,DO:A liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts. DSA07270,GSE79970,GPL16791,523,Juvenile Idiopathic Arthritis,C3890205,Blood,GEO,RNA-Seq,Homo sapiens,16|23,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA07271,GSE80008,GPL6244,427,Cutaneous Leishmaniasis,C0023283,,GEO,Microarray,Homo sapiens,12|18,"DO:A leishmaniasis that involves skin infection caused by Leishmania species, resulting in one or more cutaneous lesions." DSA07272,GSE80009,GPL16951,1,Vitiligo,C0042900,Blood,GEO,Microarray,Homo sapiens,4|4,DO:An autoimmune disease that causes depigmentation of patches of skin resulting from loss of function or death of melanoctyes. DSA07273,GSE80009,GPL16951,0,Vitiligo,C0042900,Blood,GEO,Microarray,Homo sapiens,4|4,DO:An autoimmune disease that causes depigmentation of patches of skin resulting from loss of function or death of melanoctyes. DSA07274,GSE80060,GPL570,1000,Systemic Juvenile Idiopathic Arthritis,C1384600,Whole blood,GEO,Microarray,Homo sapiens,22|33,"EFO:Juvenile idiopathic arthritis (JIA), also known as juvenile rheumatoid arthritis (JRA), is the most common form of arthritis in children and adolescents. (Juvenile in this context refers to an onset before age 16, idiopathic refers to a condition with no defined cause, and arthritis is the inflammation of the synovium of a joint.) JIA is an autoimmune, non-infective, inflammatory joint disease of more than 6 weeks duration in children less than 16 years of age. The disease commonly occurs in children from the ages of 7 to 12, but it may occur in adolescents as old as 15 years of age, as well as in infants. It is a subset of arthritis seen in childhood, which may be transient and self-limited or chronic. It differs significantly from arthritis commonly seen in adults (osteoarthritis, rheumatoid arthritis), and other types of arthritis that can present in childhood which are chronic conditions (e.g. psoriatic arthritis and ankylosing spondylitis). Aetiopathology is similar to rheumatoid arthritis but with less marked cartilage erosion, and joint instability and absent rheumatoid factor. JIA affects approximately 1 in 1,000 children in any given year, with about 1 in 10,000 having a more severe form." DSA07275,GSE80062,GPL11154,1000,Paroxysmal Nocturnal Hemoglobinuria,C0024790,Blood,GEO,RNA-Seq,Homo sapiens,3|1,"DO:An aquired hemolytic anemia that is characterized by abdominal pain, hematuria, esophageal dysmotility and thrombosis, has_material_basis_in defect in the cell membrane glycosyl phosphatidylinositols that protect red blood cells from the innate complement immune system." DSA07276,GSE80163,GPL16791,29,Schizophrenia,C0036341,,GEO,RNA-Seq,Homo sapiens,6|5,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA07277,GSE80163,GPL16791,409,Schizophrenia,C0036341,,GEO,RNA-Seq,Homo sapiens,6|6,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA07278,GSE80183,GPL11154,503,Systemic Lupus Erythematosus,C0024141,Blood,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA07279,GSE80183,GPL11154,648,Systemic Lupus Erythematosus,C0024141,Blood,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA07280,GSE80183,GPL11154,417,Systemic Lupus Erythematosus,C0024141,Blood,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA07281,GSE8030,GPL339,0,Parkinson's Disease,C0030567,Striatum,GEO,Microarray,Mus musculus,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA07282,GSE8030,GPL339,0,Parkinson's Disease,C0030567,Striatum,GEO,Microarray,Mus musculus,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA07283,GSE182410,GPL24676,1000,Ataxia-Telangiectasia,C0004135,Skin,GEO,RNA-Seq,Homo sapiens,7|9,"DO:An autosomal recessive cerebellar ataxia that is characterized by cerebellar ataxia, telangiectases, immune defects, and a predisposition to malignancy and that has_material_basis_in homozygous or compound heterozygous mutation in the ATM gene on chromosome 11q22." DSA07284,GSE185911,GPL17021,183,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,3|2,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA07285,GSE194313,GPL21697,1000,Alpha-1 Antitrypsin Deficiency,C0221757,Lung,GEO,RNA-Seq,Homo sapiens,6|4,"DO:A plasma protein metabolism disease that has_material_basis_in defective production of the protease inhibitor alpha 1-antitrypsin (A1AT), leading to decreased A1AT activity in the blood and lungs, and deposition of excessive abnormal A1AT protein in liver cells." DSA07286,GSE197702,GPL20301,1000,Eosinophilic Esophagitis,C0341106,Esophageal mucosal,GEO,RNA-Seq,Homo sapiens,7|11,DO:An esophagitis characterized by inflammation involving eosinophils located_in esophagus. DSA07287,GSE80496,GPL6883,1000,Sepsis,C0243026,Whole blood,GEO,Microarray,Homo sapiens,21|21,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07288,GSE80506,GPL10558,0,Malignant Breast Neoplasm,C0006142,,GEO,Microarray,Homo sapiens,6|10,DO:A thoracic cancer that originates in the mammary gland. DSA07289,GSE197702,GPL20301,1000,Eosinophilic Esophagitis,C0341106,Esophageal mucosal,GEO,RNA-Seq,Homo sapiens,7|8,DO:An esophagitis characterized by inflammation involving eosinophils located_in esophagus. DSA07290,GSE80608,GPL5175,175,Monoclonal Gammopathy of Undetermined Significance,C0026470,,GEO,Microarray,Homo sapiens,10|10,DO:A blood protein disease that is characterized by the presence of an abnormal protein called monoclonal protein in the blood. DSA07291,GSE80608,GPL5175,1000,Multiple Myeloma,C0026764,,GEO,Microarray,Homo sapiens,10|10,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA07292,GSE80715,GPL11154,1000,Chronic Periodontitis,C0266929,Gingiva,GEO,RNA-Seq,Homo sapiens,1|1,"EFO:Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology)" DSA07293,GSE80751,GPL17692,109,Injury of Liver,C0160390,,GEO,Microarray,Homo sapiens,5|5,NCI:Damage to liver structure or function due to trauma or toxicity. DSA07294,GSE80751,GPL17692,898,Acute Liver Failure,C0162557,,GEO,Microarray,Homo sapiens,5|12,"HPO:Hepatic failure refers to the inability of the liver to perform its normal synthetic and metabolic functions, which can result in coagulopathy and alteration in the mental status of a previously healthy individual. Hepatic failure is defined as fulminant if there is onset of encephalopathy within 4 weeks of the onset of symptoms in a patient with a previously healthy liver." DSA07295,GSE80759,GPL17077,0,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07296,GSE80759,GPL17077,0,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07297,GSE80759,GPL17077,1,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07298,GSE80759,GPL17077,0,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07299,GSE80759,GPL17077,0,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07300,GSE80975,GPL1261,1000,Pneumocystis Pneumonia,C1535939,Lung,GEO,Microarray,Mus musculus,4|5,"DO:An opportunistic mycosis that is located in lungs, but can also occur in eyes, ears, skin, thyroid, pituitary, palate, parathyroid, esophagus, pleura, heart, liver, spleen, small intestine, adrenals, kidneys, bone marrow, and lymph nodes, has_material_basis_in Pneumocystis jirovecii that effects interstitial and alveolar tissues and has symptom nonproductive cough, has symptom shortness of breath, and has symptom fever." DSA07301,GSE81010,GPL6246,1000,Leukemia,C0023418,Bone marrow,GEO,Microarray,Mus musculus,9|18,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA07302,GSE81071,GPL19983,1000,Cutaneous Lupus Erythematosus,C0024137,Skin,GEO,Microarray,Homo sapiens,7|26,DO:A lupus erythematosus that causes skin lesions on parts of the body that are exposed to sunlight. DSA07303,GSE81071,GPL19983,1000,Subacute Cutaneous Lupus Erythematosus,C0024140,Skin,GEO,Microarray,Homo sapiens,7|23,"MONDO:Subacute cutaneous lupus erythematosus (SCLE) is a form of cutaneous lupus erythematosus (CLE) that can present either as a non-scarring, annular photo-distributed dermatosis or psoriasiform plaques. SCLE is associated with anti-Ro/SSA antibodies and can be drug-induced." DSA07304,GSE81071,GPL19983,287,Cutaneous Lupus Erythematosus,C0024137,Skin,GEO,Microarray,Homo sapiens,6|21,DO:A lupus erythematosus that causes skin lesions on parts of the body that are exposed to sunlight. DSA07305,GSE81071,GPL19983,172,Subacute Cutaneous Lupus Erythematosus,C0024140,Skin,GEO,Microarray,Homo sapiens,6|20,"MONDO:Subacute cutaneous lupus erythematosus (SCLE) is a form of cutaneous lupus erythematosus (CLE) that can present either as a non-scarring, annular photo-distributed dermatosis or psoriasiform plaques. SCLE is associated with anti-Ro/SSA antibodies and can be drug-induced." DSA07306,GSE202069,GPL24676,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,RNA-Seq,Homo sapiens,25|24,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07307,GSE203150,GPL24247,1000,Myocardial Infarction,C0027051,Heart,GEO,RNA-Seq,Mus musculus,1|2,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07308,GSE81156,GPL570,44,Schimke Immuno-Osseous Dysplasia,C0877024,,GEO,Microarray,Homo sapiens,2|3,"DO:A spondyloepiphyseal dysplasia characterized by short stature with hyperpigmented macules, unusual facies, proteinuria with progressive renal failure, lymphopenia with recurrent infections, and cerebral ischaemia. It has_material_basis_in mutations in the SMARCAL1 gene." DSA07309,GSE81245,GPL6887,1,Spinal Muscular Atrophy,C0026847,Spinal cord,GEO,Microarray,Mus musculus,3|3,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA07310,GSE81245,GPL6887,0,Spinal Muscular Atrophy,C0026847,Spinal cord,GEO,Microarray,Mus musculus,3|3,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA07311,GSE81245,GPL6887,1,Spinal Muscular Atrophy,C0026847,Dorsal root ganglion,GEO,Microarray,Mus musculus,3|3,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA07312,GSE81245,GPL6887,5,Spinal Muscular Atrophy,C0026847,Brain,GEO,Microarray,Mus musculus,3|3,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA07313,GSE81259,GPL16791,1000,Juvenile Idiopathic Arthritis,C3890205,,GEO,RNA-Seq,Homo sapiens,14|47,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA07314,GSE81279,GPL21847,9,Multiple Sclerosis,C0026769,Blood,GEO,Microarray,Homo sapiens,20|7,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA07315,GSE81279,GPL21847,21,Multiple Sclerosis,C0026769,Blood,GEO,Microarray,Homo sapiens,17|6,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA07316,GSE81292,GPL18991,1000,Systemic Sclerosis With Lung Involvement,C0339904,Lung,GEO,Microarray,Homo sapiens,5|15,HPO:It is a bilateral reticular pattern of linear or lineonodular densities that are most pronounced in basilar portions of the lungs on standard chest x-ray. It is the third minor criterion for scleroderma diagnosis. DSA07317,GSE81376,GPL16570,1000,Arthrogryposis With Renal Dysfunction And Cholestasis Syndrome,C4551984,Kidney,GEO,Microarray,Mus musculus,3|3,"DO:An arthrogryposis, renal dysfunction, and cholestasis that has_material_basis_in homozygous or compound heterozygous mutation in VPS33B on 15q26.1." DSA07318,GSE81376,GPL16570,1000,Arthrogryposis With Renal Dysfunction And Cholestasis Syndrome,C4551984,Kidney,GEO,Microarray,Mus musculus,3|3,"DO:An arthrogryposis, renal dysfunction, and cholestasis that has_material_basis_in homozygous or compound heterozygous mutation in VPS33B on 15q26.1." DSA07319,GSE81376,GPL16570,1000,Arthrogryposis With Renal Dysfunction And Cholestasis Syndrome,C4551984,Kidney,GEO,Microarray,Mus musculus,3|3,"DO:An arthrogryposis, renal dysfunction, and cholestasis that has_material_basis_in homozygous or compound heterozygous mutation in VPS33B on 15q26.1." DSA07320,GSE81396,GPL11154,1,Bipolar Disorder,C0005586,Brain,GEO,RNA-Seq,Homo sapiens,4|4,DO:A mood disorder that involves alternating periods of mania and depression. DSA07321,GSE81396,GPL11154,24,Bipolar Disorder,C0005586,Brain,GEO,RNA-Seq,Homo sapiens,4|4,DO:A mood disorder that involves alternating periods of mania and depression. DSA07322,GSE81587,GPL13112,142,Depression,C0011581,Prefrontal cortex,GEO,RNA-Seq,Mus musculus,2|2,DO:A mood disorder that involves the presence of a low mood almost daily over a span of at least two years. DSA07323,GSE81624,GPL17586,288,Autism Spectrum Disorder,C1510586,,GEO,Microarray,Homo sapiens,8|9,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA07324,GSE81937,GPL16699,0,Chronic Lymphocytic Leukemia,C0023434,Whole blood,GEO,Microarray,Homo sapiens,2|11,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA07325,GSE81937,GPL16699,0,Chronic Lymphocytic Leukemia,C0023434,Whole blood,GEO,Microarray,Homo sapiens,2|10,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA07326,GSE81965,GPL16791,1000,Type 2 Diabetes,C0011860,Vastus lateralis,GEO,RNA-Seq,Homo sapiens,18|11,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA07327,GSE81965,GPL16791,1000,Obesity,C0028754,Vastus lateralis,GEO,RNA-Seq,Homo sapiens,18|16,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07328,GSE81979,GPL20188,0,Multiple Myeloma,C0026764,Oral buccal mucosa,GEO,Microarray,Homo sapiens,10|10,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA07329,GSE81979,GPL20188,345,Multiple Myeloma,C0026764,Blood,GEO,Microarray,Homo sapiens,10|7,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA07330,GSE82107,GPL570,5,Osteoarthritis,C0157946,Synovium,GEO,Microarray,Homo sapiens,7|10,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA07331,GSE82140,GPL17692,358,Sebaceous Hyperplasia,C0406484,Skin,GEO,Microarray,Homo sapiens,3|5,NCI:Enlargement of the sebaceous glands. DSA07332,GSE82177,GPL11154,0,Hepatocellular Carcinoma,C0334287,Liver,GEO,RNA-Seq,Homo sapiens,9|8,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07333,GSE82188,GPL10192,1000,Dilated Cardiomyopathy,C0007193,Heart,GEO,Microarray,Mus musculus,3|3,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA07334,GSE82221,GPL10558,1000,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,25|15,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA07335,GSE82221,GPL10558,1000,Lupus Nephritis,C0024143,Blood,GEO,Microarray,Homo sapiens,25|15,DO:A glomerulonephritis that is characterized by inflammation of the kidneys resulting from systemic lupus erythematosus. DSA07336,GSE82290,GPL10558,0,Dilated Cardiomyopathy 1A,C1449563,,GEO,Microarray,Homo sapiens,4|7,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LMNA gene on chromosome 1q21. DSA07337,GSE82340,GPL11154,45,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,7|4,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA07338,GSE83192,GPL16570,650,AIDS related complex,C0001857,Liver,GEO,Microarray,Mus musculus,4|6,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA07339,GSE83256,GPL11154,1000,Paroxysmal Kinesigenic Dyskinesia,C1868682,,GEO,RNA-Seq,Homo sapiens,7|16,DO:A dystonia characterized by recurrent brief involuntary hyperkinesias triggered by sudden movements that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the proline-rich transmembrane protein 2 gene (PRRT2) on chromosome 16p11. DSA07340,GSE83318,GPL7202,1000,Hepatocellular Adenoma,C0206669,Liver,GEO,Microarray,Mus musculus,10|10,"EFO:A benign epithelial neoplasm arising from the hepatocytes. Grossly, it appears as a soft, round mass which often contains areas of hemorrhage and necrosis. Morphologically, the neoplastic cells resemble normal hepatocytes and form plates separated by sinusoids. Most patients have a history of contraceptive or anabolic steroids use." DSA07341,GSE83353,GPL10739,0,Adenoma,C0001430,Blood,GEO,Microarray,Homo sapiens,3|4,DO:A pancreatic cystadenoma that is characterized by innumerable small cysts lined by bland clear cells. DSA07342,GSE83353,GPL10739,0,Colorectal Carcinoma,C0009402,Blood,GEO,Microarray,Homo sapiens,3|3,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA07343,GSE83374,GPL16686,249,Alexander Disease,C0270726,,GEO,Microarray,Homo sapiens,3|1,DO:A leukodystrophy that is characterized by the destruction of white matter and the formation of Rosenthal fibers consisting of abnormal clumps of protein that accumulate in astrocytes. DSA07344,GSE83381,GPL11154,857,Crohn's Disease,C0010346,,GEO,RNA-Seq,Homo sapiens,4|4,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA07345,GSE83448,GPL18134,1000,Crohn's Disease,C0010346,Intestine,GEO,Microarray,Homo sapiens,14|39,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA07346,GSE83456,GPL10558,1000,Extrapulmonary Tuberculosis,C0679362,Blood,GEO,Microarray,Homo sapiens,61|47,MONDO:A tuberculosis that occurs at body sites other than the lung. DSA07347,GSE83456,GPL10558,1000,Pulmonary Tuberculosis,C0041327,Blood,GEO,Microarray,Homo sapiens,61|45,"DO:A tuberculosis that is a contagious disease located_in lungs. The infection has_symptom fever, has_symptom cough, has_symptom difficulty in breathing, has_symptom inflammatory infiltrations, has_symptom formation of tubercles, has_symptom caseation, has_symptom pleural effusion, and has_symptom fibrosis." DSA07348,GSE83456,GPL10558,1000,Sarcoidosis,C0036202,Blood,GEO,Microarray,Homo sapiens,61|49,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA07349,GSE83505,GPL16791,585,Dyskeratosis Congenita,C0265965,,GEO,RNA-Seq,Homo sapiens,95|48,"DO:A skin disease characterized by cutaneous pigmentation, premature graying, dystrophy of the nails, leukoplakia of the oral mucosa, continuous lacrimation due to atresia of the lacrimal ducts, often thrombocytopenia, anemia, testicular atrophy in the male carriers and predisposition to cancer." DSA07350,GSE83505,GPL16791,562,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,RNA-Seq,Homo sapiens,95|27,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA07351,GSE83505,GPL16791,812,Scleroderma,C0011644,,GEO,RNA-Seq,Homo sapiens,95|49,"DO:A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies." DSA07352,GSE83558,GPL570,4,Primary Sjogren Syndrome,C0151449,,GEO,Microarray,Homo sapiens,2|3,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA07353,GSE83558,GPL570,0,Primary Sjogren Syndrome,C0151449,,GEO,Microarray,Homo sapiens,2|2,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA07354,GSE83572,GPL6246,1000,Preleukemia,C0033027,Thymus,GEO,Microarray,Mus musculus,4|5,"EFO:A clonal hematopoietic disorder characterized by dysplasia and ineffective hematopoiesis in one or more of the hematopoietic cell lines. The dysplasia may be accompanied by an increase in myeloblasts, but the number is less than 20%, which, according to the WHO guidelines, is the requisite threshold for the diagnosis of acute myeloid leukemia. It may occur de novo or as a result of exposure to alkylating agents and/or radiotherapy. (WHO, 2001)" DSA07355,GSE83572,GPL6246,1000,Preleukemia,C0033027,Thymus,GEO,Microarray,Mus musculus,4|5,"EFO:A clonal hematopoietic disorder characterized by dysplasia and ineffective hematopoiesis in one or more of the hematopoietic cell lines. The dysplasia may be accompanied by an increase in myeloblasts, but the number is less than 20%, which, according to the WHO guidelines, is the requisite threshold for the diagnosis of acute myeloid leukemia. It may occur de novo or as a result of exposure to alkylating agents and/or radiotherapy. (WHO, 2001)" DSA07356,GSE83572,GPL6246,1000,Leukemia,C0023418,Thymus,GEO,Microarray,Mus musculus,4|11,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA07357,GSE83582,GPL19983,1000,Plaque Psoriasis,C0263361,Skin,GEO,Microarray,Homo sapiens,20|12, DSA07358,GSE83582,GPL19983,174,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,20|30,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA07359,GSE83582,GPL19983,114,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,20|40,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA07360,GSE83596,GPL21810,125,Steatosis,C2711227,Liver,GEO,Microarray,Mus musculus,3|3,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA07361,GSE83596,GPL21810,289,Steatosis,C2711227,Liver,GEO,Microarray,Mus musculus,3|3,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA07362,GSE83596,GPL21810,1000,Steatosis,C2711227,Liver,GEO,Microarray,Mus musculus,4|4,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA07363,GSE83596,GPL21810,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Mus musculus,4|4,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07364,GSE83596,GPL21810,26,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Mus musculus,4|4,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07365,GSE83601,GPL11154,1000,Post-Traumatic Stress Disorder,C0038436,Peripheral blood,GEO,RNA-Seq,Homo sapiens,5|5,DO:An anxiety disorder which results from a traumatic experience that results in psychological trauma. DSA07366,GSE83632,GPL5175,1000,Diffuse Large B-Cell Lymphoma,C0079744,Blood,GEO,Microarray,Homo sapiens,87|76,DO:A B-cell lymphoma that is a cancer of B cells presenting as an aggressive tumour which can arise in virtually any part of the body. DSA07367,GSE83670,GPL570,0,Multiple Sclerosis,C0026769,Brain,GEO,Microarray,Homo sapiens,3|4,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA07368,GSE83675,GPL17077,0,Bicuspid Aortic Valve,C0149630,Wall of ascending aorta,GEO,Microarray,Homo sapiens,7|9,DO:An aortic valve disease that is characterized by the presence of abnormal two-leaflet aortic valve in at least 2 first-degree relatives. DSA07369,GSE83686,GPL6244,0,Nijmegen Breakage Syndrome,C0398791,,GEO,Microarray,Homo sapiens,2|2,"DO:A syndrome characterized by chromosomal instability, microcephaly, growth retardation, immunodeficiency, cellular hypersensitivity to X-rays, and predisposition to cancer that has_material_basis_in homozygous or compound heterozygous mutation in NBN on chromosome 8q21.3." DSA07370,GSE83687,GPL16791,1000,Ulcerative Colitis,C0009324,Rectum,GEO,RNA-Seq,Homo sapiens,2|3,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA07371,GSE83687,GPL16791,1000,Crohn's Disease,C0010346,Colon,GEO,RNA-Seq,Homo sapiens,17|1,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA07372,GSE83687,GPL16791,47,Ulcerative Colitis,C0009324,Colon,GEO,RNA-Seq,Homo sapiens,17|3,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA07373,GSE83687,GPL16791,237,Crohn's Disease,C0010346,Sigmoid colon,GEO,RNA-Seq,Homo sapiens,10|2,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA07374,GSE83687,GPL16791,1000,Ulcerative Colitis,C0009324,Sigmoid colon,GEO,RNA-Seq,Homo sapiens,10|1,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA07375,GSE83687,GPL16791,0,Crohn's Disease,C0010346,Small bowel,GEO,RNA-Seq,Homo sapiens,7|11,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA07376,GSE83687,GPL16791,1000,Ulcerative Colitis,C0009324,Small bowel,GEO,RNA-Seq,Homo sapiens,7|1,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA07377,GSE83717,GPL11154,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,RNA-Seq,Homo sapiens,5|6,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA07378,GSE83808,GPL11154,606,Paroxysmal Nocturnal Hemoglobinuria,C0024790,Blood,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An aquired hemolytic anemia that is characterized by abdominal pain, hematuria, esophageal dysmotility and thrombosis, has_material_basis_in defect in the cell membrane glycosyl phosphatidylinositols that protect red blood cells from the innate complement immune system." DSA07379,GSE83808,GPL11154,387,Paroxysmal Nocturnal Hemoglobinuria,C0024790,Blood,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An aquired hemolytic anemia that is characterized by abdominal pain, hematuria, esophageal dysmotility and thrombosis, has_material_basis_in defect in the cell membrane glycosyl phosphatidylinositols that protect red blood cells from the innate complement immune system." DSA07380,GSE83808,GPL11154,147,Paroxysmal Nocturnal Hemoglobinuria,C0024790,Blood,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An aquired hemolytic anemia that is characterized by abdominal pain, hematuria, esophageal dysmotility and thrombosis, has_material_basis_in defect in the cell membrane glycosyl phosphatidylinositols that protect red blood cells from the innate complement immune system." DSA07381,GSE83808,GPL11154,35,Paroxysmal Nocturnal Hemoglobinuria,C0024790,Blood,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An aquired hemolytic anemia that is characterized by abdominal pain, hematuria, esophageal dysmotility and thrombosis, has_material_basis_in defect in the cell membrane glycosyl phosphatidylinositols that protect red blood cells from the innate complement immune system." DSA07382,GSE83920,GPL570,3,Hermansky-Pudlak Syndrome,C0079504,,GEO,Microarray,Homo sapiens,3|3,"DO:A syndrome characterized by oculocutaneous albinism, bleeding problems due to platelet storage pool defect, visual impairment and lysosomal accumulation of ceroid lipofuscin." DSA07383,GSE83946,GPL10558,358,Congenital Anomalies of Kidney And Urinary Tract 1,C1835826,Ureter,GEO,Microarray,Homo sapiens,7|19,DO:A CAKUT that has_material_basis_in heterozygous mutation in the DSTYK gene on chromosome 1q32. DSA07384,GSE8397,GPL96,0,Parkinson's Disease,C0030567,Superior frontal gyrus,GEO,Microarray,Homo sapiens,3|5,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA07385,GSE8397,GPL96,195,Parkinson's Disease,C0030567,Substantia nigra,GEO,Microarray,Homo sapiens,5|9,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA07386,GSE8397,GPL96,254,Parkinson's Disease,C0030567,Brain,GEO,Microarray,Homo sapiens,6|15,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA07387,GSE205021,GPL24247,1000,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,RNA-Seq,Mus musculus,3|4,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA07388,GSE84013,GPL16791,109,Huntington's Disease,C0020179,,GEO,RNA-Seq,Homo sapiens,8|8,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA07389,GSE84073,GPL18460,547,Hepatocellular Carcinoma,C0334287,Liver,GEO,RNA-Seq,Homo sapiens,4|3,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07390,GSE84073,GPL18460,1000,Cholangiocarcinoma,C0206698,Liver,GEO,RNA-Seq,Homo sapiens,4|4,DO:A bile duct carcinoma that derives_from epithelial cells of glandular origin. DSA07391,GSE84073,GPL18460,1000,Mixed Hcc/Cc Tumours,,Liver,GEO,RNA-Seq,Homo sapiens,4|3, DSA07392,GSE84073,GPL18460,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,RNA-Seq,Homo sapiens,6|3,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07393,GSE84073,GPL18460,1000,Cholangiocarcinoma,C0206698,Liver,GEO,RNA-Seq,Homo sapiens,6|7,DO:A bile duct carcinoma that derives_from epithelial cells of glandular origin. DSA07394,GSE84073,GPL18460,1000,Mixed Hcc/Cc Tumours,,Liver,GEO,RNA-Seq,Homo sapiens,6|5, DSA07395,GSE84076,GPL16791,347,Active Tuberculosis,C0151332,Whole blood,GEO,RNA-Seq,Homo sapiens,4|6,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA07396,GSE84076,GPL16791,52,Latent Tuberculosis,C1609538,Whole blood,GEO,RNA-Seq,Homo sapiens,4|5,"MONDO:Mycobacterium tuberculosis infection that does not induce infectious expression of the disease in the affected person, although it can cause continuous immune response generated towards TB antigens; person having LTBI are asymptomatic and acting as a reservoir of active tuberculosis tuberculosis cases and Mycobacterium tuberculosis and run a 5-10% risk of reactivating tuberculosis throughout their lives." DSA07397,GSE84331,GPL570,1000,Dengue Hemorrhagic Fever,C0019100,,GEO,Microarray,Homo sapiens,5|7,"DO:A dengue disease that occurs when a person experiences a second infection with a heterologous Dengue virus serotype, which is transmitted_by Aedes mosquito bite. The infection has_symptom hemorrhagic lesions of the skin, has_symptom thrombocytopenia, has_symptom reduction in the fluid part of the blood, and has_symptom high fever." DSA07398,GSE84445,GPL16791,141,Tuberculosis Infection,C1609538,,GEO,RNA-Seq,Homo sapiens,10|10,"MONDO:Mycobacterium tuberculosis infection that does not induce infectious expression of the disease in the affected person, although it can cause continuous immune response generated towards TB antigens; person having LTBI are asymptomatic and acting as a reservoir of active tuberculosis tuberculosis cases and Mycobacterium tuberculosis and run a 5-10% risk of reactivating tuberculosis throughout their lives." DSA07399,GSE84445,GPL16791,37,Tuberculosis Infection,C1609538,,GEO,RNA-Seq,Homo sapiens,10|10,"MONDO:Mycobacterium tuberculosis infection that does not induce infectious expression of the disease in the affected person, although it can cause continuous immune response generated towards TB antigens; person having LTBI are asymptomatic and acting as a reservoir of active tuberculosis tuberculosis cases and Mycobacterium tuberculosis and run a 5-10% risk of reactivating tuberculosis throughout their lives." DSA07400,GSE84504,GPL18573,1000,Teratoma,C0039538,,GEO,RNA-Seq,Homo sapiens,2|2,DO:A germ cell and embryonal cancer that is an encapsulated tumor with tissue or organ components resembling normal derivatives of all three germ layers. DSA07401,GSE84504,GPL18573,1000,Teratoma,C0039538,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A germ cell and embryonal cancer that is an encapsulated tumor with tissue or organ components resembling normal derivatives of all three germ layers. DSA07402,GSE84538,GPL21290,1000,Chronic Thromboembolic Pulmonary Hypertension,C2363973,Pulmonary artery,GEO,RNA-Seq,Homo sapiens,4|3,MONDO:Chronic thromboembolic pulmonary hypertension (CTEPH) is characterized by the persistence of thromboemboli in the form of organized tissue obstructing the pulmonary arteries. The consequence is an increase in pulmonary vascular resistance (PVR) resulting in pulmonary hypertension (PH) and progressive right heart failure. DSA07403,GSE84538,GPL21290,928,Pulmonary Arterial Hypertension,C2973725,Pulmonary artery,GEO,RNA-Seq,Homo sapiens,4|4,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA07404,GSE84546,GPL13497,1000,Metastatic Adenocarcinoma,C0334277,Kidney,GEO,Microarray,Homo sapiens,3|3,NCI:An adenocarcinoma that has spread from its original site of growth to another anatomic site. DSA07405,GSE84546,GPL13497,1000,Papillary Renal Cell Carcinoma,C1306837,Kidney,GEO,Microarray,Homo sapiens,3|3,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA07406,GSE84616,GPL13497,24,Multicentric Carpotarsal Osteolysis Syndrome,C2674705,,GEO,Microarray,Homo sapiens,2|2,"DO:A syndrome characterized by progressive loss of bone, typically involving the capsal and tarsal bones, and in many cases chronic renal failure that has_material_basis_in heterozygous mutation in MAFB on chromosome 20q12." DSA07407,GSE84626,GPL16699,0,Critical Limb Ischemia,,Whole blood,GEO,Microarray,Homo sapiens,6|6, DSA07408,GSE84638,GPL10558,0,Primary Myelofibrosis,C0001815,Blood,GEO,Microarray,Homo sapiens,7|17,DO:A myeloid neoplasm that is located in the bone marrow which results in bone marrow being replaced by fibrous (scar) tissue. DSA07409,GSE84684,GPL11154,97,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,2|2,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA07410,GSE84787,GPL17077,0,Gastric Cancer,C0699791,Stomach,GEO,Microarray,Homo sapiens,10|10,DO:A gastrointestinal system cancer that is located_in the stomach. DSA07411,GSE84796,GPL14550,1000,Chagas Cardiomyopathy,C0007930,Left ventricle,GEO,Microarray,Homo sapiens,7|10,"EFO:a form of cardiomyopathy that develops as a result of Chagas disease, an infection with the protozoan parasite Trypanosoma Cruzi" DSA07412,GSE205748,GPL18573,1000,Psoriatic Arthritis,C0003872,Skin,GEO,RNA-Seq,Homo sapiens,6|8,DO:An arthritis that is characterized by joint inflammation that usually occurs in combination with psoriasis. DSA07413,GSE84844,GPL570,1000,Primary Sjogren Syndrome,C0151449,Whole blood,GEO,Microarray,Homo sapiens,30|30,NCI:Sjogren syndrome without a concomitant systemic autoimmune disorder. DSA07414,GSE84881,GPL570,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,4|19,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA07415,GSE84887,GPL570,7,Down Syndrome,C0013080,,GEO,Microarray,Homo sapiens,1|7,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA07416,GSE84988,GPL17021,1000,Acute Leukemia,C0085669,Bone marrow,GEO,RNA-Seq,Mus musculus,3|3,"DO:A lymphoid leukemia that occurs when a hematopoietic stem cell undergoes malignant transformation into a primitive, undifferentiated cell with abnormal longevity producing large numbers of white blood cells to be produced and enter the blood stream." DSA07417,GSE84988,GPL17021,1000,Acute Leukemia,C0085669,Bone marrow,GEO,RNA-Seq,Mus musculus,3|3,"DO:A lymphoid leukemia that occurs when a hematopoietic stem cell undergoes malignant transformation into a primitive, undifferentiated cell with abnormal longevity producing large numbers of white blood cells to be produced and enter the blood stream." DSA07418,GSE84988,GPL17021,1000,Acute Leukemia,C0085669,Bone marrow,GEO,RNA-Seq,Mus musculus,3|3,"DO:A lymphoid leukemia that occurs when a hematopoietic stem cell undergoes malignant transformation into a primitive, undifferentiated cell with abnormal longevity producing large numbers of white blood cells to be produced and enter the blood stream." DSA07419,GSE205748,GPL18573,6,Psoriatic Arthritis,C0003872,Skin,GEO,RNA-Seq,Homo sapiens,6|9,DO:An arthritis that is characterized by joint inflammation that usually occurs in combination with psoriasis. DSA07420,GSE85126,GPL13912,686,Huntington's Disease,C0020179,Striatum,GEO,Microarray,Mus musculus,5|5,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA07421,GSE85148,GPL17021,1000,Osteoarthritis,C0157946,Cartilage,GEO,RNA-Seq,Mus musculus,3|3,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA07422,GSE85195,GPL6480,10,Oral Leukoplakia,C0023532,,GEO,Microarray,Homo sapiens,1|15,DO:A skin disease characterized by a defect in the normal process of keratinization of the mucosa. DSA07423,GSE85195,GPL6480,166,Oral Squamous Cell Carcinoma,C0585362,Gingiva,GEO,Microarray,Homo sapiens,1|34,"EFO:A squamous cell carcinoma arising from the oral cavity. It affects predominantly adults in their fifth and sixth decades of life and is associated with alcohol and tobacco use. Human papillomavirus is present in approximately half of the cases. It is characterized by a tendency to metastasize early to the lymph nodes. When the tumor is small, patients are often asymptomatic. Physical examination may reveal erythematous or white lesions or plaques. The majority of patients present with signs and symptoms of locally advanced disease including mucosal ulceration, pain, difficulty with speaking, chewing, and swallowing, bleeding, weight loss, and neck swelling. Patients may also present with swollen neck lymph nodes without any symptoms from the oropharyngeal tumor. The most significant prognostic factors are the size of the tumor and the lymph nodes status." DSA07424,GSE85214,GPL16791,12,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,5|8,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA07425,GSE85214,GPL16791,13,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,5|8,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA07426,GSE85307,GPL6244,0,Pre-Eclampsia,C0032914,Whole blood,GEO,Microarray,Homo sapiens,110|47,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA07427,GSE85349,GPL20844,42,Spinocerebellar Ataxia Type 6 (Disorder),C0752124,,GEO,Microarray,Homo sapiens,4|6,"DO:An autosomal dominant cerebellar ataxia that is characterized by progresive ataxia, has_material_basis_in mutation in the CACNA1A gene." DSA07428,GSE85349,GPL21185,1000,Spinocerebellar Ataxia Type 6 (Disorder),C0752124,,GEO,Microarray,Homo sapiens,4|4,"DO:An autosomal dominant cerebellar ataxia that is characterized by progresive ataxia, has_material_basis_in mutation in the CACNA1A gene." DSA07429,GSE85417,GPL16791,0,Autism Spectrum Disorder,C1510586,Cerebellum,GEO,RNA-Seq,Homo sapiens,2|4,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA07430,GSE85426,GPL14550,1000,Alzheimer's Disease,C0002395,Whole blood,GEO,Microarray,Homo sapiens,90|90,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA07431,GSE85567,GPL11154,1000,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,28|57,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA07432,GSE85598,GPL16791,952,Charcot-Marie-Tooth Disease Type 1A,C0007959,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A hereditary sensory neuropathy characterized by progressively reduced sensation to pain, temperature, and touch, loss of myelinated and unmyelinated fibers, and hypotonia with onset at birth or in early childhood." DSA07433,GSE85598,GPL16791,1000,Charcot-Marie-Tooth Disease Type 1A,C0007959,,GEO,RNA-Seq,Homo sapiens,4|3,"DO:A hereditary sensory neuropathy characterized by progressively reduced sensation to pain, temperature, and touch, loss of myelinated and unmyelinated fibers, and hypotonia with onset at birth or in early childhood." DSA07434,GSE85599,GPL17586,1000,Infectious Mononucleosis,C0021345,,GEO,Microarray,Homo sapiens,6|6,"DO:A viral infectious disease that results in inflammation, located in pharynx, has_material_basis_in Human herpesvirus 4 and has symptom fever, has symptom fatigue, has symptom lymphadenopathy, and has symptom splenomegaly." DSA07435,GSE85649,GPL10558,0,Myasthenia Gravis,C0026896,Blood,GEO,Microarray,Homo sapiens,3|3,"DO:An autoimmune disease of the nervous system that has_material_basis_in antibodies to acetylcholine receptors at the neuromuscular junction, has_symptom ptosis, has_symptom diplopia, has_symptom dysphagia, has_symptom dysarthria, has_symptom muscle weakness and has_symptom shortness of breath." DSA07436,GSE85716,GPL19612,1000,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Homo sapiens,6|6,DO:A respiratory system cancer that is located_in the lung. DSA07437,GSE85804,GPL10558,32,Adrenomyeloneuropathy,C1527231,,GEO,Microarray,Homo sapiens,3|3,"DO:A leukodystrophy that disrupts the breakdown of very-long-chain fatty acids resulting in progressive brain damage, failure of the adrenal glands and eventually death." DSA07438,GSE85804,GPL10558,106,Cerebral Adrenoleukodystrophy,C4684865,,GEO,Microarray,Homo sapiens,3|3,"NCI:A subtype of adrenoleukodystrophy (ALD) occurring in approximately 40 percent of boys with ALD, primarily affecting the cerebrum, resulting in rapidly declining neurocognitive function and in most patients, premature death." DSA07439,GSE85817,GPL6244,0,Non syndromic cleft lip/palate (NSCL/P),,Orbicularis Oris Muscle,GEO,Microarray,Homo sapiens,4|42, DSA07440,GSE85837,GPL10558,0,Asymptomatic Myeloma,C1531608,Bone marrow,GEO,Microarray,Homo sapiens,13|15,EFO:A plasma cell myeloma lacking clinical manifestations and organ impairment. DSA07441,GSE85902,GPL10787,2,Congenital Heart Disease,C0152021,Heart,GEO,Microarray,Mus musculus,3|3,"EFO:any form of heart disease that is present at birth, including defects to the structure and function of the heart and great vessels" DSA07442,GSE85984,GPL15433,170,Myotonic Dystrophy Type 1,C0027126,Skeletal muscle,GEO,RNA-Seq,Homo sapiens,3|2,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA07443,GSE86095,GPL11154,1000,Clear Cell Renal Cell Carcinoma,C0007134,Kidney,GEO,RNA-Seq,Homo sapiens,10|10,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA07444,GSE86356,GPL11154,260,Myotonic Dystrophy Type 1,C0027126,Heart,GEO,RNA-Seq,Homo sapiens,3|11,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA07445,GSE86356,GPL11154,432,Myotonic Dystrophy Type 1,C0027126,Quadriceps,GEO,RNA-Seq,Homo sapiens,12|19,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA07446,GSE86356,GPL11154,1000,Duchenne Muscular Dystrophy,C0013264,Quadriceps,GEO,RNA-Seq,Homo sapiens,12|1,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA07447,GSE86356,GPL11154,1000,Myotonic Dystrophy Type 1,C0027126,Tibialis anterior,GEO,RNA-Seq,Homo sapiens,11|31,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA07448,GSE86356,GPL11154,1000,Duchenne Muscular Dystrophy,C0013264,Tibialis anterior muscle,GEO,RNA-Seq,Homo sapiens,9|1,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA07449,GSE86373,GPL17586,1000,Melanoma,C0025202,,GEO,Microarray,Homo sapiens,3|3,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA07450,GSE86418,GPL13112,547,Sickle Cell Disease,C0002895,Dorsal root ganglion,GEO,RNA-Seq,Mus musculus,6|5,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA07451,GSE86418,GPL13112,154,Sickle Cell Disease,C0002895,Dorsal root ganglion,GEO,RNA-Seq,Mus musculus,7|5,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA07452,GSE86418,GPL13112,486,Sickle Cell Disease,C0002895,Dorsal root ganglion,GEO,RNA-Seq,Mus musculus,6|5,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA07453,GSE86418,GPL13112,718,Sickle Cell Disease,C0002895,Dorsal root ganglion,GEO,RNA-Seq,Mus musculus,6|4,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA07454,GSE206614,GPL16791,1000,Oxidation Resistance 1 Mutation,,,GEO,RNA-Seq,Homo sapiens,3|3, DSA07455,GSE8650,GPL96,1000,Systemic-Onset Juvenile Idiopathic Arthritis,C0087031,,GEO,Microarray,Homo sapiens,21|58,"MONDO:Systemic-onset juvenile idiopathic arthritis is marked by the severity of the extra-articular manifestations (fever, cutaneous eruptions) and by an equal sex ratio." DSA07456,GSE86618,GPL18573,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,RNA-Seq,Homo sapiens,215|325,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA07457,GSE86906,GPL16791,1000,Schizophrenia,C0036341,Brain,GEO,RNA-Seq,Homo sapiens,14|22,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA07458,GSE86959,GPL16791,1000,Invasive Mucinous Lung Adenocarcinoma,C4522160,Lung,GEO,RNA-Seq,Homo sapiens,6|2,"NCI:An invasive adenocarcinoma that arises from the lung. It is characterized by the presence of tall columnar cells and mucin production. This category refers to cases formerly classified as mucinous bronchioloalveolar carcinoma, excluding cases that meet the criteria for adenocarcinoma in situ or mucinous minimally invasive adenocarcinoma." DSA07459,GSE86984,GPL17930,0,Diffuse Scleroderma,C1258104,,GEO,Microarray,Homo sapiens,4|4,"EFO:A variant of systemic scleroderma characterized by sclerosis of the skin, Raynaud phenomenon, and organ involvement, including pulmonary fibrosis, renal disease, and gastrointestinal tract involvement." DSA07460,GSE87024,GPL6887,1000,Acute Kidney Injury,C2609414,Kidney,GEO,Microarray,Mus musculus,3|3,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA07461,GSE87024,GPL6887,1000,Acute Kidney Injury,C2609414,Kidney,GEO,Microarray,Mus musculus,3|3,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA07462,GSE87024,GPL6887,1000,Acute Kidney Injury,C2609414,Kidney,GEO,Microarray,Mus musculus,3|3,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA07463,GSE87098,GPL16686,1000,Chronic Obstructive Pulmonary Disease,C0024117,Lung,GEO,Microarray,Homo sapiens,4|4,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA07464,GSE87098,GPL16686,381,Chronic Obstructive Pulmonary Disease,C0024117,Lung,GEO,Microarray,Homo sapiens,3|4,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA07465,GSE87187,GPL16791,1000,Acute Monocytic Leukemia,C0023465,Peripheral blood,GEO,RNA-Seq,Homo sapiens,4|9,DO:A monocytic leukemia where the majority of monocytic cells are promonocytes. DSA07466,GSE87194,GPL13393,0,Schizophrenia,C0036341,Dorsal lateral prefrontal cortex,GEO,RNA-Seq,Homo sapiens,19|19,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA07467,GSE87211,GPL13497,1000,Colorectal Carcinoma,C0009402,Rectum,GEO,Microarray,Homo sapiens,160|203,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA07468,GSE87295,GPL10558,0,Gestational Diabetes,C0085207,Infant umbilical cord,GEO,Microarray,Homo sapiens,5|5,DO:A diabetes mellitus that manifests during pregnancy. DSA07469,GSE87317,GPL1261,1000,Inflammatory Bowel Disease,C0021390,Colon,GEO,Microarray,Mus musculus,4|3,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA07470,GSE87317,GPL1261,1000,Inflammatory Bowel Disease,C0021390,Colon,GEO,Microarray,Mus musculus,4|3,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA07471,GSE87433,GPL20710,0,Diabetes,C0011847,Retina,GEO,Microarray,Mus musculus,6|6,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA07472,GSE87473,GPL13158,1000,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,21|87,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA07473,GSE87473,GPL13158,1000,Ulcerative Colitis,C0009324,Colon,GEO,Microarray,Homo sapiens,21|19,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA07474,GSE87493,GPL6244,1,Obesity,C0028754,,GEO,Microarray,Homo sapiens,20|12,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07475,GSE87535,GPL16791,159,Glioblastoma Multiforme,C1621958,Brain,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA07476,GSE87546,GPL6246,0,Lymphoma,C0024299,Spleen,GEO,Microarray,Mus musculus,6|6,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA07477,GSE87546,GPL6246,1000,Lymphoma,C0024299,Lymph node,GEO,Microarray,Mus musculus,6|6,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA07478,GSE87650,GPL10558,68,Crohn's Disease,C0010346,,GEO,Microarray,Homo sapiens,49|94,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA07479,GSE87650,GPL10558,0,Irritable Bowel Syndrome,C0022104,Whole blood,GEO,Microarray,Homo sapiens,49|21,"DO:An intestinal disease that is characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause." DSA07480,GSE87650,GPL10558,1000,Inflammatory Bowel Disease,C0021390,,GEO,Microarray,Homo sapiens,49|4,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA07481,GSE87650,GPL10558,2,Ulcerative Colitis,C0009324,,GEO,Microarray,Homo sapiens,49|79,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA07482,GSE87666,GPL17077,0,High Grade Gastric Cancer,C0699791,Stomach,GEO,Microarray,Homo sapiens,7|9,DO:A gastrointestinal system cancer that is located_in the stomach. DSA07483,GSE87806,GPL16987,1,Chronic Myeloid Leukemia,C0023473,Bone marrow,GEO,Microarray,Homo sapiens,10|6,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA07484,GSE87806,GPL16987,0,Myeloproliferative Neoplasm,C0027022,Bone marrow,GEO,Microarray,Homo sapiens,10|4,"DO:A myeloid neoplasm that is characterized by a group of slow growing blood cancers in which large numbers of abnormal red blood cells, white blood cells, or platelets grow and spread in the bone marrow and the peripheral blood." DSA07485,GSE87806,GPL16987,0,Myeloproliferative Neoplasm,C0027022,Bone marrow,GEO,Microarray,Homo sapiens,10|4,"DO:A myeloid neoplasm that is characterized by a group of slow growing blood cancers in which large numbers of abnormal red blood cells, white blood cells, or platelets grow and spread in the bone marrow and the peripheral blood." DSA07486,GSE87809,GPL11154,1000,Endometriosis,C0014175,Endometrium,GEO,RNA-Seq,Homo sapiens,3|2,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA07487,GSE87899,GPL17021,65,Diabetes,C0011847,Kidney,GEO,RNA-Seq,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA07488,GSE8836,GPL1261,0,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Mus musculus,3|12,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA07489,GSE8836,GPL1261,1,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Mus musculus,4|12,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA07490,GSE88710,GPL16791,1000,Enteritis,C0014335,Sigmoid colon,GEO,RNA-Seq,Homo sapiens,6|4,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA07491,GSE88721,GPL17692,1000,Meningeal Tumor,C0025284,,GEO,Microarray,Homo sapiens,1|14,DO:A central nervous system cancer that are manifested in the central nervous system and arise from the arachnoid cap cells of the arachnoid villi in the meninges. DSA07492,GSE88805,GPL11154,1000,Cervical Squamous Cell Carcinoma,C0279671,Cervix,GEO,RNA-Seq,Homo sapiens,3|3,DO:A cervix carcinoma that has_material_basis_in squamous cells of the cervix. DSA07493,GSE88805,GPL11154,479,Cervical Squamous Cell Carcinoma,C0279671,Cervix,GEO,RNA-Seq,Homo sapiens,3|3,DO:A cervix carcinoma that has_material_basis_in squamous cells of the cervix. DSA07494,GSE88805,GPL11154,1000,Esophageal Squamous Cell Carcinoma,C0279626,Esophagus,GEO,RNA-Seq,Homo sapiens,3|3,DO:An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus. DSA07495,GSE88805,GPL11154,0,Esophageal Squamous Cell Carcinoma,C0279626,Esophagus,GEO,RNA-Seq,Homo sapiens,3|3,DO:An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus. DSA07496,GSE88805,GPL11154,869,Gastric Adenocarcinoma,C0278701,Stomach,GEO,RNA-Seq,Homo sapiens,3|3,DO:A stomach carcinoma that derives_from epithelial cells of glandular origin. DSA07497,GSE88805,GPL11154,1000,Gastric Adenocarcinoma,C0278701,Stomach,GEO,RNA-Seq,Homo sapiens,3|3,DO:A stomach carcinoma that derives_from epithelial cells of glandular origin. DSA07498,GSE88805,GPL11154,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07499,GSE88805,GPL11154,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07500,GSE88805,GPL11154,157,Lung Adenocarcinoma,C0152013,Lung,GEO,RNA-Seq,Homo sapiens,3|3,DO:A respiratory system cancer that is located_in the lung. DSA07501,GSE88805,GPL11154,1000,Lung Adenocarcinoma,C0152013,Lung,GEO,RNA-Seq,Homo sapiens,3|3,DO:A respiratory system cancer that is located_in the lung. DSA07502,GSE88805,GPL11154,1000,Lung Squamous Cell Carcinoma,C0149782,Lung,GEO,RNA-Seq,Homo sapiens,3|3,DO:A non-small cell lung carcinoma that has_material_basis_in the squamous cell. DSA07503,GSE88805,GPL11154,1000,Lung Squamous Cell Carcinoma,C0149782,Lung,GEO,RNA-Seq,Homo sapiens,3|3,DO:A non-small cell lung carcinoma that has_material_basis_in the squamous cell. DSA07504,GSE88805,GPL11154,243,Signet Ring Cell Carcinoma,C0206696,Stomach,GEO,RNA-Seq,Homo sapiens,3|2,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which have signet ring appearance." DSA07505,GSE88805,GPL11154,1000,Small Cell Lung Cancer,C0149925,Lung,GEO,RNA-Seq,Homo sapiens,3|3,DO:A lung carcinoma that has_material_basis_in primitive-appearing cells that are smaller than normal cells and is located_in the lung. DSA07506,GSE88805,GPL11154,23,Small Cell Lung Cancer,C0149925,Lung,GEO,RNA-Seq,Homo sapiens,3|3,DO:A lung carcinoma that has_material_basis_in primitive-appearing cells that are smaller than normal cells and is located_in the lung. DSA07507,GSE206614,GPL16791,1000,Oxidation Resistance 1 Mutation,,Neural aggregates,GEO,RNA-Seq,Homo sapiens,3|3, DSA07508,GSE88888,GPL11154,160,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,10|10,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA07509,GSE89047,GPL17077,1000,Lung Cancer,C0684249,Lung,GEO,Microarray,Homo sapiens,8|8,DO:A respiratory system cancer that is located_in the lung. DSA07510,GSE89063,GPL11154,1000,Non-Alcoholic Steatohepatitis,C3241937,,GEO,RNA-Seq,Homo sapiens,9|8,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA07511,GSE89077,GPL11202,1000,Colorectal Polyps,C0949059,Colorectum,GEO,Microarray,Mus musculus,4|4,HPO:Multiple abnormal growths that arise from the lining of the large intestine (colon or rectum) and protrude into the intestinal lumen. DSA07512,GSE206614,GPL16791,1000,Oxidation Resistance 1 Mutation,,,GEO,RNA-Seq,Homo sapiens,3|3, DSA07513,GSE206677,GPL24676,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,2|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07514,GSE89270,GPL13112,1000,Cleft Palate,C0008925,Mouse Embryonic Pharyngeal Arch,GEO,RNA-Seq,Mus musculus,3|1,"DO:A cleft palate seen as an isolated malformation, distinct from cleft lip with or without cleft palate." DSA07515,GSE89270,GPL13112,1000,Cleft Palate,C0008925,,GEO,RNA-Seq,Mus musculus,3|1,"DO:A cleft palate seen as an isolated malformation, distinct from cleft lip with or without cleft palate." DSA07516,GSE89373,GPL16570,35,Sickle Cell Disease,C0002895,Left ventricle,GEO,Microarray,Mus musculus,3|3,"DO:A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape." DSA07517,GSE89377,GPL6947,0,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,13|8,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07518,GSE89377,GPL6947,476,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,13|12,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07519,GSE89377,GPL6947,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,13|12,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07520,GSE89377,GPL6947,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,13|11,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07521,GSE89377,GPL6947,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,13|11,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07522,GSE89377,GPL6947,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,13|5,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07523,GSE89377,GPL6947,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,13|9,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07524,GSE89377,GPL6947,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,13|12,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07525,GSE89377,GPL6947,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,13|14,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07526,GSE89408,GPL11154,1000,Arthritis,C0003864,Synovium,GEO,RNA-Seq,Homo sapiens,28|20,DO:A bone disease that is located_in the joint. DSA07527,GSE89408,GPL11154,1000,Arthritis,C0003864,Synovium,GEO,RNA-Seq,Homo sapiens,28|10,DO:A bone disease that is located_in the joint. DSA07528,GSE89408,GPL11154,1000,Arthritis,C0003864,Synovium,GEO,RNA-Seq,Homo sapiens,28|6,DO:A bone disease that is located_in the joint. DSA07529,GSE89408,GPL11154,1000,Arthritis,C0003864,Synovium,GEO,RNA-Seq,Homo sapiens,28|150,DO:A bone disease that is located_in the joint. DSA07530,GSE89462,GPL13912,1000,Skin Carcinoma,C0699893,Skin,GEO,Microarray,Mus musculus,3|3,DO:A skin cancer that is located_in tissues of the skin and develops from epithelial cells. DSA07531,GSE89475,GPL20301,600,Diabetes,C0011847,Vascular organoids,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA07532,GSE89509,GPL16790,1000,Skin Carcinoma,C0699893,Skin,GEO,RNA-Seq,Mus musculus,1|1,DO:A skin cancer that is located_in tissues of the skin and develops from epithelial cells. DSA07533,GSE89509,GPL16790,1000,Skin Carcinoma,C0699893,Skin,GEO,RNA-Seq,Mus musculus,1|1,DO:A skin cancer that is located_in tissues of the skin and develops from epithelial cells. DSA07534,GSE89509,GPL16790,1000,Skin Carcinoma,C0699893,Skin,GEO,RNA-Seq,Mus musculus,1|2,DO:A skin cancer that is located_in tissues of the skin and develops from epithelial cells. DSA07535,GSE89509,GPL16790,1000,Skin Carcinoma,C0699893,Skin,GEO,RNA-Seq,Mus musculus,1|1,DO:A skin cancer that is located_in tissues of the skin and develops from epithelial cells. DSA07536,GSE89594,GPL16699,5,Autism Spectrum Disorder,C1510586,Whole blood,GEO,Microarray,Homo sapiens,30|32,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA07537,GSE89594,GPL16699,598,Williams Syndrome,C0175702,Whole blood,GEO,Microarray,Homo sapiens,30|32,"DO:A syndrome that is characterized by mild to moderate intellectual disability, a broad forehead, a short nose with a broad tip, full cheeks, and a wide mouth with full lips and difficulty with visual-spatial tasks and has_material_basis_in hemizygous deletion of 1.5 to 1.8 Mb on chromosome 7q11.23." DSA07538,GSE89632,GPL14951,1000,Steatosis,C2711227,Liver,GEO,Microarray,Homo sapiens,24|19,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA07539,GSE89632,GPL14951,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Homo sapiens,24|20,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA07540,GSE89714,GPL11154,1000,Hypertrophic Cardiomyopathy,C0007194,Heart,GEO,RNA-Seq,Homo sapiens,4|5,DO:A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations. DSA07541,GSE89775,GPL16791,1000,Hepatoblastoma,C0206624,Liver,GEO,RNA-Seq,Homo sapiens,3|10,DO:A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver. DSA07542,GSE89809,GPL13158,0,Asthma,C0004096,Bronchus,GEO,Microarray,Homo sapiens,15|14,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA07543,GSE89809,GPL13158,5,Asthma,C0004096,Epidermis,GEO,Microarray,Homo sapiens,18|14,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA07544,GSE89809,GPL13158,0,Asthma,C0004096,Sputum,GEO,Microarray,Homo sapiens,10|10,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA07545,GSE89809,GPL13158,0,Asthma,C0004096,Bronchus,GEO,Microarray,Homo sapiens,15|14,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA07546,GSE89809,GPL13158,0,Asthma,C0004096,Epidermis,GEO,Microarray,Homo sapiens,18|13,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA07547,GSE89809,GPL13158,0,Asthma,C0004096,Sputum,GEO,Microarray,Homo sapiens,10|6,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA07548,GSE89809,GPL13158,0,Asthma,C0004096,Bronchus,GEO,Microarray,Homo sapiens,15|11,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA07549,GSE89809,GPL13158,6,Asthma,C0004096,Epidermis,GEO,Microarray,Homo sapiens,18|11,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA07550,GSE89809,GPL13158,4,Asthma,C0004096,Sputum,GEO,Microarray,Homo sapiens,10|9,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA07551,GSE89843,GPL16791,109,Multiple Sclerosis,C0026769,Blood,GEO,RNA-Seq,Homo sapiens,228|54,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA07552,GSE89843,GPL16791,249,Pulmonary Hypertension,C0020542,Blood,GEO,RNA-Seq,Homo sapiens,228|30,"DO:A hypertension characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein or pulmonary capillaries." DSA07553,GSE89843,GPL16791,76,Chronic Pancreatitis,C0149521,Blood,GEO,RNA-Seq,Homo sapiens,228|5,"EFO:INFLAMMATION of the PANCREAS that is characterized by recurring or persistent ABDOMINAL PAIN with or without STEATORRHEA or DIABETES MELLITUS. It is characterized by the irregular destruction of the pancreatic parenchyma which may be focal, segmental, or diffuse." DSA07554,GSE89843,GPL16791,93,Epilepsy,C0014544,Blood,GEO,RNA-Seq,Homo sapiens,228|20,"DO:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions." DSA07555,GSE89843,GPL16791,505,Atherosclerosis,C0004153,Blood,GEO,RNA-Seq,Homo sapiens,228|11,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA07556,GSE89843,GPL16791,0,Stable Angina Pectoris,C0340288,Blood,GEO,RNA-Seq,Homo sapiens,228|4,"EFO:The symptom of paroxysmal pain consequent to MYOCARDIAL ISCHEMIA usually of distinctive character, location and radiation. It is thought to be provoked by a transient stressful situation during which the oxygen requirements of the MYOCARDIUM exceed that supplied by the CORONARY CIRCULATION." DSA07557,GSE89843,GPL16791,1000,Unstable Angina Pectoris,C0002965,Blood,GEO,RNA-Seq,Homo sapiens,228|6,"MONDO:Angina pectoris (or equivalent type of ischemic discomfort) which has recently changed in frequency, duration, intensity, or occurs at rest." DSA07558,GSE89843,GPL16791,1000,Pulmonary Hypertension,C0020542,Blood,GEO,RNA-Seq,Homo sapiens,228|1,"DO:A hypertension characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein or pulmonary capillaries." DSA07559,GSE89843,GPL16791,1000,Non-Small Cell Lung Cancer,C0007131,Blood,GEO,RNA-Seq,Homo sapiens,228|368,DO:A respiratory system cancer that is located_in the lung. DSA07560,GSE89851,GPL16570,1000,Colitis,C0009319,Colon,GEO,Microarray,Mus musculus,4|4,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA07561,GSE89886,GPL10558,0,Parkinson's Disease,C0030567,,GEO,Microarray,Homo sapiens,4|6,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA07562,GSE89886,GPL10558,0,Parkinson's Disease,C0030567,,GEO,Microarray,Homo sapiens,4|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA07563,GSE89956,GPL6246,0,Lymphoma,C0024299,Spleen,GEO,Microarray,Mus musculus,3|3,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA07564,GSE89996,GPL16570,539,Oculopharyngeal Muscular Dystrophy,C0270952,Tibialis anterior,GEO,Microarray,Mus musculus,3|2,"MONDO:Oculopharyngeal muscular dystrophy (OPMD) is an adult-onset progressive myopathy characterized by progressive eyelid ptosis, dysphagia, dysarthria and proximal limb weakness." DSA07565,GSE90010,GPL17692,1000,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,Microarray,Homo sapiens,4|4,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA07566,GSE90010,GPL17692,1000,Respiratory Bronchiolitis Interstitial Lung Disease,C0238378,,GEO,Microarray,Homo sapiens,4|4,DO:An idiopathic interstitial pneumonia that is characterized by the accumulation of bronchiolocentric alveolar macrophages in alveolar spaces and interstitial inflammation and involves mild bronchiolar fibrosis and chronic inflammation. DSA07567,GSE90062,GPL15207,1000,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA07568,GSE90081,GPL11154,1000,Rheumatoid Arthritis,C0003873,Whole blood,GEO,RNA-Seq,Homo sapiens,12|4,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA07569,GSE90153,GPL17021,1000,Colon Tumor,C0009375,Colon,GEO,RNA-Seq,Mus musculus,2|3,DO:A colorectal cancer that is located_in the colon. DSA07570,GSE90153,GPL17021,1000,Colon Tumor,C0009375,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:A colorectal cancer that is located_in the colon. DSA07571,GSE90153,GPL17021,1000,Colon Tumor,C0009375,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:A colorectal cancer that is located_in the colon. DSA07572,GSE90153,GPL17021,1000,Colon Tumor,C0009375,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:A colorectal cancer that is located_in the colon. DSA07573,GSE90450,GPL16570,0,Autoinflammatory Syndrome,C3890737,Skin,GEO,Microarray,Mus musculus,5|5,MONDO:A group of disorders of the innate immune system characterized by attacks of seemingly unprovoked inflammation without significant levels of either autoantibodies or autoreactive T cells more characteristic of autoimmune disease. DSA07574,GSE90466,GPL13112,903,Charge Syndrome,C0265354,,GEO,RNA-Seq,Mus musculus,2|2,"DO:A syndrome that is characterized by a pattern of congenital anomalies including choanal atresia and malformations of the heart, inner ear, and retina." DSA07575,GSE90489,GPL21290,852,Posterior Polymorphous Corneal Dystrophy,C0339284,Cornea,GEO,RNA-Seq,Homo sapiens,2|2,DO:A corneal dystrophy that is characterised by changes in Descemet's membrane and endothelial layer. DSA07576,GSE90497,GPL17021,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,12|9,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA07577,GSE90497,GPL17021,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,RNA-Seq,Mus musculus,12|11,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07578,GSE90514,GPL11154,677,Parkinson's Disease,C0030567,,GEO,RNA-Seq,Homo sapiens,4|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA07579,GSE90594,GPL17077,991,Androgenetic Alopecia,C0162311,Scalp skin,GEO,Microarray,Homo sapiens,14|14,DO:An alopecia that is characterized by M-shaped hair line recession and thinning of hair at the crown of the head in males. DSA07580,GSE90604,GPL17692,1000,Glioblastoma Multiforme,C1621958,Brain,GEO,Microarray,Homo sapiens,7|16,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA07581,GSE90627,GPL17077,1000,Rectal Cancer,C0007113,Rectum,GEO,Microarray,Homo sapiens,32|32,DO:A colorectal cancer that is located_in the rectum. DSA07582,GSE90627,GPL17077,1000,Rectal Cancer,C0007113,Rectum,GEO,Microarray,Homo sapiens,32|32,DO:A colorectal cancer that is located_in the rectum. DSA07583,GSE90627,GPL17077,1000,Rectal Cancer,C0007113,Rectum,GEO,Microarray,Homo sapiens,32|32,DO:A colorectal cancer that is located_in the rectum. DSA07584,GSE90689,GPL6480,1000,Metastatic Neuroblastoma,C0027819,,GEO,Microarray,Homo sapiens,13|20,DO:An autonomic nervous system neoplasm that derives_from immature nerve cells. DSA07585,GSE90689,GPL6480,0,Neuroblastoma,C0027819,Bone marrow,GEO,Microarray,Homo sapiens,14|10,DO:An autonomic nervous system neoplasm that derives_from immature nerve cells. DSA07586,GSE90708,GPL17077,1000,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,1|20,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA07587,GSE90727,GPL21810,665,Sepsis,C0243026,Whole blood,GEO,Microarray,Mus musculus,8|8,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07588,GSE90727,GPL21810,1000,Sepsis,C0243026,Whole blood,GEO,Microarray,Mus musculus,8|8,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07589,GSE90836,GPL6246,2,Kabuki Syndrome,C3275495,Hippocampus,GEO,Microarray,Mus musculus,4|3,"DO:A syndrome characterized by multiple congenital anomalies and mental retardation. Other characteristics include a peculiar facial gestalt, short stature, skeletal and visceral abnormalities, cardiac anomalies, and immunological defects." DSA07590,GSE90836,GPL6246,0,Kabuki Syndrome,C3275495,Hippocampus,GEO,Microarray,Mus musculus,3|3,"DO:A syndrome characterized by multiple congenital anomalies and mental retardation. Other characteristics include a peculiar facial gestalt, short stature, skeletal and visceral abnormalities, cardiac anomalies, and immunological defects." DSA07591,GSE90880,GPL8300,0,Vitiligo,C0042900,Whole blood,GEO,Microarray,Homo sapiens,6|8,DO:An autoimmune disease that causes depigmentation of patches of skin resulting from loss of function or death of melanoctyes. DSA07592,GSE90889,GPL18573,1000,Age Related Macular Degeneration,C0242383,Retinal pigment epithelium,GEO,RNA-Seq,Homo sapiens,1|4,DO:A degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision. DSA07593,GSE90889,GPL18573,1000,Age Related Macular Degeneration,C0242383,Retinal pigment epithelium,GEO,RNA-Seq,Homo sapiens,1|4,DO:A degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision. DSA07594,GSE90977,GPL13112,1000,Sporadic Creutzfeldt-Jakob Disease,C1852467,Brain,GEO,RNA-Seq,Mus musculus,4|4,"MONDO:Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease characterized by typical CJD features (rapidly progressive dementia, personality/behavioral changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia." DSA07595,GSE90977,GPL13112,790,Sporadic Creutzfeldt-Jakob Disease,C1852467,Brain,GEO,RNA-Seq,Mus musculus,4|4,"MONDO:Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease characterized by typical CJD features (rapidly progressive dementia, personality/behavioral changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia." DSA07596,GSE91077,GPL13497,12,Pre-Eclampsia,C0032914,Endometrium,GEO,Microarray,Homo sapiens,5|5,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA07597,GSE91077,GPL13497,0,Pre-Eclampsia,C0032914,Endometrium,GEO,Microarray,Homo sapiens,7|3,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA07598,GSE206677,GPL24676,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,2|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07599,GSE91393,GPL6246,1000,Glioblastoma,C0017636,,GEO,Microarray,Mus musculus,3|9,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA07600,GSE208535,GPL24676,1000,Hepatitis B,C0019163,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus, which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice." DSA07601,GSE92293,GPL11154,137,Juvenile Idiopathic Arthritis,C3890205,,GEO,RNA-Seq,Homo sapiens,2|3,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA07602,GSE92340,GPL20301,1000,Frontotemporal Dementia,C0338451,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA07603,GSE92387,GPL11154,1000,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,12|12,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA07604,GSE92415,GPL13158,1000,Ulcerative Colitis,C0009324,Colon mucosa,GEO,Microarray,Homo sapiens,21|162,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA07605,GSE92447,GPL20301,1000,Hypoplastic Left Heart Syndrome,C0152101,,GEO,RNA-Seq,Homo sapiens,1|2,DO:A congenital heart disease characterized by abnormal development of the left-sided structures of the heart. DSA07606,GSE92472,GPL21290,1000,Ulcerative Colitis,C0009324,Whole blood,GEO,RNA-Seq,Homo sapiens,1|1,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA07607,GSE92472,GPL21290,1000,Crohn's Disease,C0010346,Whole blood,GEO,RNA-Seq,Homo sapiens,1|1,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA07608,GSE92472,GPL21290,1000,Irritable Bowel Syndrome,C0022104,Whole blood,GEO,RNA-Seq,Homo sapiens,1|1,"DO:An intestinal disease that is characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause." DSA07609,GSE92472,GPL21290,1000,Coeliac Disease,C0007570,Whole blood,GEO,RNA-Seq,Homo sapiens,1|1,"DO:An autoimmune disease of gastrointestinal tract that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite." DSA07610,GSE92472,GPL21290,1000,Fibromyalgia Syndrome,C0016053,Whole blood,GEO,RNA-Seq,Homo sapiens,1|1,"DO:A syndrome that is is characterized by chronic widespread musculoskeletal pain, fatigue, sleep disturbances, cognitive dysfunction and depression." DSA07611,GSE92472,GPL21290,1000,Clinically Isolated Syndrome,C2921627,Whole blood,GEO,RNA-Seq,Homo sapiens,1|1, DSA07612,GSE92472,GPL21290,1000,Multiple Sclerosis,C0026769,Whole blood,GEO,RNA-Seq,Homo sapiens,1|1,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA07613,GSE92472,GPL21290,1000,Multiple Sclerosis,C0026769,Whole blood,GEO,RNA-Seq,Homo sapiens,1|1,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA07614,GSE92472,GPL21290,1000,Rheumatoid Arthritis,C0003873,Whole blood,GEO,RNA-Seq,Homo sapiens,1|1,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA07615,GSE92472,GPL21290,1000,Systemic Lupus Erythematosus,C0024141,Whole blood,GEO,RNA-Seq,Homo sapiens,1|1,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA07616,GSE92472,GPL21290,1000,Psoriasis,C0033860,Whole blood,GEO,RNA-Seq,Homo sapiens,1|1,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA07617,GSE92472,GPL21290,1000,Psoriatic Arthritis,C0003872,Whole blood,GEO,RNA-Seq,Homo sapiens,1|1,DO:An arthritis that is characterized by joint inflammation that usually occurs in combination with psoriasis. DSA07618,GSE92472,GPL21290,1000,Sjogren's Syndrome,C1527336,Whole blood,GEO,RNA-Seq,Homo sapiens,1|1,DO:An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. DSA07619,GSE92592,GPL11154,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,RNA-Seq,Homo sapiens,19|20,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA07620,GSE92624,GPL16699,0,Chronic Myeloid Leukemia,C0023473,,GEO,Microarray,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA07621,GSE92624,GPL16699,0,Chronic Myeloid Leukemia,C0023473,,GEO,Microarray,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA07622,GSE92624,GPL16699,1000,Chronic Myeloid Leukemia,C0023473,,GEO,Microarray,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA07623,GSE92624,GPL16699,1000,Chronic Myeloid Leukemia,C0023473,,GEO,Microarray,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA07624,GSE92724,GPL20301,821,Type 2 Diabetes,C0011860,,GEO,RNA-Seq,Homo sapiens,6|4,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA07625,GSE92778,GPL6244,7,Acute Myeloid Leukemia (Aml-M2),C1879321,Bone marrow,GEO,Microarray,Homo sapiens,6|6,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA07626,GSE92874,GPL16791,1000,Schizophrenia,C0036341,,GEO,RNA-Seq,Homo sapiens,4|4,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA07627,GSE92926,GPL16570,111,Alzheimer's Disease,C0002395,Cortex,GEO,Microarray,Mus musculus,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA07628,GSE92935,GPL17077,2,Keratoconus,C0022578,Corneal epithelium,GEO,Microarray,Homo sapiens,1|5,"DO:A corneal disease characterized by structural changes within the cornea causing it to thin and change, leading to a protruding conical shape." DSA07629,GSE9297,GPL1261,85,Colitis,C0009319,Colon,GEO,Microarray,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA07630,GSE9297,GPL1261,1000,Colitis,C0009319,Colon,GEO,Microarray,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA07631,GSE9297,GPL1261,40,Colitis,C0009319,Colon,GEO,Microarray,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA07632,GSE93138,GPL6244,1000,Acutely Injured,,Whole venous blood,GEO,Microarray,Homo sapiens,4|8, DSA07633,GSE143253,GPL6885,1000,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Mus musculus,2|5,DO:A respiratory system cancer that is located_in the lung. DSA07634,GSE143253,GPL6885,1000,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Mus musculus,2|5,DO:A respiratory system cancer that is located_in the lung. DSA07635,GSE143253,GPL6885,1000,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Mus musculus,2|4,DO:A respiratory system cancer that is located_in the lung. DSA07636,GSE143253,GPL6887,0,Kidney Tumor,C0022665,Kidney,GEO,Microarray,Mus musculus,3|3,DO:A urinary system cancer that is located_in the kidney. DSA07637,GSE143253,GPL6887,5,Kidney Tumor,C0022665,Kidney,GEO,Microarray,Mus musculus,3|3,DO:A urinary system cancer that is located_in the kidney. DSA07638,GSE143253,GPL6887,128,Kidney Clear Cell Carcinoma,C0279702,Kidney,GEO,Microarray,Mus musculus,3|3,DO:A hereditary renal cell carcinoma that has_material_basis_in a loss of 3p13-pter sequences. DSA07639,GSE143253,GPL6887,622,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Mus musculus,4|6,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07640,GSE143351,GPL19057,1000,Obesity,C0028754,Colon,GEO,scRNA-Seq,Mus musculus,2|2,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07641,GSE143560,GPL17021,1000,Epilepsy,C0014544,Hippocampus,GEO,snRNA-Seq,Mus musculus,1|1,"DO:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions." DSA07642,GSE143912,GPL19057,482,Cleft Secondary Palate,C4317218,Anterior palate mesenchyme,GEO,RNA-Seq,Mus musculus,3|3, DSA07643,GSE143979,GPL21290,1000,Hepatocellular Carcinoma,C0334287,Adductor muscle,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07644,GSE143979,GPL21290,19,Diabetic Peripheral Angiopathy,C0011871,Gastrocnemius muscle,GEO,RNA-Seq,Homo sapiens,4|5,MONDO:Diabetic angiopathy is a form of angiopathy associated with diabetic complications. DSA07645,GSE209567,GPL570,0,Behcet's Disease,C0004943,Peripheral blood,GEO,Microarray,Homo sapiens,15|8,"DO:A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis." DSA07646,GSE144335,GPL17021,468,Obesity,C0028754,Bone marrow,GEO,RNA-Seq,Mus musculus,4|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07647,GSE144622,GPL19057,43,Acute Kidney Injury,C2609414,Kidney,GEO,RNA-Seq,Mus musculus,2|3,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA07648,GSE144622,GPL19057,1000,Acute Kidney Injury,C2609414,Kidney,GEO,RNA-Seq,Mus musculus,3|3,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA07649,GSE144622,GPL19057,558,Acute Kidney Injury,C2609414,Kidney,GEO,RNA-Seq,Mus musculus,3|3,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA07650,GSE144622,GPL19057,1000,Acute Kidney Injury,C2609414,Kidney,GEO,RNA-Seq,Mus musculus,4|3,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA07651,GSE144853,GPL21103,1000,Cleft Lip With Or Without Cleft Palate,C0008924,,GEO,RNA-Seq,Mus musculus,4|4,DO:An orofacial cleft that is characterized by a congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences. DSA07652,GSE144853,GPL21103,1000,Cleft Lip With Or Without Cleft Palate,C0008924,Mesenchyme,GEO,RNA-Seq,Mus musculus,4|4,DO:An orofacial cleft that is characterized by a congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences. DSA07653,GSE146401,GPL19057,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,RNA-Seq,Mus musculus,3|2,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07654,GSE146483,GPL17077,1000,Oral Squamous Cell Carcinoma,C0585362,,GEO,Microarray,Homo sapiens,3|8,"EFO:A squamous cell carcinoma arising from the oral cavity. It affects predominantly adults in their fifth and sixth decades of life and is associated with alcohol and tobacco use. Human papillomavirus is present in approximately half of the cases. It is characterized by a tendency to metastasize early to the lymph nodes. When the tumor is small, patients are often asymptomatic. Physical examination may reveal erythematous or white lesions or plaques. The majority of patients present with signs and symptoms of locally advanced disease including mucosal ulceration, pain, difficulty with speaking, chewing, and swallowing, bleeding, weight loss, and neck swelling. Patients may also present with swollen neck lymph nodes without any symptoms from the oropharyngeal tumor. The most significant prognostic factors are the size of the tumor and the lymph nodes status." DSA07655,GSE146560,GPL6480,0,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,4|4,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA07656,GSE146560,GPL6480,1000,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,4|4,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA07657,GSE146627,GPL21273,63,Liver Steatosis,C2711227,Liver,GEO,RNA-Seq,Mus musculus,3|3,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA07658,GSE146629,GPL17021,1000,Peripheral Neuropathy,C0031117,Sciatic nerve,GEO,RNA-Seq,Mus musculus,3|3,DO:A nervous system disease that affects the peripheral nervous system. DSA07659,GSE146884,GPL17303,125,Acute Wounding,,,GEO,RNA-Seq,Homo sapiens,3|3, DSA07660,GSE146884,GPL17303,49,Acute Wounding,,,GEO,RNA-Seq,Homo sapiens,3|3, DSA07661,GSE146884,GPL17303,1000,Chronic Wounding,,,GEO,RNA-Seq,Homo sapiens,3|3, DSA07662,GSE146884,GPL17303,261,Chronic Wounding,,,GEO,RNA-Seq,Homo sapiens,3|3, DSA07663,GSE146890,GPL18573,79,Meningitis,C0025289,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A central nervous system disease that is characterized by an inflammation of the pia-arachnoid meninges. It can be caused by growth of bacteria, fungi, or parasites within the subarachnoid space or by the growth of bacteria or viruses within the meningeal or ependymal cells." DSA07664,GSE146890,GPL18573,43,Meningitis,C0025289,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A central nervous system disease that is characterized by an inflammation of the pia-arachnoid meninges. It can be caused by growth of bacteria, fungi, or parasites within the subarachnoid space or by the growth of bacteria or viruses within the meningeal or ependymal cells." DSA07665,GSE146890,GPL18573,218,Meningitis,C0025289,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A central nervous system disease that is characterized by an inflammation of the pia-arachnoid meninges. It can be caused by growth of bacteria, fungi, or parasites within the subarachnoid space or by the growth of bacteria or viruses within the meningeal or ependymal cells." DSA07666,GSE147044,GPL21103,1000,Colon Tumor,C0009375,Liver,GEO,RNA-Seq,Mus musculus,5|9,DO:A colorectal cancer that is located_in the colon. DSA07667,GSE147044,GPL21103,1000,Colon Tumor,C0009375,Liver,GEO,RNA-Seq,Mus musculus,5|9,DO:A colorectal cancer that is located_in the colon. DSA07668,GSE147078,GPL10787,7,Aortic Dissection,C0340643,Aorta,GEO,Microarray,Mus musculus,3|3,HPO:Aortic dissection refers to a tear in the intimal layer of the aorta causing a separation between the intima and the medial layers of the aorta. DSA07669,GSE209567,GPL570,0,Behcet's Disease,C0004943,Peripheral blood,GEO,Microarray,Homo sapiens,15|5,"DO:A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis." DSA07670,GSE209567,GPL570,1000,Behcet's Disease,C0004943,Peripheral blood,GEO,Microarray,Homo sapiens,15|9,"DO:A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis." DSA07671,GSE147265,GPL24247,1000,Acute Erythroid Leukemia,C4520840,Spleen,GEO,RNA-Seq,Mus musculus,6|8,NCI:Acute erythroid leukemia characterised by the presence of at least 50% erythroid precursors and at least 20% myeloblasts in the bone marrow. DSA07672,GSE147265,GPL24247,1000,Acute Erythroid Leukemia,C4520840,Spleen,GEO,RNA-Seq,Mus musculus,6|2,NCI:Acute erythroid leukemia characterised by the presence of at least 50% erythroid precursors and at least 20% myeloblasts in the bone marrow. DSA07673,GSE147265,GPL24247,1000,Acute Erythroid Leukemia,C4520840,Spleen,GEO,RNA-Seq,Mus musculus,6|3,NCI:Acute erythroid leukemia characterised by the presence of at least 50% erythroid precursors and at least 20% myeloblasts in the bone marrow. DSA07674,GSE147265,GPL24247,1000,Acute Erythroid Leukemia,C4520840,Spleen,GEO,RNA-Seq,Mus musculus,6|12,NCI:Acute erythroid leukemia characterised by the presence of at least 50% erythroid precursors and at least 20% myeloblasts in the bone marrow. DSA07675,GSE147265,GPL24247,1000,Acute Erythroid Leukemia,C4520840,Spleen,GEO,RNA-Seq,Mus musculus,6|2,NCI:Acute erythroid leukemia characterised by the presence of at least 50% erythroid precursors and at least 20% myeloblasts in the bone marrow. DSA07676,GSE147265,GPL24247,1000,Acute Erythroid Leukemia,C4520840,Spleen,GEO,RNA-Seq,Mus musculus,6|2,NCI:Acute erythroid leukemia characterised by the presence of at least 50% erythroid precursors and at least 20% myeloblasts in the bone marrow. DSA07677,GSE147265,GPL24247,1000,Acute Erythroid Leukemia,C4520840,Spleen,GEO,RNA-Seq,Mus musculus,6|2,NCI:Acute erythroid leukemia characterised by the presence of at least 50% erythroid precursors and at least 20% myeloblasts in the bone marrow. DSA07678,GSE147265,GPL24247,1000,Acute Erythroid Leukemia,C4520840,Spleen,GEO,RNA-Seq,Mus musculus,6|2,NCI:Acute erythroid leukemia characterised by the presence of at least 50% erythroid precursors and at least 20% myeloblasts in the bone marrow. DSA07679,GSE147265,GPL24247,1000,Acute Erythroid Leukemia,C4520840,Spleen,GEO,RNA-Seq,Mus musculus,6|3,NCI:Acute erythroid leukemia characterised by the presence of at least 50% erythroid precursors and at least 20% myeloblasts in the bone marrow. DSA07680,GSE147265,GPL24247,1000,Acute Erythroid Leukemia,C4520840,Spleen,GEO,RNA-Seq,Mus musculus,6|3,NCI:Acute erythroid leukemia characterised by the presence of at least 50% erythroid precursors and at least 20% myeloblasts in the bone marrow. DSA07681,GSE147265,GPL24247,1000,Acute Erythroid Leukemia,C4520840,Spleen,GEO,RNA-Seq,Mus musculus,6|3,NCI:Acute erythroid leukemia characterised by the presence of at least 50% erythroid precursors and at least 20% myeloblasts in the bone marrow. DSA07682,GSE147265,GPL24247,1000,Acute Erythroid Leukemia,C4520840,Spleen,GEO,RNA-Seq,Mus musculus,6|2,NCI:Acute erythroid leukemia characterised by the presence of at least 50% erythroid precursors and at least 20% myeloblasts in the bone marrow. DSA07683,GSE147265,GPL24247,758,Acute Erythroid Leukemia,C4520840,Spleen,GEO,RNA-Seq,Mus musculus,6|3,NCI:Acute erythroid leukemia characterised by the presence of at least 50% erythroid precursors and at least 20% myeloblasts in the bone marrow. DSA07684,GSE147265,GPL24247,1000,Acute Erythroid Leukemia,C4520840,Spleen,GEO,RNA-Seq,Mus musculus,6|3,NCI:Acute erythroid leukemia characterised by the presence of at least 50% erythroid precursors and at least 20% myeloblasts in the bone marrow. DSA07685,GSE147365,GPL24247,1000,Myocardial Infarction,C0027051,Heart,GEO,RNA-Seq,Mus musculus,6|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07686,GSE147581,GPL21103,1000,Liver Cirrhosis,C0023890,Liver,GEO,scRNA-Seq,Mus musculus,1|1,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA07687,GSE147786,GPL23126,1000,Pituitary Tumor,C0032019,Pituitary gland,GEO,Microarray,Homo sapiens,8|20,DO:An endocrine gland cancer located_in the pituitary gland located at the base of the brain. DSA07688,GSE147786,GPL23126,1000,Pituitary Tumor,C0032019,Pituitary gland,GEO,Microarray,Homo sapiens,8|16,DO:An endocrine gland cancer located_in the pituitary gland located at the base of the brain. DSA07689,GSE147786,GPL23126,1000,Pituitary Tumor,C0032019,Pituitary gland,GEO,Microarray,Homo sapiens,8|6,DO:An endocrine gland cancer located_in the pituitary gland located at the base of the brain. DSA07690,GSE147950,GPL21273,1000,Rosacea,C0035854,Skin,GEO,RNA-Seq,Mus musculus,3|2,"HPO:Redness of the skin of the face, caused by hyperemia of the capillaries in the lower layers of the skin." DSA07691,GSE147950,GPL21273,1000,Rosacea,C0035854,Skin,GEO,RNA-Seq,Mus musculus,3|3,"HPO:Redness of the skin of the face, caused by hyperemia of the capillaries in the lower layers of the skin." DSA07692,GSE148139,GPL21103,632,Pancreatic Ductal Adenocarcinoma,C1335302,Liver,GEO,RNA-Seq,Mus musculus,3|6,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA07693,GSE148505,GPL24247,1000,Colitis,C0009319,Colon,GEO,RNA-Seq,Mus musculus,4|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA07694,GSE148505,GPL24247,1000,Colitis,C0009319,Colon,GEO,RNA-Seq,Mus musculus,3|4,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA07695,GSE210610,GPL30173,1000,Facioscapulohumeral Muscular Dystrophy,C0238288,Skeletal muscle,GEO,RNA-Seq,Homo sapiens,1|1,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA07696,GSE213709,GPL21103,1000,Pulmonary Fibrosis,C0034069,Lung,GEO,RNA-Seq,Mus musculus,1|4,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA07697,GSE213709,GPL21103,1000,Pulmonary Fibrosis,C0034069,Lung,GEO,RNA-Seq,Mus musculus,2|5,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA07698,GSE213709,GPL21103,1000,Pulmonary Fibrosis,C0034069,Lung,GEO,RNA-Seq,Mus musculus,1|4,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA07699,GSE213709,GPL21103,1000,Pulmonary Fibrosis,C0034069,Lung,GEO,RNA-Seq,Mus musculus,1|5,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA07700,GSE217814,GPL21103,1000,Pulmonary Fibrosis,C0034069,Lung,GEO,RNA-Seq,Mus musculus,3|4,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA07701,GSE220533,GPL24247,38,Obesity,C0028754,Hypothalamus,GEO,RNA-Seq,Mus musculus,6|7,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07702,GSE149019,GPL21103,860,Rathke Cleft Cysts,C0752244,Pituitary gland,GEO,RNA-Seq,Mus musculus,6|6,"MSH:Congenital or acquired cysts of the brain, spinal cord, or meninges which may remain stable in size or undergo progressive enlargement." DSA07703,GSE149508,GPL21103,1000,Fibrosis; Liver,C0239946,,GEO,RNA-Seq,Mus musculus,3|3,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA07704,GSE149612,GPL20301,1000,Esophageal Squamous Cell Carcinoma,C0279626,Esophagus,GEO,RNA-Seq,Homo sapiens,10|10,DO:An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus. DSA07705,GSE149669,GPL11180,864,Spinal Cord Disorder,C0037928,Spinal cord,GEO,Microarray,Mus musculus,6|6,EFO:A disease involving the spinal cord. DSA07706,GSE220533,GPL24247,22,Obesity,C0028754,Hypothalamus,GEO,RNA-Seq,Mus musculus,8|8,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07707,GSE150640,GPL19057,1000,Ovarian Serous Carcinoma,C1335177,Fallopian tube,GEO,RNA-Seq,Mus musculus,3|3,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA07708,GSE150640,GPL19057,1000,Ovarian Serous Carcinoma,C1335177,Fallopian tube,GEO,RNA-Seq,Mus musculus,3|3,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA07709,GSE150640,GPL19057,1000,Ovarian Serous Carcinoma,C1335177,Fallopian tube,GEO,RNA-Seq,Mus musculus,3|3,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA07710,GSE150640,GPL19057,1000,Ovarian Serous Carcinoma,C1335177,Fallopian tube,GEO,RNA-Seq,Mus musculus,3|3,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA07711,GSE150640,GPL19057,1000,Ovarian Serous Carcinoma,C1335177,Fallopian tube,GEO,RNA-Seq,Mus musculus,3|3,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA07712,GSE150640,GPL19057,1000,Ovarian Serous Carcinoma,C1335177,Fallopian tube,GEO,RNA-Seq,Mus musculus,3|3,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA07713,GSE150640,GPL19057,1000,Ovarian Serous Carcinoma,C1335177,Fallopian tube,GEO,RNA-Seq,Mus musculus,3|3,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA07714,GSE150640,GPL19057,1000,Ovarian Serous Carcinoma,C1335177,Fallopian tube,GEO,RNA-Seq,Mus musculus,3|3,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA07715,GSE150640,GPL19057,113,Metastatic Ovarian Serous Carcinoma,C1335177,Fallopian tube,GEO,RNA-Seq,Mus musculus,3|3,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA07716,GSE150640,GPL19057,0,Metastatic Ovarian Serous Carcinoma,C1335177,Fallopian tube,GEO,RNA-Seq,Mus musculus,3|3,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA07717,GSE222576,GPL22598,468,Fibrosis; Liver,C0239946,Liver,GEO,Microarray,Mus musculus,3|3,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA07718,GSE222576,GPL22598,158,Fibrosis; Liver,C0239946,Liver,GEO,Microarray,Mus musculus,3|3,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA07719,GSE222576,GPL22598,1000,Fibrosis; Liver,C0239946,Liver,GEO,Microarray,Mus musculus,3|3,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA07720,GSE151188,GPL20795,209,Genital Prolapse,C0156349,Vaginal wall,GEO,RNA-Seq,Homo sapiens,2|13, DSA07721,GSE222576,GPL22598,321,Fibrosis; Liver,C0239946,Liver,GEO,Microarray,Mus musculus,3|3,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA07722,GSE151550,GPL11154,1000,Breast Cancer,C0678222,,GEO,RNA-Seq,Homo sapiens,2|2,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07723,GSE151550,GPL11154,1000,Breast Cancer,C0678222,,GEO,RNA-Seq,Homo sapiens,2|2,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07724,GSE151550,GPL11154,1000,Breast Cancer,C0678222,,GEO,RNA-Seq,Homo sapiens,2|2,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07725,GSE151550,GPL11154,1000,Breast Cancer,C0678222,,GEO,RNA-Seq,Homo sapiens,2|2,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07726,GSE151580,GPL20795,1000,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,RNA-Seq,Homo sapiens,6|13,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA07727,GSE151580,GPL20795,1000,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,RNA-Seq,Homo sapiens,6|14,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA07728,GSE151580,GPL20795,1000,Metastatic Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,RNA-Seq,Homo sapiens,13|14,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA07729,GSE151728,GPL13112,344,Inflammation,C0021368,Placenta,GEO,RNA-Seq,Mus musculus,4|4,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA07730,GSE151728,GPL13112,539,Inflammation,C0021368,Placenta,GEO,RNA-Seq,Mus musculus,4|4,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA07731,GSE151888,GPL28635,219,Bladder Cancer,C0699885,,GEO,Microarray,Mus musculus,3|3,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07732,GSE151888,GPL28635,0,Bladder Cancer,C0699885,,GEO,Microarray,Mus musculus,3|3,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07733,GSE151888,GPL28635,146,Bladder Cancer,C0699885,,GEO,Microarray,Mus musculus,3|3,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07734,GSE151888,GPL28635,1000,Bladder Cancer,C0699885,,GEO,Microarray,Mus musculus,3|3,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA07735,GSE152494,GPL1261,1000,Cholestasis,C0008370,Liver,GEO,Microarray,Mus musculus,6|6,DO:A bile duct disease that is characterized by where bile cannot flow from the liver to the duodenum. DSA07736,GSE222576,GPL22598,745,Fibrosis; Liver,C0239946,Liver,GEO,Microarray,Mus musculus,3|3,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA07737,GSE223137,GPL24247,1000,Multiple Sclerosis,C0026769,,GEO,RNA-Seq,Mus musculus,2|3,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA07738,GSE152972,GPL21493,1000,Ischemia Reperfusion Injury,C0035126,Kidney,GEO,RNA-Seq,Mus musculus,3|3,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA07739,GSE153077,GPL19057,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,RNA-Seq,Mus musculus,5|4,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07740,GSE153097,GPL16173,1000,Aneurysm,C0002940,Aorta,GEO,RNA-Seq,Mus musculus,4|4,"DO:A cardiovascular system disease that primarily affects the blood vessels which includes the arteries, veins and capillaries that carry blood to and from the heart." DSA07741,GSE153097,GPL16173,535,Aneurysm,C0002940,Aorta,GEO,RNA-Seq,Mus musculus,4|4,"DO:A cardiovascular system disease that primarily affects the blood vessels which includes the arteries, veins and capillaries that carry blood to and from the heart." DSA07742,GSE153485,GPL24247,1000,Myocardial Infarction,C0027051,Heart,GEO,RNA-Seq,Mus musculus,5|5,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07743,GSE153485,GPL24247,937,Myocardial Infarction,C0027051,Heart,GEO,RNA-Seq,Mus musculus,5|5,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07744,GSE153485,GPL24247,201,Myocardial Infarction,C0027051,Liver,GEO,RNA-Seq,Mus musculus,5|5,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07745,GSE153485,GPL24247,1,Myocardial Infarction,C0027051,Liver,GEO,RNA-Seq,Mus musculus,5|5,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07746,GSE153485,GPL24247,722,Myocardial Infarction,C0027051,Muscle,GEO,RNA-Seq,Mus musculus,4|4,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07747,GSE153485,GPL24247,2,Myocardial Infarction,C0027051,Muscle,GEO,RNA-Seq,Mus musculus,4|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07748,GSE153485,GPL24247,5,Myocardial Infarction,C0027051,White adipose tissue,GEO,RNA-Seq,Mus musculus,4|4,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07749,GSE153485,GPL24247,185,Myocardial Infarction,C0027051,White adipose tissue,GEO,RNA-Seq,Mus musculus,4|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07750,GSE153988,GPL21103,296,Heart Failure,C0018801,Heart,GEO,RNA-Seq,Mus musculus,2|3,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA07751,GSE153988,GPL21103,651,Heart Failure,C0018801,Heart,GEO,RNA-Seq,Mus musculus,2|2,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA07752,GSE154194,GPL26644,98,Non-Alcoholic Fatty Liver Disease,C0400966,,GEO,Microarray,Mus musculus,3|3,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA07753,GSE154194,GPL26644,5,Non-Alcoholic Fatty Liver Disease,C0400966,,GEO,Microarray,Mus musculus,3|3,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA07754,GSE154219,GPL21103,1000,Cachexia,C0006625,Liver,GEO,RNA-Seq,Mus musculus,7|3,"HPO:Severe weight loss, wasting of muscle, loss of appetite, and general debility related to a chronic disease." DSA07755,GSE154247,GPL19057,1000,Fracture,,Bone,GEO,RNA-Seq,Mus musculus,4|4, DSA07756,GSE154418,GPL28038,143,Down Syndrome,C0013080,,GEO,RNA-Seq,Homo sapiens,6|11,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA07757,GSE154504,GPL21103,447,Dilated Cardiomyopathy,C0007193,Left ventricle,GEO,RNA-Seq,Mus musculus,3|3,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA07758,GSE154733,GPL11202,0,Myocardial Infarction,C0027051,Spleen,GEO,Microarray,Mus musculus,1|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07759,GSE154733,GPL11202,0,Myocardial Infarction,C0027051,Bone marrow,GEO,Microarray,Mus musculus,1|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07760,GSE154892,GPL24242,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Mus musculus,8|8,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA07761,GSE154934,GPL26963,0,Brain Damage,C0006109,Cerebellum,GEO,Microarray,Homo sapiens,4|4,MONDO:Chronic form of encephalitis. DSA07762,GSE154939,GPL24247,917,Ischemia Reperfusion Injury,C0035126,Lung,GEO,RNA-Seq,Mus musculus,3|3,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA07763,GSE154959,GPL24247,1000,Pulmonary Arterial Hypertension,C2973725,Lung,GEO,scRNA-Seq,Mus musculus,3|3,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA07764,GSE155012,GPL17021,11,Ischemia,C0022116,Hindlimb muscle,GEO,RNA-Seq,Mus musculus,2|3,DO:A vascular disease that is characterized by a restriction in blood supply to tissues. DSA07765,GSE155071,GPL24247,1000,Asthma,C0004096,Lung,GEO,RNA-Seq,Mus musculus,3|1,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA07766,GSE155516,GPL24247,1000,Systemic Inflammatory Response Syndrome,C0242966,Cerebral vessel,GEO,RNA-Seq,Mus musculus,3|1,"MSH:A systemic inflammatory response to a variety of clinical insults, characterized by two or more of the following conditions: (1) fever >38 degrees C or HYPOTHERMIA <36 degrees C; (2) TACHYCARDIA >90 beat/minute; (3) tachypnea >24 breaths/minute; (4) LEUKOCYTOSIS >12,000 cells/cubic mm or 10% immature forms. While usually related to infection, SIRS can also be associated with noninfectious insults such as TRAUMA; BURNS; or PANCREATITIS. If infection is involved, a patient with SIRS is said to have SEPSIS." DSA07767,GSE155516,GPL24247,1000,Systemic Inflammatory Response Syndrome,C0242966,Cerebral vessel,GEO,RNA-Seq,Mus musculus,3|3,"MSH:A systemic inflammatory response to a variety of clinical insults, characterized by two or more of the following conditions: (1) fever >38 degrees C or HYPOTHERMIA <36 degrees C; (2) TACHYCARDIA >90 beat/minute; (3) tachypnea >24 breaths/minute; (4) LEUKOCYTOSIS >12,000 cells/cubic mm or 10% immature forms. While usually related to infection, SIRS can also be associated with noninfectious insults such as TRAUMA; BURNS; or PANCREATITIS. If infection is involved, a patient with SIRS is said to have SEPSIS." DSA07768,GSE155516,GPL24247,1000,Systemic Inflammatory Response Syndrome,C0242966,Cerebral vessel,GEO,RNA-Seq,Mus musculus,3|3,"MSH:A systemic inflammatory response to a variety of clinical insults, characterized by two or more of the following conditions: (1) fever >38 degrees C or HYPOTHERMIA <36 degrees C; (2) TACHYCARDIA >90 beat/minute; (3) tachypnea >24 breaths/minute; (4) LEUKOCYTOSIS >12,000 cells/cubic mm or 10% immature forms. While usually related to infection, SIRS can also be associated with noninfectious insults such as TRAUMA; BURNS; or PANCREATITIS. If infection is involved, a patient with SIRS is said to have SEPSIS." DSA07769,GSE223137,GPL24247,1000,Multiple Sclerosis,C0026769,,GEO,RNA-Seq,Mus musculus,2|3,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA07770,GSE223740,GPL24247,162,Epilepsy,C0014544,Hippocampus,GEO,RNA-Seq,Mus musculus,5|5,"DO:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions." DSA07771,GSE223740,GPL24247,72,Epilepsy,C0014544,Hippocampus,GEO,RNA-Seq,Mus musculus,5|10,"DO:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions." DSA07772,GSE223740,GPL24247,81,Epilepsy,C0014544,Hippocampus,GEO,RNA-Seq,Mus musculus,5|4,"DO:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions." DSA07773,GSE223740,GPL24247,31,Epilepsy,C0014544,Hippocampus,GEO,RNA-Seq,Mus musculus,5|8,"DO:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions." DSA07774,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07775,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07776,GSE156174,GPL19057,1000,Disuse Osteoporosis,C0152256,Bone marrow,GEO,RNA-Seq,Mus musculus,1|1, DSA07777,GSE156174,GPL19057,1000,Disuse Osteoporosis,C0152256,Bone marrow,GEO,RNA-Seq,Mus musculus,1|1, DSA07778,GSE156174,GPL19057,1000,Disuse Osteoporosis,C0152256,Bone marrow,GEO,RNA-Seq,Mus musculus,1|1, DSA07779,GSE156174,GPL19057,1000,Disuse Osteoporosis,C0152256,Bone marrow,GEO,RNA-Seq,Mus musculus,1|1, DSA07780,GSE156197,GPL1261,334,Inflammation,C0021368,Skin,GEO,Microarray,Mus musculus,4|4,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA07781,GSE156197,GPL1261,1000,Papilloma,C0030354,Skin,GEO,Microarray,Mus musculus,4|4,DO:A cell type benign neoplam that is composed of epithelial tissue on papillae of vascularized connective tissue. DSA07782,GSE156856,GPL17021,1000,Malnutrition,C0162429,Liver,GEO,RNA-Seq,Mus musculus,4|5,"DO:A nutritional deficiency disease that is characterized by inadequate dietary protein and calories, which can have profound systemic effects including decreased metabolism, altered tissue distribution, compromised immunity, and impaired growth, and has_material_basis_in dietary deprivation." DSA07783,GSE156856,GPL17021,1000,Malnutrition,C0162429,Liver,GEO,RNA-Seq,Mus musculus,5|5,"DO:A nutritional deficiency disease that is characterized by inadequate dietary protein and calories, which can have profound systemic effects including decreased metabolism, altered tissue distribution, compromised immunity, and impaired growth, and has_material_basis_in dietary deprivation." DSA07784,GSE156891,GPL13112,1000,Tuberous Sclerosis,C0041341,Cortex,GEO,RNA-Seq,Mus musculus,3|4,DO:A tuberous sclerosis that is characterized by hamartomas in multiple organ systems and has_material_basis_in heterozygous mutation in the TSC1 gene on chromosome 9q34. DSA07785,GSE156891,GPL13112,458,Tuberous Sclerosis,C0041341,Cortex,GEO,RNA-Seq,Mus musculus,5|5,DO:A tuberous sclerosis that is characterized by hamartomas in multiple organ systems and has_material_basis_in heterozygous mutation in the TSC1 gene on chromosome 9q34. DSA07786,GSE156895,GPL13112,1000,Polycystic Ovary Syndrome,C0032460,Ovary,GEO,RNA-Seq,Mus musculus,2|2,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA07787,GSE157008,GPL21103,40,Exencephaly,C0266453,Forebrain,GEO,RNA-Seq,Mus musculus,6|3,HPO:A malformation of the neural tube with a large amount of protruding brain tissue and absence of calvarium. DSA07788,GSE157008,GPL21103,51,Cranial Defect,C4025787,Forebrain,GEO,RNA-Seq,Mus musculus,6|3,"HPO:A localized defect in the bone of the skull resulting from abnormal embryological development. The defect is covered by normal skin. In some cases, skull x-rays have shown underlying lytic bone lesions which have closed before the age of one year." DSA07789,GSE157008,GPL21103,47,Exencephaly,C0266453,Forebrain,GEO,RNA-Seq,Mus musculus,6|4,HPO:A malformation of the neural tube with a large amount of protruding brain tissue and absence of calvarium. DSA07790,GSE157008,GPL21103,37,Exencephaly,C0266453,Midbrain,GEO,RNA-Seq,Mus musculus,6|3,HPO:A malformation of the neural tube with a large amount of protruding brain tissue and absence of calvarium. DSA07791,GSE157008,GPL21103,40,Cranial Defect,C4025787,Midbrain,GEO,RNA-Seq,Mus musculus,6|3,"HPO:A localized defect in the bone of the skull resulting from abnormal embryological development. The defect is covered by normal skin. In some cases, skull x-rays have shown underlying lytic bone lesions which have closed before the age of one year." DSA07792,GSE157008,GPL21103,34,Exencephaly,C0266453,Midbrain,GEO,RNA-Seq,Mus musculus,6|4,HPO:A malformation of the neural tube with a large amount of protruding brain tissue and absence of calvarium. DSA07793,GSE157035,GPL19057,491,Hypertrophy,C0020564,Heart,GEO,RNA-Seq,Mus musculus,4|4,EFO:Hypertrophy is the increase in the volume of an organ or tissue due to the enlargement of its component cells. DSA07794,GSE157035,GPL19057,645,Heart Failure,C0018801,Heart,GEO,RNA-Seq,Mus musculus,4|4,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA07795,GSE157132,GPL17021,5,Influenza,C0021400,Placenta,GEO,RNA-Seq,Mus musculus,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA07796,GSE157132,GPL17021,0,Influenza,C0021400,Placenta,GEO,RNA-Seq,Mus musculus,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA07797,GSE157132,GPL17021,1000,Influenza,C0021400,Thymus,GEO,RNA-Seq,Mus musculus,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA07798,GSE157460,GPL21493,1000,Stress Fracture,,Ulna,GEO,RNA-Seq,Mus musculus,6|9, DSA07799,GSE157460,GPL21493,1000,Stress Fracture,,Ulna,GEO,RNA-Seq,Mus musculus,6|7, DSA07800,GSE157569,GPL21103,245,Obesity,C0028754,Brown adipose tissue,GEO,RNA-Seq,Mus musculus,4|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07801,GSE157569,GPL21103,82,Obesity,C0028754,Brown adipose tissue,GEO,RNA-Seq,Mus musculus,4|2,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07802,GSE157569,GPL21103,1000,Obesity,C0028754,Brown adipose tissue,GEO,RNA-Seq,Mus musculus,4|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07803,GSE157569,GPL21103,566,Obesity,C0028754,Brown adipose tissue,GEO,RNA-Seq,Mus musculus,4|2,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07804,GSE157569,GPL21103,31,Obesity,C0028754,Brown adipose tissue,GEO,RNA-Seq,Mus musculus,4|2,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07805,GSE157569,GPL21103,132,Obesity,C0028754,Brown adipose tissue,GEO,RNA-Seq,Mus musculus,4|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07806,GSE157569,GPL21103,1000,Obesity,C0028754,Brown adipose tissue,GEO,RNA-Seq,Mus musculus,3|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07807,GSE157569,GPL21103,364,Obesity,C0028754,Brown adipose tissue,GEO,RNA-Seq,Mus musculus,2|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07808,GSE157569,GPL21103,255,Obesity,C0028754,Brown adipose tissue,GEO,RNA-Seq,Mus musculus,2|2,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07809,GSE157569,GPL21103,861,Obesity,C0028754,Brown adipose tissue,GEO,RNA-Seq,Mus musculus,1|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07810,GSE157569,GPL21103,1000,Obesity,C0028754,Brown adipose tissue,GEO,RNA-Seq,Mus musculus,3|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07811,GSE157569,GPL21103,566,Obesity,C0028754,Brown adipose tissue,GEO,RNA-Seq,Mus musculus,2|2,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07812,GSE157569,GPL21103,98,Obesity,C0028754,Brown adipose tissue,GEO,RNA-Seq,Mus musculus,4|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07813,GSE157569,GPL21103,37,Obesity,C0028754,Brown adipose tissue,GEO,RNA-Seq,Mus musculus,2|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07814,GSE157569,GPL21103,1000,Obesity,C0028754,Brown adipose tissue,GEO,RNA-Seq,Mus musculus,3|2,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07815,GSE157569,GPL21103,225,Obesity,C0028754,Brown adipose tissue,GEO,RNA-Seq,Mus musculus,4|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07816,GSE158270,GPL21163,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,10|4,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA07817,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|4,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07818,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|4,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07819,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07820,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|4,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07821,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07822,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07823,GSE158662,GPL22755,10,Gastric Cancer,C0699791,Stomach,GEO,Microarray,Homo sapiens,3|3,DO:A gastrointestinal system cancer that is located_in the stomach. DSA07824,GSE158790,GPL21493,1000,Spinal Muscular Atrophy,C0026847,Skeletal muscle,GEO,RNA-Seq,Mus musculus,5|4,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA07825,GSE158967,GPL19057,1000,Colitis,C0009319,Colon,GEO,RNA-Seq,Mus musculus,2|2,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA07826,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07827,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07828,GSE158994,GPL11180,268,Myocardial Infarction,C0027051,Heart,GEO,Microarray,Mus musculus,4|4,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07829,GSE158994,GPL11180,51,Myocardial Infarction,C0027051,Heart,GEO,Microarray,Mus musculus,3|4,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07830,GSE158994,GPL11180,5,Myocardial Infarction,C0027051,Heart,GEO,Microarray,Mus musculus,3|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07831,GSE158994,GPL11180,0,Myocardial Infarction,C0027051,Heart,GEO,Microarray,Mus musculus,4|4,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07832,GSE158994,GPL11180,1000,Myocardial Infarction,C0027051,Heart,GEO,Microarray,Mus musculus,4|4,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07833,GSE158994,GPL11180,201,Myocardial Infarction,C0027051,Heart,GEO,Microarray,Mus musculus,4|4,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07834,GSE158994,GPL11180,631,Myocardial Infarction,C0027051,Heart,GEO,Microarray,Mus musculus,4|4,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07835,GSE158994,GPL11180,586,Myocardial Infarction,C0027051,Heart,GEO,Microarray,Mus musculus,4|4,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07836,GSE158994,GPL11180,737,Myocardial Infarction,C0027051,Heart,GEO,Microarray,Mus musculus,4|4,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07837,GSE159219,GPL13112,1000,Hepatic Steatosis,C2711227,Liver,GEO,RNA-Seq,Mus musculus,1|1,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA07838,GSE159851,GPL20301,1000,Glioblastoma,C0017636,,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA07839,GSE159851,GPL20301,1000,Adenocarcinoma; Metastatic,C0334277,,GEO,RNA-Seq,Homo sapiens,5|5,NCI:An adenocarcinoma that has spread from its original site of growth to another anatomic site. DSA07840,GSE159851,GPL20301,1000,Adenocarcinoma; Metastatic,C0334277,,GEO,RNA-Seq,Homo sapiens,5|5,NCI:An adenocarcinoma that has spread from its original site of growth to another anatomic site. DSA07841,GSE159895,GPL21103,29,Inflammatory Pain,,Dorsal spinal cord,GEO,RNA-Seq,Mus musculus,3|3, DSA07842,GSE159895,GPL21103,23,Inflammatory Pain,,Dorsal spinal cord,GEO,RNA-Seq,Mus musculus,2|3, DSA07843,GSE159895,GPL21103,5,Inflammatory Pain,,Dorsal spinal cord,GEO,RNA-Seq,Mus musculus,2|3, DSA07844,GSE160078,GPL21103,1000,Autosomal Dominant Centronuclear Myopathy,C1834558,Tibialis anterior,GEO,RNA-Seq,Mus musculus,3|6,DO:A centronuclear myopathy that has_material_basis_in autosomal dominant inheritance. DSA07845,GSE160078,GPL21103,939,Autosomal Dominant Centronuclear Myopathy,C1834558,Tibialis anterior,GEO,RNA-Seq,Mus musculus,3|4,DO:A centronuclear myopathy that has_material_basis_in autosomal dominant inheritance. DSA07846,GSE160081,GPL21103,1000,X-Linked Myotubular Myopathy,C0410203,Tibialis anterior,GEO,RNA-Seq,Mus musculus,3|4,DO:A centronuclear myopathy that has_material_basis_in X-linked inheritance of mutations in MTM1 on Xq28. DSA07847,GSE160151,GPL17021|GPL19057,20,Tauopathy,C0949664,Hippocampus,GEO,RNA-Seq,Mus musculus,2|2,DO:A neurodegenerative disease that has_material_basis_in the pathological aggregation of tau protein in so-called neurofibrillary tangles (NFT) in the human brain. DSA07848,GSE160650,GPL24247,6,Melanoma,C0025202,Blood,GEO,RNA-Seq,Mus musculus,5|5,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA07849,GSE160650,GPL24247,221,Melanoma,C0025202,Blood,GEO,RNA-Seq,Mus musculus,5|5,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA07850,GSE160650,GPL24247,9,Melanoma,C0025202,Blood,GEO,RNA-Seq,Mus musculus,5|5,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA07851,GSE160650,GPL24247,14,Melanoma,C0025202,Blood,GEO,RNA-Seq,Mus musculus,5|5,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA07852,GSE160650,GPL24247,232,Progressive Melanoma,C0025202,Blood,GEO,RNA-Seq,Mus musculus,5|5,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA07853,GSE160650,GPL24247,236,Progressive Melanoma,C0025202,Blood,GEO,RNA-Seq,Mus musculus,5|5,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA07854,GSE160651,GPL29331,34,Brain Damage,C0006109,Cortex,GEO,Microarray,Mus musculus,7|6,MONDO:Chronic form of encephalitis. DSA07855,GSE160651,GPL29331,0,Brain Damage,C0006109,Cortex,GEO,Microarray,Mus musculus,7|7,MONDO:Chronic form of encephalitis. DSA07856,GSE160651,GPL29331,0,Brain Damage,C0006109,Cortex,GEO,Microarray,Mus musculus,7|5,MONDO:Chronic form of encephalitis. DSA07857,GSE160651,GPL29331,15,Brain Damage,C0006109,Cortex,GEO,Microarray,Mus musculus,6|8,MONDO:Chronic form of encephalitis. DSA07858,GSE160651,GPL29331,0,Brain Damage,C0006109,Cortex,GEO,Microarray,Mus musculus,6|9,MONDO:Chronic form of encephalitis. DSA07859,GSE160651,GPL29331,0,Brain Damage,C0006109,Cortex,GEO,Microarray,Mus musculus,6|7,MONDO:Chronic form of encephalitis. DSA07860,GSE160763,GPL13112,1000,Brain Damage,C0006109,Cortex,GEO,scRNA-Seq,Mus musculus,2|2,MONDO:Chronic form of encephalitis. DSA07861,GSE160763,GPL13112,1000,Brain Damage,C0006109,Cortex,GEO,scRNA-Seq,Mus musculus,2|2,MONDO:Chronic form of encephalitis. DSA07862,GSE160880,GPL21273,1000,Injury of Liver,C0160390,Liver,GEO,RNA-Seq,Mus musculus,3|3,NCI:Damage to liver structure or function due to trauma or toxicity. DSA07863,GSE160905,GPL1261,0,Polytrauma,,Peripheral blood,GEO,Microarray,Mus musculus,3|3, DSA07864,GSE160905,GPL1261,77,Hemorrhagic Shock,C0036982,Peripheral blood,GEO,Microarray,Mus musculus,3|3,MSH:Acute hemorrhage or excessive fluid loss resulting in HYPOVOLEMIA. DSA07865,GSE161151,GPL20775,0,Myocardial Ischemia,C0151744,Heart,GEO,Microarray,Mus musculus,3|3,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA07866,GSE161693,GPL24247,1000,Muscle Atrophy,C0026846,Gastrocnemius muscle,GEO,RNA-Seq,Mus musculus,4|4,EFO:The loss of muscle tissue due to inactivity or disease. DSA07867,GSE161693,GPL24247,1000,Muscle Atrophy,C0026846,Gastrocnemius muscle,GEO,RNA-Seq,Mus musculus,4|4,EFO:The loss of muscle tissue due to inactivity or disease. DSA07868,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07869,GSE162185,GPL21103,30,Obesity,C0028754,Heart,GEO,RNA-Seq,Mus musculus,4|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07870,GSE162246,GPL19057,2,Multiple Sclerosis,C0026769,Spleen;lymph node,GEO,RNA-Seq,Mus musculus,3|3,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA07871,GSE162274,GPL21273,203,Psoriasis,C0033860,Epidermis,GEO,RNA-Seq,Mus musculus,2|3,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA07872,GSE162493,GPL21103,1000,Iron-Deficiency Anemia,C0162316,Heart,GEO,RNA-Seq,Mus musculus,10|10,"MONDO:Anemia caused by low iron intake, inefficient iron absorption in the gastrointestinal tract, or chronic blood loss." DSA07873,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07874,GSE162535,GPL24247,1000,Cerebral Malaria,C0024534,Brain,GEO,RNA-Seq,Mus musculus,4|4,"DO:A malaria that involves neurologic damage resulting from blockage of the blood vessels, caused due to the infection of the red blood cells by Plasmodium species." DSA07875,GSE162574,GPL24247,652,Chronic Pain,C0150055,Spinal cord,GEO,RNA-Seq,Mus musculus,2|2,"HPO:Persistent pain, usually defined as pain that has lasted longer than 3 to 6 months." DSA07876,GSE162795,GPL21103,923,Thyroid Proliferative Lesion,,Thyroid,GEO,RNA-Seq,Mus musculus,9|9, DSA07877,GSE162795,GPL21103,404,Thyroid Proliferative Lesion,,Thyroid,GEO,RNA-Seq,Mus musculus,9|9, DSA07878,GSE162876,GPL21103,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,4|4,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA07879,GSE162876,GPL21103,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,4|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA07880,GSE162876,GPL21103,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,4|4,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA07881,GSE162876,GPL21103,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,4|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA07882,GSE162876,GPL21103,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,4|4,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA07883,GSE162876,GPL21103,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,4|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA07884,GSE162876,GPL21103,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,4|4,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA07885,GSE162876,GPL21103,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,4|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA07886,GSE162953,GPL26962,0,Obesity,C0028754,Submandibular gland,GEO,Microarray,Mus musculus,4|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07887,GSE163071,GPL24676,277,Glioblastoma,C0017636,Brain,GEO,RNA-Seq,Homo sapiens,8|4,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA07888,GSE163071,GPL24676,1000,Pilocytic Astrocytoma,C0334583,Brain,GEO,RNA-Seq,Homo sapiens,8|32,DO:A childhood low-grade glioma that is characterized by cells that look like fibers when viewed under a microscope and is located_in the brain. DSA07889,GSE163359,GPL16791,1000,Hemangiosarcoma,C0018923,Breast,GEO,RNA-Seq,Homo sapiens,1|2,DO:A vascular cancer that derives_from the cells that line the walls of blood vessels or lymphatic vessels. DSA07890,GSE163359,GPL16791,1000,Hemangiosarcoma,C0018923,Lung,GEO,RNA-Seq,Homo sapiens,1|2,DO:A vascular cancer that derives_from the cells that line the walls of blood vessels or lymphatic vessels. DSA07891,GSE163444,GPL24247,1000,Alcoholic Hepatitis,C0019187,Liver,GEO,RNA-Seq,Mus musculus,4|4,MONDO:Acute hepatitis resulting from ingestion of alcohol. DSA07892,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07893,GSE163537,GPL17021,1000,Wart,C3665596,Ear,GEO,RNA-Seq,Mus musculus,3|3,"DO:A viral infectious disease that results_in infection located_in skin, has_material_basis_in human papillomavirus (types 2 and 4). This infection is characterized by a raised wart with roughened surface, most common on hands, but can grow anywhere on the body." DSA07894,GSE163762,GPL17021,1000,Obesity,C0028754,Visceral adipose tissue,GEO,scRNA-Seq,Mus musculus,3|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA07895,GSE163956,GPL21103,1000,Myocardial Infarction,C0027051,Heart,GEO,RNA-Seq,Mus musculus,1|4,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA07896,GSE164300,GPL13112,1000,Colorectal Carcinoma,C0009402,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA07897,GSE164636,GPL21493,199,Hepatic Steatosis,C2711227,Liver,GEO,RNA-Seq,Mus musculus,10|10,HPO:Steatosis is a term used to denote lipid accumulation within hepatocytes. DSA07898,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|1,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07899,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07900,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07901,GSE165286,GPL20301,0,Glioblastoma,C0017636,Brain,GEO,RNA-Seq,Homo sapiens,4|9,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA07902,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07903,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07904,GSE165493,GPL18480,475,Major Depressive Disorder,C1269683,Prefrontal cortex,GEO,RNA-Seq,Mus musculus,2|5,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA07905,GSE165493,GPL18480,7,Major Depressive Disorder,C1269683,Hippocampus,GEO,RNA-Seq,Mus musculus,2|6,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA07906,GSE166403,GPL24247,1000,Heart Failure,C0018801,Heart,GEO,scRNA-Seq,Mus musculus,1|1,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA07907,GSE166403,GPL24247,1000,Heart Failure,C0018801,Heart,GEO,scRNA-Seq,Mus musculus,1|1,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA07908,GSE166403,GPL24247,1000,Heart Failure,C0018801,Heart,GEO,scRNA-Seq,Mus musculus,1|1,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA07909,GSE166403,GPL24247,1000,Heart Failure,C0018801,Heart,GEO,scRNA-Seq,Mus musculus,1|1,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA07910,GSE166403,GPL24247,1000,Heart Failure,C0018801,Heart,GEO,scRNA-Seq,Mus musculus,1|1,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA07911,GSE166403,GPL24247,370,Heart Failure,C0018801,Heart,GEO,scRNA-Seq,Mus musculus,1|1,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA07912,GSE166488,GPL1261,256,Injury of Liver,C0160390,Liver,GEO,Microarray,Mus musculus,3|5,NCI:Damage to liver structure or function due to trauma or toxicity. DSA07913,GSE166655,GPL24247,1000,Spinal And Bulbar Muscular Atrophy,C1839259,Tibialis anterior,GEO,RNA-Seq,Mus musculus,3|3,DO:A spinal muscular dystrophy that has_material_basis_in an X-linked recessive expansion of CAG triplet repeats (glutamine) in exon 1 of AR gene encoding the androgen receptor. DSA07914,GSE166671,GPL17021,667,T-Cell Lymphoma,C0079772,Spleen,GEO,RNA-Seq,Mus musculus,3|3,HPO:A type of lymphoma that originates in T-cells. DSA07915,GSE166671,GPL17021,1000,T-Cell Lymphoma,C0079772,Spleen,GEO,RNA-Seq,Mus musculus,3|3,HPO:A type of lymphoma that originates in T-cells. DSA07916,GSE166671,GPL17021,359,T-Cell Lymphoma,C0079772,,GEO,RNA-Seq,Mus musculus,4|3,HPO:A type of lymphoma that originates in T-cells. DSA07917,GSE166671,GPL17021,1000,T-Cell Lymphoma,C0079772,,GEO,RNA-Seq,Mus musculus,4|3,HPO:A type of lymphoma that originates in T-cells. DSA07918,GSE166671,GPL17021,286,T-Cell Lymphoma,C0079772,,GEO,RNA-Seq,Mus musculus,4|2,HPO:A type of lymphoma that originates in T-cells. DSA07919,GSE166671,GPL17021,1000,T-Cell Lymphoma,C0079772,,GEO,RNA-Seq,Mus musculus,3|4,HPO:A type of lymphoma that originates in T-cells. DSA07920,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07921,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07922,GSE166751,GPL19057,1000,Basal Cell Carcinoma,C0007117,Skin,GEO,RNA-Seq,Mus musculus,3|4,DO:A skin carcinoma affecting basal cells. DSA07923,GSE166751,GPL19057,1000,Merkel Cell Carcinoma,C0007129,Skin,GEO,RNA-Seq,Mus musculus,3|3,"HPO:A malignant cutaneous tumor of the elderly that is characterized by an aggressive course with regional nodal involvement, distant metastases and a high rate of recurrence. Most patients present with rapidly growing, painless, firm, non-tender, dome-shaped red, occasionally ulcerated skin nodules, which have a red or bluish color, measuring up to several centimeters, on predominantly sun-exposed areas of the body. The overlying skin is smooth and shiny, sometimes exhibiting ulcerative, acneiform or telangiectatic features." DSA07924,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|4,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07925,GSE167033,GPL1261,1000,Injury of Liver,C0160390,Liver,GEO,Microarray,Mus musculus,5|5,NCI:Damage to liver structure or function due to trauma or toxicity. DSA07926,GSE167033,GPL1261,1000,Injury of Liver,C0160390,Liver,GEO,Microarray,Mus musculus,5|5,NCI:Damage to liver structure or function due to trauma or toxicity. DSA07927,GSE167033,GPL1261,51,Injury of Liver,C0160390,Liver,GEO,Microarray,Mus musculus,5|6,NCI:Damage to liver structure or function due to trauma or toxicity. DSA07928,GSE167033,GPL1261,1000,Injury of Liver,C0160390,Liver,GEO,Microarray,Mus musculus,5|5,NCI:Damage to liver structure or function due to trauma or toxicity. DSA07929,GSE167033,GPL1261,1000,Injury of Liver,C0160390,Liver,GEO,Microarray,Mus musculus,5|5,NCI:Damage to liver structure or function due to trauma or toxicity. DSA07930,GSE167033,GPL1261,1000,Injury of Liver,C0160390,Liver,GEO,Microarray,Mus musculus,5|5,NCI:Damage to liver structure or function due to trauma or toxicity. DSA07931,GSE167033,GPL1261,0,Injury of Liver,C0160390,Liver,GEO,Microarray,Mus musculus,5|5,NCI:Damage to liver structure or function due to trauma or toxicity. DSA07932,GSE167033,GPL1261,8,Injury of Liver,C0160390,Liver,GEO,Microarray,Mus musculus,5|5,NCI:Damage to liver structure or function due to trauma or toxicity. DSA07933,GSE167088,GPL19057,79,Gastrointestinal Inflammation,C1535950,Ileum,GEO,RNA-Seq,Mus musculus,2|4,HPO:Inflammation of the alimentary part of the gastrointestinal system. DSA07934,GSE167190,GPL1261,1000,Arthritis,C0003864,Ankle,GEO,Microarray,Mus musculus,4|4,DO:A bone disease that is located_in the joint. DSA07935,GSE167216,GPL17021,1000,Liver Cirrhosis,C0023890,Liver,GEO,RNA-Seq,Mus musculus,6|6,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA07936,GSE167216,GPL17021,1000,Liver Cirrhosis,C0023890,Liver,GEO,RNA-Seq,Mus musculus,6|6,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA07937,GSE167568,GPL21103,83,Emphysema,C0034067,Lung,GEO,RNA-Seq,Mus musculus,4|3,DO:A chronic obstructive pulmonary disease that is characterized by permanent enlargement of air spaces distal to the terminal bronchioles and the destruction of the alveolar walls. DSA07938,GSE167568,GPL21103,5,Emphysema,C0034067,Lung,GEO,RNA-Seq,Mus musculus,5|3,DO:A chronic obstructive pulmonary disease that is characterized by permanent enlargement of air spaces distal to the terminal bronchioles and the destruction of the alveolar walls. DSA07939,GSE168494,GPL28457,1000,Epithelioid Hemangioendothelioma,C0206732,Liver,GEO,RNA-Seq,Mus musculus,3|3,"DO:A malignant hemangioma characterized by the presence of epithelioid endothelial cells. The neoplastic cells are arranged in cords and nests, which are embedded in a myxoid to hyalinized stroma." DSA07940,GSE168789,GPL21103,898,Damaged Optic Nerve,C3887709,Retina,GEO,RNA-Seq,Mus musculus,5|5,"DO:An optic neuritis that is characterized by nutritional deficiency causing optic nerve dysfunction, has_symptom painless bilateral progressive decrease in visual acuity and color perception, and has_material_basis_in nuritional deficits, especially of folate and vitamin B, which can be associated with restrictive diets and alcohol abuse." DSA07941,GSE168904,GPL21185,1000,Anaplastic Pleomorphic Xanthoastrocytoma,C4283858,Brain,GEO,Microarray,Homo sapiens,4|6,NCI:A WHO grade 3 pleomorphic xanthoastrocytoma characterized by the presence of five or more mitoses per 10 high-power fields. Necrosis may be present. Patients have shorter survival rates when compared to those with WHO grade 2 pleomorphic xanthoastrocytoma. DSA07942,GSE168904,GPL21185,1000,Pleomorphic Xanthoastrocytoma,C0334586,Brain,GEO,Microarray,Homo sapiens,4|14,DO:A low grade glioma that is characterized by pleomorphic and lipidized cells expressing GFAP often surrounded by a reticulin network and eosinophilic granular bodies. DSA07943,GSE168983,GPL18635,424,Duchenne Muscular Dystrophy,C0013264,Muscle,GEO,RNA-Seq,Mus musculus,2|2,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA07944,GSE168984,GPL19057,1000,Duchenne Muscular Dystrophy,C0013264,Muscle,GEO,RNA-Seq,Mus musculus,3|2,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA07945,GSE169411,GPL18635,482,Skeletal Muscle Acute Injury,C0410158,Tibialis anterior,GEO,RNA-Seq,Mus musculus,2|3, DSA07946,GSE169527,GPL24247,1000,Retinitis Pigmentosa,C0035334,Retina,GEO,RNA-Seq,Mus musculus,2|3,DO:A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss. DSA07947,GSE225601,GPL24676,933,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|4,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07948,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|4,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07949,GSE119132,GPL17021,1000,Peripheral Neuropathy,C0031117,Sciatic nerve,GEO,RNA-Seq,Mus musculus,3|3,DO:A nervous system disease that affects the peripheral nervous system. DSA07950,GSE119265,GPL18573,0,Pre-Eclampsia,C0032914,,GEO,RNA-Seq,Homo sapiens,8|14,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA07951,GSE119265,GPL18573,0,Pre-Eclampsia,C0032914,,GEO,RNA-Seq,Homo sapiens,8|14,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA07952,GSE225601,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,9|8,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA07953,GSE225904,GPL23159,11,Behcet's Disease,C0004943,,GEO,Microarray,Homo sapiens,5|4,"DO:A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis." DSA07954,GSE226869,GPL16791,1000,Melanoma,C0025202,Skin,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA07955,GSE119303,GPL17021|GPL19057,1000,Leukemia,C0023418,,GEO,RNA-Seq,Mus musculus,3|3,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA07956,GSE119844,GPL21273,1000,Acute Pancreatitis,C0001339,Pancreas,GEO,RNA-Seq,Mus musculus,2|2,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA07957,GSE119946,GPL11154,1000,Hepatocellular Carcinoma,C0334287,,GEO,RNA-Seq,Homo sapiens,1|1,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07958,GSE119974,GPL18573,1000,Ewing Sarcoma,C0553580,,GEO,RNA-Seq,Homo sapiens,2|3,"DO:A connective tissue cancer that has_material_basis_in neural crest cells derives_from undeveloped, undifferentiated neuroectoderm." DSA07959,GSE119974,GPL18573,1000,Ewing Sarcoma,C0553580,,GEO,RNA-Seq,Homo sapiens,2|1,"DO:A connective tissue cancer that has_material_basis_in neural crest cells derives_from undeveloped, undifferentiated neuroectoderm." DSA07960,GSE120326,GPL21783,0,Brain Damage,C0006109,Lung,GEO,Microarray,Mus musculus,3|2,MONDO:Chronic form of encephalitis. DSA07961,GSE227329,GPL571,1000,Lupus Erythematosus,C0409974,Skin,GEO,Microarray,Homo sapiens,7|7,"DO:An autoimmune disease that is characterized by a constellation of findings that include elevated antibodies to nuclear antigens, antiphospholipids, low complement levels, ulcers, non-scarring alopecia, renal or neurologic damage, and low white blood cell and platelet counts, has_symptom rashes, fatigue, arthritis, hair loss, seizures, and symptoms related to affected organs." DSA07962,GSE4612,GPL339,96,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Mus musculus,3|3,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA07963,GSE121123,GPL21273,1000,Leukemia,C0023418,Bone marrow,GEO,RNA-Seq,Mus musculus,7|9,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA07964,GSE121123,GPL21273,1000,Leukemia,C0023418,Bone marrow,GEO,RNA-Seq,Mus musculus,5|5,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA07965,GSE121186,GPL15103,1000,Melanoma,C0025202,,GEO,RNA-Seq,Mus musculus,3|3,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA07966,GSE121276,GPL16791,1000,Liver Cancer,C2239176,,GEO,RNA-Seq,Homo sapiens,1|1,DO:A hepatobiliary system cancer that is located_in the liver. DSA07967,GSE121276,GPL16791,1000,Liver Cancer,C2239176,,GEO,RNA-Seq,Homo sapiens,1|1,DO:A hepatobiliary system cancer that is located_in the liver. DSA07968,GSE121276,GPL16791,1000,Liver Cancer,C2239176,,GEO,RNA-Seq,Homo sapiens,1|1,DO:A hepatobiliary system cancer that is located_in the liver. DSA07969,GSE121276,GPL16791,1000,Liver Cancer,C2239176,,GEO,RNA-Seq,Homo sapiens,1|1,DO:A hepatobiliary system cancer that is located_in the liver. DSA07970,GSE121276,GPL16791,1000,Liver Cancer,C2239176,,GEO,RNA-Seq,Homo sapiens,1|1,DO:A hepatobiliary system cancer that is located_in the liver. DSA07971,GSE121276,GPL16791,1000,Liver Cancer,C2239176,,GEO,RNA-Seq,Homo sapiens,1|1,DO:A hepatobiliary system cancer that is located_in the liver. DSA07972,GSE121359,GPL19057,754,Pseudomonas Aeruginosa Infection,C0854135,Lung,GEO,RNA-Seq,Mus musculus,3|3,MSH:Infections with bacteria of the genus PSEUDOMONAS. DSA07973,GSE121467,GPL1261,0,Albinism,C0001916,Retinal pigment epithelium,GEO,Microarray,Mus musculus,3|3,"DO:A syndrome characterized by abnormal pigmentation of the skin, hair and eyes." DSA07974,GSE121847,GPL16570,1000,Sepsis,C0243026,Liver,GEO,Microarray,Mus musculus,6|6,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07975,GSE121847,GPL16570,1000,Sepsis,C0243026,Liver,GEO,Microarray,Mus musculus,6|6,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA07976,GSE122089,GPL17021,1000,Metachondromatosis,C0410530,Articular cartilage,GEO,RNA-Seq,Mus musculus,1|1,DO:An osteochondrodysplasia characterized by the presence of both multiple multiple enchondromas and exostoses that has_material_basis_in heterozygous mutation in PTPN11 on chromosome 12q24.13. DSA07977,GSE122089,GPL17021,1000,Metachondromatosis,C0410530,Articular cartilage,GEO,RNA-Seq,Mus musculus,1|1,DO:An osteochondrodysplasia characterized by the presence of both multiple multiple enchondromas and exostoses that has_material_basis_in heterozygous mutation in PTPN11 on chromosome 12q24.13. DSA07978,GSE122165,GPL21493,967,Injury of Liver,C0160390,Liver,GEO,RNA-Seq,Mus musculus,2|1,NCI:Damage to liver structure or function due to trauma or toxicity. DSA07979,GSE122183,GPL17586,0,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,5|5,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA07980,GSE122183,GPL17586,0,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,5|5,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA07981,GSE122183,GPL17586,1000,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,5|5,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA07982,GSE122183,GPL17586,0,Progressive Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,5|5,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA07983,GSE122225,GPL19057,118,Skin Tumor,C0037286,Skin,GEO,RNA-Seq,Mus musculus,2|2,DO:An integumentary system cancer located_in the skin that is the uncontrolled growth of abnormal skin cells. DSA07984,GSE122660,GPL13158,1000,Hepatoma,C2239176,,GEO,Microarray,Homo sapiens,3|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA07985,GSE122660,GPL13158,1000,Hepatoma,C2239176,,GEO,Microarray,Homo sapiens,3|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA07986,GSE122660,GPL13158,1000,Hepatoma,C2239176,,GEO,Microarray,Homo sapiens,3|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA07987,GSE122660,GPL13158,1000,Hepatoma,C2239176,,GEO,Microarray,Homo sapiens,3|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA07988,GSE122660,GPL13158,1000,Hepatoma,C2239176,,GEO,Microarray,Homo sapiens,3|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA07989,GSE122660,GPL13158,1000,Hepatoma,C2239176,,GEO,Microarray,Homo sapiens,3|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA07990,GSE12305,GPL570,1000,Glioblastoma,C0017636,,GEO,Microarray,Homo sapiens,3|3,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA07991,GSE123114,GPL1261,168,Alcohol Dependence,C2751719,Prefrontal cortex,GEO,Microarray,Mus musculus,3|3,"DO:A substance dependence that is characterized by tolerance, withdrawal symptoms, increasing use, persistent desire to decrease consumption, time spent obtaining or recovering from alcohol caused by a physical and psychological dependence on alcohol." DSA07992,GSE123114,GPL1261,0,Alcohol Dependence,C2751719,Striatum,GEO,Microarray,Mus musculus,3|3,"DO:A substance dependence that is characterized by tolerance, withdrawal symptoms, increasing use, persistent desire to decrease consumption, time spent obtaining or recovering from alcohol caused by a physical and psychological dependence on alcohol." DSA07993,GSE123281,GPL13112,1000,Neuroblastoma,C0027819,,GEO,RNA-Seq,Mus musculus,3|4,DO:An autonomic nervous system neoplasm that derives_from immature nerve cells. DSA07994,GSE123281,GPL13112,1000,Neuroblastoma,C0027819,,GEO,RNA-Seq,Mus musculus,3|6,DO:An autonomic nervous system neoplasm that derives_from immature nerve cells. DSA07995,GSE123427,GPL13112,1000,Liver Cancer,C2239176,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA07996,GSE123427,GPL13112,519,Liver Cancer,C2239176,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA07997,GSE123737,GPL13912,1000,Liver Cancer,C2239176,Liver,GEO,Microarray,Mus musculus,3|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA07998,GSE124029,GPL21103,1000,Colorectal Carcinoma,C0009402,,GEO,RNA-Seq,Mus musculus,3|3,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA07999,GSE124357,GPL11154,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,RNA-Seq,Mus musculus,6|6,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA08000,GSE124357,GPL11154,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,RNA-Seq,Mus musculus,5|5,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA08001,GSE131145,GPL13112,1000,Left Ventricular Hypertrophy,C0149721,Heart,GEO,RNA-Seq,Mus musculus,3|3,EFO:Enlargement of the LEFT VENTRICLE of the heart. This increase in ventricular mass is attributed to sustained abnormal pressure or volume loads and is a contributor to cardiovascular morbidity and mortality. DSA08002,GSE131154,GPL16417,1000,Cardiomyopathy,C0878544,Heart,GEO,RNA-Seq,Mus musculus,1|1,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA08003,GSE229188,GPL24247,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,9|15,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA08004,GSE131536,GPL19057,1000,Neural Tube Defects,C0027794,Brain,GEO,RNA-Seq,Mus musculus,2|2,"HPO:A neural tube defect arises when the neural tube, the embryonic precursor of the brain and spinal cord, fails to close during neurulation. The cranial region (anencephaly) or the low spine (open spina bifida; myelomeningocele) are most commonly affected although, in the severe NTD craniorachischisis, almost the entire neural tube remains open, from midbrain to low spine." DSA08005,GSE131845,GPL21103,1000,Prostate Cancer,C0600139,Prostate,GEO,RNA-Seq,Mus musculus,2|2,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08006,GSE131845,GPL21103,1000,Prostate Cancer,C0600139,Prostate,GEO,RNA-Seq,Mus musculus,2|2,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08007,GSE131845,GPL21103,1000,Prostate Cancer,C0600139,Prostate,GEO,RNA-Seq,Mus musculus,2|2,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08008,GSE131845,GPL21103,1000,Prostate Cancer,C0600139,Prostate,GEO,RNA-Seq,Mus musculus,2|4,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08009,GSE131854,GPL17021,1000,Experimental Autoimmune Encephalomyelitis,C0014072,Spinal cord,GEO,RNA-Seq,Mus musculus,3|3,"EFO:An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)" DSA08010,GSE131883,GPL21103,473,Colitis,C0009319,Spleen;lymph node,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA08011,GSE221990,GPL24247,1000,Periapical Periodontitis,C0031030,Alveolar bone,GEO,RNA-Seq,Mus musculus,1|2,"MONDO:Inflammation of the periapical tissue. It includes general, unspecified, or acute nonsuppurative inflammation. Chronic nonsuppurative inflammation is periapical granuloma. Suppurative inflammation is periapical abscess." DSA08012,GSE132103,GPL17021,1000,Alcoholic Liver Disease,C0023896,Liver,GEO,RNA-Seq,Mus musculus,18|18,"EFO:A disorder caused by damage to the liver parenchyma due to alcohol consumption. It may present with an acute onset or follow a chronic course, leading to cirrhosis." DSA08013,GSE132103,GPL17021,605,Alcoholic Liver Disease,C0023896,Liver,GEO,RNA-Seq,Mus musculus,18|18,"EFO:A disorder caused by damage to the liver parenchyma due to alcohol consumption. It may present with an acute onset or follow a chronic course, leading to cirrhosis." DSA08014,GSE132108,GPL21273,313,Amyotrophic Lateral Sclerosis,C0002736,Cerebellum,GEO,RNA-Seq,Mus musculus,6|5,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA08015,GSE132108,GPL21273,75,Amyotrophic Lateral Sclerosis,C0002736,Cortex,GEO,RNA-Seq,Mus musculus,3|2,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA08016,GSE132108,GPL21273,78,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,RNA-Seq,Mus musculus,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA08017,GSE132120,GPL19057,1000,Lung Cancer,C0684249,Gastrocnemius muscle,GEO,RNA-Seq,Mus musculus,3|3,DO:A respiratory system cancer that is located_in the lung. DSA08018,GSE132242,GPL26743,1000,Spinal Cord Contusion Injury,,Spinal cord,GEO,Microarray,Mus musculus,4|4, DSA08019,GSE221791,GPL23038,0,Cognitive Impairment,C0338656,Brain,GEO,Microarray,Mus musculus,2|2,"HPO:Abnormal cognition with deficits in thinking, reasoning, or remembering." DSA08020,GSE132330,GPL17021,1000,Pancreatic Cancer,C0235974,Pancreas,GEO,RNA-Seq,Mus musculus,3|3,DO:An endocrine gland cancer located_in the pancreas. DSA08021,GSE132330,GPL17021,1000,Pancreatic Cancer,C0235974,Pancreas,GEO,RNA-Seq,Mus musculus,3|4,DO:An endocrine gland cancer located_in the pancreas. DSA08022,GSE132330,GPL17021,1000,Pancreatic Cancer,C0235974,Pancreas,GEO,RNA-Seq,Mus musculus,3|5,DO:An endocrine gland cancer located_in the pancreas. DSA08023,GSE132528,GPL13112,1000,Mammary Carcinoma,C0678222,Mammary gland,GEO,RNA-Seq,Mus musculus,3|14,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08024,GSE132528,GPL13112,1000,Mammary Carcinoma,C0678222,Mammary gland,GEO,RNA-Seq,Mus musculus,3|4,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08025,GSE132575,GPL1261,1000,Hepatocellular Carcinoma,C0334287,,GEO,Microarray,Mus musculus,6|6,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA08026,GSE132575,GPL1261,1000,Hepatocellular Carcinoma,C0334287,,GEO,Microarray,Mus musculus,6|6,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA08027,GSE132583,GPL19057,1000,Melanoma,C0025202,,GEO,RNA-Seq,Mus musculus,1|1,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA08028,GSE133179,GPL17021,1000,Female Sterility,C0917730,Ovary,GEO,RNA-Seq,Mus musculus,3|3,MSH:Diminished or absent ability of a female to achieve conception. DSA08029,GSE133269,GPL21493,1,Atherosclerosis,C0004153,Aorta,GEO,RNA-Seq,Mus musculus,2|2,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA08030,GSE133485,GPL26860,1000,Papillary Thyroid Carcinoma,C0238463,,GEO,Microarray,Homo sapiens,3|3,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA08031,GSE133485,GPL26860,1000,Papillary Thyroid Carcinoma,C0238463,,GEO,Microarray,Homo sapiens,3|3,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA08032,GSE186542,GPL24676,8,Intervertebral Disc Degeneration,C0158266,Nucleus pulposus,GEO,RNA-Seq,Homo sapiens,3|2,DO:A bone deterioration disease that has_material_basis_in gradual dehydration and tears located_in intervertebral disc. DSA08033,GSE134375,GPL20301,1000,Ovarian Cancer,C1140680,Ovary,GEO,RNA-Seq,Homo sapiens,3|2,DO:A female reproductive organ cancer that is located_in the ovary. DSA08034,GSE134375,GPL20301,1000,Ovarian Cancer,C1140680,Ovary,GEO,RNA-Seq,Homo sapiens,3|3,DO:A female reproductive organ cancer that is located_in the ovary. DSA08035,GSE134375,GPL20301,1000,Ovarian Cancer,C1140680,Ovary,GEO,RNA-Seq,Homo sapiens,3|3,DO:A female reproductive organ cancer that is located_in the ovary. DSA08036,GSE134384,GPL17021,62,Diabetic Cataract,C0011876,,GEO,RNA-Seq,Mus musculus,2|1,DO:A cataract that is characterized by loss of lens transparency secondary to hyperglycemia related to diabetes mellitus. DSA08037,GSE194388,GPL24676,156,Myocardial Infarction,C0027051,,GEO,RNA-Seq,Homo sapiens,5|5,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA08038,GSE194388,GPL24676,1000,Myocardial Infarction,C0027051,,GEO,RNA-Seq,Homo sapiens,5|5,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA08039,GSE190451,GPL24676,1000,Temporal Lobe Epilepsy,C0014556,Brain,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A focal epilepsy that is characterized by recurrent, unprovoked focal seizures that originate in the temporal lobe of the brain and last about one or two minutes." DSA08040,GSE224776,GPL570,124,Chordoma,C0008487,,GEO,Microarray,Homo sapiens,3|4,DO:A notochordal cancer that derives_from cellular remnants of the notochord. DSA08041,GSE134741,GPL19057,1000,Pulmonary Fibrosis,C0034069,Lung,GEO,RNA-Seq,Mus musculus,3|3,DO:A pneumonia located_in the lung parenchyma of unknown cause. DSA08042,GSE135590,GPL21103,1000,High Grade Serous Carcinoma,,Oviduct,GEO,RNA-Seq,Mus musculus,4|12, DSA08043,GSE135590,GPL21103,1000,Malignant Mixed Mullerian Tumor,C1334603,Oviduct,GEO,RNA-Seq,Mus musculus,4|9,DO:A mixed cell type cancer that has_material_basis_in carcinomatous (epithelial tissue) and sarcomatous (connective tissue) components. DSA08044,GSE135590,GPL21103,1000,Endometrial Cancer,C0476089,Oviduct,GEO,RNA-Seq,Mus musculus,4|6,DO:A uterine cancer that is located_in tissues lining the uterus. DSA08045,GSE135623,GPL11154,1000,Prostate Cancer,C0600139,Prostate gland,GEO,RNA-Seq,Homo sapiens,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08046,GSE135623,GPL11154,93,Prostate Cancer,C0600139,Prostate gland,GEO,RNA-Seq,Homo sapiens,1|1,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08047,GSE217709,GPL20301,1000,Diabetic Kidney Disease,C0011881,Adipose tissue,GEO,RNA-Seq,Homo sapiens,9|27,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA08048,GSE224052,GPL24247,1000,Injury of Liver,C0160390,Liver,GEO,RNA-Seq,Mus musculus,4|5,NCI:Damage to liver structure or function due to trauma or toxicity. DSA08049,GSE136062,GPL17021,1000,Breast Cancer,C0678222,Mammary gland,GEO,RNA-Seq,Mus musculus,1|2,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08050,GSE136062,GPL21103,1000,Breast Cancer,C0678222,Mammary gland,GEO,RNA-Seq,Mus musculus,1|1,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08051,GSE136308,GPL1261,1000,Heart Failure,C0018801,Heart,GEO,Microarray,Mus musculus,5|4,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA08052,GSE136311,GPL13112,1000,Gastrointestinal Inflammation,C1535950,Colon,GEO,RNA-Seq,Mus musculus,1|2,HPO:Inflammation of the alimentary part of the gastrointestinal system. DSA08053,GSE136657,GPL17021,705,Atopic Dermatitis,C0011615,Skin,GEO,RNA-Seq,Mus musculus,3|3,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA08054,GSE48812,GPL11154,1000,Prostate Cancer,C0600139,Prostate,GEO,RNA-Seq,Homo sapiens,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08055,GSE48812,GPL11154,1000,Prostate Cancer,C0600139,Prostate,GEO,RNA-Seq,Homo sapiens,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08056,GSE48812,GPL11154,1000,Prostate Cancer,C0600139,Prostate,GEO,RNA-Seq,Homo sapiens,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08057,GSE48812,GPL11154,1000,Prostate Cancer,C0600139,Prostate,GEO,RNA-Seq,Homo sapiens,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08058,GSE48812,GPL11154,1000,Prostate Cancer,C0600139,Prostate,GEO,RNA-Seq,Homo sapiens,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08059,GSE48812,GPL11154,1000,Prostate Cancer,C0600139,Prostate,GEO,RNA-Seq,Homo sapiens,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08060,GSE48812,GPL11154,1000,Prostate Cancer,C0600139,Prostate,GEO,RNA-Seq,Homo sapiens,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08061,GSE48812,GPL11154,1000,Prostate Cancer,C0600139,Prostate,GEO,RNA-Seq,Homo sapiens,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08062,GSE48818,GPL6885,931,B-Cell Lymphomas,C0079731,Spleen,GEO,Microarray,Mus musculus,4|3,DO:A non-Hodgkin lymphoma that has_material_basis_in B cells. DSA08063,GSE49122,GPL1261,1000,Otitis Media,C0029882,Ear,GEO,Microarray,Mus musculus,5|8,DO:A otitis which involves inflammation of the middle ear. DSA08064,GSE49128,GPL1261,1000,Otitis Media,C0029882,Middle ear,GEO,Microarray,Mus musculus,8|9,DO:A otitis which involves inflammation of the middle ear. DSA08065,GSE49524,GPL7020,0,Gestational Diabetes,C0085207,Umbilical cord,GEO,Microarray,Homo sapiens,3|3,DO:A diabetes mellitus that manifests during pregnancy. DSA08066,GSE50195,GPL17629,0,Age Related Macular Degeneration,C0242383,Retinal pigment epithelium,GEO,Microarray,Homo sapiens,7|9,DO:A degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision. DSA08067,GSE50627,GPL6244,1000,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Homo sapiens,6|6,DO:A respiratory system cancer that is located_in the lung. DSA08068,GSE50627,GPL6244,1000,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Homo sapiens,6|3,DO:A respiratory system cancer that is located_in the lung. DSA08069,GSE224052,GPL24247,1000,Injury of Liver,C0160390,Liver,GEO,RNA-Seq,Mus musculus,5|5,NCI:Damage to liver structure or function due to trauma or toxicity. DSA08070,GSE50901,GPL13607,354,Thyroid Carcinoma,C0549473,Thyroid,GEO,Microarray,Homo sapiens,4|4,DO:A thyroid gland cancer that has_material_basis_in epithelial cells. DSA08071,GSE51925,GPL1261,279,Sepsis,C0243026,Blood,GEO,Microarray,Mus musculus,8|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08072,GSE51925,GPL1261,1000,Sepsis,C0243026,Blood,GEO,Microarray,Mus musculus,8|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08073,GSE51925,GPL1261,841,Sepsis,C0243026,Blood,GEO,Microarray,Mus musculus,8|5,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08074,GSE51925,GPL1261,938,Sepsis,C0243026,Blood,GEO,Microarray,Mus musculus,8|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08075,GSE51925,GPL1261,1000,Sepsis,C0243026,Blood,GEO,Microarray,Mus musculus,8|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08076,GSE51925,GPL1261,0,Sepsis,C0243026,Blood,GEO,Microarray,Mus musculus,8|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08077,GSE224052,GPL24247,1000,Injury of Liver,C0160390,Liver,GEO,RNA-Seq,Mus musculus,5|5,NCI:Damage to liver structure or function due to trauma or toxicity. DSA08078,GSE224052,GPL24247,138,Injury of Liver,C0160390,Liver,GEO,RNA-Seq,Mus musculus,5|5,NCI:Damage to liver structure or function due to trauma or toxicity. DSA08079,GSE52682,GPL13912,0,Acute Lung Injury,C0242488,Lung,GEO,Microarray,Mus musculus,3|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08080,GSE52682,GPL13912,0,Acute Lung Injury,C0242488,Lung,GEO,Microarray,Mus musculus,2|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08081,GSE52682,GPL13912,0,Acute Lung Injury,C0242488,Lung,GEO,Microarray,Mus musculus,2|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08082,GSE52682,GPL13912,0,Acute Lung Injury,C0242488,Lung,GEO,Microarray,Mus musculus,2|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08083,GSE52682,GPL13912,0,Acute Lung Injury,C0242488,Lung,GEO,Microarray,Mus musculus,2|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08084,GSE52682,GPL13912,0,Acute Lung Injury,C0242488,Lung,GEO,Microarray,Mus musculus,2|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08085,GSE52683,GPL13912,0,Acute Lung Injury,C0242488,Brain,GEO,Microarray,Mus musculus,3|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08086,GSE52683,GPL13912,0,Acute Lung Injury,C0242488,Brain,GEO,Microarray,Mus musculus,3|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08087,GSE52683,GPL13912,0,Acute Lung Injury,C0242488,Brain,GEO,Microarray,Mus musculus,2|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08088,GSE52683,GPL13912,0,Acute Lung Injury,C0242488,Brain,GEO,Microarray,Mus musculus,2|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08089,GSE52683,GPL13912,1,Acute Lung Injury,C0242488,Brain,GEO,Microarray,Mus musculus,2|2,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08090,GSE52683,GPL13912,2,Acute Lung Injury,C0242488,Brain,GEO,Microarray,Mus musculus,2|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08091,GSE52684,GPL13912,0,Acute Lung Injury,C0242488,,GEO,Microarray,Mus musculus,3|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08092,GSE52684,GPL13912,6,Acute Lung Injury,C0242488,,GEO,Microarray,Mus musculus,3|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08093,GSE52684,GPL13912,0,Acute Lung Injury,C0242488,,GEO,Microarray,Mus musculus,2|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08094,GSE52684,GPL13912,0,Acute Lung Injury,C0242488,,GEO,Microarray,Mus musculus,1|2,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08095,GSE52684,GPL13912,0,Acute Lung Injury,C0242488,,GEO,Microarray,Mus musculus,2|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08096,GSE52684,GPL13912,0,Acute Lung Injury,C0242488,,GEO,Microarray,Mus musculus,2|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08097,GSE53520,GPL7202,0,Malnutrition,C0162429,Tibialis anterior,GEO,Microarray,Mus musculus,4|4,"DO:A nutritional deficiency disease that is characterized by inadequate dietary protein and calories, which can have profound systemic effects including decreased metabolism, altered tissue distribution, compromised immunity, and impaired growth, and has_material_basis_in dietary deprivation." DSA08098,GSE53520,GPL7202,0,Malnutrition,C0162429,Tibialis anterior,GEO,Microarray,Mus musculus,4|4,"DO:A nutritional deficiency disease that is characterized by inadequate dietary protein and calories, which can have profound systemic effects including decreased metabolism, altered tissue distribution, compromised immunity, and impaired growth, and has_material_basis_in dietary deprivation." DSA08099,GSE53737,GPL17021,419,White Matter Abnormalities,C0948163,,GEO,RNA-Seq,Mus musculus,10|7,HPO:An abnormality of the cerebral white matter. DSA08100,GSE53737,GPL17021,363,White Matter Abnormalities,C0948163,,GEO,RNA-Seq,Mus musculus,10|6,HPO:An abnormality of the cerebral white matter. DSA08101,GSE53769,GPL16686,0,Acute Kidney Injury,C2609414,Kidney,GEO,Microarray,Homo sapiens,10|8,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA08102,GSE53769,GPL16686,0,Acute Kidney Injury,C2609414,Kidney,GEO,Microarray,Homo sapiens,10|8,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA08103,GSE53996,GPL10333,51,Obesity,C0028754,Kidney,GEO,Microarray,Mus musculus,4|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA08104,GSE53996,GPL10333,1000,Obesity,C0028754,Kidney,GEO,Microarray,Mus musculus,4|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA08105,GSE5455,GPL81,49,Tumor,C0006826,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A disease of cellular proliferation that is malignant and primary, characterized by uncontrolled cellular proliferation, local cell invasion and metastasis." DSA08106,GSE5455,GPL81,7,Tumor,C0006826,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A disease of cellular proliferation that is malignant and primary, characterized by uncontrolled cellular proliferation, local cell invasion and metastasis." DSA08107,GSE55238,GPL1261,1000,Sepsis,C0243026,,GEO,Microarray,Mus musculus,4|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08108,GSE55238,GPL1261,907,Sepsis,C0243026,,GEO,Microarray,Mus musculus,4|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08109,GSE55238,GPL1261,441,Sepsis,C0243026,,GEO,Microarray,Mus musculus,4|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08110,GSE55238,GPL1261,304,Sepsis,C0243026,,GEO,Microarray,Mus musculus,4|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08111,GSE55238,GPL1261,1000,Sepsis,C0243026,,GEO,Microarray,Mus musculus,4|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08112,GSE55238,GPL1261,0,Sepsis,C0243026,,GEO,Microarray,Mus musculus,4|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08113,GSE55271,GPL15433,568,Inflammation,C0021368,,GEO,RNA-Seq,Homo sapiens,1|1,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA08114,GSE55271,GPL15433,53,Inflammation,C0021368,,GEO,RNA-Seq,Homo sapiens,1|1,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA08115,GSE55276,GPL10558,159,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08116,GSE55276,GPL10558,927,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08117,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08118,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08119,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08120,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08121,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08122,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08123,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08124,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08125,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08126,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08127,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08128,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08129,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08130,GSE55276,GPL10558,229,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08131,GSE55276,GPL10558,767,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08132,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08133,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08134,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08135,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08136,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08137,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08138,GSE55276,GPL10558,282,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08139,GSE55276,GPL10558,972,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08140,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08141,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08142,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08143,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08144,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08145,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08146,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08147,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08148,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08149,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08150,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08151,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08152,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08153,GSE55276,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08154,GSE55277,GPL10558,624,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08155,GSE55277,GPL10558,884,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08156,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08157,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08158,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08159,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08160,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08161,GSE55277,GPL10558,43,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08162,GSE55277,GPL10558,154,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08163,GSE55277,GPL10558,493,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08164,GSE55277,GPL10558,453,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08165,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08166,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08167,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08168,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08169,GSE55277,GPL10558,127,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08170,GSE55277,GPL10558,782,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08171,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08172,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08173,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08174,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08175,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08176,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08177,GSE55277,GPL10558,227,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08178,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08179,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08180,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08181,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08182,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08183,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08184,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08185,GSE55277,GPL10558,328,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08186,GSE55277,GPL10558,913,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08187,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08188,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08189,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08190,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08191,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08192,GSE55277,GPL10558,1000,Influenza,C0021400,,GEO,Microarray,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08193,GSE55546,GPL17077,792,Oropharyngeal Cancer,C2349952,Tonsil,GEO,Microarray,Homo sapiens,4|12,DO:A pharynx cancer that is located_in the oropharynx. DSA08194,GSE55547,GPL17077,857,Oropharyngeal Cancer,C2349952,Tonsil,GEO,Microarray,Homo sapiens,4|16,DO:A pharynx cancer that is located_in the oropharynx. DSA08195,GSE55597,GPL10558,0,Prostate Carcinoma,C0600139,Prostate,GEO,Microarray,Homo sapiens,16|16,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08196,GSE55909,GPL16699,1000,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,2|2,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08197,GSE55909,GPL16699,1000,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,2|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08198,GSE55909,GPL16699,1000,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,2|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08199,GSE56256,GPL13607,0,Inflammation,C0021368,Lung,GEO,Microarray,Homo sapiens,3|3,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA08200,GSE207805,GPL24247,19,Oligoasthenoteratozoospermia,,Testis,GEO,RNA-Seq,Mus musculus,3|4, DSA08201,GSE207805,GPL24247,1,Oligospermia,C0028960,Testis,GEO,RNA-Seq,Mus musculus,3|4,DO:A Sertoli cell-only syndrome that has_material_basis_in deletions in the Yq11 chromosomal region. DSA08202,GSE56584,GPL6885,13,Inflammation,C0021368,,GEO,Microarray,Mus musculus,4|4,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA08203,GSE56584,GPL6885,164,Inflammation,C0021368,,GEO,Microarray,Mus musculus,4|4,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA08204,GSE56584,GPL6885,82,Inflammation,C0021368,,GEO,Microarray,Mus musculus,4|4,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA08205,GSE56584,GPL6885,18,Inflammation,C0021368,,GEO,Microarray,Mus musculus,4|4,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA08206,GSE56584,GPL6885,272,Inflammation,C0021368,,GEO,Microarray,Mus musculus,4|4,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA08207,GSE56584,GPL6885,66,Inflammation,C0021368,,GEO,Microarray,Mus musculus,4|3,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA08208,GSE56584,GPL6885,45,Inflammation,C0021368,,GEO,Microarray,Mus musculus,4|4,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA08209,GSE57130,GPL10558,1000,Esophageal Cancer,C0152018,Esophagus,GEO,Microarray,Homo sapiens,3|3,DO:A esophageal cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08210,GSE57130,GPL10558,1000,Esophageal Cancer,C0152018,Esophagus,GEO,Microarray,Homo sapiens,3|3,DO:A esophageal cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08211,GSE57130,GPL10558,1000,Esophageal Cancer,C0152018,Esophagus,GEO,Microarray,Homo sapiens,3|3,DO:A esophageal cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08212,GSE57130,GPL10558,1000,Esophageal Cancer,C0152018,Esophagus,GEO,Microarray,Homo sapiens,3|3,DO:A esophageal cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08213,GSE57130,GPL10558,1000,Esophageal Cancer,C0152018,Esophagus,GEO,Microarray,Homo sapiens,3|3,DO:A esophageal cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08214,GSE57130,GPL10558,1000,Esophageal Cancer,C0152018,Esophagus,GEO,Microarray,Homo sapiens,3|3,DO:A esophageal cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08215,GSE57130,GPL10558,1000,Esophageal Cancer,C0152018,Esophagus,GEO,Microarray,Homo sapiens,3|3,DO:A esophageal cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08216,GSE57130,GPL10558,1000,Esophageal Cancer,C0152018,Esophagus,GEO,Microarray,Homo sapiens,3|3,DO:A esophageal cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08217,GSE57150,GPL18619,1000,B-Cell Lymphomas,C0079731,Spleen,GEO,Microarray,Mus musculus,10|4,DO:A non-Hodgkin lymphoma that has_material_basis_in B cells. DSA08218,GSE57150,GPL18619,1000,B-Cell Lymphomas,C0079731,Spleen,GEO,Microarray,Mus musculus,10|4,DO:A non-Hodgkin lymphoma that has_material_basis_in B cells. DSA08219,GSE57150,GPL18619,1000,B-Cell Lymphomas,C0079731,Spleen,GEO,Microarray,Mus musculus,10|4,DO:A non-Hodgkin lymphoma that has_material_basis_in B cells. DSA08220,GSE175900,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,1|1,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA08221,GSE175900,GPL24676,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,1|1,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA08222,GSE57533,GPL13112,960,Colitis,C0009319,Colon,GEO,RNA-Seq,Mus musculus,2|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA08223,GSE57533,GPL13112,1000,Intestinal Tumor,C0021841,Colon,GEO,RNA-Seq,Mus musculus,2|3,DO:A gastrointestinal system cancer that is located_in the intestine. DSA08224,GSE57572,GPL13912,11,Cytomegalovirus Infection,C0010823,Lung,GEO,Microarray,Mus musculus,4|4,"EFO:Infection with CYTOMEGALOVIRUS, characterized by enlarged cells bearing intranuclear inclusions. Infection may be in almost any organ, but the salivary glands are the most common site in children, as are the lungs in adults." DSA08225,GSE58014,GPL6246,2,Listeria Monocytogenes,,Spleen,GEO,Microarray,Mus musculus,3|3, DSA08226,GSE58014,GPL6246,162,Listeria Monocytogenes,,Spleen,GEO,Microarray,Mus musculus,3|3, DSA08227,GSE58484,GPL1261,66,Traumatic Brain Injury,,Neocortex,GEO,Microarray,Mus musculus,3|3, DSA08228,GSE85496,GPL6887,0,Diabetes,C0011847,,GEO,Microarray,Mus musculus,2|2,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA08229,GSE59034,GPL11532,1000,Obesity,C0028754,White adipose tissue,GEO,Microarray,Homo sapiens,16|16,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA08230,GSE59070,GPL4134,0,Stress; Psychological,C0038443,Hippocampus,GEO,Microarray,Mus musculus,3|3,MSH:Stress wherein emotional factors predominate. DSA08231,GSE59070,GPL4134,4,Stress; Psychological,C0038443,Hippocampus,GEO,Microarray,Mus musculus,3|3,MSH:Stress wherein emotional factors predominate. DSA08232,GSE59070,GPL4134,0,Stress; Psychological,C0038443,Hippocampus,GEO,Microarray,Mus musculus,3|3,MSH:Stress wherein emotional factors predominate. DSA08233,GSE59070,GPL4134,0,Stress; Psychological,C0038443,Hippocampus,GEO,Microarray,Mus musculus,3|3,MSH:Stress wherein emotional factors predominate. DSA08234,GSE59128,GPL10558,0,Airway Injury,,Lung,GEO,Microarray,Homo sapiens,8|4, DSA08235,GSE59128,GPL10558,0,Airway Injury,,Lung,GEO,Microarray,Homo sapiens,8|4, DSA08236,GSE59128,GPL10558,167,Airway Injury,,Lung,GEO,Microarray,Homo sapiens,8|4, DSA08237,GSE59128,GPL10558,1,Airway Injury,,Lung,GEO,Microarray,Homo sapiens,8|8, DSA08238,GSE59128,GPL10558,0,Airway Injury,,Lung,GEO,Microarray,Homo sapiens,4|4, DSA08239,GSE59128,GPL10558,1000,Airway Injury,,Lung,GEO,Microarray,Homo sapiens,8|4, DSA08240,GSE59128,GPL10558,1000,Airway Injury,,Lung,GEO,Microarray,Homo sapiens,8|4, DSA08241,GSE59128,GPL10558,0,Airway Injury,,Lung,GEO,Microarray,Homo sapiens,8|8, DSA08242,GSE59128,GPL10558,0,Airway Injury,,Lung,GEO,Microarray,Homo sapiens,4|4, DSA08243,GSE59362,GPL13912,0,Brain Damage,C0006109,Brain,GEO,Microarray,Mus musculus,2|2,MONDO:Chronic form of encephalitis. DSA08244,GSE59362,GPL13912,711,Brain Damage,C0006109,Brain,GEO,Microarray,Mus musculus,2|1,MONDO:Chronic form of encephalitis. DSA08245,GSE59362,GPL13912,1000,Brain Damage,C0006109,Brain,GEO,Microarray,Mus musculus,2|2,MONDO:Chronic form of encephalitis. DSA08246,GSE59362,GPL13912,0,Brain Damage,C0006109,Brain,GEO,Microarray,Mus musculus,2|2,MONDO:Chronic form of encephalitis. DSA08247,GSE59831,GPL13112,1000,Lung Cancer,C0684249,Lung,GEO,RNA-Seq,Mus musculus,2|3,DO:A respiratory system cancer that is located_in the lung. DSA08248,GSE59831,GPL13112,817,Lung Cancer,C0684249,Lung,GEO,RNA-Seq,Mus musculus,2|2,DO:A respiratory system cancer that is located_in the lung. DSA08249,GSE59831,GPL13112,1000,Lung Cancer,C0684249,Lung,GEO,RNA-Seq,Mus musculus,3|3,DO:A respiratory system cancer that is located_in the lung. DSA08250,GSE59831,GPL13112,1000,Lung Cancer,C0684249,Lung,GEO,RNA-Seq,Mus musculus,3|3,DO:A respiratory system cancer that is located_in the lung. DSA08251,GSE59831,GPL13112,1000,Lung Cancer,C0684249,Lung,GEO,RNA-Seq,Mus musculus,3|3,DO:A respiratory system cancer that is located_in the lung. DSA08252,GSE59872,GPL6246,1000,Mammary Tumor,C1512981,Mammary gland,GEO,Microarray,Mus musculus,2|10,NCI:Production of a new growth or growths in the mammary gland. DSA08253,GSE59872,GPL6246,64,Mammary Tumor,C1512981,Mammary gland,GEO,Microarray,Mus musculus,3|10,NCI:Production of a new growth or growths in the mammary gland. DSA08254,GSE60349,GPL6887,305,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Mus musculus,4|4,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA08255,GSE61211,GPL5175,1000,Infection By Leishmania Braziliensis,C0023288,,GEO,Microarray,Homo sapiens,9|9,"DO:A leishmaniasis that involves a chronic inflammatory process involving the nasal, pharyngeal, and laryngeal mucosa, which can lead to extensive tissue destruction, caused by protozoan parasites belonging to the genus Leishmania. The infection is characterized by granulomatous lesion which can destroy upper respiratory tract mucosa." DSA08256,GSE61306,GPL16570,151,Embryopathies,C0013949,,GEO,Microarray,Mus musculus,3|3,MSH:Pathophysiological conditions of the FETUS in the UTERUS. Some fetal diseases may be treated with FETAL THERAPIES. DSA08257,GSE61306,GPL16570,296,Embryopathies,C0013949,,GEO,Microarray,Mus musculus,3|3,MSH:Pathophysiological conditions of the FETUS in the UTERUS. Some fetal diseases may be treated with FETAL THERAPIES. DSA08258,GSE61306,GPL16570,0,Embryopathies,C0013949,,GEO,Microarray,Mus musculus,3|3,MSH:Pathophysiological conditions of the FETUS in the UTERUS. Some fetal diseases may be treated with FETAL THERAPIES. DSA08259,GSE61460,GPL1261,1000,Colitis,C0009319,Spleen,GEO,Microarray,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA08260,GSE142615,GPL27951,1000,Cardiomyopathy,C0878544,Heart,GEO,Microarray,Mus musculus,4|4,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA08261,GSE216128,GPL24247,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,1|1,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA08262,GSE216128,GPL24247,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,1|1,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA08263,GSE62157,GPL17791,436,Immune Dysfunction,C0021053,Brown adipose tissue,GEO,Microarray,Mus musculus,3|3,DO:A disease of anatomical entity that is located_in the immune system. DSA08264,GSE62165,GPL13667,1000,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,Microarray,Homo sapiens,13|18,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA08265,GSE62165,GPL13667,1000,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,Microarray,Homo sapiens,13|38,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA08266,GSE62165,GPL13667,1000,Pancreatic Ductal Adenocarcinoma,C1335302,Pancreas,GEO,Microarray,Homo sapiens,13|62,DO:A pancreatic adenocarcinoma that derives_from pancreatic duct cells. DSA08267,GSE62817,GPL1261,25,Lung Cancer,C0684249,Lung,GEO,Microarray,Mus musculus,5|4,DO:A respiratory system cancer that is located_in the lung. DSA08268,GSE62817,GPL1261,2,Lung Cancer,C0684249,Lung,GEO,Microarray,Mus musculus,5|5,DO:A respiratory system cancer that is located_in the lung. DSA08269,GSE192392,GPL24247,151,Leishmaniasis,C0023281,,GEO,RNA-Seq,Mus musculus,5|4,"DO:A parasitic protozoa infectious disease that involves infection caused by protozoan parasite of the genus Leishmania, which is transmitted by the bite of sand fly (subfamily Phlebotominae)." DSA08270,GSE165142,GPL24247,1000,Ebola Virus Disease,C0282687,,GEO,RNA-Seq,Mus musculus,8|12,"DO:A viral infectious disease that is a hemorrhagic fever, has_material_basis_in Zaire ebolavirus, has_material_basis_in Sudan ebolavirus, has_material_basis_in Cote d'Ivoire ebolavirus, or has_material_basis_in Bundibugyo ebolavirus, which are transmitted_by contact with the body fluids of an infected animal or person, transmitted by contaminated fomites, or transmitted by infected medical equipment. The infection has_symptom fever, has_symptom headache, has_symptom joint pain, has_symptom muscle aches, has_symptom sore throat, has_symptom weakness, has_symptom diarrhea, has_symptom vomiting, has_symptom stomach pain, has_symptom rash, has_symptom red eyes, has_symptom hiccups, and has_symptom internal and external bleeding." DSA08271,GSE165142,GPL24247,1000,Ebola Virus Disease,C0282687,,GEO,RNA-Seq,Mus musculus,8|14,"DO:A viral infectious disease that is a hemorrhagic fever, has_material_basis_in Zaire ebolavirus, has_material_basis_in Sudan ebolavirus, has_material_basis_in Cote d'Ivoire ebolavirus, or has_material_basis_in Bundibugyo ebolavirus, which are transmitted_by contact with the body fluids of an infected animal or person, transmitted by contaminated fomites, or transmitted by infected medical equipment. The infection has_symptom fever, has_symptom headache, has_symptom joint pain, has_symptom muscle aches, has_symptom sore throat, has_symptom weakness, has_symptom diarrhea, has_symptom vomiting, has_symptom stomach pain, has_symptom rash, has_symptom red eyes, has_symptom hiccups, and has_symptom internal and external bleeding." DSA08272,GSE184383,GPL24676,29,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,30|7,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08273,GSE184383,GPL24676,11,Lower Respiratory Tract Infections,C0149725,,GEO,RNA-Seq,Homo sapiens,30|13,HPO:An increased susceptibility to lower respiratory tract infections as manifested by a history of recurrent lower respiratory tract infections. DSA08274,GSE184383,GPL24676,0,Asthma;Respiratory Tract Infections,,,GEO,RNA-Seq,Homo sapiens,30|9, DSA08275,GSE208395,GPL17021,1000,Colitis,C0009319,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA08276,GSE208395,GPL17021,1000,Colitis,C0009319,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA08277,GSE208395,GPL17021,1000,Colitis,C0009319,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA08278,GSE208395,GPL17021,1000,Colitis,C0009319,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA08279,GSE208395,GPL17021,1000,Colitis,C0009319,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA08280,GSE208395,GPL17021,1000,Colitis,C0009319,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA08281,GSE208395,GPL17021,1000,Colitis,C0009319,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA08282,GSE208395,GPL17021,1000,Colitis,C0009319,Colon,GEO,RNA-Seq,Mus musculus,3|4,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA08283,GSE205540,GPL24247,1000,Fibrosis; Liver,C0239946,Liver,GEO,RNA-Seq,Mus musculus,3|3,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA08284,GSE63169,GPL19146,0,Diabetes;Obesity,,,GEO,Microarray,Mus musculus,1|2, DSA08285,GSE184052,GPL21163,0,Neuropathic Pain,C3714625,Spinal cord,GEO,Microarray,Mus musculus,2|2,NCI:Chronic pain caused by damage to nerve fibers. It is usually associated with tissue injury. DSA08286,GSE203554,GPL17021,22,Alzheimer's Disease,C0002395,Hippocampal dentate gyrus,GEO,RNA-Seq,Mus musculus,5|5,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA08287,GSE160292,GPL21103,1000,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,RNA-Seq,Mus musculus,2|3,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA08288,GSE102812,GPL16791,1000,Facioscapulohumeral Muscular Dystrophy,C0238288,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA08289,GSE100202,GPL6246,164,Epileptic Syndromes,C4505072,Brain,GEO,Microarray,Mus musculus,3|3,"MSH:EPILEPTIC SEIZURES that are of similar type and age of onset and have other similar features (e.g., clinical course, EEG findings, genetic association and neuropathology)." DSA08290,GSE100202,GPL6246,1000,Epileptic Syndromes,C4505072,Brain,GEO,Microarray,Mus musculus,3|3,"MSH:EPILEPTIC SEIZURES that are of similar type and age of onset and have other similar features (e.g., clinical course, EEG findings, genetic association and neuropathology)." DSA08291,GSE92506,GPL15433,4,Atherosclerosis,C0004153,,GEO,RNA-Seq,Homo sapiens,2|2,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA08292,GSE92506,GPL15433,4,Atherosclerosis,C0004153,,GEO,RNA-Seq,Homo sapiens,2|2,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA08293,GSE92506,GPL15433,17,Atherosclerosis,C0004153,,GEO,RNA-Seq,Homo sapiens,2|2,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA08294,GSE92506,GPL15433,8,Atherosclerosis,C0004153,,GEO,RNA-Seq,Homo sapiens,2|2,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA08295,GSE92506,GPL15433,31,Atherosclerosis,C0004153,,GEO,RNA-Seq,Homo sapiens,2|2,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA08296,GSE92506,GPL15433,29,Atherosclerosis,C0004153,,GEO,RNA-Seq,Homo sapiens,2|2,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA08297,GSE92506,GPL15433,88,Atherosclerosis,C0004153,,GEO,RNA-Seq,Homo sapiens,2|2,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA08298,GSE92506,GPL15433,39,Atherosclerosis,C0004153,,GEO,RNA-Seq,Homo sapiens,2|2,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA08299,GSE97344,GPL13112,97,Hepatic Fibrosis,C0239946,,GEO,RNA-Seq,Mus musculus,3|2,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA08300,GSE96047,GPL1261,1000,Amyotrophic Lateral Sclerosis,C0002736,,GEO,Microarray,Mus musculus,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA08301,GSE229279,GPL24676,1000,Cutaneous Lichenoid Immune-Related Adverse Events,,Skin,GEO,RNA-Seq,Homo sapiens,1|2, DSA08302,GSE229279,GPL24676,1000,Cutaneous Lichenoid Immune-Related Adverse Events,,Skin,GEO,RNA-Seq,Homo sapiens,1|2, DSA08303,GSE174074,GPL21626,1000,Drug Induced Liver Injury,C0860207,Liver,GEO,RNA-Seq,Mus musculus,4|4,"MSH:INFLAMMATION of the LIVER due to hepatocellular toxicity, caused by drug metabolites and chemicals from the environment." DSA08304,GSE174074,GPL21626,339,Liver Cancer,C2239176,Liver,GEO,RNA-Seq,Mus musculus,4|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA08305,GSE174074,GPL21626,1000,Drug Induced Liver Injury;Liver Cancer,,Liver,GEO,RNA-Seq,Mus musculus,4|4, DSA08306,GSE174074,GPL21626,1000,Liver Cancer,C2239176,Liver,GEO,RNA-Seq,Mus musculus,4|1,DO:A hepatobiliary system cancer that is located_in the liver. DSA08307,GSE190023,GPL24676,10,Adhesive Capsulitis,C0158300,Synovitis and thickening joint capsule,GEO,RNA-Seq,Homo sapiens,3|4,MSH:Inflammation or irritation of a JOINT CAPSULE. DSA08308,GSE190023,GPL24676,38,Adhesive Capsulitis,C0158300,Synovitis and thickening joint capsule,GEO,RNA-Seq,Homo sapiens,3|4,MSH:Inflammation or irritation of a JOINT CAPSULE. DSA08309,GSE205450,GPL24676,1000,Parkinson's Disease,C0030567,Brain,GEO,RNA-Seq,Homo sapiens,38|32,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA08310,GSE205450,GPL24676,1000,Parkinson's Disease,C0030567,Brain,GEO,RNA-Seq,Homo sapiens,39|33,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA08311,GSE151325,GPL21273,1000,Diabetic Kidney Disease,C0011881,Renal cortex,GEO,RNA-Seq,Mus musculus,4|2,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA08312,GSE222530,GPL24247,1000,Arthritis,C0003864,Whole blood,GEO,RNA-Seq,Mus musculus,8|15,DO:A bone disease that is located_in the joint. DSA08313,GSE222530,GPL24247,1000,Arthritis,C0003864,Whole blood,GEO,RNA-Seq,Mus musculus,8|15,DO:A bone disease that is located_in the joint. DSA08314,GSE221521,GPL24676,1000,Diabetic Retinopathy,C0011884,Blood,GEO,RNA-Seq,Homo sapiens,47|69,"EFO:Disease of the RETINA as a complication of DIABETES MELLITUS. It is characterized by the progressive microvascular complications, such as ANEURYSM, interretinal EDEMA, and intraocular PATHOLOGIC NEOVASCULARIZATION." DSA08315,GSE221521,GPL24676,18,Diabetic Retinopathy,C0011884,Blood,GEO,RNA-Seq,Homo sapiens,47|73,"EFO:Disease of the RETINA as a complication of DIABETES MELLITUS. It is characterized by the progressive microvascular complications, such as ANEURYSM, interretinal EDEMA, and intraocular PATHOLOGIC NEOVASCULARIZATION." DSA08316,GSE222019,GPL24247,1000,"Atopic Dermatitis, Chronic",C0011615,Skin,GEO,RNA-Seq,Mus musculus,2|3,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA08317,GSE222019,GPL24247,204,"Atopic Dermatitis, Chronic",C0011615,Lung,GEO,RNA-Seq,Mus musculus,2|3,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA08318,GSE186198,GPL11154,0,Systemic Sclerosis,C0036421,,GEO,RNA-Seq,Homo sapiens,11|12,"DO:A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies." DSA08319,GSE186198,GPL11154,2,Systemic Sclerosis,C0036421,,GEO,RNA-Seq,Homo sapiens,11|11,"DO:A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies." DSA08320,GSE186198,GPL11154,0,Limited Systemic Sclerosis,C0748540,,GEO,RNA-Seq,Homo sapiens,11|11,"MONDO:Limited cutaneous systemic sclerosis (lcSSc) is a subtype of systemic sclerosis (SSc) characterized by the association of Raynaud's phenomenon with skin fibrosis limited to the hands, face, feet and forearms." DSA08321,GSE186198,GPL11154,46,Diffuse Sclerosis,C0036421,,GEO,RNA-Seq,Homo sapiens,11|11,"DO:A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies." DSA08322,GSE209762,GPL24247,1000,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,RNA-Seq,Mus musculus,6|9,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA08323,GSE190125,GPL24676,1000,Down Syndrome,C0013080,Whole blood,GEO,RNA-Seq,Homo sapiens,92|281,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA08324,GSE147256,GPL21103,1000,Acute Kidney Injury,C2609414,Kidney,GEO,RNA-Seq,Mus musculus,3|3,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA08325,GSE147834,GPL24247,1000,Cardiomyopathy,C0878544,Heart,GEO,RNA-Seq,Mus musculus,1|1,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA08326,GSE147834,GPL24247,1000,Cardiomyopathy,C0878544,Heart,GEO,RNA-Seq,Mus musculus,1|1,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA08327,GSE147834,GPL24247,1000,Cardiomyopathy,C0878544,Heart,GEO,RNA-Seq,Mus musculus,1|1,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA08328,GSE147834,GPL24247,1000,Cardiomyopathy,C0878544,Heart,GEO,RNA-Seq,Mus musculus,1|1,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA08329,GSE148287,GPL24676,1000,Pulp Inflammation,,,GEO,RNA-Seq,Homo sapiens,6|2, DSA08330,GSE63174,GPL19146,0,Diabetes;Obesity,,Hippocampus,GEO,Microarray,Mus musculus,1|3, DSA08331,GSE63174,GPL19146,3,Diabetes;Obesity,,Hippocampus,GEO,Microarray,Mus musculus,3|3, DSA08332,GSE63174,GPL19146,0,Diabetes;Obesity,,Hippocampus,GEO,Microarray,Mus musculus,3|3, DSA08333,GSE63174,GPL19146,1000,Diabetes;Obesity,,Hippocampus,GEO,Microarray,Mus musculus,3|3, DSA08334,GSE63174,GPL19146,8,Diabetes;Obesity,,Hippocampus,GEO,Microarray,Mus musculus,3|3, DSA08335,GSE63174,GPL19146,0,Diabetes;Obesity,,Hippocampus,GEO,Microarray,Mus musculus,3|3, DSA08336,GSE63174,GPL19146,8,Diabetes;Obesity,,Hippocampus,GEO,Microarray,Mus musculus,3|3, DSA08337,GSE63174,GPL19146,0,Diabetes;Obesity,,Hippocampus,GEO,Microarray,Mus musculus,3|3, DSA08338,GSE63174,GPL19146,0,Diabetes;Obesity,,Hippocampus,GEO,Microarray,Mus musculus,3|3, DSA08339,GSE63174,GPL19146,0,Diabetes;Obesity,,Hippocampus,GEO,Microarray,Mus musculus,3|3, DSA08340,GSE63174,GPL19146,1,Diabetes;Obesity,,Hippocampus,GEO,Microarray,Mus musculus,3|3, DSA08341,GSE63175,GPL19146,145,Diabetes;Obesity,,Liver,GEO,Microarray,Mus musculus,3|3, DSA08342,GSE63175,GPL19146,0,Diabetes;Obesity,,Liver,GEO,Microarray,Mus musculus,3|3, DSA08343,GSE63175,GPL19146,0,Diabetes;Obesity,,Liver,GEO,Microarray,Mus musculus,3|3, DSA08344,GSE63175,GPL19146,6,Diabetes;Obesity,,Liver,GEO,Microarray,Mus musculus,3|3, DSA08345,GSE63175,GPL19146,479,Diabetes;Obesity,,Liver,GEO,Microarray,Mus musculus,2|3, DSA08346,GSE63175,GPL19146,1000,Diabetes;Obesity,,Liver,GEO,Microarray,Mus musculus,3|3, DSA08347,GSE63175,GPL19146,1,Diabetes;Obesity,,Liver,GEO,Microarray,Mus musculus,3|3, DSA08348,GSE63175,GPL19146,33,Diabetes;Obesity,,Liver,GEO,Microarray,Mus musculus,3|3, DSA08349,GSE63175,GPL19146,0,Diabetes;Obesity,,Liver,GEO,Microarray,Mus musculus,3|3, DSA08350,GSE63175,GPL19146,1,Diabetes;Obesity,,Liver,GEO,Microarray,Mus musculus,3|3, DSA08351,GSE63175,GPL19146,0,Diabetes;Obesity,,Liver,GEO,Microarray,Mus musculus,3|3, DSA08352,GSE63176,GPL19146,1000,Diabetes;Obesity,,Skeletal muscle,GEO,Microarray,Mus musculus,3|3, DSA08353,GSE63176,GPL19146,0,Diabetes;Obesity,,Skeletal muscle,GEO,Microarray,Mus musculus,3|3, DSA08354,GSE63176,GPL19146,0,Diabetes;Obesity,,Skeletal muscle,GEO,Microarray,Mus musculus,3|3, DSA08355,GSE63176,GPL19146,168,Diabetes;Obesity,,Skeletal muscle,GEO,Microarray,Mus musculus,3|3, DSA08356,GSE63176,GPL19146,0,Diabetes;Obesity,,Skeletal muscle,GEO,Microarray,Mus musculus,3|3, DSA08357,GSE63176,GPL19146,1,Diabetes;Obesity,,Skeletal muscle,GEO,Microarray,Mus musculus,3|3, DSA08358,GSE63176,GPL19146,53,Diabetes;Obesity,,Skeletal muscle,GEO,Microarray,Mus musculus,3|3, DSA08359,GSE148552,GPL18573,1000,Melanoma,C0025202,Skin,GEO,RNA-Seq,Homo sapiens,9|15,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA08360,GSE63176,GPL19146,0,Diabetes;Obesity,,Skeletal muscle,GEO,Microarray,Mus musculus,3|3, DSA08361,GSE63176,GPL19146,0,Diabetes;Obesity,,Skeletal muscle,GEO,Microarray,Mus musculus,3|3, DSA08362,GSE63177,GPL19146,1000,Diabetes;Obesity,,Spleen,GEO,Microarray,Mus musculus,3|3, DSA08363,GSE63177,GPL19146,0,Diabetes;Obesity,,Spleen,GEO,Microarray,Mus musculus,3|3, DSA08364,GSE63177,GPL19146,767,Diabetes;Obesity,,Spleen,GEO,Microarray,Mus musculus,3|3, DSA08365,GSE63177,GPL19146,591,Diabetes;Obesity,,Spleen,GEO,Microarray,Mus musculus,3|3, DSA08366,GSE63177,GPL19146,1000,Diabetes;Obesity,,Spleen,GEO,Microarray,Mus musculus,3|3, DSA08367,GSE63177,GPL19146,1000,Diabetes;Obesity,,Spleen,GEO,Microarray,Mus musculus,3|3, DSA08368,GSE63177,GPL19146,0,Diabetes;Obesity,,Spleen,GEO,Microarray,Mus musculus,2|2, DSA08369,GSE63177,GPL19146,0,Diabetes;Obesity,,Spleen,GEO,Microarray,Mus musculus,3|3, DSA08370,GSE63177,GPL19146,0,Diabetes;Obesity,,Spleen,GEO,Microarray,Mus musculus,3|3, DSA08371,GSE63177,GPL19146,0,Diabetes;Obesity,,Spleen,GEO,Microarray,Mus musculus,3|3, DSA08372,GSE63177,GPL19146,0,Diabetes;Obesity,,Spleen,GEO,Microarray,Mus musculus,3|3, DSA08373,GSE63357,GPL570,131,Pituitary Adenoma,C0032019,Pituitary gland,GEO,Microarray,Homo sapiens,5|5,DO:An endocrine gland cancer located_in the pituitary gland located at the base of the brain. DSA08374,GSE63357,GPL570,1000,Pituitary Adenoma,C0032019,Pituitary gland,GEO,Microarray,Homo sapiens,5|11,DO:An endocrine gland cancer located_in the pituitary gland located at the base of the brain. DSA08375,GSE63574,GPL13912,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Mus musculus,4|5,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA08376,GSE63876,GPL11180,1,Lymphocytic Choriomeningitis,C0024266,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A viral infectious disease that results in infection located in brain, or located in meninges, or located in brain and meninges, has_material_basis_in Lymphocytic choriomeningitis virus, which is transmitted by common house mouse, Mus musculus. The infection has symptom fever, has symptom lack of appetite, has symptom headache, has symptom muscle aches, has symptom malaise, has symptom nausea, and has symptom vomiting." DSA08377,GSE63876,GPL11180,1000,Lymphocytic Choriomeningitis,C0024266,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A viral infectious disease that results in infection located in brain, or located in meninges, or located in brain and meninges, has_material_basis_in Lymphocytic choriomeningitis virus, which is transmitted by common house mouse, Mus musculus. The infection has symptom fever, has symptom lack of appetite, has symptom headache, has symptom muscle aches, has symptom malaise, has symptom nausea, and has symptom vomiting." DSA08378,GSE64004,GPL1261,2,Depression,C0011581,Teminal ileum,GEO,Microarray,Mus musculus,5|5,DO:A mood disorder that involves the presence of a low mood almost daily over a span of at least two years. DSA08379,GSE64498,GPL13912,0,Sepsis,C0243026,Bone marrow,GEO,Microarray,Mus musculus,4|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08380,GSE64640,GPL6246,1000,Duodenal Tumor,C0013291,Duodenum,GEO,Microarray,Mus musculus,5|6,DO:A small intestine cancer that is located_in the beginning section of the small intestine. DSA08381,GSE64734,GPL10333,0,Stress,C0038443,Prefrontal cortex,GEO,Microarray,Mus musculus,3|2,MSH:Stress wherein emotional factors predominate. DSA08382,GSE64734,GPL10333,0,Stress,C0038443,Prefrontal cortex,GEO,Microarray,Mus musculus,3|2,MSH:Stress wherein emotional factors predominate. DSA08383,GSE64734,GPL10333,0,Stress,C0038443,Prefrontal cortex,GEO,Microarray,Mus musculus,3|2,MSH:Stress wherein emotional factors predominate. DSA08384,GSE64734,GPL10333,0,Stress,C0038443,Prefrontal cortex,GEO,Microarray,Mus musculus,3|2,MSH:Stress wherein emotional factors predominate. DSA08385,GSE64798,GPL8833,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,4|8,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08386,GSE64798,GPL8833,556,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,4|8,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08387,GSE64798,GPL8833,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,4|8,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08388,GSE64798,GPL8833,121,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,3|7,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08389,GSE64798,GPL8833,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,3|8,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08390,GSE64798,GPL8833,855,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,4|8,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08391,GSE64799,GPL8833,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08392,GSE64799,GPL8833,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08393,GSE64799,GPL8833,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08394,GSE64799,GPL8833,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08395,GSE64799,GPL8833,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,2|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08396,GSE64799,GPL8833,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08397,GSE65055,GPL17930,1,Trisomy 13,C0152095,,GEO,Microarray,Homo sapiens,9|2,"MONDO:Trisomy 13 is a chromosomal anomaly caused by the presence of an extra chromosome 13 and is characterized by brain malformations (holoprosencephaly), facial dysmorphism, ocular anomalies, postaxial polydactyly, visceral malformations (cardiopathy) and severe psychomotor retardation." DSA08398,GSE65055,GPL17930,1,Trisomy 18,C4317091,,GEO,Microarray,Homo sapiens,9|2,DO:A chromosomal duplciation syndrome that is characterized by slow growth before birth and a low birth weight and that has_material_basis_in three copies of chromosome 18. DSA08399,GSE65055,GPL17930,0,Down Syndrome,C0013080,,GEO,Microarray,Homo sapiens,5|5,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA08400,GSE65075,GPL16570,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,5|5,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08401,GSE65107,GPL16791,303,Lymphocytic Colitis,C0400822,Colorectum,GEO,RNA-Seq,Homo sapiens,2|4,DO:A colitis characterized by an accumulation of lymphocytes in the colonic epithelium and connective tissue (lamina propria). DSA08402,GSE65893,GPL6885,0,Salmonella Infection Nos,C0036117,Spleen,GEO,Microarray,Mus musculus,3|3,MONDO:Infections with bacteria of the genus salmonella. DSA08403,GSE65893,GPL6885,25,Salmonella Infection Nos,C0036117,Spleen,GEO,Microarray,Mus musculus,3|3,MONDO:Infections with bacteria of the genus salmonella. DSA08404,GSE65893,GPL6885,0,Salmonella Infection Nos,C0036117,Spleen,GEO,Microarray,Mus musculus,3|3,MONDO:Infections with bacteria of the genus salmonella. DSA08405,GSE65893,GPL6885,51,Salmonella Infection Nos,C0036117,Spleen,GEO,Microarray,Mus musculus,3|3,MONDO:Infections with bacteria of the genus salmonella. DSA08406,GSE65893,GPL6885,52,Salmonella Infection Nos,C0036117,Spleen,GEO,Microarray,Mus musculus,3|3,MONDO:Infections with bacteria of the genus salmonella. DSA08407,GSE171809,GPL18573,127,Acute Alcoholic Hepatitis,C0001306,,GEO,RNA-Seq,Homo sapiens,3|7,MONDO:Acute hepatitis resulting from ingestion of alcohol. DSA08408,GSE173160,GPL24676,0,Polycystic Ovary Syndrome,C0032460,,GEO,RNA-Seq,Homo sapiens,6|6,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA08409,GSE212719,GPL24676,1000,Irritable Bowel Syndrome With Diarrhea,C0348898,Intestinal tissue,GEO,RNA-Seq,Homo sapiens,4|3, DSA08410,GSE144302,GPL16791,1000,Eosinophilic Granulomatosis With Polyangiitis,C0008728,Lung,GEO,RNA-Seq,Homo sapiens,4|3,"DO:A vasculitits that is systemic vasculitis realized as blood vessel inflammation and has_symptom asthma along with hay fever, rash and gastrointestinal bleeding." DSA08411,GSE137420,GPL18573,1000,Juvenile Neuronal Ceroid Lipofuscinosis,C0751383,,GEO,RNA-Seq,Homo sapiens,6|6,"DO:A neuronal ceroid lipofuscinosis that is characterized by autosomal dominant inhetitance, onset of symptoms (psychiatric manifestations, seizures, cerebellar ataxia, and cognitive decline) in adulthood and has_material_basis_in heterozygous mutation in the DNAJC5 gene (611203) on chromosome 20q13." DSA08412,GSE136198,GPL16699,0,Microtia,C3850155,,GEO,Microarray,Homo sapiens,4|3,MSH:Malformation of external portion of EAR AURICLE. DSA08413,GSE136198,GPL16699,0,Microtia,C3850155,,GEO,Microarray,Homo sapiens,4|4,MSH:Malformation of external portion of EAR AURICLE. DSA08414,GSE142591,GPL20301,1000,Age Related Macular Degeneration,C0242383,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision. DSA08415,GSE66141,GPL1261,0,Otitis Media,C0029882,Middle ear,GEO,Microarray,Mus musculus,2|2,DO:A otitis which involves inflammation of the middle ear. DSA08416,GSE66141,GPL1261,0,Otitis Media,C0029882,Middle ear,GEO,Microarray,Mus musculus,2|2,DO:A otitis which involves inflammation of the middle ear. DSA08417,GSE66141,GPL1261,0,Otitis Media,C0029882,Middle ear,GEO,Microarray,Mus musculus,2|2,DO:A otitis which involves inflammation of the middle ear. DSA08418,GSE66141,GPL1261,0,Otitis Media,C0029882,Middle ear,GEO,Microarray,Mus musculus,2|2,DO:A otitis which involves inflammation of the middle ear. DSA08419,GSE66141,GPL1261,0,Otitis Media,C0029882,Middle ear,GEO,Microarray,Mus musculus,2|2,DO:A otitis which involves inflammation of the middle ear. DSA08420,GSE66141,GPL1261,0,Otitis Media,C0029882,Middle ear,GEO,Microarray,Mus musculus,2|2,DO:A otitis which involves inflammation of the middle ear. DSA08421,GSE66141,GPL1261,0,Otitis Media,C0029882,Middle ear,GEO,Microarray,Mus musculus,2|2,DO:A otitis which involves inflammation of the middle ear. DSA08422,GSE66405,GPL17077,1000,Wilms Tumor,C2930471,Kidney,GEO,Microarray,Homo sapiens,4|15,"MSH:A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN." DSA08423,GSE66405,GPL17077,1000,Wilms Tumor,C2930471,Kidney,GEO,Microarray,Homo sapiens,4|1,"MSH:A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN." DSA08424,GSE66405,GPL17077,1000,Wilms Tumor,C2930471,Kidney,GEO,Microarray,Homo sapiens,4|4,"MSH:A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN." DSA08425,GSE66405,GPL17077,1000,Wilms Tumor,C2930471,Kidney,GEO,Microarray,Homo sapiens,4|5,"MSH:A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN." DSA08426,GSE66405,GPL17077,1000,Wilms Tumor,C2930471,Kidney,GEO,Microarray,Homo sapiens,4|1,"MSH:A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN." DSA08427,GSE66405,GPL17077,1000,Wilms Tumor,C2930471,Kidney,GEO,Microarray,Homo sapiens,4|1,"MSH:A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN." DSA08428,GSE66405,GPL17077,1000,Wilms Tumor,C2930471,Kidney,GEO,Microarray,Homo sapiens,4|1,"MSH:A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN." DSA08429,GSE67241,GPL6885,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,2|4,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08430,GSE67241,GPL6885,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,2|4,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08431,GSE67316,GPL1261,1000,Hepatoblastoma,C0206624,Liver,GEO,Microarray,Mus musculus,6|6,DO:A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver. DSA08432,GSE67316,GPL1261,25,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Mus musculus,6|6,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA08433,GSE67688,GPL13112,1000,Vulvovaginal Candidiasis,C0006852,Vagina,GEO,RNA-Seq,Mus musculus,1|3,"DO:A candidiasis that involves fungal infection of the vaginal mucous membranes in women caused by Candida albicans. The symptoms include intense vulval pruritus, burning, erythema and dyspareunia associated with a creamy white, curd-like discharge." DSA08434,GSE67815,GPL6246,0,Cardiac Hypertrophy,C1383860,Heart,GEO,Microarray,Mus musculus,3|2,"EFO:an increase in size of the cardiac tissue, not due to increased cell number" DSA08435,GSE141455,GPL17400,457,Polyuria,C0032617,Kidney,GEO,Microarray,Mus musculus,3|3,HPO:An increased rate of urine production. DSA08436,GSE68750,GPL16570,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Mus musculus,5|5,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA08437,GSE68750,GPL16570,947,Psoriasis,C0033860,Skin,GEO,Microarray,Mus musculus,5|5,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA08438,GSE69201,GPL13112,38,Myocardial Infarction,C0027051,Heart,GEO,RNA-Seq,Mus musculus,3|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA08439,GSE69201,GPL13112,1000,Myocardial Infarction,C0027051,Heart,GEO,RNA-Seq,Mus musculus,3|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA08440,GSE69345,GPL1261,1000,Sepsis,C0243026,,GEO,Microarray,Mus musculus,4|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08441,GSE69345,GPL1261,0,Sepsis,C0243026,,GEO,Microarray,Mus musculus,4|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08442,GSE69345,GPL1261,328,Sepsis,C0243026,,GEO,Microarray,Mus musculus,4|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08443,GSE69359,GPL8321,806,Medulloblastoma,C0025149,,GEO,Microarray,Mus musculus,3|3,DO:An infratentorial cancer that is located_in the lower part of the brain and is a type of primitive neuroectodermal tumor. DSA08444,GSE70123,GPL17021,77,Insulin Resistance,C0021655,White adipose tissue,GEO,RNA-Seq,Mus musculus,3|3,EFO:diminished effectiveness of insulin in lowering plasma glucose levels DSA08445,GSE70418,GPL1261,1000,Polytrauma,,,GEO,Microarray,Mus musculus,4|4, DSA08446,GSE70418,GPL1261,1000,Polytrauma,,,GEO,Microarray,Mus musculus,4|4, DSA08447,GSE70418,GPL1261,0,Polytrauma,,,GEO,Microarray,Mus musculus,4|6, DSA08448,GSE70418,GPL1261,1000,Polytrauma,,,GEO,Microarray,Mus musculus,4|3, DSA08449,GSE70418,GPL1261,1000,Polytrauma,,,GEO,Microarray,Mus musculus,4|4, DSA08450,GSE70418,GPL1261,1000,Polytrauma,,,GEO,Microarray,Mus musculus,4|4, DSA08451,GSE70418,GPL1261,1000,Polytrauma,,Bone marrow,GEO,Microarray,Mus musculus,4|4, DSA08452,GSE70418,GPL1261,842,Polytrauma,,Bone marrow,GEO,Microarray,Mus musculus,4|4, DSA08453,GSE70418,GPL1261,82,Polytrauma,,Bone marrow,GEO,Microarray,Mus musculus,4|4, DSA08454,GSE70418,GPL1261,0,Polytrauma,,Bronchus,GEO,Microarray,Mus musculus,4|5, DSA08455,GSE70418,GPL1261,0,Polytrauma,,Bronchus,GEO,Microarray,Mus musculus,4|4, DSA08456,GSE70544,GPL11154,1000,Kidney Injury,C2609414,,GEO,RNA-Seq,Homo sapiens,1|3,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA08457,GSE71363,GPL570,1000,Breast Cancer,C0678222,,GEO,Microarray,Homo sapiens,2|4,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08458,GSE71363,GPL570,1000,Breast Cancer,C0678222,,GEO,Microarray,Homo sapiens,2|4,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08459,GSE71363,GPL570,1000,Breast Cancer,C0678222,,GEO,Microarray,Homo sapiens,2|4,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08460,GSE71534,GPL17021,174,Hypercholesterolemia,C0020443,Aortic valve,GEO,RNA-Seq,Mus musculus,2|4,HPO:An increased concentration of cholesterol in the blood. DSA08461,GSE71534,GPL17021,5,Hypertension,C0020538,Aortic valve,GEO,RNA-Seq,Mus musculus,2|4,DO:An artery disease characterized by chronic elevated blood pressure in the arteries. DSA08462,GSE72227,GPL6885,263,Type 1 Diabetes,C0011854,Hypothalamus,GEO,Microarray,Mus musculus,2|3,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA08463,GSE72227,GPL6885,249,Type 1 Diabetes,C0011854,Hypothalamus,GEO,Microarray,Mus musculus,2|3,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA08464,GSE72874,GPL10558,1000,Adenocarcinoma of Esophagus,C0279628,Esophagus,GEO,Microarray,Homo sapiens,10|34,DO:An esophageal carcinoma that derives_from epithelial cells of glandular origin. DSA08465,GSE72874,GPL10558,1000,Adenocarcinoma of Esophagus,C0279628,Stomach,GEO,Microarray,Homo sapiens,7|14,DO:An esophageal carcinoma that derives_from epithelial cells of glandular origin. DSA08466,GSE73402,GPL17077,0,Lung Squamous Cell Carcinoma,C0149782,Lung,GEO,Microarray,Homo sapiens,5|18,DO:A non-small cell lung carcinoma that has_material_basis_in the squamous cell. DSA08467,GSE73402,GPL17077,0,Lung Squamous Cell Carcinoma,C0149782,Lung,GEO,Microarray,Homo sapiens,5|11,DO:A non-small cell lung carcinoma that has_material_basis_in the squamous cell. DSA08468,GSE73402,GPL17077,1000,Lung Squamous Cell Carcinoma,C0149782,Lung,GEO,Microarray,Homo sapiens,5|13,DO:A non-small cell lung carcinoma that has_material_basis_in the squamous cell. DSA08469,GSE73402,GPL17077,459,Lung Squamous Cell Carcinoma,C0149782,Lung,GEO,Microarray,Homo sapiens,5|8,DO:A non-small cell lung carcinoma that has_material_basis_in the squamous cell. DSA08470,GSE73402,GPL17077,58,Lung Squamous Cell Carcinoma,C0149782,Lung,GEO,Microarray,Homo sapiens,5|7,DO:A non-small cell lung carcinoma that has_material_basis_in the squamous cell. DSA08471,GSE74604,GPL6104,1000,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,30|30,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA08472,GSE75091,GPL10558,0,Obesity,C0028754,,GEO,Microarray,Homo sapiens,13|11,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA08473,GSE140201,GPL17021,118,Prediabetes,C0362046,Sciatic nerve,GEO,RNA-Seq,Mus musculus,5|7,"DO:A glucose metabolism disease that is characterized by blood glucose levels are high, but not high enough to be classified as type 2 diabetes." DSA08474,GSE140201,GPL17021,330,Prediabetes,C0362046,Sciatic nerve,GEO,RNA-Seq,Mus musculus,8|7,"DO:A glucose metabolism disease that is characterized by blood glucose levels are high, but not high enough to be classified as type 2 diabetes." DSA08475,GSE140201,GPL17021,52,Type 2 Diabetes,C0011860,Sciatic nerve,GEO,RNA-Seq,Mus musculus,5|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA08476,GSE75300,GPL9250,1000,Malignant Glioma,C0555198,Brain,GEO,RNA-Seq,Mus musculus,1|6,DO:A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine. DSA08477,GSE140201,GPL17021,62,Type 2 Diabetes,C0011860,Sciatic nerve,GEO,RNA-Seq,Mus musculus,8|8,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA08478,GSE106897,GPL17021,207,Cardiac Hypertrophy,C1383860,Heart,GEO,RNA-Seq,Mus musculus,2|2,"EFO:an increase in size of the cardiac tissue, not due to increased cell number" DSA08479,GSE103166,GPL23961,141,Asthma,C0004096,,GEO,Microarray,Homo sapiens,31|56,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08480,GSE75524,GPL11154,702,Multiple Suture Craniosynostosis,C4021161,,GEO,RNA-Seq,Homo sapiens,6|15,"HPO:Craniosynostosis involving at least 2 cranial sutures, where the exact pattern of sutures fused has not been precisely specified." DSA08481,GSE75677,GPL13112,1000,Liver Tumor,C0345904,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA08482,GSE75815,GPL6887,55,Hypertension,C0020538,Superior mesenteric artery,GEO,Microarray,Mus musculus,5|6,DO:An artery disease characterized by chronic elevated blood pressure in the arteries. DSA08483,GSE75815,GPL6887,1000,Hypertension,C0020538,Thoracic aorta,GEO,Microarray,Mus musculus,3|3,DO:An artery disease characterized by chronic elevated blood pressure in the arteries. DSA08484,GSE75815,GPL6887,23,Hypertension,C0020538,Abdominal aorta,GEO,Microarray,Mus musculus,3|3,DO:An artery disease characterized by chronic elevated blood pressure in the arteries. DSA08485,GSE76049,GPL15520,1000,Colorectal Carcinoma,C0009402,Colon,GEO,RNA-Seq,Homo sapiens,1|2,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA08486,GSE76062,GPL13112,1000,Liver Tumor,C0345904,Liver,GEO,RNA-Seq,Mus musculus,6|16,DO:A hepatobiliary system cancer that is located_in the liver. DSA08487,GSE76062,GPL13112,1000,Liver Tumor,C0345904,Liver,GEO,RNA-Seq,Mus musculus,6|8,DO:A hepatobiliary system cancer that is located_in the liver. DSA08488,GSE76062,GPL13112,1000,Liver Tumor,C0345904,Liver,GEO,RNA-Seq,Mus musculus,6|11,DO:A hepatobiliary system cancer that is located_in the liver. DSA08489,GSE83865,GPL13112,1000,Liver Tumor,C0345904,Liver,GEO,RNA-Seq,Mus musculus,3|8,DO:A hepatobiliary system cancer that is located_in the liver. DSA08490,GSE84663,GPL6885,118,Diabetes,C0011847,,GEO,Microarray,Mus musculus,4|4,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA08491,GSE84663,GPL6885,0,Diabetes,C0011847,,GEO,Microarray,Mus musculus,4|4,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA08492,GSE84917,GPL16570,1000,Mammary Tumor,C1512981,Breast,GEO,Microarray,Mus musculus,3|3,NCI:Production of a new growth or growths in the mammary gland. DSA08493,GSE84917,GPL16570,0,Mammary Tumor,C1512981,Breast,GEO,Microarray,Mus musculus,3|3,NCI:Production of a new growth or growths in the mammary gland. DSA08494,GSE110512,GPL20301,1000,Dengue Disease,C0011311,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A viral infectious disease that results in infection, has_material_basis_in Dengue virus" DSA08495,GSE117898,GPL1261,0,Allergy,C1527304,Peyer's Patches,GEO,Microarray,Mus musculus,1|2,"DO:An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods." DSA08496,GSE117898,GPL1261,0,Allergy,C1527304,Peyer's Patches,GEO,Microarray,Mus musculus,1|4,"DO:An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods." DSA08497,GSE85955,GPL18535,1000,Circulating Tumor,,,GEO,Microarray,Mus musculus,3|3, DSA08498,GSE85955,GPL18535,1000,Circulating Tumor,,,GEO,Microarray,Mus musculus,3|3, DSA08499,GSE8642,GPL339,0,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Mus musculus,6|6,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA08500,GSE86501,GPL11180,1000,Alveolar Soft Part Sarcoma,C0206657,,GEO,Microarray,Mus musculus,4|19,DO:A soft tissue cancer that is a slow growing tumor of an unknown origin that effects children and effects young adults. DSA08501,GSE86522,GPL16686,1000,Non-Small Cell Lung Cancer,C0007131,,GEO,Microarray,Homo sapiens,3|3,DO:A respiratory system cancer that is located_in the lung. DSA08502,GSE86917,GPL6244,1000,Prostate Cancer,C0600139,,GEO,Microarray,Homo sapiens,2|2,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08503,GSE87025,GPL6887,1000,Acute Kidney Injury,C2609414,Kidney,GEO,Microarray,Mus musculus,6|12,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA08504,GSE93167,GPL17021,1000,Facioscapulohumeral Dystrophy,C0238288,,GEO,RNA-Seq,Mus musculus,3|3,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA08505,GSE87266,GPL17021,1000,Facioscapulohumeral Dystrophy,C0238288,,GEO,RNA-Seq,Mus musculus,3|3,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA08506,GSE87266,GPL17021,1000,Facioscapulohumeral Dystrophy,C0238288,,GEO,RNA-Seq,Mus musculus,3|3,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA08507,GSE87266,GPL17021,1000,Facioscapulohumeral Dystrophy,C0238288,,GEO,RNA-Seq,Mus musculus,3|3,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA08508,GSE85461,GPL18460,1000,Facioscapulohumeral Dystrophy,C0238288,Immortalized primary myoblasts,GEO,RNA-Seq,Homo sapiens,3|3,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA08509,GSE75793,GPL16686,349,Pulmonary Hypertension,C0020542,,GEO,Microarray,Homo sapiens,6|6,"DO:A hypertension characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein or pulmonary capillaries." DSA08510,GSE75699,GPL11154,1000,Influenza,C0021400,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08511,GSE88804,GPL6244,1000,Adenoid Cystic Carcinoma,C0010606,Lacrimal gland,GEO,Microarray,Homo sapiens,7|13,DO:An adenocarcinoma that is characterized by bands or cylinders of hyalinized or mucinous stroma separating or surrounded by nests or cords of small epithelial cells. DSA08512,GSE88804,GPL6244,1000,Adenoid Cystic Carcinoma,C0010606,Lung,GEO,Microarray,Homo sapiens,7|2,DO:An adenocarcinoma that is characterized by bands or cylinders of hyalinized or mucinous stroma separating or surrounded by nests or cords of small epithelial cells. DSA08513,GSE169717,GPL24247,437,Mir-424/503 Deficiency,,Bone marrow,GEO,RNA-Seq,Mus musculus,3|3, DSA08514,GSE169717,GPL24247,1000,Mir-424/503 Deficiency,,Bone marrow,GEO,RNA-Seq,Mus musculus,3|3, DSA08515,GSE171874,GPL21103,1000,Injury of Liver,C0160390,Liver,GEO,RNA-Seq,Mus musculus,2|2,NCI:Damage to liver structure or function due to trauma or toxicity. DSA08516,GSE171878,GPL24247,1000,Squamous Cell Carcinoma,C0007137,,GEO,RNA-Seq,Mus musculus,2|2,DO:A carcinoma that derives_from squamous epithelial cells. DSA08517,GSE172297,GPL24247,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,1|1,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA08518,GSE75699,GPL11154,1000,Influenza,C0021400,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08519,GSE173900,GPL21697,685,Keloid,C0022548,Skin,GEO,RNA-Seq,Homo sapiens,4|4,"EFO:An irregularly shaped, elevated mark on the skin caused by deposits of excessive amounts of collagen during wound healing. It extends beyond the original boundaries of the wound and may enlarge progressively." DSA08520,GSE173963,GPL6887,1,Liver Neoplasm,C0023903,Liver,GEO,Microarray,Mus musculus,9|5,DO:A hepatobiliary system cancer that is located_in the liver. DSA08521,GSE173963,GPL6887,1000,Liver Tumor,C0345904,Liver,GEO,Microarray,Mus musculus,9|1,DO:A hepatobiliary system cancer that is located_in the liver. DSA08522,GSE173963,GPL6887,0,Liver Neoplasm,C0023903,Liver,GEO,Microarray,Mus musculus,9|5,DO:A hepatobiliary system cancer that is located_in the liver. DSA08523,GSE173963,GPL6887,1000,Liver Tumor,C0345904,Liver,GEO,Microarray,Mus musculus,9|5,DO:A hepatobiliary system cancer that is located_in the liver. DSA08524,GSE84429,GPL6246,0,Hepatitis B,C0019163,Liver,GEO,Microarray,Mus musculus,3|3,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus, which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice." DSA08525,GSE84429,GPL6246,1000,Hepatitis B,C0019163,Liver,GEO,Microarray,Mus musculus,3|3,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus, which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice." DSA08526,GSE84429,GPL6246,1000,Hepatitis B,C0019163,Liver,GEO,Microarray,Mus musculus,3|3,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus, which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice." DSA08527,GSE174382,GPL24247,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Mus musculus,4|5,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA08528,GSE174382,GPL24247,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Mus musculus,4|5,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA08529,GSE174430,GPL28457,842,Spared Nerve Injury,,Dorsal root ganglion,GEO,scRNA-Seq,Mus musculus,1|1, DSA08530,GSE174430,GPL28457,1000,Spared Nerve Injury,,Dorsal root ganglion,GEO,scRNA-Seq,Mus musculus,1|1, DSA08531,GSE174540,GPL21103,1000,Pleomorphic Sarcoma,,Contralateral muscle,GEO,RNA-Seq,Mus musculus,2|3, DSA08532,GSE178663,GPL19057,283,Colitis,C0009319,Intestine,GEO,RNA-Seq,Mus musculus,2|2,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA08533,GSE178930,GPL19057,1000,Spinal Cord Disorder,C0037928,Spinal cord,GEO,RNA-Seq,Mus musculus,3|3,EFO:A disease involving the spinal cord. DSA08534,GSE179098,GPL30215,1000,Injury of Liver,C0160390,Liver,GEO,RNA-Seq,Mus musculus,3|3,NCI:Damage to liver structure or function due to trauma or toxicity. DSA08535,GSE179102,GPL28457,1000,Obesity,C0028754,Visceral white adipose tissue,GEO,RNA-Seq,Mus musculus,3|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA08536,GSE179102,GPL28457,1000,Obesity,C0028754,Visceral white adipose tissue,GEO,RNA-Seq,Mus musculus,3|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA08537,GSE179125,GPL21163,0,Liver Tumor,C0345904,Liver,GEO,Microarray,Mus musculus,3|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA08538,GSE179125,GPL21163,0,Liver Tumor,C0345904,Liver,GEO,Microarray,Mus musculus,3|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA08539,GSE179135,GPL24676,1000,Microtia,C3850155,Auricular cartilage,GEO,scRNA-Seq,Homo sapiens,6|3,MSH:Malformation of external portion of EAR AURICLE. DSA08540,GSE179231,GPL24247,1000,Type 2 Diabetes,C0011860,Lacrimal gland,GEO,RNA-Seq,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA08541,GSE179782,GPL21103,1000,Liver Cirrhosis,C0023890,Liver,GEO,RNA-Seq,Mus musculus,2|4,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA08542,GSE179782,GPL21103,67,Liver Cirrhosis,C0023890,Liver,GEO,RNA-Seq,Mus musculus,2|4,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA08543,GSE179782,GPL21103,1000,Liver Cirrhosis,C0023890,Liver,GEO,RNA-Seq,Mus musculus,1|4,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA08544,GSE179782,GPL21103,1000,Liver Cirrhosis,C0023890,Liver,GEO,RNA-Seq,Mus musculus,1|3,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA08545,GSE179782,GPL21103,766,Liver Cirrhosis,C0023890,Liver,GEO,RNA-Seq,Mus musculus,2|4,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA08546,GSE179782,GPL21103,206,Liver Cirrhosis,C0023890,Liver,GEO,RNA-Seq,Mus musculus,2|3,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA08547,GSE179782,GPL21103,552,Liver Cirrhosis,C0023890,Liver,GEO,RNA-Seq,Mus musculus,2|3,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA08548,GSE179782,GPL21103,381,Liver Cirrhosis,C0023890,Liver,GEO,RNA-Seq,Mus musculus,2|3,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA08549,GSE180008,GPL19057,1000,Severe Periodontitis,C4025886,Bone marrow,GEO,RNA-Seq,Mus musculus,3|3,HPO:A severe form of periodontitis. DSA08550,GSE180169,GPL21103,1000,Pulmonary Arterial Hypertension,C2973725,Lung,GEO,RNA-Seq,Mus musculus,5|4,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA08551,GSE180189,GPL21163,139,Obesity,C0028754,Liver,GEO,Microarray,Mus musculus,4|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA08552,GSE70852,GPL16368,529,Diabetic Peripheral Neuropathy,C0740447,Sciatic nerve,GEO,Microarray,Mus musculus,5|5, DSA08553,GSE70852,GPL16368,1000,Diabetic Peripheral Neuropathy,C0740447,Dorsal root ganglion,GEO,Microarray,Mus musculus,5|5, DSA08554,GSE180317,GPL21103,1000,Beta-Cell Dysfunction,C1969875,Pancreatic islet,GEO,RNA-Seq,Mus musculus,4|4, DSA08555,GSE180476,GPL23038,1000,Kidney Injury,C2609414,Kidney,GEO,Microarray,Mus musculus,4|4,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA08556,GSE180476,GPL23038,1000,Kidney Injury,C2609414,Kidney,GEO,Microarray,Mus musculus,4|4,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA08557,GSE180763,GPL17021,6,Obesity,C0028754,Heart,GEO,RNA-Seq,Mus musculus,10|10,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA08558,GSE181246,GPL24247,908,H1N1 Influenza,C2076600,Lung,GEO,RNA-Seq,Mus musculus,4|4,"EFO:An influenza that results_in infection located_in respiratory tract of pigs and humans, has_material_basis_in Influenza C virus, or has_material_basis_in Influenza A virus subtypes (H1N1, H1N2, H3N1, H3N2, and H2N3), which are transmitted_by direct contact with infected pigs. The infection in humans has_symptom fever, has_symptom lethargy, has_symptom lack of appetite, has_symptom coughing, has_symptom runny nose, has_symptom sore throat, has_symptom nausea, has_symptom vomiting, and has_symptom diarrhea." DSA08559,GSE181246,GPL24247,516,H1N1 Influenza,C2076600,Lung,GEO,RNA-Seq,Mus musculus,4|4,"EFO:An influenza that results_in infection located_in respiratory tract of pigs and humans, has_material_basis_in Influenza C virus, or has_material_basis_in Influenza A virus subtypes (H1N1, H1N2, H3N1, H3N2, and H2N3), which are transmitted_by direct contact with infected pigs. The infection in humans has_symptom fever, has_symptom lethargy, has_symptom lack of appetite, has_symptom coughing, has_symptom runny nose, has_symptom sore throat, has_symptom nausea, has_symptom vomiting, and has_symptom diarrhea." DSA08560,GSE182132,GPL16791,1000,Endometrial Cancer,C0476089,Endometrium,GEO,RNA-Seq,Homo sapiens,1|1,DO:A uterine cancer that is located_in tissues lining the uterus. DSA08561,GSE182350,GPL18573,1000,Reactive Oxygen Injury,,Kidney,GEO,RNA-Seq,Homo sapiens,4|4, DSA08562,GSE182350,GPL18573,1000,Reactive Oxygen Injury,,Kidney,GEO,RNA-Seq,Homo sapiens,4|4, DSA08563,GSE182793,GPL21103,1000,Ischemia Reperfusion Injury,C0035126,Kidney,GEO,RNA-Seq,Mus musculus,4|4,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA08564,GSE182793,GPL21103,1000,Ischemia Reperfusion Injury,C0035126,Kidney,GEO,RNA-Seq,Mus musculus,4|4,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA08565,GSE183158,GPL17021,1000,Acute Pancreatitis,C0001339,Liver,GEO,RNA-Seq,Mus musculus,6|6,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA08566,GSE183320,GPL20301|GPL24676,1000,Age Related Macular Degeneration,C0242383,Choroid,GEO,scRNA-Seq,Homo sapiens,10|11,DO:A degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision. DSA08567,GSE79782,GPL16791,73,Pre-Eclampsia,C0032914,Amnion,GEO,RNA-Seq,Homo sapiens,11|17,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA08568,GSE183979,GPL23479,1000,Pulmonary Aspergillosis,C2350529,Lung,GEO,RNA-Seq,Mus musculus,3|3,MONDO:A aspergillosis that involves the lung. DSA08569,GSE183979,GPL23479,1000,Pulmonary Aspergillosis,C2350529,Lung,GEO,RNA-Seq,Mus musculus,3|3,MONDO:A aspergillosis that involves the lung. DSA08570,GSE184021,GPL30215,1000,Injury of Liver,C0160390,Liver,GEO,RNA-Seq,Mus musculus,3|3,NCI:Damage to liver structure or function due to trauma or toxicity. DSA08571,GSE184023,GPL30215,428,Injury of Liver,C0160390,Spleen,GEO,RNA-Seq,Mus musculus,3|3,NCI:Damage to liver structure or function due to trauma or toxicity. DSA08572,GSE82062,GPL17586,1000,Lung Carcinoma,C0684249,,GEO,Microarray,Homo sapiens,3|3,DO:A respiratory system cancer that is located_in the lung. DSA08573,GSE184390,GPL24676,13,COVID-19,D8888888,Stomach,GEO,RNA-Seq,Homo sapiens,4|4,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA08574,GSE184390,GPL24676,583,COVID-19,D8888888,Stomach,GEO,RNA-Seq,Homo sapiens,4|4,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA08575,GSE71560,GPL16791,1000,Cardiac Hypoxia,,,GEO,RNA-Seq,Homo sapiens,5|5, DSA08576,GSE76333,GPL21061,0,Hepatitis C,C0019196,,GEO,Microarray,Homo sapiens,2|2,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA08577,GSE184563,GPL24247|GPL30661|GPL30662,1000,Metabolic Diseases,C0025517,Lung,GEO,RNA-Seq,Mus musculus,2|3,DO:A disease that involving errors in metabolic processes of building or degradation of molecules. DSA08578,GSE184563,GPL24247|GPL30661|GPL30662,1000,Metabolic Diseases,C0025517,Lung,GEO,RNA-Seq,Mus musculus,3|4,DO:A disease that involving errors in metabolic processes of building or degradation of molecules. DSA08579,GSE184761,GPL6887,2,Lung Injury,C0273115,Lung,GEO,Microarray,Mus musculus,2|3,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA08580,GSE184761,GPL6887,0,Lung Injury,C0273115,Lung,GEO,Microarray,Mus musculus,1|2,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA08581,GSE184761,GPL6887,0,Lung Injury,C0273115,Lung,GEO,Microarray,Mus musculus,2|3,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA08582,GSE184995,GPL30680,2,Neonatal Hypoxic And Ischemic Brain Injury,C0752304,Cerebellum,GEO,Microarray,Mus musculus,4|4,"MONDO:A disorder caused by a lack of blood flow or gas exchange to or from the fetus in the period immediately before, during, or after the birth process." DSA08583,GSE184995,GPL30680,5,Neonatal Hypoxic And Ischemic Brain Injury,C0752304,Cortex,GEO,Microarray,Mus musculus,4|4,"MONDO:A disorder caused by a lack of blood flow or gas exchange to or from the fetus in the period immediately before, during, or after the birth process." DSA08584,GSE184995,GPL30680,15,Neonatal Hypoxic And Ischemic Brain Injury,C0752304,Striatum,GEO,Microarray,Mus musculus,4|4,"MONDO:A disorder caused by a lack of blood flow or gas exchange to or from the fetus in the period immediately before, during, or after the birth process." DSA08585,GSE185901,GPL16791,1000,Bladder Cancer,C0699885,Bladder,GEO,RNA-Seq,Homo sapiens,3|3,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08586,GSE186067,GPL20301,539,Rift Valley Fever,C0035613,,GEO,RNA-Seq,Homo sapiens,1|2,"DO:A viral infectious disease that results_in infection, has_material_basis_in Rift Valley fever virus, which is transmitted_by Aedes mosquitoes. The virus affects domestic animals (cattle, buffalo, sheep, goats, and camels) and humans. The infection has_symptom jaundice, has_symptom vomiting blood, has_symptom passing blood in the feces, has_symptom ecchymoses (caused by bleeding in the skin), has_symptom bleeding from the nose or gums, has_symptom menorrhagia and has_symptom bleeding from venepuncture sites." DSA08587,GSE186067,GPL20301,1000,Rift Valley Fever,C0035613,,GEO,RNA-Seq,Homo sapiens,1|2,"DO:A viral infectious disease that results_in infection, has_material_basis_in Rift Valley fever virus, which is transmitted_by Aedes mosquitoes. The virus affects domestic animals (cattle, buffalo, sheep, goats, and camels) and humans. The infection has_symptom jaundice, has_symptom vomiting blood, has_symptom passing blood in the feces, has_symptom ecchymoses (caused by bleeding in the skin), has_symptom bleeding from the nose or gums, has_symptom menorrhagia and has_symptom bleeding from venepuncture sites." DSA08588,GSE186067,GPL20301,1000,Rift Valley Fever,C0035613,,GEO,RNA-Seq,Homo sapiens,1|2,"DO:A viral infectious disease that results_in infection, has_material_basis_in Rift Valley fever virus, which is transmitted_by Aedes mosquitoes. The virus affects domestic animals (cattle, buffalo, sheep, goats, and camels) and humans. The infection has_symptom jaundice, has_symptom vomiting blood, has_symptom passing blood in the feces, has_symptom ecchymoses (caused by bleeding in the skin), has_symptom bleeding from the nose or gums, has_symptom menorrhagia and has_symptom bleeding from venepuncture sites." DSA08589,GSE186278,GPL28383,0,Neurogenic Inflammation,C0600467,Brain,GEO,Microarray,Mus musculus,6|6,MSH:Inflammation caused by an injurious stimulus of peripheral neurons and resulting in release of neuropeptides which affect vascular permeability and help initiate proinflammatory and immune reactions at the site of injury. DSA08590,GSE186421,GPL24247,1000,Inflammation,C0021368,Tirgeminal ganglion,GEO,RNA-Seq,Mus musculus,1|1,"MSH:A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function." DSA08591,GSE186798,GPL23038,0,Internal Carotid Artery Stenosis,C0340569,,GEO,Microarray,Mus musculus,5|5,"EFO:Carotid stenosis is a narrowing or constriction of the inner surface (lumen) of the carotid artery, usually caused by atherosclerosis. The internal carotid artery supplies the brain. Plaque often builds up at that division, and causes a narrowing (stenosis). Pieces of plaque can break off and block the small arteries above in the brain, which causes a stroke. Plaque can also build up at the origin of the carotid artery at the aorta." DSA08592,GSE186798,GPL23159,0,Dementia,C0497327,,GEO,Microarray,Homo sapiens,10|10,"DO:A cognitive disorder resulting from a loss of brain function affecting memory, thinking, language, judgement and behavior." DSA08593,GSE186798,GPL23159,0,Post-Stroke Non Dementia,,,GEO,Microarray,Homo sapiens,10|10, DSA08594,GSE186798,GPL23159,0,Dementia,C0497327,,GEO,Microarray,Homo sapiens,10|10,"DO:A cognitive disorder resulting from a loss of brain function affecting memory, thinking, language, judgement and behavior." DSA08595,GSE186798,GPL23159,1,Post-Stroke Non Dementia,,,GEO,Microarray,Homo sapiens,10|10, DSA08596,GSE186798,GPL23159,0,Dementia,C0497327,,GEO,Microarray,Homo sapiens,10|10,"DO:A cognitive disorder resulting from a loss of brain function affecting memory, thinking, language, judgement and behavior." DSA08597,GSE186798,GPL23159,0,Post-Stroke Non Dementia,,,GEO,Microarray,Homo sapiens,10|10, DSA08598,GSE187015,GPL13112,1000,Granulosa Cell Tumor,C0018206,Ovary,GEO,RNA-Seq,Mus musculus,5|5,DO:A sex cord-gonadal stromal tumor that has_material_basis_in granulosa cells and arises from the sex cord stroma. DSA08599,GSE188554,GPL24676,1000,Undifferentiated Soft Tissue Sarcoma,C2188153,Kidney,GEO,RNA-Seq,Homo sapiens,1|1,"NCI:A term that refers to a heterogeneous group of uncommon soft tissue sarcomas that do not show an identifiable line of differentiation using currently available technologies. This is a diagnosis of exclusion and includes undifferentiated pleomorphic sarcoma (also known as malignant fibrous histiocytoma), undifferentiated spindle cell sarcoma, undifferentiated round cell sarcoma, and undifferentiated epithelioid sarcoma." DSA08600,GSE189015,GPL24247,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Mus musculus,4|4,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA08601,GSE189221,GPL23038,1000,Lymphoma,C0024299,Spleen,GEO,Microarray,Mus musculus,4|4,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA08602,GSE189327,GPL23479,435,Lung Cysts,,Lung,GEO,RNA-Seq,Mus musculus,3|3, DSA08603,GSE189330,GPL21626,0,Behavioral Abnormality,C0233514,Amygdala,GEO,RNA-Seq,Mus musculus,8|8,"HPO:An abnormality of mental functioning including various affective, behavioral, cognitive, and perceptual abnormalities." DSA08604,GSE189409,GPL24247,1000,Liver Cirrhosis,C0023890,Liver,GEO,RNA-Seq,Mus musculus,3|3,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA08605,GSE189530,GPL17021,1000,Kidney Damage,C1408258,Kidney,GEO,RNA-Seq,Mus musculus,6|6,HPO:A nonspecific term referring to disease or damage of the kidneys. DSA08606,GSE189530,GPL17021,1000,Kidney Damage,C1408258,Kidney,GEO,RNA-Seq,Mus musculus,6|6,HPO:A nonspecific term referring to disease or damage of the kidneys. DSA08607,GSE189530,GPL17021,301,Kidney Damage,C1408258,Kidney,GEO,RNA-Seq,Mus musculus,6|6,HPO:A nonspecific term referring to disease or damage of the kidneys. DSA08608,GSE189530,GPL17021,1000,Kidney Damage,C1408258,Kidney,GEO,RNA-Seq,Mus musculus,6|6,HPO:A nonspecific term referring to disease or damage of the kidneys. DSA08609,GSE78730,GPL13112,1000,Amyotrophic Lateral Sclerosis,C0002736,Brain,GEO,RNA-Seq,Mus musculus,5|10,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA08610,GSE78730,GPL13112,1000,Amyotrophic Lateral Sclerosis,C0002736,Brain,GEO,RNA-Seq,Mus musculus,5|9,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA08611,GSE70422,GPL14951,0,Sudden Infant Death Syndrome,C0038644,Brain,GEO,Microarray,Homo sapiens,8|10,DO:A syndrome that is characterized by the sudden death of an infant that is not predicted by medical history and remains unexplained after a thorough forensic autopsy and detailed death scene investigation. DSA08612,GSE191077,GPL21103|GPL24247,1000,Macular Degeneration,C0024437,Retinal pigment epithelium,GEO,RNA-Seq,Mus musculus,3|2,DO:A retinitis pigmentosa that has_material_basis_in mutation in the FSCN2 gene on chromosome 17q25. DSA08613,GSE191183,GPL13112,1000,Disorder of Skull,C1290854,Skull,GEO,RNA-Seq,Mus musculus,3|3,MONDO:A non-neoplastic or neoplastic disorder that affects structures of the skull. DSA08614,GSE191183,GPL13112,1000,Disorder of Skull,C1290854,Skull,GEO,RNA-Seq,Mus musculus,3|3,MONDO:A non-neoplastic or neoplastic disorder that affects structures of the skull. DSA08615,GSE191183,GPL13112,1000,Brain Ischemia,C0007786,Brain,GEO,RNA-Seq,Mus musculus,3|3,DO:An ischemia that is characterized by insufficient blood flow to the brain to meet metabolic demand. DSA08616,GSE191183,GPL13112,1000,Brain Ischemia,C0007786,Brain,GEO,RNA-Seq,Mus musculus,3|3,DO:An ischemia that is characterized by insufficient blood flow to the brain to meet metabolic demand. DSA08617,GSE192522,GPL24247,17,Dysbiosis,C3658208,Testis,GEO,RNA-Seq,Mus musculus,3|3,MSH:Changes in quantitative and qualitative composition of MICROBIOTA. The changes may lead to altered host microbial interaction or homeostatic imbalance that can contribute to a disease state often with inflammation. DSA08618,GSE192791,GPL24247,1000,Renal Fibrosis,C0151650,Kidney,GEO,RNA-Seq,Mus musculus,3|2,HPO:Renal fibrosis is the consequence of an excessive accumulation of extracellular matrix that occurs in virtually every type of chronic kidney disease. DSA08619,GSE192791,GPL24247,1000,Renal Fibrosis,C0151650,Kidney,GEO,RNA-Seq,Mus musculus,3|3,HPO:Renal fibrosis is the consequence of an excessive accumulation of extracellular matrix that occurs in virtually every type of chronic kidney disease. DSA08620,GSE193322,GPL21103,1000,Sepsis,C0243026,Bone marrow,GEO,scRNA-Seq,Mus musculus,2|2,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08621,GSE193322,GPL21103,1000,Sepsis,C0243026,Bone marrow,GEO,scRNA-Seq,Mus musculus,1|2,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08622,GSE193322,GPL21103,1000,Sepsis,C0243026,Bone marrow,GEO,scRNA-Seq,Mus musculus,2|2,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08623,GSE193322,GPL21103,1000,Sepsis,C0243026,Bone marrow,GEO,scRNA-Seq,Mus musculus,2|2,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08624,GSE193322,GPL21103,1000,Sepsis,C0243026,Bone marrow,GEO,scRNA-Seq,Mus musculus,1|1,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08625,GSE193322,GPL21103,823,Sepsis,C0243026,Bone marrow,GEO,scRNA-Seq,Mus musculus,1|1,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08626,GSE193322,GPL21103,1000,Sepsis,C0243026,Bone marrow,GEO,scRNA-Seq,Mus musculus,1|1,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08627,GSE193322,GPL21103,628,Sepsis,C0243026,Bone marrow,GEO,scRNA-Seq,Mus musculus,1|1,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08628,GSE70422,GPL14951,0,Sudden Infant Death Syndrome,C0038644,Liver,GEO,Microarray,Homo sapiens,10|10,DO:A syndrome that is characterized by the sudden death of an infant that is not predicted by medical history and remains unexplained after a thorough forensic autopsy and detailed death scene investigation. DSA08629,GSE70422,GPL14951,0,Sudden Infant Death Syndrome,C0038644,Heart,GEO,Microarray,Homo sapiens,7|10,DO:A syndrome that is characterized by the sudden death of an infant that is not predicted by medical history and remains unexplained after a thorough forensic autopsy and detailed death scene investigation. DSA08630,GSE73482,GPL20171,766,Asthma,C0004096,,GEO,Microarray,Homo sapiens,24|22,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08631,GSE73482,GPL20171,0,Asthma,C0004096,,GEO,Microarray,Homo sapiens,26|22,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08632,GSE193703,GPL19057,0,Intestinal Tumor,C0021841,Small intestine,GEO,RNA-Seq,Mus musculus,5|5,DO:A gastrointestinal system cancer that is located_in the intestine. DSA08633,GSE194075,GPL24247,18,Obesity,C0028754,,GEO,RNA-Seq,Mus musculus,4|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA08634,GSE194075,GPL24247,3,Obesity,C0028754,,GEO,RNA-Seq,Mus musculus,3|4,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA08635,GSE194334,GPL19057,1000,Pyogranulomas,,Small intestine,GEO,RNA-Seq,Mus musculus,3|3, DSA08636,GSE195664,GPL18573,1000,Influenza,C0021400,Liver,GEO,RNA-Seq,Homo sapiens,3|4,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08637,GSE195786,GPL21103,1000,Acute Kidney Injury,C2609414,Kidney,GEO,RNA-Seq,Mus musculus,6|6,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA08638,GSE195786,GPL21103,355,Acute Kidney Injury,C2609414,Kidney,GEO,RNA-Seq,Mus musculus,7|5,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA08639,GSE196488,GPL24247,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Mus musculus,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA08640,GSE196488,GPL24247,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Mus musculus,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA08641,GSE196488,GPL24247,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Mus musculus,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA08642,GSE196708,GPL21103,1000,Pneumonia,C0032285,Lung,GEO,RNA-Seq,Mus musculus,3|3,"DO:A lung disease that involves lung parenchyma or alveolar inflammation and abnormal alveolar filling with fluid (consolidation and exudation). It results from a variety of causes including infection with bacteria, viruses, fungi or parasites, and chemical or physical injury to the lungs. It is accompanied by fever, chills, cough, and difficulty in breathing." DSA08643,GSE196708,GPL21103,1000,Influenza A (H1N1),C2076600,Lung,GEO,RNA-Seq,Mus musculus,3|3,"EFO:An influenza that results_in infection located_in respiratory tract of pigs and humans, has_material_basis_in Influenza C virus, or has_material_basis_in Influenza A virus subtypes (H1N1, H1N2, H3N1, H3N2, and H2N3), which are transmitted_by direct contact with infected pigs. The infection in humans has_symptom fever, has_symptom lethargy, has_symptom lack of appetite, has_symptom coughing, has_symptom runny nose, has_symptom sore throat, has_symptom nausea, has_symptom vomiting, and has_symptom diarrhea." DSA08644,GSE197266,GPL24247,1000,Acute Kidney Injury,C2609414,Kidney,GEO,scRNA-Seq,Mus musculus,2|2,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA08645,GSE197266,GPL24247,1000,Acute Kidney Injury,C2609414,Kidney,GEO,scRNA-Seq,Mus musculus,2|2,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA08646,GSE197266,GPL24247,1000,Acute Kidney Injury,C2609414,Kidney,GEO,scRNA-Seq,Mus musculus,2|2,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA08647,GSE197266,GPL24247,1000,Acute Kidney Injury,C2609414,Kidney,GEO,scRNA-Seq,Mus musculus,2|2,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA08648,GSE197266,GPL24247,1000,Acute Kidney Injury,C2609414,Kidney,GEO,scRNA-Seq,Mus musculus,2|2,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA08649,GSE198331,GPL21273,1000,Proctitis,C0033246,Rectum,GEO,RNA-Seq,Mus musculus,3|3,"DO:A rectal disease that involves inflammation of the rectal mucosa, which results from infection, inflammatory bowel disease, or radiation. Sexually transmitted pathogens (Neisseria gonorrhoeae, Chlamydia trachomatis, herpes simplex virus 1 and 2, Treponema pallidum) and enteric pathogens (Campylobacter, Shigella, Salmonella) are involved in the disease. Symptoms are rectal discomfort and bleeding." DSA08650,GSE198331,GPL21273,1000,Proctitis,C0033246,Rectum,GEO,RNA-Seq,Mus musculus,3|3,"DO:A rectal disease that involves inflammation of the rectal mucosa, which results from infection, inflammatory bowel disease, or radiation. Sexually transmitted pathogens (Neisseria gonorrhoeae, Chlamydia trachomatis, herpes simplex virus 1 and 2, Treponema pallidum) and enteric pathogens (Campylobacter, Shigella, Salmonella) are involved in the disease. Symptoms are rectal discomfort and bleeding." DSA08651,GSE198331,GPL21273,1000,Proctitis,C0033246,Rectum,GEO,RNA-Seq,Mus musculus,3|3,"DO:A rectal disease that involves inflammation of the rectal mucosa, which results from infection, inflammatory bowel disease, or radiation. Sexually transmitted pathogens (Neisseria gonorrhoeae, Chlamydia trachomatis, herpes simplex virus 1 and 2, Treponema pallidum) and enteric pathogens (Campylobacter, Shigella, Salmonella) are involved in the disease. Symptoms are rectal discomfort and bleeding." DSA08652,GSE198331,GPL21273,1000,Proctitis,C0033246,Rectum,GEO,RNA-Seq,Mus musculus,3|3,"DO:A rectal disease that involves inflammation of the rectal mucosa, which results from infection, inflammatory bowel disease, or radiation. Sexually transmitted pathogens (Neisseria gonorrhoeae, Chlamydia trachomatis, herpes simplex virus 1 and 2, Treponema pallidum) and enteric pathogens (Campylobacter, Shigella, Salmonella) are involved in the disease. Symptoms are rectal discomfort and bleeding." DSA08653,GSE198372,GPL24247,1000,Necrotizing Enterocolitis,C0520459,Terminal ileum,GEO,RNA-Seq,Mus musculus,3|3,"EFO:Necrotizing enterocolitis (NEC) is a devastating disease that affects mostly the intestine of premature infants. The wall of the intestine is invaded by bacteria, which cause local infection and inflammation that can ultimately destroy the wall of the bowel (intestine). Such bowel wall destruction can lead to perforation of the intestine and spillage of stool into the infant's abdomen, which can result in an overwhelming infection and death." DSA08654,GSE198836,GPL19057,1000,Type 1 Diabetes,C0011854,Knee joint,GEO,RNA-Seq,Mus musculus,4|4,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA08655,GSE73482,GPL20171,0,Asthma,C0004096,,GEO,Microarray,Homo sapiens,26|22,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08656,GSE73482,GPL20171,1000,Asthma,C0004096,,GEO,Microarray,Homo sapiens,26|22,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08657,GSE19295,GPL571,1000,Breast Cancer,C0678222,Kidney,GEO,Microarray,Homo sapiens,4|4,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08658,GSE199286,GPL18573,130,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,5|5,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA08659,GSE199545,GPL24247,389,COVID-19,D8888888,Hippocampus,GEO,RNA-Seq,Mus musculus,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA08660,GSE199888,GPL18573,617,Hepatoblastoma,C0206624,Liver,GEO,RNA-Seq,Homo sapiens,5|14,DO:A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver. DSA08661,GSE199891,GPL21626,1000,Congenital Melanocytic Nevus,C1318558,Ear,GEO,RNA-Seq,Mus musculus,3|3,DO:A skin disease characterized by the presence at birth of a pigmented skin lesion composed of melanocytes of more than 20 cm in projected adult diameter that has_material_basis_in somatic mutation in NRAS on chromosome 11p15.5. DSA08662,GSE68849,GPL10558,733,Influenza,C0021400,,GEO,Microarray,Homo sapiens,5|5,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08663,GSE199905,GPL16570,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,7|6,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08664,GSE199905,GPL16570,1000,Sarcomatoid Carcinoma,C0007097,Lung,GEO,Microarray,Mus musculus,7|6,DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08665,GSE199907,GPL21103,1000,Obesity,C0028754,Pancreatic islet,GEO,RNA-Seq,Mus musculus,3|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA08666,GSE200279,GPL24247,228,Hypertensive Heart Failure,C0264652,Heart,GEO,RNA-Seq,Mus musculus,3|3, DSA08667,GSE200409,GPL13912,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Mus musculus,2|2,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA08668,GSE200409,GPL13912,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Mus musculus,2|2,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA08669,GSE200409,GPL13912,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Mus musculus,2|2,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA08670,GSE200611,GPL24247,2,Obesity,C0028754,Hypothalamus,GEO,RNA-Seq,Mus musculus,8|7,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA08671,GSE200611,GPL24247,3,Obesity,C0028754,Hypothalamus,GEO,RNA-Seq,Mus musculus,8|8,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA08672,GSE20065,GPL1261,1000,Basal Cell Carcinoma,C0007117,Epidermis,GEO,Microarray,Mus musculus,2|2,DO:A skin carcinoma affecting basal cells. DSA08673,GSE200838,GPL13112,1000,Adenosquamous Carcinoma,C0206623,Mammary gland,GEO,RNA-Seq,Mus musculus,3|2,DO:A squamous cell carcinoma that contains squamous cells and gland-like cells. DSA08674,GSE200838,GPL13112,1000,Spindle Cell Carcinoma,C0205697,Mammary gland,GEO,RNA-Seq,Mus musculus,3|1,DO:A carcinoma that is characterized by the presence of spindle cells and anaplastic morphologic features. DSA08675,GSE200838,GPL13112,1000,Papillary Carcinoma,C0007133,Mammary gland,GEO,RNA-Seq,Mus musculus,3|1,DO:A carcinoma that is derives_from epithelial cells with finger like projections. DSA08676,GSE201955,GPL16791|GPL20301,65,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,18|22,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08677,GSE201955,GPL16791|GPL20301,305,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,21|24,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08678,GSE205014,GPL24247,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Mus musculus,4|10,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA08679,GSE205014,GPL24247,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Mus musculus,4|10,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA08680,GSE11889,GPL571,0,Chronic Myeloid Leukemia,C0023473,Bone Marrow,GEO,Microarray,Homo sapiens,5|6,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA08681,GSE205772,GPL29792,0,Viral Encephalitis,C0243010,Spinal cord,GEO,Microarray,Mus musculus,3|4,EFO:Encephalitis resulting from viral infection. DSA08682,GSE11889,GPL571,0,Chronic Myeloid Leukemia,C0023473,Bone Marrow,GEO,Microarray,Homo sapiens,5|7,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA08683,GSE205772,GPL29792,0,Viral Encephalitis,C0243010,Bladder,GEO,Microarray,Mus musculus,4|5,EFO:Encephalitis resulting from viral infection. DSA08684,GSE205839,GPL7202,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,4|4,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08685,GSE205839,GPL7202,965,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,4|4,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08686,GSE205839,GPL7202,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,4|4,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08687,GSE205839,GPL7202,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,4|4,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08688,GSE205839,GPL7202,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08689,GSE205839,GPL7202,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08690,GSE205839,GPL7202,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,6|4,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08691,GSE205839,GPL7202,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,6|4,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08692,GSE205839,GPL7202,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,4|4,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08693,GSE205839,GPL7202,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,4|4,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08694,GSE205839,GPL7202,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08695,GSE205839,GPL7202,1000,Influenza,C0021400,Lung,GEO,Microarray,Mus musculus,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08696,GSE206068,GPL24247,1000,Mammary Tumor,C1512981,Mammary gland,GEO,RNA-Seq,Mus musculus,3|5,NCI:Production of a new growth or growths in the mammary gland. DSA08697,GSE206068,GPL24247,1000,Mammary Tumor,C1512981,Mammary gland,GEO,RNA-Seq,Mus musculus,3|5,NCI:Production of a new growth or growths in the mammary gland. DSA08698,GSE206068,GPL24247,1000,Mammary Tumor,C1512981,Mammary gland,GEO,RNA-Seq,Mus musculus,3|5,NCI:Production of a new growth or growths in the mammary gland. DSA08699,GSE206091,GPL23479,496,Acute Kidney Injury,C2609414,Blood,GEO,RNA-Seq,Mus musculus,2|2,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA08700,GSE206091,GPL23479,1000,Acute Kidney Injury,C2609414,Kidney,GEO,RNA-Seq,Mus musculus,3|2,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA08701,GSE206426,GPL21493,1000,Radiation Injury,C0034535,Lung,GEO,scRNA-Seq,Mus musculus,1|1,MONDO:Harmful effects of non-experimental exposure to ionizing or non-ionizing radiation in VERTEBRATES. DSA08702,GSE206426,GPL21493,1000,Radiation Injury,C0034535,Lung,GEO,scRNA-Seq,Mus musculus,1|1,MONDO:Harmful effects of non-experimental exposure to ionizing or non-ionizing radiation in VERTEBRATES. DSA08703,GSE207363,GPL24247,1000,Sepsis,C0243026,Heart,GEO,RNA-Seq,Mus musculus,1|1,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08704,GSE207928,GPL24247,283,Glaucoma,C0017601,Retina,GEO,RNA-Seq,Mus musculus,3|3,DO:An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. DSA08705,GSE207928,GPL24247,568,Glaucoma,C0017601,Retina,GEO,RNA-Seq,Mus musculus,3|3,DO:An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. DSA08706,GSE11889,GPL571,0,Chronic Myeloid Leukemia,C0023473,Bone Marrow,GEO,Microarray,Homo sapiens,5|7,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA08707,GSE20916,GPL570,1000,Colon Tumor,C0009375,Colon,GEO,Microarray,Homo sapiens,5|5,DO:A colorectal cancer that is located_in the colon. DSA08708,GSE20916,GPL570,1000,Colon Tumor,C0009375,Colon,GEO,Microarray,Homo sapiens,5|5,DO:A colorectal cancer that is located_in the colon. DSA08709,GSE20916,GPL570,1000,Colon Tumor,C0009375,Colon,GEO,Microarray,Homo sapiens,5|5,DO:A colorectal cancer that is located_in the colon. DSA08710,GSE20916,GPL570,1000,Colon Tumor,C0009375,Colon,GEO,Microarray,Homo sapiens,5|5,DO:A colorectal cancer that is located_in the colon. DSA08711,GSE20916,GPL570,1000,Colon Tumor,C0009375,Colon,GEO,Microarray,Homo sapiens,5|5,DO:A colorectal cancer that is located_in the colon. DSA08712,GSE20916,GPL570,1000,Colon Tumor,C0009375,Colon,GEO,Microarray,Homo sapiens,5|5,DO:A colorectal cancer that is located_in the colon. DSA08713,GSE20916,GPL570,1000,Colon Tumor,C0009375,Colon,GEO,Microarray,Homo sapiens,5|5,DO:A colorectal cancer that is located_in the colon. DSA08714,GSE20916,GPL570,1000,Colon Tumor,C0009375,Colon,GEO,Microarray,Homo sapiens,5|5,DO:A colorectal cancer that is located_in the colon. DSA08715,GSE20916,GPL570,1000,Colon Tumor,C0009375,Colon,GEO,Microarray,Homo sapiens,7|45,DO:A colorectal cancer that is located_in the colon. DSA08716,GSE20916,GPL570,1000,Colon Tumor,C0009375,Colon,GEO,Microarray,Homo sapiens,17|36,DO:A colorectal cancer that is located_in the colon. DSA08717,GSE141623,GPL17586,0,Asthma,C0004096,Whole blood,GEO,Microarray,Homo sapiens,100|32,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08718,GSE141623,GPL17586,0,Dermatitis,C0011603,Whole blood,GEO,Microarray,Homo sapiens,100|22,"DO:A skin disease characterized by itchy, erythematous, vesicular, weeping and crusting patches of skin." DSA08719,GSE141623,GPL17586,0,Rhinitis,C0035455,Whole blood,GEO,Microarray,Homo sapiens,100|23,"DO:A upper respiratory infectious disease which involves irritation and inflammation of the mucous membrane of the nose due to viruses, bacteria or irritants. The inflammation results in generation of excessive amounts of mucus leading to runny nose, as well as nasal congestion and post-nasal drip." DSA08720,GSE141623,GPL17586,0,Asthma;Dermatitis;Rhinitis,,Whole blood,GEO,Microarray,Homo sapiens,100|16, DSA08721,GSE141623,GPL17586,0,Allergy,C1527304,Whole blood,GEO,Microarray,Homo sapiens,100|156,"DO:An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods." DSA08722,GSE141631,GPL17586,0,Asthma,C0004096,Whole blood,GEO,Microarray,Homo sapiens,109|18,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08723,GSE141631,GPL17586,0,Dermatitis,C0011603,Whole blood,GEO,Microarray,Homo sapiens,109|48,"DO:A skin disease characterized by itchy, erythematous, vesicular, weeping and crusting patches of skin." DSA08724,GSE141631,GPL17586,0,Rhinitis,C0035455,Whole blood,GEO,Microarray,Homo sapiens,109|4,"DO:A upper respiratory infectious disease which involves irritation and inflammation of the mucous membrane of the nose due to viruses, bacteria or irritants. The inflammation results in generation of excessive amounts of mucus leading to runny nose, as well as nasal congestion and post-nasal drip." DSA08725,GSE141631,GPL17586,0,Allergy,C1527304,Whole blood,GEO,Microarray,Homo sapiens,109|92,"DO:An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods." DSA08726,GSE141721,GPL17021,1000,Experimental Autoimmune Encephalomyelitis,C0014072,Spinal cord,GEO,RNA-Seq,Mus musculus,3|7,"EFO:An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)" DSA08727,GSE141721,GPL17021,371,Experimental Autoimmune Encephalomyelitis,C0014072,Spinal cord,GEO,RNA-Seq,Mus musculus,2|5,"EFO:An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)" DSA08728,GSE141725,GPL21103,916,Ocular Hypertension,C0028840,Retina,GEO,RNA-Seq,Mus musculus,3|3,DO:An eye disease that is characterized by elevated intraocular pressure in the absence of optic nerve damage or visual field loss. DSA08729,GSE141725,GPL21103,1000,Ocular Hypertension,C0028840,Retina,GEO,RNA-Seq,Mus musculus,3|3,DO:An eye disease that is characterized by elevated intraocular pressure in the absence of optic nerve damage or visual field loss. DSA08730,GSE141797,GPL18573,0,Multiple Sclerosis,C0026769,,GEO,RNA-Seq,Homo sapiens,9|9,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA08731,GSE141801,GPL13667,1000,Vestibular Schwannoma,C0027859,Vestibular nerve,GEO,Microarray,Homo sapiens,7|36,"DO:A neurofibromatosis characterized by usually bilateral tumors of the eighth cranial nerve, meningiomas of the brain, and schwannomas of the dorsal roots of the spinal cord that has_material_basis_in heterozygous of mutation in NF2 on 22q12.2." DSA08732,GSE141801,GPL13667,1000,Vestibular Schwannoma,C0027859,Vestibular nerve,GEO,Microarray,Homo sapiens,7|9,"DO:A neurofibromatosis characterized by usually bilateral tumors of the eighth cranial nerve, meningiomas of the brain, and schwannomas of the dorsal roots of the spinal cord that has_material_basis_in heterozygous of mutation in NF2 on 22q12.2." DSA08733,GSE141801,GPL13667,1000,Vestibular Schwannoma,C0027859,Vestibular nerve,GEO,Microarray,Homo sapiens,7|13,"DO:A neurofibromatosis characterized by usually bilateral tumors of the eighth cranial nerve, meningiomas of the brain, and schwannomas of the dorsal roots of the spinal cord that has_material_basis_in heterozygous of mutation in NF2 on 22q12.2." DSA08734,GSE141801,GPL13667,1000,Vestibular Schwannoma,C0027859,Vestibular nerve,GEO,Microarray,Homo sapiens,7|9,"DO:A neurofibromatosis characterized by usually bilateral tumors of the eighth cranial nerve, meningiomas of the brain, and schwannomas of the dorsal roots of the spinal cord that has_material_basis_in heterozygous of mutation in NF2 on 22q12.2." DSA08735,GSE141804,GPL571,5,Multiple Sclerosis,C0026769,,GEO,Microarray,Homo sapiens,7|15,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA08736,GSE141804,GPL571,1000,Psoriasis,C0033860,,GEO,Microarray,Homo sapiens,7|12,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA08737,GSE141804,GPL571,0,Multiple Sclerosis Nos,C0026769,,GEO,Microarray,Homo sapiens,7|12,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA08738,GSE141828,GPL20301,1,Breast Cancer,C0678222,Epidermis,GEO,RNA-Seq,Homo sapiens,18|7,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08739,GSE141828,GPL20301,1,Breast Cancer,C0678222,Breast,GEO,RNA-Seq,Homo sapiens,13|7,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08740,GSE141828,GPL20301,0,Breast Cancer,C0678222,Adipose tissue,GEO,RNA-Seq,Homo sapiens,11|5,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08741,GSE141835,GPL16791,529,Plaa-Associated Neurodevelopmental Disorder,C4479631,,GEO,RNA-Seq,Homo sapiens,4|3,"ORDO:A rare genetic neurological disorder characterized by infantile onset of progressive leukoencephalopathy, microcephaly, severe global developmental delay, and spasticity resulting in quadriparesis and posture deformation. Additional features include an abnormally exaggerated startle reflex, seizures, dystonia, and hypomimia or amimia, as well as progressive chest deformities and contractures of large and hyperextensibility of small joints, among others. Thin corpus callosum is a prominent feature in brain imaging, in addition to white matter abnormalities consistent with leukoencephalopathy." DSA08742,GSE141836,GPL16791,1000,Rheumatoid Arthritis,C0003873,,GEO,RNA-Seq,Homo sapiens,2|1,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA08743,GSE141836,GPL16791,24,Rheumatoid Arthritis,C0003873,,GEO,RNA-Seq,Homo sapiens,2|2,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA08744,GSE141864,GPL17586,0,Meningococcal Infection,C0025303,Heart,GEO,Microarray,Homo sapiens,2|8,EFO:Infections with bacteria of the species neisseria meningitidis. DSA08745,GSE141864,GPL17586,0,Meningococcal Infection,C0025303,Kidney,GEO,Microarray,Homo sapiens,2|7,EFO:Infections with bacteria of the species neisseria meningitidis. DSA08746,GSE141864,GPL17586,69,Meningococcal Infection,C0025303,Liver,GEO,Microarray,Homo sapiens,1|6,EFO:Infections with bacteria of the species neisseria meningitidis. DSA08747,GSE141864,GPL17586,1,Meningococcal Infection,C0025303,Lung,GEO,Microarray,Homo sapiens,2|9,EFO:Infections with bacteria of the species neisseria meningitidis. DSA08748,GSE141864,GPL17586,0,Meningococcal Infection,C0025303,Spleen,GEO,Microarray,Homo sapiens,1|6,EFO:Infections with bacteria of the species neisseria meningitidis. DSA08749,GSE141910,GPL16791,1000,Peripartum Cardiomyopathy,C0877208,Left ventricle,GEO,RNA-Seq,Homo sapiens,166|6,DO:A dilated cardiomyopathy that is characterized by a weakness of the heart muscle that begins sometime during the final month of pregnancy through about five months after delivery. DSA08750,GSE141910,GPL16791,1000,Hypertrophic Cardiomyopathy,C0007194,Left ventricle,GEO,RNA-Seq,Homo sapiens,166|28,DO:A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations. DSA08751,GSE141910,GPL16791,1000,Dilated Cardiomyopathy,C0007193,Left Ventricle,GEO,RNA-Seq,Homo sapiens,155|163,DO:A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. DSA08752,GSE141956,GPL6246,0,Diabetes,C0011847,Skin,GEO,Microarray,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA08753,GSE142025,GPL20301,1000,Diabetic Kidney Disease,C0011881,Kidney,GEO,RNA-Seq,Homo sapiens,9|6,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA08754,GSE142025,GPL20301,1000,Diabetic Kidney Disease,C0011881,Kidney,GEO,RNA-Seq,Homo sapiens,8|21,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA08755,GSE142025,GPL20301,1000,Progressive Diabetic Kidney Disease,C0011881,Kidney,GEO,RNA-Seq,Homo sapiens,6|21,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA08756,GSE142041,GPL11154,1000,22Q11.2 Deletion Syndrome,C2936346,Cortical spheroid,GEO,RNA-Seq,Homo sapiens,21|14,"MONDO:22q11.2 deletion syndrome (DS) is a chromosomal anomaly which causes a congenital malformation disorder whose common features include cardiac defects, palatal anomalies, facial dysmorphism, developmental delay and immune deficiency." DSA08757,GSE142041,GPL11154,1000,22Q11.2 Deletion Syndrome,C2936346,Cortical spheroid,GEO,RNA-Seq,Homo sapiens,20|16,"MONDO:22q11.2 deletion syndrome (DS) is a chromosomal anomaly which causes a congenital malformation disorder whose common features include cardiac defects, palatal anomalies, facial dysmorphism, developmental delay and immune deficiency." DSA08758,GSE142041,GPL11154,1000,22Q11.2 Deletion Syndrome,C2936346,Cortical spheroid,GEO,RNA-Seq,Homo sapiens,23|24,"MONDO:22q11.2 deletion syndrome (DS) is a chromosomal anomaly which causes a congenital malformation disorder whose common features include cardiac defects, palatal anomalies, facial dysmorphism, developmental delay and immune deficiency." DSA08759,GSE142041,GPL11154,1000,22Q11.2 Deletion Syndrome,C2936346,Cortical spheroid,GEO,RNA-Seq,Homo sapiens,20|17,"MONDO:22q11.2 deletion syndrome (DS) is a chromosomal anomaly which causes a congenital malformation disorder whose common features include cardiac defects, palatal anomalies, facial dysmorphism, developmental delay and immune deficiency." DSA08760,GSE142153,GPL6480,784,Diabetic Kidney Disease,C0011881,Peripheral blood,GEO,Microarray,Homo sapiens,10|23,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA08761,GSE142153,GPL6480,0,End Stage Renal Disease,C0022661,Peripheral blood,GEO,Microarray,Homo sapiens,10|7,DO:A kidney failure that is characterized by the gradual loss of kidney function. DSA08762,GSE142254,GPL23159,0,Cirrhosis,C1623038,,GEO,Microarray,Homo sapiens,5|5,"MSH:Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury." DSA08763,GSE142254,GPL23159,208,Acute-On-Chronic Liver Failure,C3850141,,GEO,Microarray,Homo sapiens,5|5,"EFO:Acute-on-chronic liver failure (ACLF) is an extreme condition during the natural history of chronic HBV infection, with a relatively high short-term mortality." DSA08764,GSE142255,GPL17586,0,Cirrhosis,C1623038,Whole blood,GEO,Microarray,Homo sapiens,5|7,"MSH:Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury." DSA08765,GSE142255,GPL17586,5,Cirrhosis,C1623038,Whole blood,GEO,Microarray,Homo sapiens,5|7,"MSH:Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury." DSA08766,GSE142255,GPL17586,1000,Acute-On-Chronic Liver Failure,C3850141,Whole blood,GEO,Microarray,Homo sapiens,5|8,"EFO:Acute-on-chronic liver failure (ACLF) is an extreme condition during the natural history of chronic HBV infection, with a relatively high short-term mortality." DSA08767,GSE142255,GPL17586,1000,Acute-On-Chronic Liver Failure,C3850141,Whole blood,GEO,Microarray,Homo sapiens,5|9,"EFO:Acute-on-chronic liver failure (ACLF) is an extreme condition during the natural history of chronic HBV infection, with a relatively high short-term mortality." DSA08768,GSE142255,GPL17586,1000,Septic Shock,C0036983,Whole blood,GEO,Microarray,Homo sapiens,5|8,"DO:A commensal bacterial infectious disease that results_in infection, has_material_basis_in Streptococcus pyogenes or has_material_basis_in Staphylococcus aureus , which produce toxins that are absorbed systemically and produce the systemic manifestations. The infection has_symptom fever, has_symptom rash, has_symptom hypotension, has_symptom multiorgan failure, has_symptom desquamation, has_symptom vomiting, has_symptom diarrhea, has_symptom headache, and has_symptom nonfocal neurologic abnormalities." DSA08769,GSE11889,GPL571,0,Chronic Myeloid Leukemia,C0023473,Bone Marrow,GEO,Microarray,Homo sapiens,5|7,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA08770,GSE142401,GPL10558,1,Metabolic Syndrome,C0524620,Adipose tissue,GEO,Microarray,Homo sapiens,10|9,"DO:An abdominal obesity-metabolic syndrome characterized by insulin resistance and hyperinsulinemia, dyslipidemia, essential hypertension, abdominal obesity, glucose intolerance or noninsulin-dependent diabetes mellitus and an increased risk of cardiovascular events." DSA08771,GSE142401,GPL10558,0,Metabolic Syndrome,C0524620,Adipose tissue,GEO,Microarray,Homo sapiens,10|9,"DO:An abdominal obesity-metabolic syndrome characterized by insulin resistance and hyperinsulinemia, dyslipidemia, essential hypertension, abdominal obesity, glucose intolerance or noninsulin-dependent diabetes mellitus and an increased risk of cardiovascular events." DSA08772,GSE142401,GPL10558,0,Metabolic Syndrome,C0524620,Adipose tissue,GEO,Microarray,Homo sapiens,10|9,"DO:An abdominal obesity-metabolic syndrome characterized by insulin resistance and hyperinsulinemia, dyslipidemia, essential hypertension, abdominal obesity, glucose intolerance or noninsulin-dependent diabetes mellitus and an increased risk of cardiovascular events." DSA08773,GSE142401,GPL10558,0,Metabolic Syndrome,C0524620,Adipose tissue,GEO,Microarray,Homo sapiens,10|9,"DO:An abdominal obesity-metabolic syndrome characterized by insulin resistance and hyperinsulinemia, dyslipidemia, essential hypertension, abdominal obesity, glucose intolerance or noninsulin-dependent diabetes mellitus and an increased risk of cardiovascular events." DSA08774,GSE8954,GPL201,1000,Hodgkin Lymphoma,C0019829,Adipose tissue,GEO,Microarray,Homo sapiens,3|4,DO:A lymphoma that is marked by the presence of a type of cell called the Reed-Sternberg cell. DSA08775,GSE142455,GPL21103,1000,Cachexia,C0006625,Muscle,GEO,RNA-Seq,Mus musculus,4|4,"HPO:Severe weight loss, wasting of muscle, loss of appetite, and general debility related to a chronic disease." DSA08776,GSE142455,GPL21103,1000,Cachexia,C0006625,Muscle,GEO,RNA-Seq,Mus musculus,4|4,"HPO:Severe weight loss, wasting of muscle, loss of appetite, and general debility related to a chronic disease." DSA08777,GSE142530,GPL11154,1000,Cirrhosis,C1623038,Liver,GEO,RNA-Seq,Homo sapiens,11|6,"MSH:Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury." DSA08778,GSE142530,GPL11154,1000,Alcoholic Hepatitis,C0019187,Liver,GEO,RNA-Seq,Homo sapiens,12|10,MONDO:Acute hepatitis resulting from ingestion of alcohol. DSA08779,GSE142538,GPL18573,816,Fuchs Endothelial Corneal Dystrophy,C0016781,Cornea,GEO,RNA-Seq,Homo sapiens,9|6,"DO:A corneal dystrophy that is characterized by corneal edema, iris atrophy, and secondary angle-closure glaucoma caused by an inflammatory or infectious insult that causes the endothelium to fail to pump aqueous humor from the cornea, leading to fluid accumulation, microcystic edema, and angle-closure glaucoma." DSA08780,GSE142538,GPL18573,1000,Fuchs Endothelial Corneal Dystrophy,C0016781,Cornea,GEO,RNA-Seq,Homo sapiens,9|10,"DO:A corneal dystrophy that is characterized by corneal edema, iris atrophy, and secondary angle-closure glaucoma caused by an inflammatory or infectious insult that causes the endothelium to fail to pump aqueous humor from the cornea, leading to fluid accumulation, microcystic edema, and angle-closure glaucoma." DSA08781,GSE142542,GPL23126,8,Myotonic Dystrophy Type 1,C0027126,,GEO,Microarray,Homo sapiens,4|6,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA08782,GSE8954,GPL201,1000,Hodgkin Lymphoma,C0019829,Bone marrow,GEO,Microarray,Homo sapiens,3|4,DO:A lymphoma that is marked by the presence of a type of cell called the Reed-Sternberg cell. DSA08783,GSE142612,GPL18573,92,Spinal And Bulbar Muscular Atrophy,C1839259,,GEO,RNA-Seq,Homo sapiens,4|4,DO:A spinal muscular dystrophy that has_material_basis_in an X-linked recessive expansion of CAG triplet repeats (glutamine) in exon 1 of AR gene encoding the androgen receptor. DSA08784,GSE142612,GPL18573,60,Spinal And Bulbar Muscular Atrophy,C1839259,,GEO,RNA-Seq,Homo sapiens,4|4,DO:A spinal muscular dystrophy that has_material_basis_in an X-linked recessive expansion of CAG triplet repeats (glutamine) in exon 1 of AR gene encoding the androgen receptor. DSA08785,GSE142654,GPL13112,15,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,RNA-Seq,Mus musculus,3|4,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA08786,GSE142670,GPL16791,52,Autism Spectrum Disorder,C1510586,,GEO,RNA-Seq,Homo sapiens,13|16,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA08787,GSE142670,GPL16791,38,Autism Spectrum Disorder,C1510586,,GEO,RNA-Seq,Homo sapiens,4|3,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA08788,GSE142670,GPL16791,3,Autism Spectrum Disorder,C1510586,,GEO,RNA-Seq,Homo sapiens,7|9,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA08789,GSE142698,GPL19956,131,Acute Myeloid Leukemia (Aml-M2),C1879321,,GEO,Microarray,Homo sapiens,24|24,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA08790,GSE142730,GPL11154,1000,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA08791,GSE142807,GPL17692,1000,Dermatomyositis,C0011633,Skin,GEO,Microarray,Homo sapiens,5|43,DO:A myositis that results_in inflammation located_in muscle or located_in skin where a skin rash is often seen prior to the onset of muscle weakness. The disease may result from either a viral infection or an autoimmune reaction. DSA08792,GSE142842,GPL18573,23,Ataxia-Telangiectasia,C0004135,,GEO,RNA-Seq,Homo sapiens,4|8,"DO:An autosomal recessive cerebellar ataxia that is characterized by cerebellar ataxia, telangiectases, immune defects, and a predisposition to malignancy and that has_material_basis_in homozygous or compound heterozygous mutation in the ATM gene on chromosome 11q22." DSA08793,GSE142853,GPL19057,366,Alzheimer's Disease,C0002395,,GEO,scRNA-Seq,Mus musculus,1|1,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA08794,GSE142987,GPL20795,1000,Liver Cancer,C2239176,,GEO,RNA-Seq,Homo sapiens,30|35,DO:A hepatobiliary system cancer that is located_in the liver. DSA08795,GSE143143,GPL20301,233,Type 1 Diabetes,C0011854,,GEO,RNA-Seq,Homo sapiens,5|5,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA08796,GSE143143,GPL20301,615,Type 1 Diabetes,C0011854,,GEO,RNA-Seq,Homo sapiens,5|5,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA08797,GSE143143,GPL20301,653,Type 1 Diabetes,C0011854,,GEO,RNA-Seq,Homo sapiens,5|5,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA08798,GSE143153,GPL13607,0,Sjogren's Syndrome,C1527336,Salivary gland,GEO,Microarray,Homo sapiens,3|2,DO:An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. DSA08799,GSE143153,GPL13607,2,Sjogren's Syndrome,C1527336,Salivary gland,GEO,Microarray,Homo sapiens,5|6,DO:An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. DSA08800,GSE143153,GPL13607,48,Sjogren's Syndrome,C1527336,Salivary gland,GEO,Microarray,Homo sapiens,7|9,DO:An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. DSA08801,GSE13732,GPL570,1000,Clinically Isolated Syndrome,C2921627,,GEO,Microarray,Homo sapiens,30|39, DSA08802,GSE143192,GPL22120,0,Asthma,C0004096,,GEO,Microarray,Homo sapiens,4|4,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08803,GSE143272,GPL10558,1000,Epilepsy,C0014544,Whole blood,GEO,Microarray,Homo sapiens,51|34,"DO:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions." DSA08804,GSE143303,GPL10558,971,Asthma,C0004096,Bronchus,GEO,Microarray,Homo sapiens,13|22,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08805,GSE143303,GPL10558,1000,Asthma,C0004096,Bronchus,GEO,Microarray,Homo sapiens,13|9,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08806,GSE143303,GPL10558,923,Asthma,C0004096,Bronchus,GEO,Microarray,Homo sapiens,13|16,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08807,GSE143378,GPL24247,1000,Colitis,C0009319,Colon,GEO,RNA-Seq,Mus musculus,8|5,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA08808,GSE143382,GPL27981,498,Dermatitis,C0011603,Skin,GEO,Microarray,Homo sapiens,12|46,"DO:A skin disease characterized by itchy, erythematous, vesicular, weeping and crusting patches of skin." DSA08809,GSE143382,GPL27981,599,Mycosis Fungoides,C0026948,Skin,GEO,Microarray,Homo sapiens,12|43,"MONDO:Classical mycosis fungoides is the most common type of mycosis fungoides (MF), a form of cutaneous T-cell lymphoma, and is characterized by slow progression from patches to more infiltrated plaques and eventually to tumors." DSA08810,GSE143382,GPL27981,590,Mycosis Fungoides,C0026948,Skin,GEO,Microarray,Homo sapiens,12|27,"MONDO:Classical mycosis fungoides is the most common type of mycosis fungoides (MF), a form of cutaneous T-cell lymphoma, and is characterized by slow progression from patches to more infiltrated plaques and eventually to tumors." DSA08811,GSE143447,GPL21103,13,Osteoarthritis,C0157946,Knee cartilage,GEO,RNA-Seq,Mus musculus,5|6,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA08812,GSE143447,GPL21103,64,Osteoarthritis,C0157946,Knee cartilage,GEO,RNA-Seq,Mus musculus,6|6,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA08813,GSE13732,GPL570,927,Clinically Isolated Syndrome,C2921627,,GEO,Microarray,Homo sapiens,10|34, DSA08814,GSE12767,GPL570,0,Pre-Eclampsia,C0032914,Chorion,GEO,Microarray,Homo sapiens,8|4,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA08815,GSE143514,GPL20795,15,Osteoarthritis,C0157946,Synovial fluid,GEO,RNA-Seq,Mus musculus,3|5,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA08816,GSE11681,GPL96,364,Limb-Girdle Muscular Dystrophy Type 2A,C1869123,Quadriceps,GEO,Microarray,Homo sapiens,10|10,DO:An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding the proteolytic enzyme calpain-3 (CAPN3) on chromosome 15q15. DSA08817,GSE143570,GPL20301,66,Ataxia With Oculomotor Apraxia Type 2,C1853761,,GEO,RNA-Seq,Homo sapiens,4|4,"DO:An autosomal recessive cerebellar ataxia that is characterized by the onset of ataxia between age three and thirty including axonal sensorimotor neuropathy, oculomotor apraxia, cerebellar atrophy and elevated alpha-fetoprotein, has_material_basis_in homozygous or compound heterozygous mutation in the SETX gene on chromosome 9q34." DSA08818,GSE14367,GPL6105,1000,Schistosomiasis,C0036323,Liver,GEO,Microarray,Mus musculus,2|2,"DO:A schistosomiasis that involves parasitic infection of the intestine caused by Schistosoma mansoni, Schistosoma intercalatum or Schistosomiasis japonicum. The symptoms include fever, cough, abdominal pain, diarrhea, hepatosplenomegaly, colonic polyposis with bloody diarrhea and eosinophilia." DSA08819,GSE14367,GPL6105,1000,Schistosomiasis,C0036323,Liver,GEO,Microarray,Mus musculus,2|2,"DO:A schistosomiasis that involves parasitic infection of the intestine caused by Schistosoma mansoni, Schistosoma intercalatum or Schistosomiasis japonicum. The symptoms include fever, cough, abdominal pain, diarrhea, hepatosplenomegaly, colonic polyposis with bloody diarrhea and eosinophilia." DSA08820,GSE14367,GPL6105,1000,Schistosomiasis,C0036323,Liver,GEO,Microarray,Mus musculus,2|2,"DO:A schistosomiasis that involves parasitic infection of the intestine caused by Schistosoma mansoni, Schistosoma intercalatum or Schistosomiasis japonicum. The symptoms include fever, cough, abdominal pain, diarrhea, hepatosplenomegaly, colonic polyposis with bloody diarrhea and eosinophilia." DSA08821,GSE143680,GPL6244,114,Oculomotor Apraxia,C3489733,,GEO,Microarray,Homo sapiens,12|12,"HPO:Ocular motor apraxia is a deficiency in voluntary, horizontal, lateral, fast eye movements (saccades) with retention of slow pursuit movements. The inability to follow objects visually is often compensated by head movements. There may be decreased smooth pursuit, and cancellation of the vestibulo-ocular reflex." DSA08822,GSE143686,GPL16791,1000,HIV-Associated Neurocognitive Disorder,C4285693,,GEO,scRNA-Seq,Homo sapiens,1|1,"EFO:HIV-associated neurocognitive disorder (HAND) remains a common complication of HIV infection in the combination antiretroviral therapy (ART) era. Although modern ART has substantially improved life expectancy and reduced the incidence of HIVassociated dementia (HAD), milder forms of HAND remain prevalent, including asymptomatic neurocognitive impairment (ANI) and mild neurocognitive disorder (MND). The overall prevalence of HAND is 30éˆ?0% among unselected HIV-infected persons." DSA08823,GSE143686,GPL16791,1000,HIV-Associated Neurocognitive Disorder,C4285693,,GEO,scRNA-Seq,Homo sapiens,1|1,"EFO:HIV-associated neurocognitive disorder (HAND) remains a common complication of HIV infection in the combination antiretroviral therapy (ART) era. Although modern ART has substantially improved life expectancy and reduced the incidence of HIVassociated dementia (HAD), milder forms of HAND remain prevalent, including asymptomatic neurocognitive impairment (ANI) and mild neurocognitive disorder (MND). The overall prevalence of HAND is 30éˆ?0% among unselected HIV-infected persons." DSA08824,GSE143731,GPL16791,211,Tuberculosis,C0041296,,GEO,RNA-Seq,Homo sapiens,4|4,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA08825,GSE143735,GPL11154,532,Diabetic Foot Ulcer,C1456868,Skin,GEO,RNA-Seq,Homo sapiens,4|5,"MSH:Common foot problems in persons with DIABETES MELLITUS, caused by any combination of factors such as DIABETIC NEUROPATHIES; PERIPHERAL VASCULAR DISEASES; and INFECTION. With the loss of sensation and poor circulation, injuries and infections often lead to severe foot ulceration, GANGRENE and AMPUTATION, SURGICAL." DSA08826,GSE143735,GPL11154,54,Diabetic Foot Ulcer,C1456868,Skin,GEO,RNA-Seq,Homo sapiens,4|4,"MSH:Common foot problems in persons with DIABETES MELLITUS, caused by any combination of factors such as DIABETIC NEUROPATHIES; PERIPHERAL VASCULAR DISEASES; and INFECTION. With the loss of sensation and poor circulation, injuries and infections often lead to severe foot ulceration, GANGRENE and AMPUTATION, SURGICAL." DSA08827,GSE143782,GPL16791,1000,Rectal Cancer,C0007113,Rectum,GEO,RNA-Seq,Homo sapiens,6|6,DO:A colorectal cancer that is located_in the rectum. DSA08828,GSE143786,GPL28009,34,Hypertrophic Cardiomyopathy,C0007194,,GEO,Microarray,Homo sapiens,7|14,DO:A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations. DSA08829,GSE143788,GPL13112,1,Graft Versus Host Disease,C0018133,,GEO,RNA-Seq,Mus musculus,3|2,MONDO:An immune system disorder that occurs after allogeneic hematopoietic stem cell transplant and is a reaction of donor immune cells against host tissues. Activated donor T cells damage host epithelial cells after an inflammatory cascade that begins with the preparative regimen. DSA08830,GSE143791,GPL20301,1000,Prostate Cancer,C0600139,Bone marrow,GEO,scRNA-Seq,Homo sapiens,7|9,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08831,GSE10161,GPL96,101,Aortic Stenosis,C0003507,Cardiac left ventricle,GEO,Microarray,Homo sapiens,7|20,DO:A bicuspid aortic valve disease that has_material_basis_in heterozygous mutation in the SMAD6 gene on chromosome 15q22. DSA08832,GSE143908,GPL21290,1000,Developmental Disability,C0008073,,GEO,RNA-Seq,Homo sapiens,4|4,"EFO:Disorders in which there is a delay in development based on that expected for a given age level or stage of development. These impairments or disabilities originate before age 18, may be expected to continue indefinitely, and constitute a substantial impairment. Biological and nonbiological factors are involved in these disorders. (From American Psychiatric Glossary, 6th ed)" DSA08833,GSE143908,GPL21290,1000,Developmental Disability,C0008073,,GEO,RNA-Seq,Homo sapiens,4|4,"EFO:Disorders in which there is a delay in development based on that expected for a given age level or stage of development. These impairments or disabilities originate before age 18, may be expected to continue indefinitely, and constitute a substantial impairment. Biological and nonbiological factors are involved in these disorders. (From American Psychiatric Glossary, 6th ed)" DSA08834,GSE143951,GPL16043;,1000,Alzheimer's Disease,C0002395,,GEO,Microarray,Homo sapiens,3|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA08835,GSE143953,GPL20301,36,Pre-Eclampsia,C0032914,Placenta,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA08836,GSE14407,GPL570,1000,Ovarian Adenocarcinoma,C0948216,Ovary,GEO,Microarray,Homo sapiens,12|12,DO:An ovarian carcinoma that derives_from epithelial cells of glandular origin. DSA08837,GSE144119,GPL16791,1000,Chronic Myelogenous Leukemia,C0023473,,GEO,RNA-Seq,Homo sapiens,17|48,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA08838,GSE144119,GPL16791,1000,Chronic Myelogenous Leukemia,C0023473,,GEO,RNA-Seq,Homo sapiens,17|32,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA08839,GSE13396,GPL570,0,Asthma,C0004096,,GEO,Microarray,Homo sapiens,6|5,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08840,GSE144168,GPL18480,46,Experimental Autoimmune Encephalomyelitis,C0014072,Retina,GEO,RNA-Seq,Mus musculus,7|9,"EFO:An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)" DSA08841,GSE144208,GPL20301,19,Hereditary Sensory Neuropathy Type 1F,C3810194,,GEO,RNA-Seq,Homo sapiens,4|3,"DO:A hereditary sensory and autonomic neuropathy type 1 characterized by distal sensory impairment becomes apparent during the second or third decade of life, resulting in painless ulceration of the feet with poor healing, which can progress to osteomyelitis, bone destruction, and amputation that has_material_basis_in heterozygous mutation in the ATL3 gene on chromosome 11q13." DSA08842,GSE144208,GPL20301,89,Hereditary Sensory Neuropathy Type 1F,C3810194,,GEO,RNA-Seq,Homo sapiens,8|6,"DO:A hereditary sensory and autonomic neuropathy type 1 characterized by distal sensory impairment becomes apparent during the second or third decade of life, resulting in painless ulceration of the feet with poor healing, which can progress to osteomyelitis, bone destruction, and amputation that has_material_basis_in heterozygous mutation in the ATL3 gene on chromosome 11q13." DSA08843,GSE144208,GPL20301,1000,Hereditary Sensory Neuropathy Type 1F,C3810194,,GEO,RNA-Seq,Homo sapiens,4|3,"DO:A hereditary sensory and autonomic neuropathy type 1 characterized by distal sensory impairment becomes apparent during the second or third decade of life, resulting in painless ulceration of the feet with poor healing, which can progress to osteomyelitis, bone destruction, and amputation that has_material_basis_in heterozygous mutation in the ATL3 gene on chromosome 11q13." DSA08844,GSE144208,GPL20301,125,Hereditary Sensory Neuropathy Type 1F,C3810194,,GEO,RNA-Seq,Homo sapiens,4|3,"DO:A hereditary sensory and autonomic neuropathy type 1 characterized by distal sensory impairment becomes apparent during the second or third decade of life, resulting in painless ulceration of the feet with poor healing, which can progress to osteomyelitis, bone destruction, and amputation that has_material_basis_in heterozygous mutation in the ATL3 gene on chromosome 11q13." DSA08845,GSE144274,GPL20301,1000,Idiopathic Pulmonary Hypertension,C0152171,,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A chronic pulmonary heart disease characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein, or pulmonary capillaries, among others, has symptoms shortness of breath, dizziness, fainting, leg swelling." DSA08846,GSE144277,GPL13112,130,2Q23.1 Microdeletion Syndrome,C4304532,Cerebellum,GEO,RNA-Seq,Mus musculus,24|9,"MONDO:The newly described 2q23.1 microdeletion syndrome includes severe intellectual deficit with pronounced speech delay, behavioral abnormalities including hyperactivity and inappropriate laughter, short stature and seizures." DSA08847,GSE144317,GPL19057,198,Multiple Sclerosis,C0026769,Spinal cord,GEO,RNA-Seq,Mus musculus,7|27,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA08848,GSE144338,GPL22321,0,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,Microarray,Homo sapiens,4|4,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA08849,GSE144338,GPL22321,0,Lung Adenocarcinoma,C0152013,,GEO,Microarray,Homo sapiens,4|4,DO:A respiratory system cancer that is located_in the lung. DSA08850,GSE144358,GPL20795,1000,Severe Fever With Thrombocytopenia Syndrome,,Whole blood,GEO,RNA-Seq,Homo sapiens,21|56, DSA08851,GSE144381,GPL20301,1000,Lynch Syndrome,C4552100,Colorectal mucosa,GEO,RNA-Seq,Homo sapiens,18|100,"DO:A syndrome that is characterized by an increased risk for colon cancer and cancers of the endometrium, ovary, stomach, small intestine, hepatobiliary tract, urinary tract, brain, and skin and has_material_basis_in mutation of mismatch repair genes that increases the risk of many types of cancers." DSA08852,GSE144390,GPL6244,24,Systemic Lupus Erythematosus,C0024141,,GEO,Microarray,Homo sapiens,3|3,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA08853,GSE144406,GPL18573,1000,Multiple Mitochondrial Dysfunctions Syndrome,C3502075,Whole blood,GEO,RNA-Seq,Homo sapiens,4|17,DO:A mitochondrial metabolism disease that is characterized by reduced function of more than one stage of of energy production resulting from mitochondria impairment. DSA08854,GSE144406,GPL18573,1000,Multiple Mitochondrial Dysfunctions Syndrome,C3502075,Whole blood,GEO,RNA-Seq,Homo sapiens,4|6,DO:A mitochondrial metabolism disease that is characterized by reduced function of more than one stage of of energy production resulting from mitochondria impairment. DSA08855,GSE144469,GPL20301,1000,Colitis,C0009319,Colon,GEO,scRNA-Seq,Homo sapiens,8|8,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA08856,GSE144477,GPL20301,1000,Huntington's Disease,C0020179,,GEO,scRNA-Seq,Homo sapiens,1|1,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA08857,GSE144498,GPL17021,6,Acute Myocardial Infarction,C0155626,Bone marrow,GEO,RNA-Seq,Mus musculus,3|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA08858,GSE144498,GPL17021,77,Atherosclerosis,C0004153,Bone marrow,GEO,RNA-Seq,Mus musculus,3|3,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA08859,GSE144521,GPL14951,0,Ulcerative Colitis,C0009324,,GEO,Microarray,Homo sapiens,14|19,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA08860,GSE144521,GPL14951,293,Cholangiocarcinoma,C0206698,,GEO,Microarray,Homo sapiens,14|12,DO:A bile duct carcinoma that derives_from epithelial cells of glandular origin. DSA08861,GSE144521,GPL14951,27,Cholangiocarcinoma,C0206698,,GEO,Microarray,Homo sapiens,12|23,DO:A bile duct carcinoma that derives_from epithelial cells of glandular origin. DSA08862,GSE144521,GPL14951,413,Cholangiocarcinoma,C0206698,,GEO,Microarray,Homo sapiens,3|41,DO:A bile duct carcinoma that derives_from epithelial cells of glandular origin. DSA08863,GSE144522,GPL17021;,1000,Acute Kidney Injury,C2609414,Epididymis,GEO,RNA-Seq,Mus musculus,3|3,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA08864,GSE144557,GPL28098,1000,Cockayne Syndrome,C0009207,Brain,GEO,Microarray,Homo sapiens,5|7,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA08865,GSE144559,GPL16791,6,Huntington's Disease,C0020179,,GEO,RNA-Seq,Homo sapiens,8|14,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA08866,GSE144561,GPL18573;,1000,Pancreatic Cancer,C0235974,,GEO,RNA-Seq,Homo sapiens,21|60,DO:An endocrine gland cancer located_in the pancreas. DSA08867,GSE144567,GPL13112,1000,Cancer,C0006625,Tibialis anterior skeletal muscle,GEO,RNA-Seq,Mus musculus,4|6,"HPO:Severe weight loss, wasting of muscle, loss of appetite, and general debility related to a chronic disease." DSA08868,GSE13396,GPL570,0,Asthma,C0004096,,GEO,Microarray,Homo sapiens,6|5,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08869,GSE144576,GPL20301,954,Asthma,C0004096,,GEO,RNA-Seq,Homo sapiens,8|8,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08870,GSE144596,GPL17021;,1000,Heart Failure,C0018801,Left ventricle,GEO,RNA-Seq,Mus musculus,2|6,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA08871,GSE144640,GPL21103,12,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,RNA-Seq,Homo sapiens,5|4,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA08872,GSE144640,GPL21103,3,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,RNA-Seq,Homo sapiens,5|4,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA08873,GSE144640,GPL21103,749,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,RNA-Seq,Homo sapiens,6|5,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA08874,GSE144640,GPL21103,8,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,RNA-Seq,Homo sapiens,3|5,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA08875,GSE144690,GPL19057,1000,Mammary Tumor,C1512981,Mammary gland,GEO,RNA-Seq,Mus musculus,4|6,NCI:Production of a new growth or growths in the mammary gland. DSA08876,GSE144701,GPL19057,1000,Unilateral Nasal Obstruction,C2350170,Kidney,GEO,RNA-Seq,Mus musculus,3|3,"MSH:Any hindrance to the passage of air into and out of the nose. The obstruction may be unilateral or bilateral, and may involve any part of the NASAL CAVITY." DSA08877,GSE144914,GPL11154,11,Leber Hereditary Optic Neuropathy,C0029125,,GEO,RNA-Seq,Homo sapiens,6|3,MONDO:A family of inherited disorders characterized by progressive loss of vision secondary to death of the retinal ganglion cell axons that comprise the optic nerve. DSA08878,GSE144932,GPL18573,1000,Pulmonary Arterial Hypertension,C2973725,Pulmonary artery,GEO,RNA-Seq,Homo sapiens,4|4,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA08879,GSE145027,GPL26381,48,Epstein-Barr Virus Infection,C0149678,,GEO,Microarray,Homo sapiens,50|18,"EFO:Infection with human herpesvirus 4 (HERPESVIRUS 4, HUMAN); which may facilitate the development of various lymphoproliferative disorders. These include BURKITT LYMPHOMA (African type), INFECTIOUS MONONUCLEOSIS, and oral hairy leukoplakia (LEUKOPLAKIA, HAIRY)." DSA08880,GSE145027,GPL26381,120,Epstein-Barr Virus Infection,C0149678,,GEO,Microarray,Homo sapiens,50|15,"EFO:Infection with human herpesvirus 4 (HERPESVIRUS 4, HUMAN); which may facilitate the development of various lymphoproliferative disorders. These include BURKITT LYMPHOMA (African type), INFECTIOUS MONONUCLEOSIS, and oral hairy leukoplakia (LEUKOPLAKIA, HAIRY)." DSA08881,GSE145065,GPL16791,162,Sjogren's Syndrome,C1527336,,GEO,RNA-Seq,Homo sapiens,5|5,DO:An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. DSA08882,GSE145069,GPL11154,143,Glaucoma,C0017601,,GEO,RNA-Seq,Homo sapiens,4|4,DO:An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. DSA08883,GSE13396,GPL201,1000,Asthma,C0004096,,GEO,Microarray,Homo sapiens,3|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08884,GSE145086,GPL24247,1000,Injury of Liver,C0160390,Liver,GEO,scRNA-Seq,Mus musculus,3|3,NCI:Damage to liver structure or function due to trauma or toxicity. DSA08885,GSE145095,GPL21103,1000,Alopecia Areata,C0002171,Skin,GEO,scRNA-Seq,Mus musculus,1|1,DO:An autoimmune disease resulting in the loss of hair on the scalp and elsewhere on the body initially causing bald spots. DSA08886,GSE145095,GPL21103,1000,Alopecia Areata,C0002171,Lymph node,GEO,scRNA-Seq,Mus musculus,1|1,DO:An autoimmune disease resulting in the loss of hair on the scalp and elsewhere on the body initially causing bald spots. DSA08887,GSE145095,GPL20301,1000,Alopecia Areata,C0002171,Skin,GEO,scRNA-Seq,Homo sapiens,1|1,DO:An autoimmune disease resulting in the loss of hair on the scalp and elsewhere on the body initially causing bald spots. DSA08888,GSE145120,GPL13667,867,Systemic Sclerosis [Scleroderma],C2364016,Blood,GEO,Microarray,Homo sapiens,26|125, DSA08889,GSE145122,GPL24676,1000,22Q11.2 Deletion Syndrome,C2936346,,GEO,scRNA-Seq,Homo sapiens,2|2,"MONDO:22q11.2 deletion syndrome (DS) is a chromosomal anomaly which causes a congenital malformation disorder whose common features include cardiac defects, palatal anomalies, facial dysmorphism, developmental delay and immune deficiency." DSA08890,GSE145170,GPL24247,1000,Kidney Fibrosis,C0151650,Kidney,GEO,scRNA-Seq,Mus musculus,1|1,HPO:Renal fibrosis is the consequence of an excessive accumulation of extracellular matrix that occurs in virtually every type of chronic kidney disease. DSA08891,GSE14520,GPL3921,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,11|10,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA08892,GSE14520,GPL571,90,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,2|41,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA08893,GSE145227,GPL23178,1000,Sepsis,C0243026,Blood,GEO,Microarray,Homo sapiens,12|10,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA08894,GSE13396,GPL201,0,Asthma,C0004096,,GEO,Microarray,Homo sapiens,3|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA08895,GSE14525,GPL1261,563,Acute Lung Injury,C0242488,Lung,GEO,Microarray,Mus musculus,3|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08896,GSE14525,GPL1261,1000,Acute Lung Injury,C0242488,Lung,GEO,Microarray,Mus musculus,3|3,"EFO:Acute lung injuryè?ALI) is a diffuse heterogeneousè½lungè½injury characterized byè½hypoxemia, non cardiogenicè½pulmonary edema, lowè½lung complianceè½and widespreadè½capillaryè½leakage. ALI is caused by any stimulus of local or systemicè½inflammation, principallyè½sepsis." DSA08897,GSE145265,GPL21493,276,Cerebral Ischemia,C0917798,Brain microglia,GEO,RNA-Seq,Mus musculus,2|2,DO:A brain ischemia that is characterized by ischemia of brief duration and without resultant tissue death. DSA08898,GSE145265,GPL21493,99,Cerebral Ischemia,C0917798,Brain microglia,GEO,RNA-Seq,Mus musculus,2|2,DO:A brain ischemia that is characterized by ischemia of brief duration and without resultant tissue death. DSA08899,GSE145286,GPL19057,1000,Arthritis,C0003864,,GEO,scRNA-Seq,Mus musculus,1|1,DO:A bone disease that is located_in the joint. DSA08900,GSE145286,GPL19057,1000,Arthritis,C0003864,,GEO,scRNA-Seq,Mus musculus,1|1,DO:A bone disease that is located_in the joint. DSA08901,GSE145348,GPL20301,1000,Noonan Syndrome,C0028326,,GEO,RNA-Seq,Homo sapiens,5|8,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA08902,GSE145358,GPL18573,15,Coeliac Disease,C0007570,Duodenum small intestine,GEO,RNA-Seq,Homo sapiens,6|15,"DO:An autoimmune disease of gastrointestinal tract that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite." DSA08903,GSE145358,GPL18573,549,Coeliac Disease,C0007570,Duodenum small intestine,GEO,RNA-Seq,Homo sapiens,6|15,"DO:An autoimmune disease of gastrointestinal tract that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite." DSA08904,GSE145360,GPL20301,1000,Cystic Fibrosis,C0010674,,GEO,scRNA-Seq,Homo sapiens,5|10,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA08905,GSE90518,GPL17586,0,Ameloblastoma,C0002448,,GEO,Microarray,Homo sapiens,4|6,DO:A cell type benign neoplasm that has_material_basis_in odontogenic epithelium. DSA08906,GSE92420,GPL1261,1000,Cleft Palate;Calvarial Defect,,Mandible,GEO,Microarray,Mus musculus,3|3, DSA08907,GSE92420,GPL1261,1000,Cleft Palate;Calvarial Defect,,Mandible,GEO,Microarray,Mus musculus,3|3, DSA08908,GSE92420,GPL1261,7,Cleft Palate;Calvarial Defect,,Maxilla,GEO,Microarray,Mus musculus,3|3, DSA08909,GSE92420,GPL1261,166,Cleft Palate;Calvarial Defect,,Maxilla,GEO,Microarray,Mus musculus,3|3, DSA08910,GSE94789,GPL6096,87,Acute Viral Encephalitis,C0546994,Brain,GEO,Microarray,Mus musculus,3|3,DO:An encephalitis that involves inflammation of the brain caused by viral infection. DSA08911,GSE94837,GPL11097,144,Melanoma,C0025202,,GEO,Microarray,Homo sapiens,2|2,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA08912,GSE94837,GPL11097,63,Melanoma,C0025202,,GEO,Microarray,Homo sapiens,2|2,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA08913,GSE13104,GPL1261,1000,Osteosarcoma,C0029463,,GEO,Microarray,Mus musculus,1|12,DO:A bone sarcoma that is located_in bone that has_material_basis_in cells of mesenchymal origin. DSA08914,GSE95278,GPL1261,0,Central Nervous System Sensitization,C2938905,Skin,GEO,Microarray,Mus musculus,2|2,MSH:An increased response to stimulation that is mediated by amplification of signaling in the CENTRAL NERVOUS SYSTEM (CNS). DSA08915,GSE95786,GPL10333,1000,Skin Injury,,,GEO,Microarray,Mus musculus,2|2, DSA08916,GSE9594,GPL8321,0,Chronic Constriction Injury,,Medulla,GEO,Microarray,Mus musculus,4|4, DSA08917,GSE9594,GPL8321,0,Chronic Constriction Injury,,Medulla,GEO,Microarray,Mus musculus,4|4, DSA08918,GSE9594,GPL8321,0,Chronic Constriction Injury,,Midbrain,GEO,Microarray,Mus musculus,4|4, DSA08919,GSE9594,GPL8321,0,Chronic Constriction Injury,,Midbrain,GEO,Microarray,Mus musculus,4|4, DSA08920,GSE96077,GPL16791,1000,Preterm Labor,C0022876,,GEO,RNA-Seq,Homo sapiens,28|10,"MSH:Onset of OBSTETRIC LABOR before term (TERM BIRTH) but usually after the FETUS has become viable. In humans, it occurs sometime during the 29th through 38th week of PREGNANCY. TOCOLYSIS inhibits premature labor and can prevent the BIRTH of premature infants (INFANT, PREMATURE)." DSA08921,GSE96083,GPL16791,1000,Preterm Labor,C0022876,Whole blood,GEO,RNA-Seq,Homo sapiens,23|15,"MSH:Onset of OBSTETRIC LABOR before term (TERM BIRTH) but usually after the FETUS has become viable. In humans, it occurs sometime during the 29th through 38th week of PREGNANCY. TOCOLYSIS inhibits premature labor and can prevent the BIRTH of premature infants (INFANT, PREMATURE)." DSA08922,GSE96597,GPL14951,1,Colorectal Carcinoma,C0009402,Peripheral blood,GEO,Microarray,Homo sapiens,4|4,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA08923,GSE96616,GPL19057,156,Microcephaly,C0025958,Brain,GEO,RNA-Seq,Mus musculus,5|5,DO:A congenital nervous system abnormality that is characterized by a significantly smaller than normal head in infants. DSA08924,GSE97013,GPL19057,1000,Colorectal Carcinoma,C0009402,,GEO,RNA-Seq,Mus musculus,2|2,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA08925,GSE97024,GPL23479,441,Fatty Liver,C0015695,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA08926,GSE97076,GPL7202,0,Neuropathic Pain,C3714625,Spinal cord,GEO,Microarray,Mus musculus,3|3,NCI:Chronic pain caused by damage to nerve fibers. It is usually associated with tissue injury. DSA08927,GSE11501,GPL6104,148,Coeliac Disease,C0007570,Peripheral blood,GEO,Microarray,Homo sapiens,22|110,"DO:An autoimmune disease of gastrointestinal tract that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite." DSA08928,GSE98407,GPL19057,1000,Colitis,C0009319,Intestine,GEO,RNA-Seq,Mus musculus,5|5,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA08929,GSE98527,GPL17021,1000,H1N1 Influenza,C2076600,Lung,GEO,RNA-Seq,Mus musculus,3|3,"EFO:An influenza that results_in infection located_in respiratory tract of pigs and humans, has_material_basis_in Influenza C virus, or has_material_basis_in Influenza A virus subtypes (H1N1, H1N2, H3N1, H3N2, and H2N3), which are transmitted_by direct contact with infected pigs. The infection in humans has_symptom fever, has_symptom lethargy, has_symptom lack of appetite, has_symptom coughing, has_symptom runny nose, has_symptom sore throat, has_symptom nausea, has_symptom vomiting, and has_symptom diarrhea." DSA08930,GSE98527,GPL17021,1000,Influenza,C0021400,Lung,GEO,RNA-Seq,Mus musculus,3|3,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA08931,GSE98527,GPL17021,1000,Influenza A/H5N1,C2076596,Lung,GEO,RNA-Seq,Mus musculus,3|3,"DO:An influenza that results in infection located in respiratory tract of humans, domestic and wild birds, has_material_basis_in Influenza A virus, which is transmitted by contact with infected poultry. Five strains of avian influenza A viruses (H5N1, H7N3, H7N2, H7N7 and H9N2) are known to cause human infections. The infection has_symptom fever, has_symptom cough, has_symptom sore throat, has_symptom muscle aches, has_symptom nausea, has_symptom diarrhea, has_symptom vomiting, has_symptom neurologic changes, has_symptom pneumonia, and has_symptom acute respiratory distress." DSA08932,GSE99189,GPL16570,1000,H1N1 Influenza,C2076600,Lung,GEO,Microarray,Mus musculus,4|4,"EFO:An influenza that results_in infection located_in respiratory tract of pigs and humans, has_material_basis_in Influenza C virus, or has_material_basis_in Influenza A virus subtypes (H1N1, H1N2, H3N1, H3N2, and H2N3), which are transmitted_by direct contact with infected pigs. The infection in humans has_symptom fever, has_symptom lethargy, has_symptom lack of appetite, has_symptom coughing, has_symptom runny nose, has_symptom sore throat, has_symptom nausea, has_symptom vomiting, and has_symptom diarrhea." DSA08933,GSE99189,GPL16570,1000,H1N1 Influenza,C2076600,Lung,GEO,Microarray,Mus musculus,4|4,"EFO:An influenza that results_in infection located_in respiratory tract of pigs and humans, has_material_basis_in Influenza C virus, or has_material_basis_in Influenza A virus subtypes (H1N1, H1N2, H3N1, H3N2, and H2N3), which are transmitted_by direct contact with infected pigs. The infection in humans has_symptom fever, has_symptom lethargy, has_symptom lack of appetite, has_symptom coughing, has_symptom runny nose, has_symptom sore throat, has_symptom nausea, has_symptom vomiting, and has_symptom diarrhea." DSA08934,GSE99467,GPL11202,0,Mammary Tumor,C1512981,Bone marrow,GEO,Microarray,Mus musculus,4|4,NCI:Production of a new growth or growths in the mammary gland. DSA08935,GSE99467,GPL11202,26,Mammary Tumor,C1512981,Bone marrow,GEO,Microarray,Mus musculus,4|4,NCI:Production of a new growth or growths in the mammary gland. DSA08936,GSE130116,GPL20301,1000,Acute Myeloblastic Leukemia,C2854122,Bone marrow,GEO,scRNA-Seq,Homo sapiens,4|7,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA08937,GSE130116,GPL20301,1000,Acute Myeloblastic Leukemia,C2854122,Bone marrow,GEO,scRNA-Seq,Homo sapiens,4|6,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA08938,GSE108497,GPL10558,319,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,38|83,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA08939,GSE108497,GPL10558,383,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,37|75,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA08940,GSE108497,GPL10558,510,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,37|70,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA08941,GSE108497,GPL10558,115,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,35|55,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA08942,GSE108497,GPL10558,10,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,17|40,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA08943,GSE144469,GPL20301,1000,Colitis,C0009319,Colon,GEO,scRNA-Seq,Homo sapiens,5|4,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA08944,GSE11309,GPL570,0,Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy,,,GEO,Microarray,Homo sapiens,3|3, DSA08945,TCGA-BLCA,,1000,Bladder Cancer,C0699885,,TCGA,RNA-Seq,Homo sapiens,19|410,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08946,TCGA-BRCA,,1000,Invasive Breast Carcinoma,C0853879,,TCGA,RNA-Seq,Homo sapiens,112|1103,"EFO:A carcinoma that infiltrates the breast parenchyma. The vast majority are adenocarcinomas arising from the terminal ductal lobular unit (TDLU). Often, the invasive adenocarcinoma co-exists with ductal or lobular carcinoma in situ. It is the most common carcinoma affecting women." DSA08947,TCGA-BRCA,,1000,Invasive Breast Carcinoma,C0853879,,TCGA,RNA-Seq,Homo sapiens,112|1096,"EFO:A carcinoma that infiltrates the breast parenchyma. The vast majority are adenocarcinomas arising from the terminal ductal lobular unit (TDLU). Often, the invasive adenocarcinoma co-exists with ductal or lobular carcinoma in situ. It is the most common carcinoma affecting women." DSA08948,TCGA-BRCA,,1000,Invasive Breast Carcinoma,C0853879,,TCGA,RNA-Seq,Homo sapiens,112|7,"EFO:A carcinoma that infiltrates the breast parenchyma. The vast majority are adenocarcinomas arising from the terminal ductal lobular unit (TDLU). Often, the invasive adenocarcinoma co-exists with ductal or lobular carcinoma in situ. It is the most common carcinoma affecting women." DSA08949,TCGA-BRCA,,587,Metastatic Invasive Breast Carcinoma,C0853879,,TCGA,RNA-Seq,Homo sapiens,1096|7,"EFO:A carcinoma that infiltrates the breast parenchyma. The vast majority are adenocarcinomas arising from the terminal ductal lobular unit (TDLU). Often, the invasive adenocarcinoma co-exists with ductal or lobular carcinoma in situ. It is the most common carcinoma affecting women." DSA08950,TCGA-CESC,,1000,Cervical Squamous Cell Carcinoma;Endocervical Adenocarcinoma,,,TCGA,RNA-Seq,Homo sapiens,3|306, DSA08951,TCGA-CESC,,1000,Cervical Squamous Cell Carcinoma;Endocervical Adenocarcinoma,,,TCGA,RNA-Seq,Homo sapiens,3|304, DSA08952,TCGA-CESC,,1000,Cervical Squamous Cell Carcinoma;Endocervical Adenocarcinoma,,,TCGA,RNA-Seq,Homo sapiens,3|2, DSA08953,TCGA-CESC,,88,Metastatic Invasive Cervical Squamous Cell Carcinoma;Endocervical Adenocarcinoma,,,TCGA,RNA-Seq,Homo sapiens,304|2, DSA08954,TCGA-CHOL,,1000,Cholangiocarcinoma,C0206698,,TCGA,RNA-Seq,Homo sapiens,9|36,DO:A bile duct carcinoma that derives_from epithelial cells of glandular origin. DSA08955,TCGA-COAD,,1000,Colon Cancer,C0699790,,TCGA,RNA-Seq,Homo sapiens,41|471,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08956,TCGA-ESCA,,1000,Esophageal Cancer,C0152018,,TCGA,RNA-Seq,Homo sapiens,11|162,DO:A esophageal cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA08957,TCGA-GBM,,1000,Glioblastoma,C0017636,,TCGA,RNA-Seq,Homo sapiens,5|168,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA08958,TCGA-GBM,,1000,Glioblastoma,C0017636,,TCGA,RNA-Seq,Homo sapiens,5|155,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA08959,TCGA-GBM,,1000,Glioblastoma,C0017636,,TCGA,RNA-Seq,Homo sapiens,5|13,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA08960,TCGA-HNSC,,1000,Head And Neck Squamous Cell Carcinoma,C1168401,,TCGA,RNA-Seq,Homo sapiens,44|502,"DO:A head and neck carcinoma that has_material_basis_in squamous cells that line the moist, mucosal surfaces inside the head and neck." DSA08961,TCGA-HNSC,,1000,Head And Neck Squamous Cell Carcinoma,C1168401,,TCGA,RNA-Seq,Homo sapiens,44|500,"DO:A head and neck carcinoma that has_material_basis_in squamous cells that line the moist, mucosal surfaces inside the head and neck." DSA08962,TCGA-HNSC,,1000,Head And Neck Squamous Cell Carcinoma,C1168401,,TCGA,RNA-Seq,Homo sapiens,44|2,"DO:A head and neck carcinoma that has_material_basis_in squamous cells that line the moist, mucosal surfaces inside the head and neck." DSA08963,TCGA-HNSC,,1000,Metastatic Invasive Head And Neck Squamous Cell Carcinoma,C1168401,,TCGA,RNA-Seq,Homo sapiens,500|2,"DO:A head and neck carcinoma that has_material_basis_in squamous cells that line the moist, mucosal surfaces inside the head and neck." DSA08964,TCGA-KICH,,1000,Kidney Chromophobe,,,TCGA,RNA-Seq,Homo sapiens,24|65, DSA08965,TCGA-KIRC,,1000,Kidney Clear Cell Carcinoma,C0279702,,TCGA,RNA-Seq,Homo sapiens,72|535,DO:A hereditary renal cell carcinoma that has_material_basis_in a loss of 3p13-pter sequences. DSA08966,TCGA-KIRP,,1000,Papillary Renal Cell Carcinoma,C1306837,,TCGA,RNA-Seq,Homo sapiens,32|289,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA08967,TCGA-LIHC,,1000,Liver Hepatocellular Carcinoma,C2239176,,TCGA,RNA-Seq,Homo sapiens,50|373,DO:A hepatobiliary system cancer that is located_in the liver. DSA08968,TCGA-LIHC,,1000,Liver Hepatocellular Carcinoma,C2239176,,TCGA,RNA-Seq,Homo sapiens,50|370,DO:A hepatobiliary system cancer that is located_in the liver. DSA08969,TCGA-LIHC,,1000,Liver Hepatocellular Carcinoma,C2239176,,TCGA,RNA-Seq,Homo sapiens,50|3,DO:A hepatobiliary system cancer that is located_in the liver. DSA08970,TCGA-LUAD,,1000,Lung Adenocarcinoma,C0152013,,TCGA,RNA-Seq,Homo sapiens,59|526,DO:A respiratory system cancer that is located_in the lung. DSA08971,TCGA-LUAD,,1000,Lung Adenocarcinoma,C0152013,,TCGA,RNA-Seq,Homo sapiens,59|524,DO:A respiratory system cancer that is located_in the lung. DSA08972,TCGA-LUAD,,1000,Lung Adenocarcinoma,C0152013,,TCGA,RNA-Seq,Homo sapiens,59|2,DO:A respiratory system cancer that is located_in the lung. DSA08973,TCGA-LUSC,,1000,Lung Squamous Cell Carcinoma,C0149782,,TCGA,RNA-Seq,Homo sapiens,49|501,DO:A non-small cell lung carcinoma that has_material_basis_in the squamous cell. DSA08974,TCGA-PAAD,,559,Pancreatic Adenocarcinoma,C0281361,,TCGA,RNA-Seq,Homo sapiens,4|178,DO:A pancreatic carcinoma that derives_from epithelial cells of glandular origin. DSA08975,TCGA-PCPG,,1000,Hereditary Pheochromocytoma-Paraganglioma,C1708353,,TCGA,RNA-Seq,Homo sapiens,3|183,MONDO:Hereditary paraganglioma-pheochromocytomas (PGL/PCC) are rare neuroendocrine tumors represented by paragangliomas (occurring in any paraganglia from the skull base to the pelvic floor) and pheochromocytomas (adrenal medullary paragangliomas). DSA08976,TCGA-PCPG,,1000,Hereditary Pheochromocytoma-Paraganglioma,C1708353,,TCGA,RNA-Seq,Homo sapiens,3|181,MONDO:Hereditary paraganglioma-pheochromocytomas (PGL/PCC) are rare neuroendocrine tumors represented by paragangliomas (occurring in any paraganglia from the skull base to the pelvic floor) and pheochromocytomas (adrenal medullary paragangliomas). DSA08977,TCGA-PCPG,,1000,Hereditary Pheochromocytoma-Paraganglioma,C1708353,,TCGA,RNA-Seq,Homo sapiens,3|2,MONDO:Hereditary paraganglioma-pheochromocytomas (PGL/PCC) are rare neuroendocrine tumors represented by paragangliomas (occurring in any paraganglia from the skull base to the pelvic floor) and pheochromocytomas (adrenal medullary paragangliomas). DSA08978,TCGA-PCPG,,43,Metastatic Invasive Hereditary Pheochromocytoma-Paraganglioma,C1708353,,TCGA,RNA-Seq,Homo sapiens,181|2,MONDO:Hereditary paraganglioma-pheochromocytomas (PGL/PCC) are rare neuroendocrine tumors represented by paragangliomas (occurring in any paraganglia from the skull base to the pelvic floor) and pheochromocytomas (adrenal medullary paragangliomas). DSA08979,TCGA-PCPG,,1000,Paraganglioma,C0030421,,TCGA,RNA-Seq,Homo sapiens,3|32,DO:A pheochromocytoma that arises in extraadrenal sympathetic ganglia. DSA08980,TCGA-PCPG,,1000,Pheochromocytoma,C0031511,,TCGA,RNA-Seq,Homo sapiens,3|151,"DO:An endocrine organ benign neoplasm that arises within the adrenal medulla, releasing epinephrines and norepinephrines hormones that cause either episodic or persistent high blood pressure." DSA08981,TCGA-PRAD,,1000,Prostate Adenocarcinoma,C0007112,,TCGA,RNA-Seq,Homo sapiens,52|499,DO:A prostate carcinoma that derives_from epithelial cells of glandular origin. DSA08982,TCGA-READ,,1000,Rectum Adenocarcinoma,C0149978,,TCGA,RNA-Seq,Homo sapiens,10|167,DO:A rectum cancer that derives_from epithelial cells of glandular origin. DSA08983,TCGA-SARC,,1000,Sarcoma,C1261473,,TCGA,RNA-Seq,Homo sapiens,2|261,DO:A sarcoma that results_in cells that are spindle-shaped. They are usually resistant to radiation therapy. DSA08984,TCGA-SARC,,1000,Sarcoma,C1261473,,TCGA,RNA-Seq,Homo sapiens,2|258,DO:A sarcoma that results_in cells that are spindle-shaped. They are usually resistant to radiation therapy. DSA08985,TCGA-SARC,,886,Sarcoma,C1261473,,TCGA,RNA-Seq,Homo sapiens,2|3,DO:A sarcoma that results_in cells that are spindle-shaped. They are usually resistant to radiation therapy. DSA08986,TCGA-SKCM,,32,Skin Cutaneous Celanoma,,,TCGA,RNA-Seq,Homo sapiens,1|471, DSA08987,TCGA-SKCM,,93,Skin Cutaneous Celanoma,,,TCGA,RNA-Seq,Homo sapiens,1|103, DSA08988,TCGA-SKCM,,10,Skin Cutaneous Celanoma,,,TCGA,RNA-Seq,Homo sapiens,1|368, DSA08989,TCGA-SKCM,,1000,Metastatic Invasive Skin Cutaneous Celanoma,,,TCGA,RNA-Seq,Homo sapiens,103|368, DSA08990,TCGA-STAD,,1000,Stomach Adenocarcinoma,C0278701,,TCGA,RNA-Seq,Homo sapiens,32|375,DO:A stomach carcinoma that derives_from epithelial cells of glandular origin. DSA08991,TCGA-THCA,,1000,Thyroid Carcinoma,C0549473,,TCGA,RNA-Seq,Homo sapiens,57|509,DO:A thyroid gland cancer that has_material_basis_in epithelial cells. DSA08992,TCGA-THCA,,1000,Thyroid Carcinoma,C0549473,,TCGA,RNA-Seq,Homo sapiens,57|501,DO:A thyroid gland cancer that has_material_basis_in epithelial cells. DSA08993,TCGA-THCA,,1000,Thyroid Carcinoma,C0549473,,TCGA,RNA-Seq,Homo sapiens,57|8,DO:A thyroid gland cancer that has_material_basis_in epithelial cells. DSA08994,TCGA-THCA,,70,Metastatic Invasive Thyroid Carcinoma,C0549473,,TCGA,RNA-Seq,Homo sapiens,501|8,DO:A thyroid gland cancer that has_material_basis_in epithelial cells. DSA08995,TCGA-THYM,,238,Thymoma,C0040100,,TCGA,RNA-Seq,Homo sapiens,2|119,"DO:A thymus cancer that derives_from epithelial cells located_in the thymus. The tumor cells in a thymoma look similar to the normal cells of the thymus, grow slowly, and rarely spread beyond the thymus." DSA08996,TCGA-UCEC,,1000,Uterine Corpus Endometrioid Carcinoma,C1336905,,TCGA,RNA-Seq,Homo sapiens,35|548,DO:An endometrial carcinoma that derives_from epithelial cells of glandular origin. DSA08997,TARGET-RT,,1000,Rhabdoid Tumor,C0206743,,TCGA,RNA-Seq,Homo sapiens,5|62,"DO:A brain cancer that is usually located in the brain, but can occur anywhere in the central nervous system." DSA08998,TARGET-WT,,1000,Wilms Tumor,C2930471,,TCGA,RNA-Seq,Homo sapiens,6|126,"MSH:A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN." DSA08999,TARGET-WT,,1000,Wilms Tumor,C2930471,,TCGA,RNA-Seq,Homo sapiens,6|121,"MSH:A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN." DSA09000,TARGET-WT,,1000,Wilms Tumor,C2930471,,TCGA,RNA-Seq,Homo sapiens,6|5,"MSH:A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN." DSA09001,GSE113210,GPL16791,1000,Bronchiolitis; Viral,C0339941,,GEO,RNA-Seq,Homo sapiens,16|15, DSA09002,GSE113210,GPL16791,147,Bronchiolitis; Viral,C0339941,,GEO,RNA-Seq,Homo sapiens,15|15, DSA09003,GSE119117,GPL16791,3,Hepatitis C,C0019196,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA09004,GSE119117,GPL16791,2,Hepatitis C,C0019196,,GEO,RNA-Seq,Homo sapiens,3|2,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA09005,GSE119117,GPL16791,2,Hepatitis C,C0019196,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA09006,GSE119117,GPL16791,0,Hepatitis C,C0019196,,GEO,RNA-Seq,Homo sapiens,3|2,"DO:A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice." DSA09007,GSE97356,GPL11154,805,Post-Traumatic Stress Disorder,C0038436,Blood,GEO,RNA-Seq,Homo sapiens,201|81,DO:An anxiety disorder which results from a traumatic experience that results in psychological trauma. DSA09008,GSE172450,GPL24676,195,Malaria,C0024530,Blood,GEO,RNA-Seq,Homo sapiens,13|46,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA09009,GSE172450,GPL24676,1000,Malaria,C0024530,Blood,GEO,RNA-Seq,Homo sapiens,13|13,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA09010,GSE172450,GPL24676,9,Malaria,C0024530,Blood,GEO,RNA-Seq,Homo sapiens,9|36,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA09011,GSE172450,GPL24676,1000,Malaria,C0024530,Blood,GEO,RNA-Seq,Homo sapiens,9|10,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA09012,GSE172450,GPL24676,93,Malaria,C0024530,Blood,GEO,RNA-Seq,Homo sapiens,6|24,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA09013,GSE172450,GPL24676,1000,Malaria,C0024530,Blood,GEO,RNA-Seq,Homo sapiens,6|6,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA09014,GSE7700,GPL570,1000,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,3|2,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09015,GSE7700,GPL570,1000,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,3|2,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09016,GSE77049,GPL6246,2,Cerebellar Malformation,C4025708,Brain,GEO,Microarray,Mus musculus,5|3, DSA09017,GSE77049,GPL6246,539,Cerebellar Malformation,C4025708,Brain,GEO,Microarray,Mus musculus,6|2, DSA09018,GSE11309,GPL570,1,Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy,,,GEO,Microarray,Homo sapiens,3|3, DSA09019,GSE8154,GPL339,0,Diabetes,C0011847,Embryonic brain,GEO,Microarray,Mus musculus,2|2,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09020,GSE78025,GPL11154,1000,Glioblastoma,C0017636,Brain,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA09021,GSE78025,GPL11154,1000,Glioblastoma,C0017636,Brain,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA09022,GSE78025,GPL11154,1000,Glioblastoma,C0017636,Brain,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA09023,GSE79416,GPL17021,1000,Subarachnoid Hemorrhage,C0038525,Brain,GEO,RNA-Seq,Mus musculus,2|3,EFO:Intracranial hemorrhage into the subarachnoid space. DSA09024,GSE12852,GPL2986,0,Pelvic Organ Prolapse,C0877015,Round ligament,GEO,Microarray,Homo sapiens,9|8,"EFO:Abnormal descent of a pelvic organ resulting in the protrusion of the organ beyond its normal anatomical confines. Symptoms often include vaginal discomfort, dyspareunia; urinary stress incontinence; and fecal incontinence." DSA09025,GSE80005,GPL1261,1000,Esophageal Squamous Cell Carcinoma,C0279626,Esophagus,GEO,Microarray,Mus musculus,3|2,DO:An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus. DSA09026,GSE80085,GPL17400,1000,Ovarian Tumor,C1140680,Oviduct,GEO,Microarray,Mus musculus,4|5,DO:A female reproductive organ cancer that is located_in the ovary. DSA09027,GSE12852,GPL2986,0,Pelvic Organ Prolapse,C0877015,Uterosacral ligament,GEO,Microarray,Homo sapiens,9|8,"EFO:Abnormal descent of a pelvic organ resulting in the protrusion of the organ beyond its normal anatomical confines. Symptoms often include vaginal discomfort, dyspareunia; urinary stress incontinence; and fecal incontinence." DSA09028,GSE80338,GPL18460,1000,Glioblastoma,C0017636,Brain,GEO,RNA-Seq,Homo sapiens,8|8,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA09029,GSE11839,GPL570,1,Interstitial Cystitis,C0282488,,GEO,Microarray,Homo sapiens,6|6,"DO:A chronic cystitis characterized by unpleasant sensation related to the bladder and lower urinary tract in the absence of identifiable causes and has_symptom pain, has_symptom pressure, has_symptom discomfort, has_symptom dysuria, and/or has_symptom urinary frequency." DSA09030,GSE82319,GPL16368,1000,Ovarian Serous Carcinoma,C1335177,Fallopian tube,GEO,Microarray,Mus musculus,3|5,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA09031,GSE4324,GPL339,0,Malaria,C0024530,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA09032,GSE4324,GPL339,106,Malaria,C0024530,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA09033,GSE4324,GPL339,1000,Malaria,C0024530,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA09034,GSE4324,GPL339,0,Malaria,C0024530,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA09035,GSE4324,GPL339,793,Malaria,C0024530,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA09036,GSE4324,GPL339,1000,Malaria,C0024530,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA09037,GSE4324,GPL339,0,Malaria,C0024530,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA09038,GSE4324,GPL339,344,Malaria,C0024530,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA09039,GSE4324,GPL339,964,Malaria,C0024530,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA09040,GSE4324,GPL339,0,Malaria,C0024530,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA09041,GSE4324,GPL339,445,Malaria,C0024530,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA09042,GSE4324,GPL339,1000,Malaria,C0024530,Spleen,GEO,Microarray,Mus musculus,3|3,"DO:A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle." DSA09043,GSE435,GPL81,0,Muscle Ache,C0231528,Skeletal muscle,GEO,Microarray,Mus musculus,2|2,"DO:A syndrome that is is characterized by chronic widespread musculoskeletal pain, fatigue, sleep disturbances, cognitive dysfunction and depression." DSA09044,GSE435,GPL81,0,Muscle Ache,C0231528,Skeletal muscle,GEO,Microarray,Mus musculus,2|2,"DO:A syndrome that is is characterized by chronic widespread musculoskeletal pain, fatigue, sleep disturbances, cognitive dysfunction and depression." DSA09045,GSE43620,GPL1261,1000,Diabetes,C0011847,Pancreatic islet,GEO,Microarray,Mus musculus,2|2,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09046,GSE43620,GPL1261,54,Diabetes,C0011847,Pancreatic islet,GEO,Microarray,Mus musculus,2|2,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09047,GSE43628,GPL6887,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Mus musculus,4|4,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA09048,GSE12648,GPL96,17,"Inclusion Body Myopathy, Autosomal Dominant",C2931820,Muscle,GEO,Microarray,Homo sapiens,10|10, DSA09049,GSE43841,GPL14951,638,Hyperplastic Polyp,C0333983,Colon,GEO,Microarray,Homo sapiens,6|6,"EFO:A polyp found mainly in the stomach and colon. Microscopically, it is characterized by elongated, serrated crypts lined by proliferative epithelium. Hyperplastic polyps are traditionally considered non-neoplastic, but ras mutation is common, clonality has been demonstrated and biochemical abnormalities and epidemiological associations that occur in colorectal adenomas and carcinomas have been found (WHO Tumors of the Digestive System, 2000)." DSA09050,GSE43841,GPL14951,876,Sessile Serrated Adenoma/Polyp,C2732618,Colon,GEO,Microarray,Homo sapiens,6|6,"EFO:A sessile serrated polyp is a serrated polyp that demonstrates abnormal cellular proliferation characterized by a proximally displaced proliferative zone, epithelial serrations, and characteristic distorted basilar crypt architecture with crypt dilation, branching, and lateral growth along the muscularis mucosa." DSA09051,GSE12484,GPL96,0,Periodontitis,C0031099,,GEO,Microarray,Homo sapiens,2|2,"EFO:Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology)" DSA09052,GSE44205,GPL6105,1000,Muscle Atrophy,C0026846,Triceps muscle,GEO,Microarray,Mus musculus,3|3,EFO:The loss of muscle tissue due to inactivity or disease. DSA09053,GSE44205,GPL6105,170,Muscle Atrophy,C0026846,Triceps surae muscle,GEO,Microarray,Mus musculus,3|3,EFO:The loss of muscle tissue due to inactivity or disease. DSA09054,GSE44205,GPL6105,1000,Muscle Atrophy,C0026846,Triceps muscle,GEO,Microarray,Mus musculus,3|3,EFO:The loss of muscle tissue due to inactivity or disease. DSA09055,GSE44205,GPL6105,1000,Muscle Atrophy,C0026846,Triceps muscle,GEO,Microarray,Mus musculus,3|3,EFO:The loss of muscle tissue due to inactivity or disease. DSA09056,GSE12216,GPL2986,0,Intrauterine Growth Restriction,C1386048,Placenta,GEO,Microarray,Homo sapiens,8|8,HPO:An abnormal restriction of fetal growth with fetal weight below the tenth percentile for gestational age. DSA09057,GSE11967,GPL5188,0,Myasthenia Gravis,C0026896,Thymus,GEO,Microarray,Homo sapiens,2|2,"DO:An autoimmune disease of the nervous system that has_material_basis_in antibodies to acetylcholine receptors at the neuromuscular junction, has_symptom ptosis, has_symptom diplopia, has_symptom dysphagia, has_symptom dysarthria, has_symptom muscle weakness and has_symptom shortness of breath." DSA09058,GSE11967,GPL5175,426,Myasthenia Gravis,C0026896,Thymus,GEO,Microarray,Homo sapiens,2|2,"DO:An autoimmune disease of the nervous system that has_material_basis_in antibodies to acetylcholine receptors at the neuromuscular junction, has_symptom ptosis, has_symptom diplopia, has_symptom dysphagia, has_symptom dysarthria, has_symptom muscle weakness and has_symptom shortness of breath." DSA09059,GSE44322,GPL6246,1000,Lymphocytic Choriomeningitis,C0024266,Spleen,GEO,Microarray,Mus musculus,4|3,"DO:A viral infectious disease that results in infection located in brain, or located in meninges, or located in brain and meninges, has_material_basis_in Lymphocytic choriomeningitis virus, which is transmitted by common house mouse, Mus musculus. The infection has symptom fever, has symptom lack of appetite, has symptom headache, has symptom muscle aches, has symptom malaise, has symptom nausea, and has symptom vomiting." DSA09060,GSE44322,GPL6246,1000,Lymphocytic Choriomeningitis,C0024266,Spleen,GEO,Microarray,Mus musculus,4|3,"DO:A viral infectious disease that results in infection located in brain, or located in meninges, or located in brain and meninges, has_material_basis_in Lymphocytic choriomeningitis virus, which is transmitted by common house mouse, Mus musculus. The infection has symptom fever, has symptom lack of appetite, has symptom headache, has symptom muscle aches, has symptom malaise, has symptom nausea, and has symptom vomiting." DSA09061,GSE44322,GPL6246,11,Lymphocytic Choriomeningitis,C0024266,Spleen,GEO,Microarray,Mus musculus,4|4,"DO:A viral infectious disease that results in infection located in brain, or located in meninges, or located in brain and meninges, has_material_basis_in Lymphocytic choriomeningitis virus, which is transmitted by common house mouse, Mus musculus. The infection has symptom fever, has symptom lack of appetite, has symptom headache, has symptom muscle aches, has symptom malaise, has symptom nausea, and has symptom vomiting." DSA09062,GSE44322,GPL6246,1000,Lymphocytic Choriomeningitis,C0024266,Spleen,GEO,Microarray,Mus musculus,4|3,"DO:A viral infectious disease that results in infection located in brain, or located in meninges, or located in brain and meninges, has_material_basis_in Lymphocytic choriomeningitis virus, which is transmitted by common house mouse, Mus musculus. The infection has symptom fever, has symptom lack of appetite, has symptom headache, has symptom muscle aches, has symptom malaise, has symptom nausea, and has symptom vomiting." DSA09063,GSE44322,GPL6246,1000,Lymphocytic Choriomeningitis,C0024266,Spleen,GEO,Microarray,Mus musculus,4|4,"DO:A viral infectious disease that results in infection located in brain, or located in meninges, or located in brain and meninges, has_material_basis_in Lymphocytic choriomeningitis virus, which is transmitted by common house mouse, Mus musculus. The infection has symptom fever, has symptom lack of appetite, has symptom headache, has symptom muscle aches, has symptom malaise, has symptom nausea, and has symptom vomiting." DSA09064,GSE44322,GPL6246,1000,Lymphocytic Choriomeningitis,C0024266,Spleen,GEO,Microarray,Mus musculus,4|4,"DO:A viral infectious disease that results in infection located in brain, or located in meninges, or located in brain and meninges, has_material_basis_in Lymphocytic choriomeningitis virus, which is transmitted by common house mouse, Mus musculus. The infection has symptom fever, has symptom lack of appetite, has symptom headache, has symptom muscle aches, has symptom malaise, has symptom nausea, and has symptom vomiting." DSA09065,GSE9460,GPL1261,1000,Osteosarcoma,C0029463,,GEO,Microarray,Mus musculus,3|15,DO:A bone sarcoma that is located_in bone that has_material_basis_in cells of mesenchymal origin. DSA09066,GSE44561,GPL11532,0,Glioma,C0017638,,GEO,Microarray,Homo sapiens,1|2,DO:A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine. DSA09067,GSE11545,GPL2986,1,Breast Cancer,C0678222,Blood,GEO,Microarray,Homo sapiens,9|11,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09068,GSE44561,GPL11532,0,Glioma,C0017638,,GEO,Microarray,Homo sapiens,1|2,DO:A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine. DSA09069,GSE44767,GPL570,0,Lymphatic Filariasis,C0013884,,GEO,Microarray,Homo sapiens,4|3,"DO:A filariasis that is characterized by the thickening of the skin and underlying tissues, especially in the legs, male genitals and female breasts, caused by thread-like parasitic worms Wuchereria bancrofti, Brugia malayi or Brugia timori, which inhabit the lymphatics. These nematodes are transmitted by mosquitoes. Acute symptoms include fever, lymphadenitis, lymphangitis, funiculitis, and epididymitis. Chronic symptoms include abscesses, hyperkeratosis, polyarthritis, hydroceles, lymphedema, and elephantiasis." DSA09070,GSE44904,GPL7202,3,Colitis,C0009319,Distal colorectal epithelium,GEO,Microarray,Mus musculus,3|3,DO:An inflammatory bowel disease that involves inflammation located_in colon. DSA09071,GSE44904,GPL7202,1000,Colorectal Carcinoma,C0009402,Distal colorectal epithelium,GEO,Microarray,Mus musculus,3|3,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA09072,GSE11545,GPL2986,0,Colon Cancer,C0699790,Blood,GEO,Microarray,Homo sapiens,9|9,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09073,GSE11545,GPL2986,0,Ovarian Cancer,C1140680,Blood,GEO,Microarray,Homo sapiens,9|10,DO:A female reproductive organ cancer that is located_in the ovary. DSA09074,GSE14924,GPL570,1000,Acute Myeloid Leukemia,C0023467,,GEO,Microarray,Homo sapiens,10|10,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA09075,GSE45156,GPL6885,0,Tibial Fracture,,,GEO,Microarray,Mus musculus,3|3, DSA09076,GSE45156,GPL6885,216,Tibial Fracture,,,GEO,Microarray,Mus musculus,3|3, DSA09077,GSE45570,GPL5175,0,Glaucoma,C0017601,Optic nerve head,GEO,Microarray,Homo sapiens,6|6,DO:An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. DSA09078,GSE45570,GPL5175,0,Ocular Hypertension,C0028840,Optic nerve head,GEO,Microarray,Homo sapiens,6|6,DO:An eye disease that is characterized by elevated intraocular pressure in the absence of optic nerve damage or visual field loss. DSA09079,GSE45577,GPL1261,1000,Disorder of Skeletal Muscle,C1533847,Tibialis anterior,GEO,Microarray,Mus musculus,5|6,DO:A muscular disease in which the muscle fibers do not function resulting in muscular weakness. DSA09080,GSE45577,GPL1261,1000,Disorder of Skeletal Muscle,C1533847,Tibialis anterior,GEO,Microarray,Mus musculus,5|6,DO:A muscular disease in which the muscle fibers do not function resulting in muscular weakness. DSA09081,GSE45577,GPL1261,1000,Disorder of Skeletal Muscle,C1533847,Tibialis anterior,GEO,Microarray,Mus musculus,5|5,DO:A muscular disease in which the muscle fibers do not function resulting in muscular weakness. DSA09082,GSE14924,GPL570,1000,Acute Myeloid Leukemia,C0023467,,GEO,Microarray,Homo sapiens,11|10,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA09083,GSE11783,GPL570,118,Interstitial Cystitis,C0282488,Bladder,GEO,Microarray,Homo sapiens,6|5,"DO:A chronic cystitis characterized by unpleasant sensation related to the bladder and lower urinary tract in the absence of identifiable causes and has_symptom pain, has_symptom pressure, has_symptom discomfort, has_symptom dysuria, and/or has_symptom urinary frequency." DSA09084,GSE45577,GPL1261,1000,Disorder of Skeletal Muscle,C1533847,Tibialis anterior,GEO,Microarray,Mus musculus,5|5,DO:A muscular disease in which the muscle fibers do not function resulting in muscular weakness. DSA09085,GSE45577,GPL1261,1000,Disorder of Skeletal Muscle,C1533847,Tibialis anterior,GEO,Microarray,Mus musculus,5|6,DO:A muscular disease in which the muscle fibers do not function resulting in muscular weakness. DSA09086,GSE45577,GPL1261,1000,Disorder of Skeletal Muscle,C1533847,Tibialis anterior,GEO,Microarray,Mus musculus,5|6,DO:A muscular disease in which the muscle fibers do not function resulting in muscular weakness. DSA09087,GSE45712,GPL14951,1000,T-Cell Lymphoma,C0079772,,GEO,Microarray,Homo sapiens,10|55,HPO:A type of lymphoma that originates in T-cells. DSA09088,GSE45712,GPL14951,1000,T-Cell Lymphoma,C0079772,,GEO,Microarray,Homo sapiens,5|55,HPO:A type of lymphoma that originates in T-cells. DSA09089,GSE45723,GPL13730,0,Asthma,C0004096,Airway smooth muscle,GEO,Microarray,Mus musculus,3|3,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA09090,GSE45744,GPL1261,1000,Lung Adenocarcinoma,C0152013,,GEO,Microarray,Mus musculus,4|4,DO:A respiratory system cancer that is located_in the lung. DSA09091,GSE45968,GPL1261,342,Microglossia,C0025988,Tongue,GEO,Microarray,Mus musculus,3|3,HPO:Decreased length and width of the tongue. DSA09092,GSE46150,GPL1261,12,Cleft Palate,C0008925,Palate mesenchyme,GEO,Microarray,Mus musculus,4|4,"DO:A cleft palate seen as an isolated malformation, distinct from cleft lip with or without cleft palate." DSA09093,GSE46211,GPL1261,1000,Submucosal Cleft Palate,C4551487,Palate,GEO,Microarray,Mus musculus,12|6, DSA09094,GSE46229,GPL6246,432,Leukemia,C0023418,Spleen,GEO,Microarray,Mus musculus,2|2,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA09095,GSE46410,GPL6887,11,Acute Kidney Injury,C2609414,Kidney,GEO,Microarray,Mus musculus,6|6,"HPO:Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia)." DSA09096,GSE46509,GPL1352,0,Schizophrenia,C0036341,Brain,GEO,Microarray,Homo sapiens,8|8,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA09097,GSE46570,GPL15207,1000,Melanoma,C0025202,,GEO,Microarray,Homo sapiens,2|2,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA09098,GSE46570,GPL15207,1000,Adenocarcinoma,C0001418,,GEO,Microarray,Homo sapiens,2|1,"DO:A carcinoma that has_material_basis_in abnormally proliferating cells, derives_from epithelial cells, which originate in glandular tissue." DSA09099,GSE46570,GPL15207,1000,Hepatocellular Carcinoma,C0334287,,GEO,Microarray,Homo sapiens,2|2,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA09100,GSE46570,GPL15207,1000,Melanoma,C0025202,,GEO,Microarray,Homo sapiens,2|2,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA09101,GSE46570,GPL15207,1000,Adenocarcinoma,C0001418,,GEO,Microarray,Homo sapiens,2|2,"DO:A carcinoma that has_material_basis_in abnormally proliferating cells, derives_from epithelial cells, which originate in glandular tissue." DSA09102,GSE46570,GPL15207,1000,Hepatocellular Carcinoma,C0334287,,GEO,Microarray,Homo sapiens,2|2,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA09103,GSE46619,GPL6244,1000,Necrotizing Enterocolitis,C0520459,Bowel,GEO,Microarray,Homo sapiens,4|5,"EFO:Necrotizing enterocolitis (NEC) is a devastating disease that affects mostly the intestine of premature infants. The wall of the intestine is invaded by bacteria, which cause local infection and inflammation that can ultimately destroy the wall of the bowel (intestine). Such bowel wall destruction can lead to perforation of the intestine and spillage of stool into the infant's abdomen, which can result in an overwhelming infection and death." DSA09104,GSE46619,GPL6244,82,Intestinal Perforation,C0021845,Bowel,GEO,Microarray,Homo sapiens,4|5,HPO:A hole (perforation) in the wall of the intestine. DSA09105,GSE46646,GPL1261,13,Hepatocellular Carcinoma,C0334287,,GEO,Microarray,Mus musculus,3|3,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA09106,GSE46967,GPL6246,1000,Biliary Atresia,C0005411,Extrahepatic bile duct and gallbladder,GEO,Microarray,Mus musculus,3|3,DO:A cholestasis characterized by blockage of the ducts that carry bile from the liver to the gallbladder. DSA09107,GSE46967,GPL6246,1000,Biliary Atresia,C0005411,Extrahepatic bile duct and gallbladder,GEO,Microarray,Mus musculus,3|3,DO:A cholestasis characterized by blockage of the ducts that carry bile from the liver to the gallbladder. DSA09108,GSE46967,GPL6246,1000,Biliary Atresia,C0005411,Extrahepatic bile duct and gallbladder,GEO,Microarray,Mus musculus,3|3,DO:A cholestasis characterized by blockage of the ducts that carry bile from the liver to the gallbladder. DSA09109,GSE47198,GPL6246,1000,Rhabdomyosarcoma,C0035412,,GEO,Microarray,Mus musculus,3|3,DO:A skeletal muscle cancer that arise from skeletal muscle progenitors. DSA09110,GSE47198,GPL6246,1000,Rhabdomyosarcoma,C0035412,,GEO,Microarray,Mus musculus,3|3,DO:A skeletal muscle cancer that arise from skeletal muscle progenitors. DSA09111,GSE47198,GPL6246,1000,Rhabdomyosarcoma,C0035412,,GEO,Microarray,Mus musculus,3|3,DO:A skeletal muscle cancer that arise from skeletal muscle progenitors. DSA09112,GSE47504,GPL6246,257,Diabetes,C0011847,Pancreatic islet,GEO,Microarray,Mus musculus,5|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09113,GSE47600,GPL6887,0,Alveolar Injury,,Lung,GEO,Microarray,Mus musculus,3|3, DSA09114,GSE47600,GPL6887,976,Alveolar Injury,,Lung,GEO,Microarray,Mus musculus,3|3, DSA09115,GSE47681,GPL1261,1000,Spinal Cord Disorder,C0037928,Thoracic spinal cord,GEO,Microarray,Mus musculus,4|4,EFO:A disease involving the spinal cord. DSA09116,GSE47681,GPL1261,1000,Spinal Cord Disorder,C0037928,Thoracic spinal cord,GEO,Microarray,Mus musculus,4|4,EFO:A disease involving the spinal cord. DSA09117,GSE47681,GPL1261,1000,Spinal Cord Disorder,C0037928,Thoracic spinal cord,GEO,Microarray,Mus musculus,4|4,EFO:A disease involving the spinal cord. DSA09118,GSE47681,GPL1261,1000,Spinal Cord Disorder,C0037928,Thoracic spinal cord,GEO,Microarray,Mus musculus,4|4,EFO:A disease involving the spinal cord. DSA09119,GSE47681,GPL1261,1000,Spinal Cord Disorder,C0037928,Thoracic spinal cord,GEO,Microarray,Mus musculus,4|5,EFO:A disease involving the spinal cord. DSA09120,GSE47681,GPL1261,1000,Spinal Cord Disorder,C0037928,Thoracic spinal cord,GEO,Microarray,Mus musculus,4|4,EFO:A disease involving the spinal cord. DSA09121,GSE48030,GPL14550,1000,Sarcoma,C1261473,,GEO,Microarray,Homo sapiens,2|2,DO:A sarcoma that results_in cells that are spindle-shaped. They are usually resistant to radiation therapy. DSA09122,GSE48030,GPL14550,1000,Sarcoma,C1261473,,GEO,Microarray,Homo sapiens,2|2,DO:A sarcoma that results_in cells that are spindle-shaped. They are usually resistant to radiation therapy. DSA09123,GSE48030,GPL14550,1000,Sarcoma,C1261473,,GEO,Microarray,Homo sapiens,2|2,DO:A sarcoma that results_in cells that are spindle-shaped. They are usually resistant to radiation therapy. DSA09124,GSE48030,GPL14550,1000,Sarcoma,C1261473,,GEO,Microarray,Homo sapiens,2|2,DO:A sarcoma that results_in cells that are spindle-shaped. They are usually resistant to radiation therapy. DSA09125,GSE48051,GPL6480,1000,Down Syndrome,C0013080,,GEO,Microarray,Homo sapiens,9|10,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA09126,GSE48072,GPL10558,0,Schizophrenia,C0036341,,GEO,Microarray,Homo sapiens,17|14,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA09127,GSE48072,GPL10558,15,Schizophrenia,C0036341,,GEO,Microarray,Homo sapiens,14|21,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA09128,GSE48167,GPL10333,0,Vitamin D Deficiency,C0042870,Ovary,GEO,Microarray,Mus musculus,4|4,"EFO:A nutritional condition produced by a deficiency of VITAMIN D in the diet, insufficient production of vitamin D in the skin, inadequate absorption of vitamin D from the diet, or abnormal conversion of vitamin D to its bioactive metabolites. It is manifested clinically as RICKETS in children and OSTEOMALACIA in adults. (From Cecil Textbook of Medicine, 19th ed, p1406)" DSA09129,GSE48167,GPL10333,1000,Vitamin D Deficiency,C0042870,Ovary,GEO,Microarray,Mus musculus,4|4,"EFO:A nutritional condition produced by a deficiency of VITAMIN D in the diet, insufficient production of vitamin D in the skin, inadequate absorption of vitamin D from the diet, or abnormal conversion of vitamin D to its bioactive metabolites. It is manifested clinically as RICKETS in children and OSTEOMALACIA in adults. (From Cecil Textbook of Medicine, 19th ed, p1406)" DSA09130,GSE48169,GPL10333,1000,Vitamin D Deficiency,C0042870,Pituitary gland,GEO,Microarray,Mus musculus,4|4,"EFO:A nutritional condition produced by a deficiency of VITAMIN D in the diet, insufficient production of vitamin D in the skin, inadequate absorption of vitamin D from the diet, or abnormal conversion of vitamin D to its bioactive metabolites. It is manifested clinically as RICKETS in children and OSTEOMALACIA in adults. (From Cecil Textbook of Medicine, 19th ed, p1406)" DSA09131,GSE48169,GPL10333,1000,Vitamin D Deficiency,C0042870,Pituitary gland,GEO,Microarray,Mus musculus,4|4,"EFO:A nutritional condition produced by a deficiency of VITAMIN D in the diet, insufficient production of vitamin D in the skin, inadequate absorption of vitamin D from the diet, or abnormal conversion of vitamin D to its bioactive metabolites. It is manifested clinically as RICKETS in children and OSTEOMALACIA in adults. (From Cecil Textbook of Medicine, 19th ed, p1406)" DSA09132,GSE48418,GPL10558,1000,Chondrosarcoma,C0008479,,GEO,Microarray,Homo sapiens,3|3,DO:A bone sarcoma that has_material_basis_in cells derived from transformed cells that produce cartilage. DSA09133,GSE11783,GPL570,1000,Interstitial Cystitis,C0282488,Bladder,GEO,Microarray,Homo sapiens,6|5,"DO:A chronic cystitis characterized by unpleasant sensation related to the bladder and lower urinary tract in the absence of identifiable causes and has_symptom pain, has_symptom pressure, has_symptom discomfort, has_symptom dysuria, and/or has_symptom urinary frequency." DSA09134,GSE11414,GPL6244,1000,Osteosarcoma,C0029463,,GEO,Microarray,Homo sapiens,2|2,DO:A bone sarcoma that is located_in bone that has_material_basis_in cells of mesenchymal origin. DSA09135,GSE48811,GPL1261,0,Obesity,C0028754,Visceral fat,GEO,Microarray,Mus musculus,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA09136,GSE48811,GPL1261,31,Obesity,C0028754,Visceral fat,GEO,Microarray,Mus musculus,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA09137,GSE37911,GPL6244,1000,Breast Cancer,C0678222,,GEO,Microarray,Homo sapiens,4|2,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09138,GSE37911,GPL6244,1000,Breast Cancer,C0678222,,GEO,Microarray,Homo sapiens,8|4,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09139,GSE38067,GPL1261,75,Diabetes,C0011847,Liver,GEO,Microarray,Mus musculus,6|6,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09140,GSE38092,GPL8321,1000,Obesity,C0028754,Lung,GEO,Microarray,Mus musculus,8|8,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA09141,GSE38092,GPL8321,1000,Obesity,C0028754,Lung,GEO,Microarray,Mus musculus,8|8,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA09142,GSE38093,GPL8321,300,Obesity,C0028754,Lung,GEO,Microarray,Mus musculus,8|8,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA09143,GSE38093,GPL8321,46,Obesity,C0028754,Lung,GEO,Microarray,Mus musculus,8|8,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA09144,GSE38093,GPL8321,378,Obesity,C0028754,Lung,GEO,Microarray,Mus musculus,8|8,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA09145,GSE38138,GPL1261,1000,Diabetes,C0011847,Liver,GEO,Microarray,Mus musculus,5|5,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09146,GSE38494,GPL570,1000,Intraosseous Ameloblastoma,C1513734,,GEO,Microarray,Homo sapiens,8|15,"NCI:An intraosseous ameloblastoma that arises from the jaw, usually the mandible. It grows slowly, invades locally, and recurs frequently. It presents with swelling of the jaw." DSA09147,GSE38494,GPL570,649,Keratocystic Odontogenic Tumor,C1708604,,GEO,Microarray,Homo sapiens,8|12,"HPO:A benign uni- or multicystic, intraosseous tumor of odontogenic origin, with a characteristic lining of parakeratinized stratified squamous epithelium and potential for aggressive, infiltrative behaviour." DSA09148,GSE38531,GPL1261,1000,Sepsis,C0243026,Whole blood,GEO,Microarray,Mus musculus,5|5,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA09149,GSE38531,GPL1261,1000,Sepsis,C0243026,Whole blood,GEO,Microarray,Mus musculus,5|5,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA09150,GSE38531,GPL1261,1000,Sepsis,C0243026,Whole blood,GEO,Microarray,Mus musculus,5|5,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA09151,GSE38531,GPL1261,1000,Sepsis,C0243026,Whole blood,GEO,Microarray,Mus musculus,5|5,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA09152,GSE38642,GPL6244,2,Type 2 Diabetes,C0011860,Pancreatic islet,GEO,Microarray,Homo sapiens,54|9,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09153,GSE38874,GPL6246,14,Skeletal Muscle Atrophy,C0541794,Soleus,GEO,Microarray,Mus musculus,2|2,HPO:The presence of skeletal muscular atrophy (which is also known as amyotrophy). DSA09154,GSE39172,GPL6193,9,Leukemia,C0023418,,GEO,Microarray,Mus musculus,3|3,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA09155,GSE39172,GPL6193,4,Leukemia,C0023418,,GEO,Microarray,Mus musculus,3|3,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA09156,GSE39172,GPL6193,9,Leukemia,C0023418,,GEO,Microarray,Mus musculus,3|3,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA09157,GSE39645,GPL6244,1000,Vestibular Schwannoma,C0027859,,GEO,Microarray,Homo sapiens,9|31,"DO:A neurofibromatosis characterized by usually bilateral tumors of the eighth cranial nerve, meningiomas of the brain, and schwannomas of the dorsal roots of the spinal cord that has_material_basis_in heterozygous of mutation in NF2 on 22q12.2." DSA09158,GSE39752,GPL6246,1000,Type 1 Diabetes,C0011854,Liver,GEO,Microarray,Mus musculus,7|6,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA09159,GSE39843,GPL570,1000,Cystic Fibrosis,C0010674,,GEO,Microarray,Homo sapiens,3|3,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA09160,GSE39843,GPL570,1000,Cystic Fibrosis,C0010674,,GEO,Microarray,Homo sapiens,3|3,"DO:A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs." DSA09161,GSE40041,GPL11533,85,Fibrosis; Liver,C0239946,Liver,GEO,Microarray,Mus musculus,3|3,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA09162,GSE40041,GPL11533,106,Fibrosis; Liver,C0239946,Liver,GEO,Microarray,Mus musculus,3|3,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA09163,GSE40334,GPL6885,65,Fatty Liver,C0015695,Liver,GEO,Microarray,Mus musculus,4|4,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA09164,GSE40359,GPL6887,1000,Embryonal Rhabdomyosarcoma,C0206656,,GEO,Microarray,Mus musculus,3|15,DO:A rhabdomyosarcoma wherein the mesenchymally-derived malignant cells resemble the primitive developing skeletal muscle of the embryo; it occurs most often in the head and neck area or in the genital or urinary organs. DSA09165,GSE40359,GPL6887,1000,Embryonal Rhabdomyosarcoma,C0206656,,GEO,Microarray,Mus musculus,3|3,DO:A rhabdomyosarcoma wherein the mesenchymally-derived malignant cells resemble the primitive developing skeletal muscle of the embryo; it occurs most often in the head and neck area or in the genital or urinary organs. DSA09166,GSE40361,GPL6887,1000,Breast Cancer,C0678222,,GEO,Microarray,Mus musculus,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09167,GSE40361,GPL6887,1000,Breast Cancer,C0678222,,GEO,Microarray,Mus musculus,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09168,GSE40508,GPL6246,1000,Tumor of Lung,C0024121,Lung,GEO,Microarray,Mus musculus,3|3,EFO:A carcinoma that arises from epithelial cells of the lung DSA09169,GSE40583,GPL571,1000,Glioma,C0017638,,GEO,Microarray,Homo sapiens,2|2,DO:A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine. DSA09170,GSE40583,GPL571,1000,Glioma,C0017638,,GEO,Microarray,Homo sapiens,2|2,DO:A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine. DSA09171,GSE40583,GPL571,1000,Glioma,C0017638,,GEO,Microarray,Homo sapiens,4|4,DO:A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine. DSA09172,GSE40583,GPL571,1000,Glioma,C0017638,,GEO,Microarray,Homo sapiens,4|4,DO:A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine. DSA09173,GSE40637,GPL6246,1000,Vascular Abnormalities,C0241657,Femoral artery,GEO,Microarray,Mus musculus,4|4,HPO:An abnormality of the vasculature. DSA09174,GSE40638,GPL6246,551,Obesity,C0028754,Liver,GEO,Microarray,Mus musculus,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA09175,GSE40638,GPL6246,394,Obesity,C0028754,Liver,GEO,Microarray,Mus musculus,5|5,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA09176,GSE40856,GPL1261,0,Small Intestine Tumor,C0345832,Small intestine,GEO,Microarray,Mus musculus,2|2,HPO:The presence of a neoplasm of the small intestine. DSA09177,GSE40856,GPL1261,0,Small Intestine Tumor,C0345832,Small intestine,GEO,Microarray,Mus musculus,2|2,HPO:The presence of a neoplasm of the small intestine. DSA09178,GSE41126,GPL7202,0,Avian Influenza,C3264382,Lung,GEO,Microarray,Mus musculus,3|3,"DO:An influenza that results in infection located in respiratory tract of humans, domestic and wild birds, has_material_basis_in Influenza A virus, which is transmitted by contact with infected poultry. Five strains of avian influenza A viruses (H5N1, H7N3, H7N2, H7N7 and H9N2) are known to cause human infections. The infection has_symptom fever, has_symptom cough, has_symptom sore throat, has_symptom muscle aches, has_symptom nausea, has_symptom diarrhea, has_symptom vomiting, has_symptom neurologic changes, has_symptom pneumonia, and has_symptom acute respiratory distress." DSA09179,GSE41126,GPL7202,3,Avian Influenza,C3264382,Lung,GEO,Microarray,Mus musculus,3|3,"DO:An influenza that results in infection located in respiratory tract of humans, domestic and wild birds, has_material_basis_in Influenza A virus, which is transmitted by contact with infected poultry. Five strains of avian influenza A viruses (H5N1, H7N3, H7N2, H7N7 and H9N2) are known to cause human infections. The infection has_symptom fever, has_symptom cough, has_symptom sore throat, has_symptom muscle aches, has_symptom nausea, has_symptom diarrhea, has_symptom vomiting, has_symptom neurologic changes, has_symptom pneumonia, and has_symptom acute respiratory distress." DSA09180,GSE4122,GPL201,0,Benign Struma Ovarii,C1511104,Ovary,GEO,Microarray,Homo sapiens,14|18,DO:An ovarian benign neoplasm struma ovarii that is not cancerous and that is composed either exclusively or predominantly of thyroid tissue. DSA09181,GSE4122,GPL201,1000,Malignant Struma Ovarii,C0334525,Ovary,GEO,Microarray,Homo sapiens,14|32,DO:A struma ovarii that is cancerous. DSA09182,GSE41293,GPL13112,1000,Osteosarcoma,C0029463,,GEO,RNA-Seq,Mus musculus,6|5,DO:A bone sarcoma that is located_in bone that has_material_basis_in cells of mesenchymal origin. DSA09183,GSE41293,GPL13112,1000,Synovial Sarcoma,C0039101,,GEO,RNA-Seq,Mus musculus,6|5,DO:A synovium cancer which develops in the synovial membrane of the joints. DSA09184,GSE41386,GPL570,0,Leiomyoma,C0042133,Uterus,GEO,Microarray,Homo sapiens,3|3,DO:An uterine benign neoplasm derived from the smooth muscle layer of the uterus. DSA09185,GSE41941,GPL6885,1000,Granuloma,C0018188,Liver,GEO,Microarray,Mus musculus,2|2,"EFO:an inflammation found in many diseases, it is a collection of immune cells known as macrophages.A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents." DSA09186,GSE41941,GPL6885,1000,Granuloma,C0018188,Liver,GEO,Microarray,Mus musculus,2|2,"EFO:an inflammation found in many diseases, it is a collection of immune cells known as macrophages.A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents." DSA09187,GSE41941,GPL6885,1000,Granuloma,C0018188,Liver,GEO,Microarray,Mus musculus,2|2,"EFO:an inflammation found in many diseases, it is a collection of immune cells known as macrophages.A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents." DSA09188,GSE41941,GPL6885,1000,Granuloma,C0018188,Liver,GEO,Microarray,Mus musculus,2|2,"EFO:an inflammation found in many diseases, it is a collection of immune cells known as macrophages.A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents." DSA09189,GSE41941,GPL6885,1000,Granuloma,C0018188,Liver,GEO,Microarray,Mus musculus,2|2,"EFO:an inflammation found in many diseases, it is a collection of immune cells known as macrophages.A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents." DSA09190,GSE41941,GPL6885,1000,Granuloma,C0018188,Liver,GEO,Microarray,Mus musculus,2|2,"EFO:an inflammation found in many diseases, it is a collection of immune cells known as macrophages.A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents." DSA09191,GSE41941,GPL6885,1000,Granuloma,C0018188,Liver,GEO,Microarray,Mus musculus,2|2,"EFO:an inflammation found in many diseases, it is a collection of immune cells known as macrophages.A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents." DSA09192,GSE42303,GPL8321,1000,Ureteral Obstruction,C0041956,Kidney,GEO,Microarray,Mus musculus,3|3,HPO:Obstruction of the flow of urine through the ureter. DSA09193,GSE42303,GPL8321,1000,Ureteral Obstruction,C0041956,Kidney,GEO,Microarray,Mus musculus,3|3,HPO:Obstruction of the flow of urine through the ureter. DSA09194,GSE42303,GPL8321,1000,Ureteral Obstruction,C0041956,Kidney,GEO,Microarray,Mus musculus,3|3,HPO:Obstruction of the flow of urine through the ureter. DSA09195,GSE42638,GPL6887,51,H1N1 Influenza,C2076600,Lung,GEO,Microarray,Mus musculus,7|7,"EFO:An influenza that results_in infection located_in respiratory tract of pigs and humans, has_material_basis_in Influenza C virus, or has_material_basis_in Influenza A virus subtypes (H1N1, H1N2, H3N1, H3N2, and H2N3), which are transmitted_by direct contact with infected pigs. The infection in humans has_symptom fever, has_symptom lethargy, has_symptom lack of appetite, has_symptom coughing, has_symptom runny nose, has_symptom sore throat, has_symptom nausea, has_symptom vomiting, and has_symptom diarrhea." DSA09196,GSE42638,GPL6887,1000,H1N1 Influenza,C2076600,Lung,GEO,Microarray,Mus musculus,7|7,"EFO:An influenza that results_in infection located_in respiratory tract of pigs and humans, has_material_basis_in Influenza C virus, or has_material_basis_in Influenza A virus subtypes (H1N1, H1N2, H3N1, H3N2, and H2N3), which are transmitted_by direct contact with infected pigs. The infection in humans has_symptom fever, has_symptom lethargy, has_symptom lack of appetite, has_symptom coughing, has_symptom runny nose, has_symptom sore throat, has_symptom nausea, has_symptom vomiting, and has_symptom diarrhea." DSA09197,GSE42638,GPL6887,813,H1N1 Influenza,C2076600,Lung,GEO,Microarray,Mus musculus,7|7,"EFO:An influenza that results_in infection located_in respiratory tract of pigs and humans, has_material_basis_in Influenza C virus, or has_material_basis_in Influenza A virus subtypes (H1N1, H1N2, H3N1, H3N2, and H2N3), which are transmitted_by direct contact with infected pigs. The infection in humans has_symptom fever, has_symptom lethargy, has_symptom lack of appetite, has_symptom coughing, has_symptom runny nose, has_symptom sore throat, has_symptom nausea, has_symptom vomiting, and has_symptom diarrhea." DSA09198,GSE42638,GPL6887,1000,H1N1 Influenza,C2076600,Lung,GEO,Microarray,Mus musculus,7|7,"EFO:An influenza that results_in infection located_in respiratory tract of pigs and humans, has_material_basis_in Influenza C virus, or has_material_basis_in Influenza A virus subtypes (H1N1, H1N2, H3N1, H3N2, and H2N3), which are transmitted_by direct contact with infected pigs. The infection in humans has_symptom fever, has_symptom lethargy, has_symptom lack of appetite, has_symptom coughing, has_symptom runny nose, has_symptom sore throat, has_symptom nausea, has_symptom vomiting, and has_symptom diarrhea." DSA09199,GSE42656,GPL6947,1000,Pilocytic Astrocytoma,C0334583,Brain,GEO,Microarray,Homo sapiens,8|14,DO:A childhood low-grade glioma that is characterized by cells that look like fibers when viewed under a microscope and is located_in the brain. DSA09200,GSE42656,GPL6947,1000,Diffuse Astrocytoma,C0280785,Brain,GEO,Microarray,Homo sapiens,8|3,"DO:A malignant glioma that is has_material_basis_in astrocyte cells, a type of star-shaped glial cell, located in the brain and spinal cord." DSA09201,GSE42656,GPL6947,1000,Anaplastic Astrocytoma,C0334579,Brain,GEO,Microarray,Homo sapiens,8|2,"DO:A malignant astrocytoma that is characterized by cells with regular, round to oval nuclei." DSA09202,GSE42656,GPL6947,1000,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,8|5,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA09203,GSE42656,GPL6947,1000,Ependymoma,C0014474,Brain,GEO,Microarray,Homo sapiens,8|14,"EFO:A well-differentiated (WHO grade II), diffusely infiltrating neuroglial tumor, typically located in the cerebral hemispheres. It is composed predominantly of cells which morphologically resemble oligodendroglia. The neoplastic cells have rounded homogeneous nuclei and, on paraffin sections, a swollen, clear cytoplasm ('honeycomb' appearance). (Adapted from WHO)" DSA09204,GSE42656,GPL6947,1000,Medulloblastoma,C0025149,Brain,GEO,Microarray,Homo sapiens,8|9,DO:An infratentorial cancer that is located_in the lower part of the brain and is a type of primitive neuroectodermal tumor. DSA09205,GSE42656,GPL6947,1000,Atypical Teratoid Rhabdoid Tumor,C1266184,Brain,GEO,Microarray,Homo sapiens,8|5,"DO:A brain cancer that is usually located in the brain, but can occur anywhere in the central nervous system." DSA09206,GSE42656,GPL6947,1000,Choroid Plexus Papilloma,C0205770,Brain,GEO,Microarray,Homo sapiens,8|4,"EFO:A benign, slow growing tumor which may cause symptoms by blocking cerebrospinal fluid pathways. It is characterized by the presence of delicate fibrovascular connective tissue fronds covered by a single layer of epithelial cells. Mitotic activity is extremely low. Surgical resection is usually curative. (Adapted from WHO)" DSA09207,GSE210936,GPL24676,0,Early Pregnancy Loss,C3830362,,GEO,RNA-Seq,Homo sapiens,2|2,MSH:A loss of PREGNANCY from natural causes before the 20th week of pregnancy. (2017/18 ICD-10-CM) DSA09208,GSE211229,GPL13112,432,Obesity,C0028754,Atria,GEO,RNA-Seq,Mus musculus,3|3,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA09209,GSE211490,GPL21103,1000,Eosinophilic Infiltration of The Esophagus,C4703646,Esophagus,GEO,RNA-Seq,Mus musculus,5|3,"HPO:Infiltration of numerous eosinophils (usually greater than 15 per high power field) into the squamous epithelium of the esophagus, and layering of eosinophils on the surface layer of the esophagus." DSA09210,GSE211804,GPL20795,127,Colorectal Carcinoma,C0009402,,GEO,RNA-Seq,Homo sapiens,4|4,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA09211,GSE214348,GPL24247,1000,Squamous Cell Carcinoma,C0007137,Spleen,GEO,RNA-Seq,Mus musculus,3|3,DO:A carcinoma that derives_from squamous epithelial cells. DSA09212,GSE214348,GPL24247,1000,Squamous Cell Carcinoma,C0007137,Spleen,GEO,RNA-Seq,Mus musculus,3|2,DO:A carcinoma that derives_from squamous epithelial cells. DSA09213,GSE215336,GPL24247,61,Spinocerebellar Ataxia Type 1,C0752120,Cerebellum,GEO,RNA-Seq,Mus musculus,3|3,"DO:An autosomal dominant cerebellar ataxia that is characterized by ataxia, dysarthria, dysphagia, dystonia and peripheral neuropathy that begins in early adulthood, has_material_basis_in the expanded (CAG)n trinucleotide repeat of ataxin-1 gene on chromosome 6p22." DSA09214,GSE215935,GPL29456,1000,Aortic Dissection,C0340643,Aorta,GEO,Microarray,Mus musculus,3|3,HPO:Aortic dissection refers to a tear in the intimal layer of the aorta causing a separation between the intima and the medial layers of the aorta. DSA09215,GSE216326,GPL13112,1000,Fibrosis; Liver,C0239946,Liver,GEO,RNA-Seq,Mus musculus,3|3,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA09216,GSE217042,GPL24247,1000,Mammary Gland Aplasia,C0266009,Mammary gland,GEO,RNA-Seq,Mus musculus,2|3,HPO:Failure to develop and congenital absence of the breast. DSA09217,GSE217622,GPL24247,882,Nerve Entrapment,C0917811,Prelimbic cortex,GEO,RNA-Seq,Mus musculus,3|3,MSH:Mechanical compression of nerves or nerve roots from internal or external causes. These may result in a conduction block to nerve impulses (due to MYELIN SHEATH dysfunction) or axonal loss. The nerve and nerve sheath injuries may be caused by ISCHEMIA; INFLAMMATION; or a direct mechanical effect. DSA09218,GSE22490,GPL570,0,Miscarriage,C4552766,Placenta,GEO,Microarray,Homo sapiens,6|4,MSH:A loss of PREGNANCY from natural causes before the 20th week of pregnancy. (2017/18 ICD-10-CM) DSA09219,GSE22798,GPL8321,1000,Myomatous Tumor,C0282606,Muscle,GEO,Microarray,Mus musculus,3|6,DO:A musculoskeletal system cancer that is located_in muscle. DSA09220,GSE23006,GPL1261,1000,Skin Wound,,Tongue,GEO,Microarray,Mus musculus,3|3, DSA09221,GSE23006,GPL1261,1000,Skin Wound,,Tongue,GEO,Microarray,Mus musculus,3|3, DSA09222,GSE23006,GPL1261,1000,Skin Wound,,Tongue,GEO,Microarray,Mus musculus,3|3, DSA09223,GSE23006,GPL1261,1000,Skin Wound,,Tongue,GEO,Microarray,Mus musculus,3|3, DSA09224,GSE23006,GPL1261,1000,Skin Wound,,Tongue,GEO,Microarray,Mus musculus,3|3, DSA09225,GSE23006,GPL1261,1000,Skin Wound,,Tongue,GEO,Microarray,Mus musculus,3|3, DSA09226,GSE23006,GPL1261,1000,Skin Wound,,Tongue,GEO,Microarray,Mus musculus,3|3, DSA09227,GSE23006,GPL1261,667,Skin Wound,,Skin,GEO,Microarray,Mus musculus,3|3, DSA09228,GSE23006,GPL1261,1000,Skin Wound,,Skin,GEO,Microarray,Mus musculus,3|3, DSA09229,GSE23006,GPL1261,1000,Skin Wound,,Skin,GEO,Microarray,Mus musculus,3|3, DSA09230,GSE23006,GPL1261,1000,Skin Wound,,Skin,GEO,Microarray,Mus musculus,3|3, DSA09231,GSE23006,GPL1261,863,Skin Wound,,Skin,GEO,Microarray,Mus musculus,3|3, DSA09232,GSE23006,GPL1261,285,Skin Wound,,Skin,GEO,Microarray,Mus musculus,3|3, DSA09233,GSE23006,GPL1261,130,Skin Wound,,Skin,GEO,Microarray,Mus musculus,3|3, DSA09234,GSE23119,GPL1261,0,Vitamin A Deficiency,C0042842,Testis,GEO,Microarray,Mus musculus,3|3,HPO:A reduced concentration of vitamin A. DSA09235,GSE23119,GPL1261,0,Vitamin A Deficiency,C0042842,Testis,GEO,Microarray,Mus musculus,3|3,HPO:A reduced concentration of vitamin A. DSA09236,GSE23160,GPL6885,256,Ischemia Reperfusion Injury,C0035126,Brain,GEO,Microarray,Mus musculus,4|4,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA09237,GSE23160,GPL6885,481,Ischemia Reperfusion Injury,C0035126,Brain,GEO,Microarray,Mus musculus,4|4,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA09238,GSE23160,GPL6885,172,Ischemia Reperfusion Injury,C0035126,Brain,GEO,Microarray,Mus musculus,4|4,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA09239,GSE23160,GPL6885,23,Ischemia Reperfusion Injury,C0035126,Brain,GEO,Microarray,Mus musculus,4|4,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA09240,GSE23160,GPL6885,97,Ischemia Reperfusion Injury,C0035126,Brain,GEO,Microarray,Mus musculus,4|4,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA09241,GSE23160,GPL6885,66,Ischemia Reperfusion Injury,C0035126,Brain,GEO,Microarray,Mus musculus,4|4,"EFO:Some of the known risk factors for cardiovascular disease (hypercholesterolaemia, hypertension, and diabetes) appear to exaggerate many of the microvascular alterations elicited by ischaemia and reperfusion (I/R). The inflammatory mediators released as a consequence of reperfusion also appear to activate endothelial cells in remote organs that are not exposed to the initial ischaemic insult. This distant response to I/R can result in leukocyte-dependent microvascular injury that is characteristic of the multiple organ dysfunction syndrome. Adaptational responses to I/R injury have been demonstrated that allow for protection of briefly ischaemic tissues against the harmful effects of subsequent, prolonged ischaemia, a phenomenon called ischaemic preconditioning." DSA09242,GSE23388,GPL6947,0,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,1|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09243,GSE23767,GPL6887,1000,Sepsis,C0243026,Liver,GEO,Microarray,Mus musculus,3|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA09244,GSE23767,GPL6887,0,Sepsis,C0243026,Liver,GEO,Microarray,Mus musculus,3|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA09245,GSE23767,GPL6887,1000,Sepsis,C0243026,Lung,GEO,Microarray,Mus musculus,3|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA09246,GSE23767,GPL6887,0,Sepsis,C0243026,Lung,GEO,Microarray,Mus musculus,3|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA09247,GSE23767,GPL6887,1000,Sepsis,C0243026,Spleen,GEO,Microarray,Mus musculus,3|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA09248,GSE23767,GPL6887,428,Sepsis,C0243026,Spleen,GEO,Microarray,Mus musculus,3|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA09249,GSE23767,GPL6887,59,Sepsis,C0243026,Blood,GEO,Microarray,Mus musculus,3|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA09250,GSE23767,GPL6887,0,Sepsis,C0243026,Blood,GEO,Microarray,Mus musculus,3|4,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA09251,GSE24242,GPL6096,0,Proximal Aortic Coarctation,C0265878,Heart ventricle,GEO,Microarray,Mus musculus,2|2,"HPO:Narrowing or constriction of the aorta localized proximal to the ductus arteriosus, i.e., to the preductal region of aortic arch." DSA09252,GSE24242,GPL6096,0,Proximal Aortic Coarctation,C0265878,Heart ventricle,GEO,Microarray,Mus musculus,2|2,"HPO:Narrowing or constriction of the aorta localized proximal to the ductus arteriosus, i.e., to the preductal region of aortic arch." DSA09253,GSE25222,GPL6887,0,Cryptorchidism,C0010417,Cremasteric sac,GEO,Microarray,Mus musculus,3|3,"EFO:The failure of one or both testes of a male fetus to descend from the abdomen into the scrotum during the late part of pregnancy. If not surgically corrected in early childhood, males may be at increased risk for testicular cancer later in life." DSA09254,GSE25680,GPL7202,1000,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Mus musculus,3|3,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA09255,GSE25713,GPL6887,1000,Schistosomiasis,C0036323,Liver,GEO,Microarray,Mus musculus,6|6,"DO:A schistosomiasis that involves parasitic infection of the intestine caused by Schistosoma mansoni, Schistosoma intercalatum or Schistosomiasis japonicum. The symptoms include fever, cough, abdominal pain, diarrhea, hepatosplenomegaly, colonic polyposis with bloody diarrhea and eosinophilia." DSA09256,GSE25713,GPL6887,1000,Schistosomiasis,C0036323,Liver,GEO,Microarray,Mus musculus,6|6,"DO:A schistosomiasis that involves parasitic infection of the intestine caused by Schistosoma mansoni, Schistosoma intercalatum or Schistosomiasis japonicum. The symptoms include fever, cough, abdominal pain, diarrhea, hepatosplenomegaly, colonic polyposis with bloody diarrhea and eosinophilia." DSA09257,GSE25713,GPL6887,1000,Schistosomiasis,C0036323,Liver,GEO,Microarray,Mus musculus,6|6,"DO:A schistosomiasis that involves parasitic infection of the intestine caused by Schistosoma mansoni, Schistosoma intercalatum or Schistosomiasis japonicum. The symptoms include fever, cough, abdominal pain, diarrhea, hepatosplenomegaly, colonic polyposis with bloody diarrhea and eosinophilia." DSA09258,GSE26509,GPL6246,1000,Urinary Tract Infection,C0042029,Bladder,GEO,Microarray,Mus musculus,5|5,"EFO:A bacterial infectious process affecting any part of the urinary tract, most commonly the bladder and the urethra. Symptoms include urinary urgency and frequency, burning sensation during urination, lower abdominal discomfort, and cloudy urine." DSA09259,GSE26671,GPL1261,1,Heart Failure,C0018801,Left ventricle,GEO,Microarray,Mus musculus,6|6,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA09260,GSE26695,GPL1261,1,Minor Trauma,,Liver,GEO,Microarray,Mus musculus,5|3, DSA09261,GSE26695,GPL1261,62,Hemorrhagic Shock,C0036982,Liver,GEO,Microarray,Mus musculus,5|4,MSH:Acute hemorrhage or excessive fluid loss resulting in HYPOVOLEMIA. DSA09262,GSE26696,GPL11579,0,Minor Trauma,,Liver,GEO,Microarray,Mus musculus,5|3, DSA09263,GSE26696,GPL11579,133,Hemorrhagic Shock,C0036982,Liver,GEO,Microarray,Mus musculus,5|4,MSH:Acute hemorrhage or excessive fluid loss resulting in HYPOVOLEMIA. DSA09264,GSE26761,GPL6244,75,Vaginal Dryness,C0241633,,GEO,Microarray,Homo sapiens,6|4,HPO:Persistent vaginal dryness. DSA09265,GSE26990,GPL6947,0,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,2|2,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09266,GSE26990,GPL6947,0,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,2|2,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09267,GSE11414,GPL6244,1000,Osteosarcoma,C0029463,,GEO,Microarray,Homo sapiens,2|2,DO:A bone sarcoma that is located_in bone that has_material_basis_in cells of mesenchymal origin. DSA09268,GSE15823,GPL8300,0,Asthma,C0004096,Lung,GEO,Microarray,Homo sapiens,4|4,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA09269,GSE15777,GPL571,1000,Chronic Lymphocytic Leukemia,C0023434,Blood,GEO,Microarray,Homo sapiens,3|10,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA09270,GSE15777,GPL571,1000,Chronic Lymphocytic Leukemia,C0023434,Blood,GEO,Microarray,Homo sapiens,3|4,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA09271,GSE15777,GPL571,1000,Chronic Lymphocytic Leukemia,C0023434,Blood,GEO,Microarray,Homo sapiens,3|8,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA09272,GSE15645,GPL570,505,Polyarticular Juvenile Idiopathic Arthritis,C0409667,Blood,GEO,Microarray,Homo sapiens,13|14,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA09273,GSE27575,GPL6246,0,Cystitis,C0010692,Bladder,GEO,Microarray,Mus musculus,5|5,DO:A bladder disease that is characterized by inflammation of the bladder. DSA09274,GSE27575,GPL6246,1000,Cystitis,C0010692,Bladder,GEO,Microarray,Mus musculus,5|10,DO:A bladder disease that is characterized by inflammation of the bladder. DSA09275,GSE27639,GPL4134,463,Infertility,C0021359,Oviduct,GEO,Microarray,Mus musculus,4|4,EFO:Inability to reproduce after a specified period of unprotected intercourse. Reproductive sterility is permanent infertility. DSA09276,GSE28731,GPL1261,851,Middle Cerebral Artery Occlusion,C0740391,Brain,GEO,Microarray,Mus musculus,2|3,"MSH:NECROSIS occurring in the MIDDLE CEREBRAL ARTERY distribution system which brings blood to the entire lateral aspects of each CEREBRAL HEMISPHERE. Clinical signs include impaired cognition; APHASIA; AGRAPHIA; weak and numbness in the face and arms, contralaterally or bilaterally depending on the infarction." DSA09277,GSE28731,GPL1261,0,Middle Cerebral Artery Occlusion,C0740391,Brain,GEO,Microarray,Mus musculus,2|3,"MSH:NECROSIS occurring in the MIDDLE CEREBRAL ARTERY distribution system which brings blood to the entire lateral aspects of each CEREBRAL HEMISPHERE. Clinical signs include impaired cognition; APHASIA; AGRAPHIA; weak and numbness in the face and arms, contralaterally or bilaterally depending on the infarction." DSA09278,GSE28938,GPL11096,174,Type 2 Diabetes,C0011860,Liver,GEO,Microarray,Mus musculus,3|3,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09279,GSE29492,GPL6480,1000,Burkitt Lymphoma,C0006413,Lymph node,GEO,Microarray,Homo sapiens,7|6,DO:A mature B-cell neoplasm of B-cells found in the germinal center. DSA09280,GSE15645,GPL570,462,Polyarticular Juvenile Idiopathic Arthritis,C0409667,Blood,GEO,Microarray,Homo sapiens,13|9,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA09281,GSE15645,GPL570,0,Polyarticular Juvenile Idiopathic Arthritis,C0409667,Blood,GEO,Microarray,Homo sapiens,13|6,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA09282,GSE29775,GPL6481,1000,Rhabdomyosarcoma,C0035412,Muscle,GEO,Microarray,Mus musculus,8|4,DO:A skeletal muscle cancer that arise from skeletal muscle progenitors. DSA09283,GSE29920,GPL6885,5,Lung Injury,C0273115,Lung,GEO,Microarray,Mus musculus,3|5,"MSH:Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES." DSA09284,GSE30126,GPL6246,0,Thymic Lymphoma,C1336745,Thymus,GEO,Microarray,Mus musculus,3|3,DO:A thymus cancer that arises from the thymus. DSA09285,GSE30292,GPL570,548,Colon Cancer,C0699790,Colon,GEO,Microarray,Homo sapiens,3|3,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09286,GSE30427,GPL6246,1000,Thyroid Tumor,C0040136,Thyroid,GEO,Microarray,Mus musculus,6|5,DO:An endocrine gland cancer located in the thryoid gland located in the neck below the thyroid cartilage. DSA09287,GSE30427,GPL6246,1000,Thyroid Tumor,C0040136,Thyroid,GEO,Microarray,Mus musculus,6|5,DO:An endocrine gland cancer located in the thryoid gland located in the neck below the thyroid cartilage. DSA09288,GSE54838,GPL6246,1000,D-2-Hydroxyglutaric Aciduria,C3152055,Heart,GEO,Microarray,Mus musculus,4|4,DO:A D-2-hydroxyglutaric aciduria that has_material_basis_in homozygous or compound heterozygous mutation in D2HGDH on 2q37.3. DSA09289,GSE3161,GPL2640,0,Hypercapnia,C0020440,Lung,GEO,Microarray,Mus musculus,4|2,HPO:Abnormally elevated blood carbon dioxide (CO2) level. DSA09290,GSE31714,GPL1261,216,Muscular Dystrophy,C0026850,,GEO,Microarray,Mus musculus,2|2,"DO:A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted." DSA09291,GSE32105,GPL6246,1000,Pneumonia,C0032285,Liver,GEO,Microarray,Mus musculus,3|3,"DO:A lung disease that involves lung parenchyma or alveolar inflammation and abnormal alveolar filling with fluid (consolidation and exudation). It results from a variety of causes including infection with bacteria, viruses, fungi or parasites, and chemical or physical injury to the lungs. It is accompanied by fever, chills, cough, and difficulty in breathing." DSA09292,GSE32105,GPL6246,136,Pneumonia,C0032285,Liver,GEO,Microarray,Mus musculus,3|3,"DO:A lung disease that involves lung parenchyma or alveolar inflammation and abnormal alveolar filling with fluid (consolidation and exudation). It results from a variety of causes including infection with bacteria, viruses, fungi or parasites, and chemical or physical injury to the lungs. It is accompanied by fever, chills, cough, and difficulty in breathing." DSA09293,GSE32230,GPL4134,470,Mantle Cell Lymphoma,C4721414,,GEO,Microarray,Mus musculus,4|4,MONDO:Mantle cell lymphoma is a rare form of malignant non-Hodgkin lymphoma affecting B lymphocytes in the lymph nodes in a region called the ``mantle zone''. DSA09294,GSE32239,GPL339,1000,Lymphoma,C0024299,Bone marrrow;spleen,GEO,Microarray,Mus musculus,4|13,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA09295,GSE32239,GPL339,820,Lymphoma,C0024299,Bone marrrow;spleen,GEO,Microarray,Mus musculus,4|5,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA09296,GSE32299,GPL14604,76,Clear Cell Renal Carcinoma,C0007134,,GEO,Microarray,Homo sapiens,3|2,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA09297,GSE32299,GPL14604,893,Clear Cell Renal Carcinoma,C0007134,,GEO,Microarray,Homo sapiens,3|2,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA09298,GSE32386,GPL1261,1000,Neuroblastoma,C0027819,,GEO,Microarray,Mus musculus,3|3,DO:An autonomic nervous system neoplasm that derives_from immature nerve cells. DSA09299,GSE32386,GPL1261,1000,Neuroblastoma,C0027819,,GEO,Microarray,Mus musculus,3|4,DO:An autonomic nervous system neoplasm that derives_from immature nerve cells. DSA09300,GSE32386,GPL1261,1000,Neuroblastoma,C0027819,,GEO,Microarray,Mus musculus,3|3,DO:An autonomic nervous system neoplasm that derives_from immature nerve cells. DSA09301,GSE32488,GPL13938,1000,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,4|35,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09302,GSE33426,GPL571,1000,Esophageal Squamous Cell Carcinoma,C0279626,,GEO,Microarray,Homo sapiens,12|59,DO:An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus. DSA09303,GSE33589,GPL14865,0,Deafness,C0011053,Cerebellum,GEO,Microarray,Mus musculus,4|4,"DO:An inner ear disease that is characterized by hearing loss resulting from damage to the cochlea, auditory nerve and/or brainstem." DSA09304,GSE33590,GPL14865,8,Deafness,C0011053,,GEO,Microarray,Mus musculus,4|3,"DO:An inner ear disease that is characterized by hearing loss resulting from damage to the cochlea, auditory nerve and/or brainstem." DSA09305,GSE34105,GPL14951,1000,Tongue Carcinoma,C0558353,Tongue,GEO,Microarray,Homo sapiens,16|62,NCI:A malignant tumor arising from the epithelium that covers the tongue. The vast majority of tongue carcinomas are moderately or poorly differentiated squamous cell carcinomas. DSA09306,GSE34106,GPL14951,1000,Tongue Carcinoma,C0558353,Tongue,GEO,Microarray,Homo sapiens,15|28,NCI:A malignant tumor arising from the epithelium that covers the tongue. The vast majority of tongue carcinomas are moderately or poorly differentiated squamous cell carcinomas. DSA09307,GSE35493,GPL570,1000,Atypical Teratoid Rhabdoid Tumor,C1266184,Brain,GEO,Microarray,Homo sapiens,9|20,"DO:A brain cancer that is usually located in the brain, but can occur anywhere in the central nervous system." DSA09308,GSE35493,GPL570,1000,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,9|12,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA09309,GSE35493,GPL570,1000,Medulloblastoma,C0025149,Brain,GEO,Microarray,Homo sapiens,9|20,DO:An infratentorial cancer that is located_in the lower part of the brain and is a type of primitive neuroectodermal tumor. DSA09310,GSE35493,GPL570,1000,Primitive Neuroectodermal Tumor,C0206663,Brain,GEO,Microarray,Homo sapiens,9|9,DO:An infratentorial cancer that is located_in the lower part of the brain and is a type of primitive neuroectodermal tumor. DSA09311,GSE36400,GPL5175,1000,Colon Cancer,C0699790,Colon,GEO,Microarray,Homo sapiens,5|9,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09312,GSE36525,GPL6246,1000,Medulloblastoma,C0025149,,GEO,Microarray,Mus musculus,1|3,DO:An infratentorial cancer that is located_in the lower part of the brain and is a type of primitive neuroectodermal tumor. DSA09313,GSE36897,GPL6246,1000,Brain Tumor,C0006118,Subcutaneous tissue,GEO,Microarray,Mus musculus,2|6,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09314,GSE37056,GPL6246,0,Epilepsy,C0014544,Hippocampus,GEO,Microarray,Mus musculus,3|3,"DO:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions." DSA09315,GSE37120,GPL571,0,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,2|2,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA09316,GSE37120,GPL571,0,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,2|2,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA09317,GSE37120,GPL571,0,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,2|2,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA09318,GSE37120,GPL571,23,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,2|2,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA09319,GSE37120,GPL571,0,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,2|2,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA09320,GSE37120,GPL571,0,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,2|2,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA09321,GSE37120,GPL571,0,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,2|2,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA09322,GSE37120,GPL571,456,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,2|2,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA09323,GSE37428,GPL6246,1000,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Mus musculus,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09324,GSE37428,GPL6246,1000,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Mus musculus,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09325,GSE37428,GPL6246,1000,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Mus musculus,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09326,GSE37428,GPL6246,1000,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Mus musculus,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09327,GSE11037,GPL891,1000,Chronic Lung Inflammation,,Lung,GEO,Microarray,Mus musculus,5|5, DSA09328,GSE11037,GPL891,1000,Chronic Lung Inflammation,,Lung,GEO,Microarray,Mus musculus,5|5, DSA09329,GSE145434,GPL24247,1000,Obstructive Sleep Apnea,C4237227,Lung,GEO,RNA-Seq,Mus musculus,6|6,"DO:A sleep apnea that is characterized by repeated collapse and obstruction of the upper airway during sleep, which results in reduced airflow (hypopnea) or complete airflow cessation (apnea), oxygen desaturation, and arousals from sleep." DSA09330,GSE145524,GPL24247,1000,Zellweger Spectrum Disorder,C4687396,Liver,GEO,RNA-Seq,Mus musculus,6|6,"MONDO:Peroxisome biogenesis disorders, Zellweger syndrome spectrum (PBD-ZSS) is a group of autosomal recessive disorders affecting the formation of functional peroxisomes, characterized by sensorineural hearing loss, pigmentary retinal degeneration, multiple organ dysfunction and psychomotor impairment, and is comprised of the phenotypic variants Zellweger syndrome (ZS), neonatal adrenoleukodystrophy (NALD) and infantile Refsum disease (IRD)." DSA09331,GSE145531,GPL20301,1000,Aplastic Anemia,C0002874,Bone marrow,GEO,RNA-Seq,Homo sapiens,86|78,"DO:An anemia that is characterized by a deficiency of red blood cells, white blood cells and platelets produced by bone marrow." DSA09332,GSE145675,GPL10999,1000,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,1|1,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA09333,GSE145676,GPL5175,1000,Amyotrophic Lateral Sclerosis,C0002736,,GEO,Microarray,Homo sapiens,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA09334,GSE145710,GPL20301,1000,Intellectual Disability,C3714756,,GEO,RNA-Seq,Homo sapiens,3|6,"DO:A specific developmental disorder that involves significant limitations both in mental functioning and in adaptive behavior such as communicating, taking care of him or herself, and social skills." DSA09335,GSE145733,GPL19395,6,Myelodysplastic Syndromes,C3463824,,GEO,Microarray,Homo sapiens,9|54,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA09336,GSE145733,GPL19395,554,Myelodysplastic Syndromes,C3463824,,GEO,Microarray,Homo sapiens,9|14,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA09337,GSE145808,GPL13684,1000,Cardiomyopathy,C0878544,Heart,GEO,Microarray,Mus musculus,6|6,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA09338,GSE145842,GPL11154,1000,Chronic Lymphocytic Leukemia,C0023434,Peripheral blood,GEO,RNA-Seq,Homo sapiens,6|5,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA09339,GSE145842,GPL11154,1000,Diffuse Large B-Cell Lymphoma,C0079744,Lymph node,GEO,RNA-Seq,Homo sapiens,6|8,DO:A B-cell lymphoma that is a cancer of B cells presenting as an aggressive tumour which can arise in virtually any part of the body. DSA09340,GSE145842,GPL11154,1000,Follicular Lymphoma,C0024301,Lymph node,GEO,RNA-Seq,Homo sapiens,6|10,DO:A B-cell lymphoma that is characterized as an indolent non-Hodgkin's lymphoma and has_material_basis_in follicle center B-cells (centrocytes and centroblasts). DSA09341,GSE145867,GPL16686,0,Gastric Cancer,C0699791,,GEO,Microarray,Homo sapiens,2|2,DO:A gastrointestinal system cancer that is located_in the stomach. DSA09342,GSE145926,GPL23227,1000,COVID-19,D8888888,Lung,GEO,scRNA-Seq,Homo sapiens,3|5,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA09343,GSE145926,GPL23227,1000,COVID-19,D8888888,Lung,GEO,scRNA-Seq,Homo sapiens,3|4,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA09344,GSE145970,GPL17021;GPL19057,718,Depression,C0011581,Cortex,GEO,RNA-Seq,Mus musculus,4|5,DO:A mood disorder that involves the presence of a low mood almost daily over a span of at least two years. DSA09345,GSE145974,GPL13667,1000,Lyme Disease,C0024198,,GEO,Microarray,Homo sapiens,21|28,"DO:A primary bacterial infectious disease that results_in infection, has_material_basis_in Borrelia burgdorferi, which is transmitted_by blacklegged tick (Ixodes scapularis) or transmitted_by western blacklegged tick (Ixodes pacificus). The infection has_symptom fever, has_symptom headache, has_symptom fatigue, and has_symptom skin rash called erythema migrans. If left untreated, infection can spread to joints, the heart, and the nervous system." DSA09346,GSE145974,GPL13667,267,Lyme Disease,C0024198,,GEO,Microarray,Homo sapiens,21|37,"DO:A primary bacterial infectious disease that results_in infection, has_material_basis_in Borrelia burgdorferi, which is transmitted_by blacklegged tick (Ixodes scapularis) or transmitted_by western blacklegged tick (Ixodes pacificus). The infection has_symptom fever, has_symptom headache, has_symptom fatigue, and has_symptom skin rash called erythema migrans. If left untreated, infection can spread to joints, the heart, and the nervous system." DSA09347,GSE146046,GPL16791,11,Allergic Asthma,C0155877,Blood,GEO,RNA-Seq,Homo sapiens,22|21,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA09348,GSE146046,GPL16791,90,Allergic Asthma,C0155877,Blood,GEO,RNA-Seq,Homo sapiens,22|30,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA09349,GSE146046,GPL16791,22,Allergy,C1527304,Blood,GEO,RNA-Seq,Homo sapiens,22|22,"DO:An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods." DSA09350,GSE146088,GPL23159,1000,Systemic Sclerosis,C0036421,,GEO,Microarray,Homo sapiens,16|48,"DO:A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies." DSA09351,GSE146091,GPL19057,1000,Parkinson's Disease,C0030567,Dorsal root ganglion,GEO,RNA-Seq,Mus musculus,8|7,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA09352,GSE146091,GPL19057,1000,Parkinson's Disease,C0030567,Dorsal root ganglion,GEO,RNA-Seq,Mus musculus,8|10,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA09353,GSE146113,GPL21103,1000,Multiple Sclerosis,C0026769,Spinal cord,GEO,scRNA-Seq,Mus musculus,2|2,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA09354,GSE146113,GPL21103,1000,Multiple Sclerosis,C0026769,Spinal cord,GEO,scRNA-Seq,Mus musculus,2|2,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA09355,GSE146190,GPL16791,1000,Coeliac Disease,C0007570,Duodenum,GEO,RNA-Seq,Homo sapiens,5|3,"DO:An autoimmune disease of gastrointestinal tract that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite." DSA09356,GSE146230,GPL23159,0,"Disorder of Vestibular Function, Unspecified",C0042594,Whole blood,GEO,Microarray,Homo sapiens,10|10,"DO:A brain disease that is characterized by vertigo caused by hemorrhagic insult, ischemic insult or mass lesion of the cerebellum, the vestibular nuclei, and the brainstem, has_symptom dizziness, has_symptom nausea, has_symptom vomiting and has_symptom difficulty walking." DSA09357,GSE11037,GPL891,1000,Chronic Lung Inflammation,,Lung,GEO,Microarray,Mus musculus,5|5, DSA09358,GSE146339,GPL18573;GPL20301,10,Fragile X Syndrome,C0016667,,GEO,RNA-Seq,Homo sapiens,6|5,"DO:A syndrome that is characterized by moderate to severe mental retardation, macroorchidism, and distinct facial features, including long face, large ears, and prominent jaw, and has_material_basis_in X-linked inheritance and a loss of FMR1 function." DSA09359,GSE146523,GPL24247,0,Smith-Lemli-Opitz Syndrome,C0175694,Liver,GEO,RNA-Seq,Mus musculus,6|6,"MONDO:Smith-Lemli-Opitz syndrome (SLOS) is characterized by multiple congenital anomalies, intellectual deficit, and behavioral problems." DSA09360,GSE146524,GPL13112,301,Desmosterolosis,C1865596,,GEO,RNA-Seq,Mus musculus,2|2,"MONDO:Desmosterolosis is a very rare sterol biosynthesis disorder characterized by multiple congenital anomalies, failure to thrive, and intellectual disability, with elevated levels of desmosterol." DSA09361,GSE146524,GPL15103,0,Desmosterolosis,C1865596,Liver,GEO,RNA-Seq,Mus musculus,2|2,"MONDO:Desmosterolosis is a very rare sterol biosynthesis disorder characterized by multiple congenital anomalies, failure to thrive, and intellectual disability, with elevated levels of desmosterol." DSA09362,GSE146532,GPL11154,1000,Rhinovirus Infection,C0276447,,GEO,RNA-Seq,Homo sapiens,20|20,"NCI:An infectious process caused by rhinovirus. The virus usually causes upper respiratory infections, but can infect the lower tract as well." DSA09363,GSE146587,GPL17077,1000,Colorectal Carcinoma,C0009402,,GEO,Microarray,Homo sapiens,6|6,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA09364,GSE146640,GPL16791,13,Angelman Syndrome,C0162635,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A syndrome that is characterized by delayed development, intellectual disability, severe speech impairment, and problems with movement and balance." DSA09365,GSE146641,GPL16791,1000,Macular Degeneration,C0024437,Retina,GEO,RNA-Seq,Homo sapiens,18|18,DO:A retinitis pigmentosa that has_material_basis_in mutation in the FSCN2 gene on chromosome 17q25. DSA09366,GSE146649,GPL570,1000,Multiple Myeloma,C0026764,,GEO,Microarray,Homo sapiens,10|12,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA09367,GSE146657,GPL20301,70,Acute Myeloid Leukemia,C0023467,,GEO,RNA-Seq,Homo sapiens,2|8,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA09368,GSE146673,GPL19057,1000,Huntington's Disease,C0020179,,GEO,RNA-Seq,Mus musculus,3|6,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA09369,GSE146763,GPL20301,210,Hypoplastic Left Heart Syndrome,C0152101,,GEO,scRNA-Seq,Homo sapiens,1|1,DO:A congenital heart disease characterized by abnormal development of the left-sided structures of the heart. DSA09370,GSE146853,GPL16791,22,Irritable Bowel Syndrome,C0022104,,GEO,RNA-Seq,Homo sapiens,18|20,"DO:An intestinal disease that is characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause." DSA09371,GSE146869,GPL11154,0,Obesity,C0028754,Whole blood,GEO,RNA-Seq,Homo sapiens,15|12,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA09372,GSE146885,GPL24247,512,Autism Spectrum Disorder,C1510586,Cerebellum,GEO,RNA-Seq,Mus musculus,4|4,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA09373,GSE146887,GPL18573,124,Age Related Macular Degeneration,C0242383,,GEO,RNA-Seq,Homo sapiens,4|4,DO:A degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision. DSA09374,GSE146912,GPL21103,1000,Toxic Nephropathy,C1404837,Kidney glomerulus,GEO,scRNA-Seq,Mus musculus,3|4,NCI:Kidney damage resulting from exposure to drugs. DSA09375,GSE11037,GPL891,1000,Chronic Lung Inflammation,,Lung,GEO,Microarray,Mus musculus,5|5, DSA09376,GSE146912,GPL21103,1000,Glomerulopathy,C0268731,Kidney glomerulus,GEO,scRNA-Seq,Mus musculus,4|1,DO:A kidney disease that is characterized by an inflammation of the kidneys. DSA09377,GSE146912,GPL21103,1000,Diabetes,C0011847,Kidney glomerulus,GEO,scRNA-Seq,Mus musculus,5|4,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09378,GSE10616,GPL5760,10,Inflammatory Bowel Disease,C0021390,Colon,GEO,Microarray,Homo sapiens,11|14,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA09379,GSE147026,GPL24676,1000,Aortic Dissection,C0340643,Aorta,GEO,RNA-Seq,Homo sapiens,4|4,HPO:Aortic dissection refers to a tear in the intimal layer of the aorta causing a separation between the intima and the medial layers of the aorta. DSA09380,GSE10616,GPL5760,1000,Inflammatory Bowel Disease,C0021390,Colon,GEO,Microarray,Homo sapiens,11|18,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA09381,GSE147236,GPL20301,1000,Heart Failure,C0018801,Left ventricle,GEO,RNA-Seq,Homo sapiens,3|3,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA09382,GSE10616,GPL5760,1000,Inflammatory Bowel Disease,C0021390,Colon,GEO,Microarray,Homo sapiens,11|8,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA09383,GSE147339,GPL20301,62,Psoriasis,C0033860,Whole blood,GEO,RNA-Seq,Homo sapiens,10|10,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09384,GSE147359,GPL16417,1000,Systemic Lupus Erythematosus,C0024141,Thymus,GEO,RNA-Seq,Mus musculus,3|3,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA09385,GSE147424,GPL16791,100,Atopic Dermatitis,C0011615,Skin,GEO,RNA-Seq,Homo sapiens,8|5,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA09386,GSE147449,GPL18573,1000,Conjunctival Squamous Cell Carcinoma,C0346359,Conjunctiva,GEO,RNA-Seq,Homo sapiens,8|7,DO:A conjunctival cancer characterized by abnormal growth of dysplastic squamous epithelial cells on the surface of the eye that arises from the conjunctiva that has infiltrated beyond the confines of the epithelial basement membrane. DSA09387,GSE147449,GPL18573,1000,Squamous Cell Papilloma,C0205874,Conjunctiva,GEO,RNA-Seq,Homo sapiens,8|7,HPO:A benign epithelial neoplasm characterized by a papillary growth pattern and a proliferation of neoplastic squamous cells without morphologic evidence of malignancy DSA09388,GSE147527,GPL17303,564,Neonatal Hypoparathyroidism,C1455734,Whole blood,GEO,RNA-Seq,Homo sapiens,3|3,HPO:Deficiency of parathyroid hormone with congenital onset. DSA09389,GSE147527,GPL17303,271,Neonatal Hypoparathyroidism,C1455734,Whole blood,GEO,RNA-Seq,Homo sapiens,3|3,HPO:Deficiency of parathyroid hormone with congenital onset. DSA09390,GSE147544,GPL20301,1000,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,4|6,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA09391,GSE147586,GPL10558,291,Hidradenitis Suppurativa,C0162836,,GEO,Microarray,Homo sapiens,5|6,"DO:A hidradenitis that is characterized by chronic inflammation of the apocrine sweat glands, has_symptom painful nodules, abscesses, sinus tract formation, scarring, erythema, pruritis, and pain, and has_material_basis_in chronic inflammation of the apocrine sweat glands leading to recurrent folliculitis and an accompanying immune response that worsens inflammation." DSA09392,GSE147608,GPL16791,1000,Systemic Juvenile Idiopathic Arthritis,C1384600,,GEO,RNA-Seq,Homo sapiens,11|16,"EFO:Juvenile idiopathic arthritis (JIA), also known as juvenile rheumatoid arthritis (JRA), is the most common form of arthritis in children and adolescents. (Juvenile in this context refers to an onset before age 16, idiopathic refers to a condition with no defined cause, and arthritis is the inflammation of the synovium of a joint.) JIA is an autoimmune, non-infective, inflammatory joint disease of more than 6 weeks duration in children less than 16 years of age. The disease commonly occurs in children from the ages of 7 to 12, but it may occur in adolescents as old as 15 years of age, as well as in infants. It is a subset of arthritis seen in childhood, which may be transient and self-limited or chronic. It differs significantly from arthritis commonly seen in adults (osteoarthritis, rheumatoid arthritis), and other types of arthritis that can present in childhood which are chronic conditions (e.g. psoriatic arthritis and ankylosing spondylitis). Aetiopathology is similar to rheumatoid arthritis but with less marked cartilage erosion, and joint instability and absent rheumatoid factor. JIA affects approximately 1 in 1,000 children in any given year, with about 1 in 10,000 having a more severe form." DSA09393,GSE147608,GPL16791,1000,Systemic Juvenile Idiopathic Arthritis,C1384600,,GEO,RNA-Seq,Homo sapiens,11|10,"EFO:Juvenile idiopathic arthritis (JIA), also known as juvenile rheumatoid arthritis (JRA), is the most common form of arthritis in children and adolescents. (Juvenile in this context refers to an onset before age 16, idiopathic refers to a condition with no defined cause, and arthritis is the inflammation of the synovium of a joint.) JIA is an autoimmune, non-infective, inflammatory joint disease of more than 6 weeks duration in children less than 16 years of age. The disease commonly occurs in children from the ages of 7 to 12, but it may occur in adolescents as old as 15 years of age, as well as in infants. It is a subset of arthritis seen in childhood, which may be transient and self-limited or chronic. It differs significantly from arthritis commonly seen in adults (osteoarthritis, rheumatoid arthritis), and other types of arthritis that can present in childhood which are chronic conditions (e.g. psoriatic arthritis and ankylosing spondylitis). Aetiopathology is similar to rheumatoid arthritis but with less marked cartilage erosion, and joint instability and absent rheumatoid factor. JIA affects approximately 1 in 1,000 children in any given year, with about 1 in 10,000 having a more severe form." DSA09394,GSE147776,GPL20844,0,Pre-Eclampsia,C0032914,Placenta,GEO,Microarray,Homo sapiens,8|7,"DO:A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy." DSA09395,GSE147776,GPL20844,0,Intrauterine Growth Restriction,C1386048,Placenta,GEO,Microarray,Homo sapiens,8|6,HPO:An abnormal restriction of fetal growth with fetal weight below the tenth percentile for gestational age. DSA09396,GSE147776,GPL20844,6,Intrauterine Growth Restriction,C1386048,Placenta,GEO,Microarray,Homo sapiens,8|7,HPO:An abnormal restriction of fetal growth with fetal weight below the tenth percentile for gestational age. DSA09397,GSE147790,GPL19057,82,Autism Spectrum Disorder,C1510586,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA09398,GSE147790,GPL19057,13,Autism Spectrum Disorder,C1510586,Cortex,GEO,RNA-Seq,Mus musculus,4|4,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA09399,GSE147851,GPL20301,1000,Atypical Teratoid Rhabdoid Tumor,C1266184,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A brain cancer that is usually located in the brain, but can occur anywhere in the central nervous system." DSA09400,GSE147851,GPL20301,1000,Atypical Teratoid Rhabdoid Tumor,C1266184,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A brain cancer that is usually located in the brain, but can occur anywhere in the central nervous system." DSA09401,GSE147878,GPL10558,116,Asthma,C0004096,Bronchus,GEO,Microarray,Homo sapiens,13|18,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA09402,GSE147880,GPL6104,0,Asthma,C0004096,Sputum,GEO,Microarray,Homo sapiens,18|8,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA09403,GSE10667,GPL4133,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,15|23,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA09404,GSE147890,GPL571,178,Diabetes,C0011847,Skin,GEO,Microarray,Homo sapiens,5|6,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09405,GSE147890,GPL571,62,Diabetes,C0011847,Skin,GEO,Microarray,Homo sapiens,7|6,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09406,GSE147930,GPL570,1000,T Cell Prolymphocytic Leukemia,C2363142,,GEO,Microarray,Homo sapiens,12|23,EFO:A slow-growing type of leukemia (blood cancer) in which too many lymphocytes are found in the bone marrow and/or blood. The T-cell is specified as the defective cell line. DSA09407,GSE10667,GPL4133,584,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,15|8,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA09408,GSE147944,GPL18573,1000,Cutaneous T Cell Lymphoma,C0079773,Skin,GEO,scRNA-Seq,Homo sapiens,4|3,DO:A non-Hodgkin's lymphoma that has_material_basis_in a mutation of T cells. DSA09409,GSE147964,GPL23126,1000,Tuberculosis,C0041296,Blood,GEO,Microarray,Homo sapiens,10|10,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA09410,GSE147964,GPL23126,1000,Tuberculosis,C0041296,Blood,GEO,Microarray,Homo sapiens,10|10,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA09411,GSE147975,GPL24676,1000,COVID-19,D8888888,,GEO,scRNA-Seq,Homo sapiens,1|1,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA09412,GSE148004,GPL13497,0,Asthma,C0004096,Sputum,GEO,Microarray,Homo sapiens,9|9,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA09413,GSE148004,GPL13497,1000,Chronic Obstructive Pulmonary Disease,C0024117,Sputum,GEO,Microarray,Homo sapiens,9|7,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA09414,GSE148020,GPL11154,1000,Vogt-Koyanagi-Harada Disease,C0042170,,GEO,scRNA-Seq,Homo sapiens,3|3,"DO:An autoimmune disease that is caused by T helper cell mediated autoimmune attack of melanocytes resulting in inflammation of the inside of the eye, whitening of hair, skin pigment loss, and meningitis." DSA09415,GSE148027,GPL570,1000,Hidradenitis Suppurativa,C0162836,Skin,GEO,Microarray,Homo sapiens,15|18,"DO:A hidradenitis that is characterized by chronic inflammation of the apocrine sweat glands, has_symptom painful nodules, abscesses, sinus tract formation, scarring, erythema, pruritis, and pain, and has_material_basis_in chronic inflammation of the apocrine sweat glands leading to recurrent folliculitis and an accompanying immune response that worsens inflammation." DSA09416,GSE148037,GPL21103,5,Acute Myeloid Leukemia,C0023467,Bone marrow,GEO,RNA-Seq,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA09417,GSE14841,GPL570,19,Irritable Bowel Syndrome With Diarrhea,C0348898,Jejunum,GEO,Microarray,Homo sapiens,4|5, DSA09418,GSE13690,GPL1261,1000,Leukemia,C0023418,,GEO,Microarray,Mus musculus,4|8,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA09419,GSE13690,GPL1261,1000,Leukemia,C0023418,,GEO,Microarray,Mus musculus,4|9,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA09420,GSE13690,GPL1261,1000,Leukemia,C0023418,,GEO,Microarray,Mus musculus,4|5,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA09421,GSE13690,GPL1261,1000,Leukemia,C0023418,,GEO,Microarray,Mus musculus,4|7,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA09422,GSE148180,GPL16791,817,Huntington's Disease,C0020179,,GEO,RNA-Seq,Homo sapiens,4|6,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA09423,GSE148180,GPL16791,1000,Myotonic Dystrophy Type 1,C0027126,,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA09424,GSE148219,GPL10999,1000,Aortic Valve Disease,C1260873,Aortic valve,GEO,RNA-Seq,Homo sapiens,8|14,DO:An aortic valve disease that is characterized by the presence of abnormal two-leaflet aortic valve in at least 2 first-degree relatives. DSA09425,GSE148240,GPL19057,1000,Asthma,C0004096,Lung,GEO,RNA-Seq,Mus musculus,6|6,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA09426,GSE148240,GPL19057,1000,Asthma,C0004096,Lung,GEO,RNA-Seq,Mus musculus,5|5,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA09427,GSE148247,GPL570,697,Tracheoesophageal Fistula,C0040588,,GEO,Microarray,Homo sapiens,3|19,HPO:An abnormal connection (fistula) between the esophagus and the trachea. DSA09428,GSE148247,GPL570,1000,Tracheoesophageal Fistula,C0040588,,GEO,Microarray,Homo sapiens,4|19,HPO:An abnormal connection (fistula) between the esophagus and the trachea. DSA09429,GSE148247,GPL570,1000,Tracheoesophageal Fistula,C0040588,,GEO,Microarray,Homo sapiens,3|19,HPO:An abnormal connection (fistula) between the esophagus and the trachea. DSA09430,GSE148300,GPL11154,346,X-Linked Retinitis Pigmentosa,,Retina,GEO,RNA-Seq,Homo sapiens,2|2, DSA09431,GSE148351,GPL13112,889,Ischemic Heart Disease,C0151744,Heart ventricle,GEO,RNA-Seq,Mus musculus,3|3,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA09432,GSE148381,GPL24676,1000,Esophagitis,C0014868,Esophagus,GEO,RNA-Seq,Homo sapiens,7|5,"EFO:Eosinophilic esophagitis (EoE) is a chronic, allergic disease of the esophagus characterized clinically by symptoms of esophageal dysfunction (including vomiting, dysphagia, feeding disorders, food impaction and abdominal pain) which persist after treatment with proton pump inhibitors (PPIs)." DSA09433,GSE148381,GPL24676,1000,Esophagitis,C0014868,Esophagus,GEO,RNA-Seq,Homo sapiens,7|13,"EFO:Eosinophilic esophagitis (EoE) is a chronic, allergic disease of the esophagus characterized clinically by symptoms of esophageal dysfunction (including vomiting, dysphagia, feeding disorders, food impaction and abdominal pain) which persist after treatment with proton pump inhibitors (PPIs)." DSA09434,GSE148381,GPL24676,658,Gastroesophageal Reflux Disease,C0017168,Esophagus,GEO,RNA-Seq,Homo sapiens,7|6,"EFO:A malignant tumor with glandular differentiation arising predominantly from Barrett mucosa in the lower third of the esophagus. Rare examples of esophageal adenocarcinoma deriving from ectopic gastric mucosa in the upper esophagus have also been reported. Grossly, esophageal adenocarcinomas are similar to esophageal squamous cell carcinomas. Microscopically, adenocarcinomas arising in the setting of Barrett esophagus are typically papillary and/or tubular. The prognosis is poor." DSA09435,GSE148381,GPL24676,1000,Esophagitis,C0014868,Esophagus,GEO,RNA-Seq,Homo sapiens,7|10,"EFO:Eosinophilic esophagitis (EoE) is a chronic, allergic disease of the esophagus characterized clinically by symptoms of esophageal dysfunction (including vomiting, dysphagia, feeding disorders, food impaction and abdominal pain) which persist after treatment with proton pump inhibitors (PPIs)." DSA09436,GSE148387,GPL18573,1000,Melanoma,C0025202,Conjunctiva,GEO,RNA-Seq,Homo sapiens,8|6,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA09437,GSE148387,GPL18573,1000,Melanoma,C0025202,Conjunctiva,GEO,RNA-Seq,Homo sapiens,8|5,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA09438,GSE148402,GPL18573,732,Preterm Birth,C0151526,Whole blood,GEO,RNA-Seq,Homo sapiens,5|5,"EFO:CHILDBIRTH before 37 weeks of PREGNANCY (259 days from the first day of the mother's last menstrual period, or 245 days after FERTILIZATION)." DSA09439,GSE148535,GPL16791,320,Systemic Lupus Erythematosus,C0024141,Skin,GEO,RNA-Seq,Homo sapiens,9|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA09440,GSE148535,GPL16791,0,Systemic Lupus Erythematosus,C0024141,Skin,GEO,RNA-Seq,Homo sapiens,9|3,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA09441,GSE148535,GPL16791,0,Systemic Lupus Erythematosus,C0024141,Skin,GEO,RNA-Seq,Homo sapiens,9|5,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA09442,GSE148590,GPL21103,1000,Allergic Disorder of Respiratory System,C1504369,,GEO,RNA-Seq,Mus musculus,5|3, DSA09443,GSE13690,GPL1261,1000,Leukemia,C0023418,,GEO,Microarray,Mus musculus,4|5,DO:A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells. DSA09444,GSE148608,GPL24247,4,Global Developmental Delay,C0557874,Cortex,GEO,RNA-Seq,Mus musculus,3|2,"HPO:A delay in the achievement of motor or mental milestones in the domains of development of a child, including motor skills, speech and language, cognitive skills, and social and emotional skills. This term should only be used to describe children younger than five years of age." DSA09445,GSE148658,GPL16791,1000,T-Cell Acute Lymphoblastic Leukemia,C1961099,,GEO,RNA-Seq,Homo sapiens,3|3,DO:An acute lymphoblastic leukemia that is characterized by too many T-cell lymphoblasts found in the bone marrow and blood. DSA09446,GSE27262,GPL570,1000,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Homo sapiens,25|25,DO:A respiratory system cancer that is located_in the lung. DSA09447,GSE14317,GPL571,1000,Adult T-Cell Leukemia,C0023493,Blood,GEO,Microarray,Homo sapiens,7|19,"DO:A T-cell acute leukemia that results_in abnormal increase of lymphocytes, derives_from T-cells, has_material_basis_in Human T-lymphotropic virus 1 (HTLV-1), which is transmitted_by sexual contact, transmitted_by contaminated needles used by intravenous-drug users, and transmitted_by breast feeding. The infection results_in_formation_of skin lesions." DSA09448,GSE27651,GPL570,1000,Borderline Ovarian Epithelial Tumor,C3665489,Ovary,GEO,Microarray,Homo sapiens,6|8,EFO:An epithelial tumor arising from the ovary without definitive morphologic characteristics of malignancy. DSA09449,GSE27651,GPL570,1000,Ovarian Serous Carcinoma,C1335177,Ovary,GEO,Microarray,Homo sapiens,6|13,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA09450,GSE27651,GPL570,1000,Ovarian Serous Carcinoma,C1335177,Ovary,GEO,Microarray,Homo sapiens,6|22,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA09451,GSE27678,GPL570,633,Squamous Cell Carcinoma,C0007137,,GEO,Microarray,Homo sapiens,3|28,DO:A carcinoma that derives_from squamous epithelial cells. DSA09452,GSE27678,GPL571,1000,High-Grade Squamous Intraepithelial Lesions,C0333875,,GEO,Microarray,Homo sapiens,12|21,DO:An uterus carcinoma in situ that is located_in the uterine cervix. DSA09453,GSE27678,GPL571,731,Low-Grade Squamous Intraepithelial Lesions,C1302773,,GEO,Microarray,Homo sapiens,12|11,"MSH:A cytological test finding often from PAP SMEARS that shows abnormal lesions of SQUAMOUS EPITHELIAL CELLS of the CERVIX. It is a diagnostic criterion used in the Bethesda System for UTERINE CERVICAL NEOPLASMS and represents the PAP TEST result that is abnormal. Although squamous intraepithelial lesions test result does not mean UTERINE CERVICAL NEOPLASMS it requires follow-ups (e.g., HPV DNA TESTS; and COLPOSCOPY)." DSA09454,GSE27838,GPL570,2,Myeloma,C0026764,,GEO,Microarray,Homo sapiens,8|8,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA09455,GSE27838,GPL570,0,Myeloma,C0026764,,GEO,Microarray,Homo sapiens,8|8,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA09456,GSE27928,GPL570,161,Follicular Lymphoma,C0024301,Lymph node,GEO,Microarray,Homo sapiens,7|12,DO:A B-cell lymphoma that is characterized as an indolent non-Hodgkin's lymphoma and has_material_basis_in follicle center B-cells (centrocytes and centroblasts). DSA09457,GSE27928,GPL570,477,Follicular Lymphoma,C0024301,Lymph node,GEO,Microarray,Homo sapiens,7|9,DO:A B-cell lymphoma that is characterized as an indolent non-Hodgkin's lymphoma and has_material_basis_in follicle center B-cells (centrocytes and centroblasts). DSA09458,GSE27949,GPL570,0,Glucose Intolerance,C0271650,Subcutaneous adipose tissue,GEO,Microarray,Homo sapiens,12|10,"DO:A glucose metabolism disease that is characterized by blood glucose levels are high, but not high enough to be classified as type 2 diabetes." DSA09459,GSE27949,GPL570,0,Diabetes Mellitus,C0011849,Subcutaneous adipose tissue,GEO,Microarray,Homo sapiens,12|11,"DO:A glucose metabolism disease that is characterized by chronic hyperglycaemia with disturbances of carbohydrate, fat and protein metabolism resulting from defects in insulin secretion, insulin action, or both." DSA09460,GSE28133,GPL570,1000,Retinal Detachment,C0035305,Retina,GEO,Microarray,Homo sapiens,19|19,HPO:Separation of the inner layers of the retina (neural retina) from the pigment epithelium. DSA09461,GSE29133,GPL570,0,Chronic Obstructive Pulmonary Disease,C0024117,Lung,GEO,Microarray,Homo sapiens,3|3,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA09462,GSE29431,GPL570,1000,Breast Cancer,C0678222,,GEO,Microarray,Homo sapiens,12|54,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09463,GSE29450,GPL570,1000,Ovarian Clear Cell Adenocarcinoma,C1518693,Ovary,GEO,Microarray,Homo sapiens,10|10,DO:A ovarian adenocarcinoma that derives_from epithelial cells which have clear cytoplasm. DSA09464,GSE29721,GPL570,1000,Hepatic Carcinosarcoma,C2007076,,GEO,Microarray,Homo sapiens,10|10,"NCI:An aggressive carcinoma with a sarcomatous component that arises from the liver. The sarcomatous component is clonally related to the more differentiated, carcinomatous component. The prognosis is usually poor." DSA09465,GSE30304,GPL570,1000,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09466,GSE30304,GPL570,1000,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09467,GSE30304,GPL570,1000,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,3|3,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09468,GSE30522,GPL570,0,Bladder Cancer,C0699885,Bladder,GEO,Microarray,Homo sapiens,3|1,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09469,GSE30522,GPL570,317,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,5|5,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09470,GSE30563,GPL570,0,Glioblastoma,C0017636,Brain,GEO,Microarray,Homo sapiens,3|1,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA09471,GSE30563,GPL570,0,Ganglioglioma,C0206716,Brain,GEO,Microarray,Homo sapiens,3|1,DO:A cell type benign neoplasm that has_material_basis_in glial-type cells. DSA09472,GSE30563,GPL570,0,Shwannoma,,Brain,GEO,Microarray,Homo sapiens,3|1, DSA09473,GSE31048,GPL570,1000,Chronic Lymphocytic Leukemia,C0023434,,GEO,Microarray,Homo sapiens,24|179,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA09474,GSE31138,GPL570,142,Breast Cancer,C0678222,Blood vessel,GEO,Microarray,Homo sapiens,3|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09475,GSE31189,GPL570,2,Bladder Cancer,C0699885,Bladder,GEO,Microarray,Homo sapiens,40|52,DO:A urinary bladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09476,GSE32676,GPL570,1000,Pancreatic Cancer,C0235974,Pancreas,GEO,Microarray,Homo sapiens,7|25,DO:An endocrine gland cancer located_in the pancreas. DSA09477,GSE33532,GPL570,1000,Non-Small Cell Lung Cancer,C0007131,Lung,GEO,Microarray,Homo sapiens,20|80,DO:A respiratory system cancer that is located_in the lung. DSA09478,GSE33810,GPL570,0,Esophageal Cancer,C0152018,Esophagus,GEO,Microarray,Homo sapiens,1|2,DO:A esophageal cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09479,GSE34248,GPL570,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,14|14,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09480,GSE35388,GPL570,1000,Melanoma,C0025202,,GEO,Microarray,Homo sapiens,2|2,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA09481,GSE35388,GPL570,1000,Melanoma,C0025202,,GEO,Microarray,Homo sapiens,2|2,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA09482,GSE36238,GPL570,735,Tuberculosis,C0041296,Blood,GEO,Microarray,Homo sapiens,9|9,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA09483,GSE36668,GPL570,504,Borderline Ovarian Epithelial Tumor,C3665489,Ovary,GEO,Microarray,Homo sapiens,4|4,EFO:An epithelial tumor arising from the ovary without definitive morphologic characteristics of malignancy. DSA09484,GSE36668,GPL570,1000,Ovarian Serous Carcinoma,C1335177,Ovary,GEO,Microarray,Homo sapiens,4|4,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA09485,GSE36895,GPL570,1000,Clear Cell Renal Cell Carcinoma,C0007134,Kidney,GEO,Microarray,Homo sapiens,23|29,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA09486,GSE37364,GPL570,1000,Colorectal Adenoma,C1302401,Colorectum,GEO,Microarray,Homo sapiens,38|13,"EFO:An adenoma that arises from the colon or rectum. The group of colorectal adenomas includes tubular, villous, and tubulovillous adenomas, traditional serrated adenomas, sessile serrated adenomas/polyps, and familial adenomatous polyposis." DSA09487,GSE37364,GPL570,1000,Colorectal Adenoma,C1302401,Colorectum,GEO,Microarray,Homo sapiens,38|16,"EFO:An adenoma that arises from the colon or rectum. The group of colorectal adenomas includes tubular, villous, and tubulovillous adenomas, traditional serrated adenomas, sessile serrated adenomas/polyps, and familial adenomatous polyposis." DSA09488,GSE37364,GPL570,1000,Colorectal Adenoma,C1302401,Colon,GEO,Microarray,Homo sapiens,38|27,"EFO:An adenoma that arises from the colon or rectum. The group of colorectal adenomas includes tubular, villous, and tubulovillous adenomas, traditional serrated adenomas, sessile serrated adenomas/polyps, and familial adenomatous polyposis." DSA09489,GSE38312,GPL570,1,Melanoma,C0025202,,GEO,Microarray,Homo sapiens,5|5,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA09490,GSE38666,GPL570,1000,Ovarian Cancer,C1140680,,GEO,Microarray,Homo sapiens,8|7,DO:A female reproductive organ cancer that is located_in the ovary. DSA09491,GSE38666,GPL570,1000,Ovarian Cancer,C1140680,,GEO,Microarray,Homo sapiens,12|18,DO:A female reproductive organ cancer that is located_in the ovary. DSA09492,GSE38941,GPL570,1000,Chronic (Viral) Hepatitis B,C0524909,Liver,GEO,Microarray,Homo sapiens,10|17,"EFO:INFLAMMATION of the LIVER in humans caused by a member of the ORTHOHEPADNAVIRUS genus, HEPATITIS B VIRUS. It is primarily transmitted by parenteral exposure, such as transfusion of contaminated blood or blood products, but can also be transmitted via sexual or intimate personal contact." DSA09493,GSE39454,GPL570,0,Dermatomyositis,C0011633,Biceps,GEO,Microarray,Homo sapiens,5|8,DO:A myositis that results_in inflammation located_in muscle or located_in skin where a skin rash is often seen prior to the onset of muscle weakness. The disease may result from either a viral infection or an autoimmune reaction. DSA09494,GSE39454,GPL570,677,Polymyositis,C0085655,Quadriceps,GEO,Microarray,Homo sapiens,5|8,EFO:Polymyositis (PM)(\ inflammation of many muscles\ ) is a type of chronic inflammation of the muscles (inflammatory myopathy) related to dermatomyositis and inclusion body myositis. DSA09495,GSE39454,GPL570,1,Necrotizing Myopathy,C4024608,Biceps,GEO,Microarray,Homo sapiens,5|5, DSA09496,GSE39454,GPL570,1000,Inclusion Body Myositis,C0238190,Biceps,GEO,Microarray,Homo sapiens,5|10,"DO:A myositis that is characterized by late onset of skeletal muscle inflammation, weakness, and atrophy with cytoplasmic granules and vacuoles in the muscle." DSA09497,GSE40562,GPL570,0,Fatal Familial Insomnia,C0206042,Thalamus,GEO,Microarray,Homo sapiens,1|3,"DO:A prion disease that is characterized by insomnia, hallucinations, dementia and death, located_in the brain." DSA09498,GSE40562,GPL570,0,Fatal Familial Insomnia,C0206042,Lobe,GEO,Microarray,Homo sapiens,1|3,"DO:A prion disease that is characterized by insomnia, hallucinations, dementia and death, located_in the brain." DSA09499,GSE40595,GPL570,1000,Ovarian Serous Carcinoma,C1335177,Ovary,GEO,Microarray,Homo sapiens,8|31,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA09500,GSE40595,GPL570,1000,Ovarian Serous Carcinoma,C1335177,,GEO,Microarray,Homo sapiens,6|32,DO:An ovary adenocarcinoma that derives_from the lining of a cavity that produces a serum-like fluid (a serous cavity). DSA09501,GSE40791,GPL570,1000,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Homo sapiens,100|94,DO:A respiratory system cancer that is located_in the lung. DSA09502,GSE41328,GPL570,1000,Colon Adenocarcinoma,C0699790,Colon,GEO,Microarray,Homo sapiens,5|5,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09503,GSE41328,GPL570,1000,Colon Adenocarcinoma,C0699790,Colon,GEO,Microarray,Homo sapiens,5|5,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09504,GSE41662,GPL570,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,24|24,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09505,GSE41663,GPL570,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,15|15,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09506,GSE10715,GPL570,1000,Colorectal Carcinoma,C0009402,Blood,GEO,Microarray,Homo sapiens,11|19,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA09507,GSE14577,GPL96,307,Chronic Fatigue Syndrome,C0015674,Blood,GEO,Microarray,Homo sapiens,7|8,"DO:A syndrome that involves prolonged and severe tiredness or weariness that is unrelated to exertion, is not relieved by rest and for a minimum of six months and is not directly caused by other conditions." DSA09508,GSE14577,GPL97,233,Chronic Fatigue Syndrome,C0015674,Blood,GEO,Microarray,Homo sapiens,7|8,"DO:A syndrome that involves prolonged and severe tiredness or weariness that is unrelated to exertion, is not relieved by rest and for a minimum of six months and is not directly caused by other conditions." DSA09509,GSE42568,GPL570,1000,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,17|104,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09510,GSE4229,GPL1211,0,Alzheimer's Disease,C0002395,Blood,GEO,Microarray,Homo sapiens,22|18,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA09511,GSE5058,GPL570,1000,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,12|6,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA09512,GSE5058,GPL570,1000,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,12|9,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA09513,GSE50683,GPL570,1000,Lymphoplasmacytic Lymphoma,C0334633,,GEO,Microarray,Homo sapiens,3|3,"EFO:Macroglobulinemia is the presence of increased levels of macroglobulins in the circulating blood. It is a Plasma cell dyscrasia, resembling leukemia, with cells of lymphocytic, plasmacytic, or intermediate morphology, which secrete a monoclonal immunoglobulin M component. There is diffuse infiltration by the malignant cells of the bone marrow and also, in many cases, of the spleen, liver, or lymph nodes. The circulating macroglobulin can produce symptoms of hyperviscosity syndrome: weakness, fatigue, bleeding disorders, and visual disturbances. Peak incidence of macroglobulinemia is in the sixth and seventh decades of life." DSA09514,GSE50738,GPL570,1000,Retinitis Pigmentosa,C0035334,,GEO,Microarray,Homo sapiens,3|27,DO:A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss. DSA09515,GSE50790,GPL570,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,4|4,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09516,GSE5081,GPL570,0,Gastritis,C0017152,Stomach,GEO,Microarray,Homo sapiens,8|8,DO:A stomach disease that is an inflammation of the lining of the stomach. DSA09517,GSE5081,GPL570,0,Gastritis,C0017152,Stomach,GEO,Microarray,Homo sapiens,8|8,DO:A stomach disease that is an inflammation of the lining of the stomach. DSA09518,GSE12685,GPL96,0,Alzheimer's Disease,C0002395,Cerebrum,GEO,Microarray,Homo sapiens,8|6,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA09519,GSE10746,GPL570,0,Acute Myeloid Leukemia,C0023467,Buccal cavity,GEO,Microarray,Homo sapiens,3|4,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA09520,GSE51021,GPL570,0,Esophageal Cancer,C0152018,Lymph node,GEO,Microarray,Homo sapiens,14|14,DO:A esophageal cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09521,GSE51024,GPL570,1000,Malignant Pleural Mesothelioma,C0812413,Pleura,GEO,Microarray,Homo sapiens,41|55,DO:A pleural cancer that has_material_basis_in mesothelium cells. DSA09522,GSE10746,GPL570,0,Acute Myeloid Leukemia,C0023467,Buccal cavity,GEO,Microarray,Homo sapiens,3|4,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA09523,GSE51401,GPL570,1000,Hepatocellular Carcinoma,C0334287,,GEO,Microarray,Homo sapiens,24|24,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA09524,GSE51472,GPL570,0,Sclerotic Aortic Valve,,Aortic valve,GEO,Microarray,Homo sapiens,5|5, DSA09525,GSE51472,GPL570,1000,Calcified Aortic Valve,,Aortic valve,GEO,Microarray,Homo sapiens,5|5, DSA09526,GSE51981,GPL570,1000,Endometriosis,C0014175,Endometrium,GEO,Microarray,Homo sapiens,81|67,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA09527,GSE52037,GPL570,1000,Ovarian Cancer,C1140680,Ovary,GEO,Microarray,Homo sapiens,10|10,DO:A female reproductive organ cancer that is located_in the ovary. DSA09528,GSE52139,GPL570,0,Multiple Sclerosis,C0026769,Spinal cord,GEO,Microarray,Homo sapiens,8|8,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA09529,GSE53157,GPL570,366,Thyroid Cancer,C0549473,Thyroid,GEO,Microarray,Homo sapiens,3|4,DO:A thyroid gland cancer that has_material_basis_in epithelial cells. DSA09530,GSE53157,GPL570,281,Thyroid Cancer,C0549473,Thyroid,GEO,Microarray,Homo sapiens,3|8,DO:A thyroid gland cancer that has_material_basis_in epithelial cells. DSA09531,GSE53157,GPL570,120,Thyroid Cancer,C0549473,Thyroid,GEO,Microarray,Homo sapiens,3|5,DO:A thyroid gland cancer that has_material_basis_in epithelial cells. DSA09532,GSE53157,GPL570,1000,Thyroid Cancer,C0549473,Thyroid,GEO,Microarray,Homo sapiens,3|7,DO:A thyroid gland cancer that has_material_basis_in epithelial cells. DSA09533,GSE53731,GPL570,0,Hepatitis,C0019158,Liver,GEO,Microarray,Homo sapiens,5|5,HPO:Inflammation of the liver. DSA09534,GSE53757,GPL570,1000,Renal Cell Carcinoma,C0007134,Kidney,GEO,Microarray,Homo sapiens,24|24,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA09535,GSE53757,GPL570,1000,Renal Cell Carcinoma,C0007134,Kidney,GEO,Microarray,Homo sapiens,15|15,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA09536,GSE53757,GPL570,1000,Renal Cell Carcinoma,C0007134,Kidney,GEO,Microarray,Homo sapiens,14|14,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA09537,GSE53757,GPL570,1000,Renal Cell Carcinoma,C0007134,Kidney,GEO,Microarray,Homo sapiens,7|7,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA09538,GSE54129,GPL570,1000,Gastric Cancer,C0699791,Stomach,GEO,Microarray,Homo sapiens,21|111,DO:A gastrointestinal system cancer that is located_in the stomach. DSA09539,GSE54495,GPL570,6,Lung Adenocarcinoma,C0152013,,GEO,Microarray,Homo sapiens,13|17,DO:A respiratory system cancer that is located_in the lung. DSA09540,GSE55092,GPL570,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,81|39,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA09541,GSE55092,GPL570,1000,Hepatocellular Carcinoma,C0334287,,GEO,Microarray,Homo sapiens,10|10,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA09542,GSE12027,GPL96,1000,Lymphangioleiomyomatosis,C0751674,,GEO,Microarray,Homo sapiens,7|14,"DO:A lung disease that is characterized by progressive cystic destruction of the lung and lymphatic abnormalities, frequently associated with renal angiomyolipomas." DSA09543,GSE10334,GPL570,1000,Periodontitis,C0031099,Gingiva,GEO,Microarray,Homo sapiens,64|183,"EFO:Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology)" DSA09544,GSE12511,GPL7191,1000,Atopic Eczema,C0013595,Skin,GEO,Microarray,Homo sapiens,12|18,"DO:A skin disease characterized by itchy, erythematous, vesicular, weeping and crusting patches of skin." DSA09545,GSE9861,GPL571,0,Cerebral Malaria,C0024534,,GEO,Microarray,Homo sapiens,2|2,"DO:A malaria that involves neurologic damage resulting from blockage of the blood vessels, caused due to the infection of the red blood cells by Plasmodium species." DSA09546,GSE5764,GPL570,36,Invasive Lobular Carcinoma,C0279565,Breast,GEO,Microarray,Homo sapiens,20|10,"EFO:An infiltrating lobular adenocarcinoma of the breast. The malignant cells lack cohesion and are arranged individually or in a linear manner (Indian files), or as narrow trabeculae within the stroma. The malignant cells are usually smaller than those of ductal carcinoma, are less pleomorphic, and have fewer mitotic figures." DSA09547,GSE58058,GPL570,1000,Colon Cancer,C0699790,Colon,GEO,Microarray,Homo sapiens,3|4,DO:A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09548,GSE9861,GPL571,0,Cerebral Malaria,C0024534,,GEO,Microarray,Homo sapiens,2|2,"DO:A malaria that involves neurologic damage resulting from blockage of the blood vessels, caused due to the infection of the red blood cells by Plasmodium species." DSA09549,GSE18920,GPL5188,20,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,Microarray,Homo sapiens,10|12,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA09550,GSE58331,GPL570,1000,Pseudotumor (Inflammatory) of Orbit,C0085270,Lacrimal gland,GEO,Microarray,Homo sapiens,7|42,MONDO:A nonspecific tumor-like inflammatory lesion in the orbit of the eye. It is usually composed of mature lymphocytes; plasma cells; macrophages; leukocytes with varying degrees of fibrosis. Orbital pseudotumors are often associated with inflammation of the extraocular muscles (orbital myositis) or inflammation of the lacrimal glands (dacryoadenitis). DSA09551,GSE58331,GPL570,1000,Pseudotumor (Inflammatory) of Orbit,C0085270,Anterior orbit,GEO,Microarray,Homo sapiens,22|33,MONDO:A nonspecific tumor-like inflammatory lesion in the orbit of the eye. It is usually composed of mature lymphocytes; plasma cells; macrophages; leukocytes with varying degrees of fibrosis. Orbital pseudotumors are often associated with inflammation of the extraocular muscles (orbital myositis) or inflammation of the lacrimal glands (dacryoadenitis). DSA09552,GSE58331,GPL570,1000,Ophthalmopathies Thyroid Assoc,C0339143,Lacrimal gland,GEO,Microarray,Homo sapiens,7|8,"MSH:An autoimmune disorder of the EYE, occurring in patients with Graves disease. Subtypes include congestive (inflammation of the orbital connective tissue), myopathic (swelling and dysfunction of the extraocular muscles), and mixed congestive-myopathic ophthalmopathy." DSA09553,GSE58331,GPL570,221,Ophthalmopathies Thyroid Assoc,C0339143,Anterior orbit,GEO,Microarray,Homo sapiens,22|27,"MSH:An autoimmune disorder of the EYE, occurring in patients with Graves disease. Subtypes include congestive (inflammation of the orbital connective tissue), myopathic (swelling and dysfunction of the extraocular muscles), and mixed congestive-myopathic ophthalmopathy." DSA09554,GSE58331,GPL570,1000,Sarcoidosis,C0036202,Lacrimal gland,GEO,Microarray,Homo sapiens,7|14,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA09555,GSE58331,GPL570,1000,Sarcoidosis,C0036202,Anterior orbit,GEO,Microarray,Homo sapiens,22|8,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA09556,GSE58331,GPL570,1000,Granulomatosis With Polyangiitis,C3495801,Anterior orbit,GEO,Microarray,Homo sapiens,22|10,"DO:An autoimmune disease that is characterized by necrotizing granulomatous inflammation of the upper and lower respiratory tract, glomerulonephritis, vasculitis, and the presence of antineutrophil cytoplasmatic autoantibodies (ANCAs) in patient sera, and is located_in lung, located_in kidney, located_in skin resulting from an autoimmune attack by antineutrophil cytoplasmic antibodies against small and medium-size blood vessels." DSA09557,GSE6004,GPL570,4,Thyroid Cancer,C0549473,Thyroid,GEO,Microarray,Homo sapiens,4|7,DO:A thyroid gland cancer that has_material_basis_in epithelial cells. DSA09558,GSE6004,GPL570,40,Thyroid Cancer,C0549473,Thyroid,GEO,Microarray,Homo sapiens,4|7,DO:A thyroid gland cancer that has_material_basis_in epithelial cells. DSA09559,GSE60403,GPL570,0,Obesity,C0028754,Umbilical cord blood,GEO,Microarray,Homo sapiens,8|8,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA09560,GSE6054,GPL570,24,Familial Hypercholesterolemia,C0020445,,GEO,Microarray,Homo sapiens,13|4,DO:A familial hyperlipidemia characterized by very high levels of low-density lipoprotein (LDL) and early cardiovascular disease. DSA09561,GSE6054,GPL570,1,Familial Hypercholesterolemia,C0020445,,GEO,Microarray,Homo sapiens,13|6,DO:A familial hyperlipidemia characterized by very high levels of low-density lipoprotein (LDL) and early cardiovascular disease. DSA09562,GSE62029,GPL570,1000,Acute Liver Failure,C0162557,Liver,GEO,Microarray,Homo sapiens,10|13,"HPO:Hepatic failure refers to the inability of the liver to perform its normal synthetic and metabolic functions, which can result in coagulopathy and alteration in the mental status of a previously healthy individual. Hepatic failure is defined as fulminant if there is onset of encephalopathy within 4 weeks of the onset of symptoms in a patient with a previously healthy liver." DSA09563,GSE62029,GPL570,1000,Hepatic Hemangioma,C0238246,Liver,GEO,Microarray,Homo sapiens,10|7,HPO:A congenital vascular malformation in the liver composed of masses of blood vessels that are atypical or irregular in arrangement and size. DSA09564,GSE6222,GPL570,18,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,2|4,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA09565,GSE6222,GPL570,23,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,2|6,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA09566,GSE62232,GPL570,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,10|81,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA09567,GSE62837,GPL570,1000,Acral Lentiginous Melanoma,C0346037,Skin,GEO,Microarray,Homo sapiens,3|2,"DO:A skin melanoma that is characterized by slow growth of a small pigmented spot on the skin with a clearly defined edge, surrounded by normal-appearing skin and occurs on occurs on non hair-bairing surfaces including hands and feet, subungual sites, and fingers or toes." DSA09568,GSE63514,GPL570,1000,Cervical Cancer,C4048328,Cervix,GEO,Microarray,Homo sapiens,24|28,DO:A female reproductive organ cancer that is located_in the cervix. DSA09569,GSE63941,GPL570,0,Esophageal Squamous Cell Carcinoma,C0279626,Esophagus,GEO,Microarray,Homo sapiens,3|1,DO:An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus. DSA09570,GSE64951,GPL570,0,Gastric Cancer,C0699791,Saliva,GEO,Microarray,Homo sapiens,31|63,DO:A gastrointestinal system cancer that is located_in the stomach. DSA09571,GSE6575,GPL570,0,Autism Spectrum Disorder,C1510586,Whole blood,GEO,Microarray,Homo sapiens,11|17,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA09572,GSE6575,GPL570,0,Autism Spectrum Disorder,C1510586,Whole blood,GEO,Microarray,Homo sapiens,11|18,"DO:A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior." DSA09573,GSE66229,GPL570,1000,Gastric Tumor,C0038356,Stomach,GEO,Microarray,Homo sapiens,100|300,DO:A gastrointestinal system cancer that is located_in the stomach. DSA09574,GSE66270,GPL570,1000,Clear Cell Renal Cell Carcinoma,C0007134,Kidney,GEO,Microarray,Homo sapiens,14|14,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA09575,GSE66271,GPL570,1000,Clear Cell Renal Cell Carcinoma,C0007134,Kidney,GEO,Microarray,Homo sapiens,13|13,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA09576,GSE66354,GPL570,1000,Brain Tumor,C0006118,,GEO,Microarray,Homo sapiens,13|2,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09577,GSE66354,GPL570,1000,Brain Tumor,C0006118,,GEO,Microarray,Homo sapiens,13|17,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09578,GSE66354,GPL570,1000,Brain Tumor,C0006118,,GEO,Microarray,Homo sapiens,13|55,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09579,GSE66354,GPL570,1000,Brain Tumor,C0006118,,GEO,Microarray,Homo sapiens,13|9,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09580,GSE66354,GPL570,1000,Brain Tumor,C0006118,,GEO,Microarray,Homo sapiens,13|19,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09581,GSE66354,GPL570,1000,Brain Tumor,C0006118,,GEO,Microarray,Homo sapiens,13|11,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09582,GSE66354,GPL570,1000,Brain Tumor,C0006118,,GEO,Microarray,Homo sapiens,13|8,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09583,GSE66354,GPL570,1000,Brain Tumor,C0006118,,GEO,Microarray,Homo sapiens,13|15,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09584,GSE66359,GPL570,1000,Cutaneous Squamous Cell Carcinoma,C0553723,Skin,GEO,Microarray,Homo sapiens,5|8,DO:A skin carcinoma that has_material_basis_in squamous cells. DSA09585,GSE66724,GPL570,0,Stroke,C0948008,,GEO,Microarray,Homo sapiens,8|8,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA09586,GSE67066,GPL570,130,Pheochromocytomas And Paragangliomas,,Adrenal gland,GEO,Microarray,Homo sapiens,40|11, DSA09587,GSE6764,GPL570,785,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,10|8,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA09588,GSE6764,GPL570,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,10|10,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA09589,GSE6764,GPL570,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,10|7,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA09590,GSE6764,GPL570,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,10|10,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA09591,GSE6764,GPL570,1000,Liver Cirrhosis,C0023890,Liver,GEO,Microarray,Homo sapiens,10|10,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA09592,GSE6764,GPL570,386,Liver Cirrhosis,C0023890,Liver,GEO,Microarray,Homo sapiens,10|3,"EFO:Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules." DSA09593,GSE6764,GPL570,489,Liver Dysplastic Nodule,C1333964,Liver,GEO,Microarray,Homo sapiens,10|10,"EFO:A premalignant neoplastic nodular lesion of the liver that usually measures less than 15 mm. It is found during microscopic examination of liver tissues, usually in cirrhotic livers. Based on the degree of atypia, it is classified as low or high grade." DSA09594,GSE6764,GPL570,173,Liver Dysplastic Nodule,C1333964,Liver,GEO,Microarray,Homo sapiens,10|7,"EFO:A premalignant neoplastic nodular lesion of the liver that usually measures less than 15 mm. It is found during microscopic examination of liver tissues, usually in cirrhotic livers. Based on the degree of atypia, it is classified as low or high grade." DSA09595,GSE67738,GPL570,0,Insulin Resistance,C0021655,Saliva,GEO,Microarray,Homo sapiens,15|23,EFO:diminished effectiveness of insulin in lowering plasma glucose levels DSA09596,GSE67853,GPL570,378,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,5|7,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09597,GSE67853,GPL570,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,8|7,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09598,GSE6791,GPL570,1000,Cervical Cancer,C4048328,Cervix,GEO,Microarray,Homo sapiens,8|20,DO:A female reproductive organ cancer that is located_in the cervix. DSA09599,GSE6791,GPL570,1000,Head And Neck Cancer,C0018671,Oral cavity,GEO,Microarray,Homo sapiens,9|42,"DO:An organ system cancer that arises in the head or neck region. This region includes the nasal cavity, sinuses, lips, mouth, salivary glands, throat, or larynx." DSA09600,GSE68015,GPL570,1000,Brain Tumor,C0006118,Brain,GEO,Microarray,Homo sapiens,16|15,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09601,GSE68015,GPL570,1000,Brain Tumor,C0006118,Brain,GEO,Microarray,Homo sapiens,16|5,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09602,GSE68015,GPL570,1000,Brain Tumor,C0006118,Brain,GEO,Microarray,Homo sapiens,16|11,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09603,GSE68015,GPL570,1000,Brain Tumor,C0006118,Brain,GEO,Microarray,Homo sapiens,16|19,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09604,GSE68015,GPL570,1000,Brain Tumor,C0006118,Brain,GEO,Microarray,Homo sapiens,16|9,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09605,GSE68015,GPL570,1000,Brain Tumor,C0006118,Brain,GEO,Microarray,Homo sapiens,16|6,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09606,GSE68015,GPL570,1000,Brain Tumor,C0006118,Brain,GEO,Microarray,Homo sapiens,16|15,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09607,GSE68015,GPL570,65,Brain Tumor,C0006118,Brain,GEO,Microarray,Homo sapiens,16|4,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09608,GSE68015,GPL570,1000,Brain Tumor,C0006118,Brain,GEO,Microarray,Homo sapiens,16|8,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09609,GSE68015,GPL570,1000,Brain Tumor,C0006118,Brain,GEO,Microarray,Homo sapiens,16|4,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA09610,GSE1297,GPL96,0,Alzheimer's Disease,C0002395,Hippocampus,GEO,Microarray,Homo sapiens,9|7,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA09611,GSE1297,GPL96,0,Alzheimer's Disease,C0002395,Hippocampus,GEO,Microarray,Homo sapiens,9|8,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA09612,GSE1297,GPL96,0,Alzheimer's Disease,C0002395,Hippocampus,GEO,Microarray,Homo sapiens,9|7,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA09613,GSE12649,GPL96,0,Schizophrenia,C0036341,Prefrontal cortex,GEO,Microarray,Homo sapiens,34|35,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA09614,GSE12649,GPL96,0,Bipolar Disorder,C1852197,Prefrontal cortex,GEO,Microarray,Homo sapiens,34|33,DO:A mood disorder that involves alternating periods of mania and depression. DSA09615,GSE1650,GPL96,2,Chronic Obstructive Pulmonary Disease,C0024117,Lung,GEO,Microarray,Homo sapiens,10|18,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA09616,GSE475,GPL96,0,Chronic Obstructive Pulmonary Disease,C0024117,Diaphragm,GEO,Microarray,Homo sapiens,4|3,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA09617,GSE5364,GPL96,1000,Lung Tumor,C0242379,Lung,GEO,Microarray,Homo sapiens,12|18,DO:A lung cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells and is located_in the lungs and has_symptom cough and has_symptom chest discomfort or pain and has_symptom weight loss and has_symptom hemoptysis. DSA09618,GSE5364,GPL96,1000,Liver Tumor,C0345904,Liver,GEO,Microarray,Homo sapiens,8|9,DO:A hepatobiliary system cancer that is located_in the liver. DSA09619,GSE5364,GPL96,880,Thyroid Tumor,C0040136,Thyroid,GEO,Microarray,Homo sapiens,16|35,DO:An endocrine gland cancer located in the thryoid gland located in the neck below the thyroid cartilage. DSA09620,GSE5364,GPL96,0,Colon Tumor,C0009375,Colon,GEO,Microarray,Homo sapiens,9|9,DO:A colorectal cancer that is located_in the colon. DSA09621,GSE5364,GPL96,1000,Breast Cancer,C0678222,Breast,GEO,Microarray,Homo sapiens,13|183,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09622,GSE5364,GPL96,1000,Malignant Neoplasm of Oesophagus,C0546837,Esophagus,GEO,Microarray,Homo sapiens,13|16,DO:A esophageal cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09623,GSE1010,GPL96,0,Familial Combined Hyperlipidemia,C0020474,,GEO,Microarray,Homo sapiens,12|11,HPO:Hyperapobetalipoproteinemia is defined as the combination of a normal low density lipoprotein (LDL) cholesterol in the face of an increased LDL apolipoprotein B (apoB) protein. DSA09624,GSE2779,GPL96,62,Myelodysplasia,C0026985,Bone marrow,GEO,Microarray,Homo sapiens,9|14,"EFO:A clonal hematopoietic disorder characterized by dysplasia and ineffective hematopoiesis in one or more of the hematopoietic cell lines. The dysplasia may be accompanied by an increase in myeloblasts, but the number is less than 20%, which, according to the WHO guidelines, is the requisite threshold for the diagnosis of acute myeloid leukemia. It may occur de novo or as a result of exposure to alkylating agents and/or radiotherapy. (WHO, 2001)" DSA09625,GSE1462,GPL96,1,Mitochondrial Encephalomyopathy,C0162666,Skeletal muscle,GEO,Microarray,Homo sapiens,3|12,"MONDO:A heterogenous group of disorders characterized by alterations of mitochondrial metabolism that result in muscle and nervous system dysfunction. These are often multisystemic and vary considerably in age at onset (usually in the first or second decade of life), distribution of affected muscles, severity, and course. (From Adams et al., Principles of Neurology, 6th ed, pp984-5)" DSA09626,GSE5090,GPL96,0,Polycystic Ovary Syndrome,C0032460,Omental adipose tissue,GEO,Microarray,Homo sapiens,8|9,"DO:An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight." DSA09627,GSE14905,GPL570,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,21|33,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09628,GSE6710,GPL96,1000,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,13|13,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09629,GSE3075,GPL339,180,Spinal Muscular Atrophy With Respiratory Distress Type 1,C1858517,Lumbar spinal cord,GEO,Microarray,Mus musculus,3|3,DO:A spinal muscular atrophy characterized by autosomal recessive inheritance of severe respiratory distress resulting from diaphragmatic paralysis that predominantly involves the upper limbs and distal muscles that has_material_basis_in homozygous or compound heterozygous mutation in the IGHMBP2 gene on chromosome 11q13. DSA09630,GSE3268,GPL96,1000,Squamous Cell Lung Carcinoma,C0149782,Lung,GEO,Microarray,Homo sapiens,5|5,DO:A non-small cell lung carcinoma that has_material_basis_in the squamous cell. DSA09631,GSE6461,GPL1261,1000,Synovial Sarcoma,C0039101,Skeletal muscle,GEO,Microarray,Mus musculus,4|5,DO:A synovium cancer which develops in the synovial membrane of the joints. DSA09632,GSE18920,GPL5188,0,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,Microarray,Homo sapiens,10|12,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA09633,GSE16161,GPL570,1000,Atopic Dermatitis,C0011615,Skin,GEO,Microarray,Homo sapiens,9|9,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA09634,GSE16532,GPL4133,99,Infertility,C0021359,Endometrium,GEO,Microarray,Homo sapiens,5|4,EFO:Inability to reproduce after a specified period of unprotected intercourse. Reproductive sterility is permanent infertility. DSA09635,GSE16174,GPL6885,312,Anaemia,C0002871,,GEO,Microarray,Mus musculus,3|5,DO:A hematopoietic system disease that is characterized by a decrease in the normal number of red blood cells. DSA09636,GSE54522,GPL570,500,Olive Pollen Allergy,,,GEO,Microarray,Homo sapiens,23|23, DSA09637,GSE54536,GPL10558,112,Parkinson's Disease,C0030567,Peripheral blood,GEO,Microarray,Homo sapiens,5|5,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA09638,GSE54538,GPL10558,50,Noonan Syndrome,C0028326,,GEO,Microarray,Homo sapiens,3|2,DO:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. DSA09639,GSE54538,GPL10558,283,Noonan/Jmml Syndrome,,,GEO,Microarray,Homo sapiens,3|4, DSA09640,GSE54562,GPL6947,0,Major Depressive Disorder,C1269683,Anterior cingulate cortex,GEO,Microarray,Homo sapiens,10|10,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA09641,GSE54563,GPL6947,0,Major Depressive Disorder,C1269683,Anterior cingulate cortex,GEO,Microarray,Homo sapiens,25|25,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA09642,GSE54564,GPL6947,0,Major Depressive Disorder,C1269683,Amygdala,GEO,Microarray,Homo sapiens,21|21,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA09643,GSE54565,GPL570,0,Major Depressive Disorder,C1269683,Anterior cingulate cortex,GEO,Microarray,Homo sapiens,16|16,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA09644,GSE54566,GPL570,0,Major Depressive Disorder,C1269683,Amygdala,GEO,Microarray,Homo sapiens,14|14,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA09645,GSE54567,GPL570,0,Major Depressive Disorder,C1269683,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,14|14,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA09646,GSE54568,GPL570,0,Major Depressive Disorder,C1269683,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,15|15,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA09647,GSE54570,GPL96,0,Major Depressive Disorder,C1269683,Dorsolateral prefrontal cortex,GEO,Microarray,Homo sapiens,13|13,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA09648,GSE54571,GPL570,0,Major Depressive Disorder,C1269683,Anterior cingulate cortex,GEO,Microarray,Homo sapiens,13|13,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA09649,GSE54572,GPL570,0,Major Depressive Disorder,C1269683,Anterior cingulate cortex,GEO,Microarray,Homo sapiens,12|12,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA09650,GSE54575,GPL96,0,Major Depressive Disorder,C1269683,Prefrontal cortex,GEO,Microarray,Homo sapiens,12|12,"DO:A depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality." DSA09651,GSE16174,GPL6885,1000,Anaemia,C0002871,,GEO,Microarray,Mus musculus,3|4,DO:A hematopoietic system disease that is characterized by a decrease in the normal number of red blood cells. DSA09652,GSE54644,GPL4685,1000,Myeloproliferative Neoplasm,C0027022,Peripheral blood,GEO,Microarray,Homo sapiens,11|47,"DO:A myeloid neoplasm that is characterized by a group of slow growing blood cancers in which large numbers of abnormal red blood cells, white blood cells, or platelets grow and spread in the bone marrow and the peripheral blood." DSA09653,GSE54644,GPL4685,1000,Myeloproliferative Neoplasm,C0027022,Peripheral blood,GEO,Microarray,Homo sapiens,11|18,"DO:A myeloid neoplasm that is characterized by a group of slow growing blood cancers in which large numbers of abnormal red blood cells, white blood cells, or platelets grow and spread in the bone marrow and the peripheral blood." DSA09654,GSE54644,GPL4685,1000,Myeloproliferative Neoplasm,C0027022,Peripheral blood,GEO,Microarray,Homo sapiens,11|28,"DO:A myeloid neoplasm that is characterized by a group of slow growing blood cancers in which large numbers of abnormal red blood cells, white blood cells, or platelets grow and spread in the bone marrow and the peripheral blood." DSA09655,GSE54729,GPL11154,1000,Alveolar Soft Part Sarcoma,C0206657,Skeletal muscle,GEO,RNA-Seq,Homo sapiens,3|2,DO:A soft tissue cancer that is a slow growing tumor of an unknown origin that effects children and effects young adults. DSA09656,GSE54729,GPL13112,1000,Alveolar Soft Part Sarcoma,C0206657,Skeletal muscle,GEO,RNA-Seq,Mus musculus,3|5,DO:A soft tissue cancer that is a slow growing tumor of an unknown origin that effects children and effects young adults. DSA09657,GSE54780,GPL8432,1000,Abnormality of The Pulmonary Veins,C0265914,Lung,GEO,Microarray,Homo sapiens,5|8,HPO:An abnormality of the pulmonary veins. DSA09658,GSE54787,GPL6885,1000,Acute Myeloid Leukemia,C0023467,Bone marrow,GEO,Microarray,Mus musculus,3|10,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA09659,GSE54787,GPL6885,1000,B-Cell Acute Lymphoblastic Leukemia,C0862030,Bone marrow,GEO,Microarray,Mus musculus,3|1,DO:A precursor lymphoblastic lymphoma/leukemia that is characterized by the presence of too many B-cell lymphoblasts in the blood and bone marrow. DSA09660,GSE54787,GPL6885,1000,T-Cell Acute Lymphoblastic Leukemia,C1961099,Spleen,GEO,Microarray,Mus musculus,3|1,DO:An acute lymphoblastic leukemia that is characterized by too many T-cell lymphoblasts found in the bone marrow and blood. DSA09661,GSE54787,GPL6885,1000,T-Cell Acute Lymphoblastic Leukemia,C1961099,Thymus,GEO,Microarray,Mus musculus,3|8,DO:An acute lymphoblastic leukemia that is characterized by too many T-cell lymphoblasts found in the bone marrow and blood. DSA09662,GSE54829,GPL81,1000,Adenocarcinoma,C0001418,Lung,GEO,Microarray,Mus musculus,4|3,"DO:A carcinoma that has_material_basis_in abnormally proliferating cells, derives_from epithelial cells, which originate in glandular tissue." DSA09663,GSE54829,GPL81,1000,Adenocarcinoma,C0001418,Lung,GEO,Microarray,Mus musculus,4|4,"DO:A carcinoma that has_material_basis_in abnormally proliferating cells, derives_from epithelial cells, which originate in glandular tissue." DSA09664,GSE54829,GPL81,1000,Adenocarcinoma,C0001418,Lung,GEO,Microarray,Mus musculus,4|3,"DO:A carcinoma that has_material_basis_in abnormally proliferating cells, derives_from epithelial cells, which originate in glandular tissue." DSA09665,GSE16174,GPL6885,1000,Anaemia,C0002871,,GEO,Microarray,Mus musculus,3|5,DO:A hematopoietic system disease that is characterized by a decrease in the normal number of red blood cells. DSA09666,GSE54838,GPL6246,1000,D-2-Hydroxyglutaric Aciduria,C3152055,Heart,GEO,Microarray,Mus musculus,4|4,DO:A D-2-hydroxyglutaric aciduria that has_material_basis_in homozygous or compound heterozygous mutation in D2HGDH on 2q37.3. DSA09667,GSE54861,GPL10558,1000,D-2-Hydroxyglutaric Aciduria 2,C1833429,Oral cavity,GEO,Microarray,Homo sapiens,2|2,HPO:An increased concentration of 2-hydroxyglutaric acid in the urine. DSA09668,GSE54873,GPL6883,670,Acute Myeloid Leukemia,C0023467,,GEO,Microarray,Homo sapiens,2|5,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA09669,GSE54873,GPL6883,1,Acute Myeloid Leukemia,C0023467,,GEO,Microarray,Homo sapiens,2|5,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA09670,GSE18383,GPL1261,0,Rubinstein-Taybi Syndrome,C0035934,Hippocampus,GEO,Microarray,Mus musculus,3|3,DO:A syndrome characterized by congenital anomalies located_in heart and located_in upper limb. DSA09671,GSE54934,GPL6244,1000,Meningioma,C0025286,Meninges,GEO,Microarray,Homo sapiens,3|22,DO:A central nervous system cancer that are manifested in the central nervous system and arise from the arachnoid cap cells of the arachnoid villi in the meninges. DSA09672,GSE54934,GPL6244,1000,Schwannoma,C0027809,Meninges,GEO,Microarray,Homo sapiens,3|31,DO:A neuroma that is characterized as a benign nerve sheath tumor that is composed of Schwann cells. DSA09673,GSE55098,GPL570,17,Type 1 Diabetes,C0011854,,GEO,Microarray,Homo sapiens,10|12,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA09674,GSE16356,GPL570,0,Kaposi Sarcoma,C0036220,,GEO,Microarray,Homo sapiens,3|3,"DO:A connective tissue cancer that derives_from lymphatic endothelium, and derives_from spindle cells, results_in_formation_of vascular channels that fill with blood cells, has_material_basis_in Human herpesvirus 8 (HHV8)." DSA09675,GSE55200,GPL17692,1000,Metabolically Healthy Obesity,C4042861,Subcutaneous adipose tissue,GEO,Microarray,Homo sapiens,7|8,EFO:Long-standing obesity without metbolic abnormalities or obesity-related comorbidities such as type 2 diabetes or heart disease DSA09676,GSE55200,GPL17692,1000,Obesity; Metabolically Benign,C4042861,Subcutaneous adipose tissue,GEO,Microarray,Homo sapiens,7|8,EFO:Long-standing obesity without metbolic abnormalities or obesity-related comorbidities such as type 2 diabetes or heart disease DSA09677,GSE55201,GPL570,481,Psoriasis,C0033860,Whole blood,GEO,Microarray,Homo sapiens,30|44,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09678,GSE55235,GPL96,1000,Osteoarthritis,C0157946,Synovium,GEO,Microarray,Homo sapiens,10|10,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA09679,GSE55235,GPL96,1000,Rheumatoid Arthritis,C0003873,Synovium,GEO,Microarray,Homo sapiens,10|10,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA09680,GSE55280,GPL13112,64,Chronic Heart Failure,C0018801,Hippocampus,GEO,RNA-Seq,Mus musculus,1|1,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA09681,GSE55280,GPL13112,8,Chronic Heart Failure,C0018801,Prefrontal cortex,GEO,RNA-Seq,Mus musculus,1|1,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA09682,GSE55280,GPL13112,1000,Chronic Heart Failure,C0018801,Myocardium,GEO,RNA-Seq,Mus musculus,1|1,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA09683,GSE55288,GPL4133,1000,Chronic Lymphocytic Leukemia,C0023434,Peripheral blood,GEO,Microarray,Homo sapiens,10|10,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA09684,GSE55288,GPL4133,1000,Chronic Lymphocytic Leukemia,C0023434,Peripheral blood,GEO,Microarray,Homo sapiens,10|23,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA09685,GSE55288,GPL4133,1000,Chronic Lymphocytic Leukemia,C0023434,Peripheral blood,GEO,Microarray,Homo sapiens,13|23,DO:A lymphocytic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood. DSA09686,GSE16355,GPL570,0,Kaposi Sarcoma,C0036220,,GEO,Microarray,Homo sapiens,3|3,"DO:A connective tissue cancer that derives_from lymphatic endothelium, and derives_from spindle cells, results_in_formation_of vascular channels that fill with blood cells, has_material_basis_in Human herpesvirus 8 (HHV8)." DSA09687,GSE16354,GPL570,1000,Kaposi Sarcoma,C0036220,,GEO,Microarray,Homo sapiens,6|6,"DO:A connective tissue cancer that derives_from lymphatic endothelium, and derives_from spindle cells, results_in_formation_of vascular channels that fill with blood cells, has_material_basis_in Human herpesvirus 8 (HHV8)." DSA09688,GSE55319,GPL6884,954,Juvenile Idiopathic Arthritis,C3890205,Whole blood,GEO,Microarray,Homo sapiens,19|26,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA09689,GSE55457,GPL96,938,Rheumatoid Arthritis,C0003873,Synovium,GEO,Microarray,Homo sapiens,10|13,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA09690,GSE55457,GPL96,801,Osteoarthritis,C0157946,Synovium,GEO,Microarray,Homo sapiens,10|10,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA09691,GSE55548,GPL17077,2,Oropharyngeal Cancer,C2349952,Tonsil,GEO,Microarray,Homo sapiens,4|4,DO:A pharynx cancer that is located_in the oropharynx. DSA09692,GSE55549,GPL17077,1000,Oropharyngeal Cancer,C2349952,Tonsil,GEO,Microarray,Homo sapiens,4|8,DO:A pharynx cancer that is located_in the oropharynx. DSA09693,GSE55617,GPL11533,0,Pck1 Deficiency; Cytosolic,C0268194,Liver,GEO,Microarray,Mus musculus,2|4,DO:A carbohydrate metabolic disorder characterized by the buildup of lactic acid in the body and a variety of neurological problems and caused by a deficiency of one of the three enzymes in the pyruvate dehydrogenase complex. DSA09694,GSE5563,GPL570,1000,Vulvar Intraepithelial Neoplasia,C0346210,Vulva biopsy,GEO,Microarray,Homo sapiens,10|9,"EFO:Intraepithelial neoplasia of the vulvar squamous epithelium. There is no evidence of invasion. This category includes vulvar high grade squamous intraepithelial lesion and vulvar intraepithelial neoplasia, differentiated type." DSA09695,GSE55650,GPL570,0,Type 2 Diabetes,C0011860,,GEO,Microarray,Homo sapiens,6|6,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09696,GSE55650,GPL570,0,Type 2 Diabetes,C0011860,,GEO,Microarray,Homo sapiens,5|6,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09697,GSE55664,GPL10558,1000,Leishmaniasis,C0023281,Skin,GEO,Microarray,Homo sapiens,10|8,"DO:A parasitic protozoa infectious disease that involves infection caused by protozoan parasite of the genus Leishmania, which is transmitted by the bite of sand fly (subfamily Phlebotominae)." DSA09698,GSE55664,GPL10558,1000,Leishmaniasis,C0023281,Skin,GEO,Microarray,Homo sapiens,10|17,"DO:A parasitic protozoa infectious disease that involves infection caused by protozoan parasite of the genus Leishmania, which is transmitted by the bite of sand fly (subfamily Phlebotominae)." DSA09699,GSE55689,GPL11154,39,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,RNA-Seq,Homo sapiens,7|13,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA09700,GSE55689,GPL11154,65,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,RNA-Seq,Homo sapiens,8|12,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA09701,GSE55689,GPL11154,84,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,RNA-Seq,Homo sapiens,7|17,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA09702,GSE55747,GPL6885,1000,Fibrosis; Liver,C0239946,Liver,GEO,Microarray,Mus musculus,4|4,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA09703,GSE55747,GPL6885,1000,Fibrosis; Liver,C0239946,Liver,GEO,Microarray,Mus musculus,4|6,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA09704,GSE55747,GPL6885,1000,Fibrosis; Liver,C0239946,Liver,GEO,Microarray,Mus musculus,4|3,HPO:The presence of excessive fibrous connective tissue in the liver. Fibrosis is a reparative or reactive process. DSA09705,GSE16354,GPL570,1000,Kaposi Sarcoma,C0036220,,GEO,Microarray,Homo sapiens,6|6,"DO:A connective tissue cancer that derives_from lymphatic endothelium, and derives_from spindle cells, results_in_formation_of vascular channels that fill with blood cells, has_material_basis_in Human herpesvirus 8 (HHV8)." DSA09706,GSE5580,GPL96,263,Severe Trauma,,,GEO,Microarray,Homo sapiens,7|7, DSA09707,GSE5580,GPL96,85,Severe Trauma,,,GEO,Microarray,Homo sapiens,7|7, DSA09708,GSE5580,GPL96,337,Severe Trauma,,,GEO,Microarray,Homo sapiens,7|7, DSA09709,GSE55801,GPL6246,0,Myeloproliferative Neoplasm,C0027022,,GEO,Microarray,Mus musculus,1|3,"DO:A myeloid neoplasm that is characterized by a group of slow growing blood cancers in which large numbers of abnormal red blood cells, white blood cells, or platelets grow and spread in the bone marrow and the peripheral blood." DSA09710,GSE55808,GPL13112,267,Anti-Basement Membrane Glomerulonephritis,C1332309,Kidney,GEO,RNA-Seq,Mus musculus,2|2,DO:A Goodpasture syndrome that is characterized by damage to only kidney capillaries. DSA09711,GSE55808,GPL13112,762,Obstructive Uropathy,C0178879,Kidney,GEO,RNA-Seq,Mus musculus,2|2,EFO:Blockage of the normal flow of contents of the urinary tract. DSA09712,GSE55808,GPL13112,1000,Anti-Basement Membrane Glomerulonephritis,C1332309,Kidney,GEO,RNA-Seq,Mus musculus,1|2,DO:A Goodpasture syndrome that is characterized by damage to only kidney capillaries. DSA09713,GSE55808,GPL13112,1000,Obstructive Uropathy,C0178879,Kidney,GEO,RNA-Seq,Mus musculus,1|2,EFO:Blockage of the normal flow of contents of the urinary tract. DSA09714,GSE55939,GPL11154,355,Turner Syndrome,C0041408,,GEO,RNA-Seq,Homo sapiens,2|2,DO:A disorder of sexual development that is characterized by a progressive loss of germ cells on the developing gonads of an embryo. DSA09715,GSE55962,GPL13667,0,Chronic Obstructive Pulmonary Disease,C0024117,,GEO,Microarray,Homo sapiens,42|24,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA09716,GSE55976,GPL18389,0,Chronic Myelogenous Leukemia,C0023473,,GEO,Microarray,Homo sapiens,5|4,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA09717,GSE13367,GPL570,1000,Ulcerative Colitis,C0009324,Colon mucosa,GEO,Microarray,Homo sapiens,10|8,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA09718,GSE55976,GPL18389,0,Essential Thrombocythemia,C0040028,,GEO,Microarray,Homo sapiens,5|3,"DO:A myeloproliferative neoplasm that is characterized by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocytes in the bone marrow, and episodes of thrombosis and/or hemorrhage and that results_in the overproduction of platelets." DSA09719,GSE55976,GPL18389,0,Polycythemia Vera,C0032463,,GEO,Microarray,Homo sapiens,5|6,"DO:A myeloproliferative neoplasm characterized by erythroid hyperplasia, myeloid leukocytosis, thrombocytosis, and splenomegaly." DSA09720,GSE55976,GPL18389,0,Primary Myelofibrosis,C0001815,,GEO,Microarray,Homo sapiens,5|2,DO:A myeloid neoplasm that is located in the bone marrow which results in bone marrow being replaced by fibrous (scar) tissue. DSA09721,GSE55976,GPL18389,0,Chronic Myelogenous Leukemia,C0023473,,GEO,Microarray,Homo sapiens,4|2,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA09722,GSE55976,GPL18389,0,Essential Thrombocythemia,C0040028,,GEO,Microarray,Homo sapiens,4|2,"DO:A myeloproliferative neoplasm that is characterized by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocytes in the bone marrow, and episodes of thrombosis and/or hemorrhage and that results_in the overproduction of platelets." DSA09723,GSE13367,GPL570,0,Ulcerative Colitis,C0009324,Colon mucosa,GEO,Microarray,Homo sapiens,10|9,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA09724,GSE13367,GPL570,270,Ulcerative Colitis,C0009324,Colon mucosa,GEO,Microarray,Homo sapiens,10|8,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA09725,GSE55976,GPL18390,533,Chronic Myelogenous Leukemia,C0023473,,GEO,Microarray,Homo sapiens,1|3,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA09726,GSE56029,GPL6885,1000,Leishmaniasis,C0023281,Ear,GEO,Microarray,Mus musculus,3|4,"DO:A parasitic protozoa infectious disease that involves infection caused by protozoan parasite of the genus Leishmania, which is transmitted by the bite of sand fly (subfamily Phlebotominae)." DSA09727,GSE56029,GPL6885,1000,Leishmaniasis,C0023281,Ear,GEO,Microarray,Mus musculus,3|5,"DO:A parasitic protozoa infectious disease that involves infection caused by protozoan parasite of the genus Leishmania, which is transmitted by the bite of sand fly (subfamily Phlebotominae)." DSA09728,GSE56029,GPL6885,1000,Leishmaniasis,C0023281,Ear,GEO,Microarray,Mus musculus,3|5,"DO:A parasitic protozoa infectious disease that involves infection caused by protozoan parasite of the genus Leishmania, which is transmitted by the bite of sand fly (subfamily Phlebotominae)." DSA09729,GSE56029,GPL6885,1000,Leishmaniasis,C0023281,Ear,GEO,Microarray,Mus musculus,3|4,"DO:A parasitic protozoa infectious disease that involves infection caused by protozoan parasite of the genus Leishmania, which is transmitted by the bite of sand fly (subfamily Phlebotominae)." DSA09730,GSE56116,GPL4133,0,Postmenopausal Osteoporosis,C0029458,Peripheral blood,GEO,Microarray,Homo sapiens,3|4,DO:A bone resorption disease characterized by decreased density of normally mineralized bone which results_in the thinning of bone tissue and decreased mechanical strength. DSA09731,GSE56116,GPL4133,0,Postmenopausal Osteoporosis,C0029458,Peripheral blood,GEO,Microarray,Homo sapiens,3|3,DO:A bone resorption disease characterized by decreased density of normally mineralized bone which results_in the thinning of bone tissue and decreased mechanical strength. DSA09732,GSE56116,GPL4133,0,Postmenopausal Osteoporosis,C0029458,Peripheral blood,GEO,Microarray,Homo sapiens,3|3,DO:A bone resorption disease characterized by decreased density of normally mineralized bone which results_in the thinning of bone tissue and decreased mechanical strength. DSA09733,GSE56426,GPL11533,0,Mucositis,C0333355,Jejunum,GEO,Microarray,Mus musculus,3|3,DO:A gastrointestinal system disease that is characterized by painful inflammation and ulceration of the mucous membranes lining the digestive tract. DSA09734,GSE56426,GPL11533,407,Mucositis,C0333355,Jejunum,GEO,Microarray,Mus musculus,3|3,DO:A gastrointestinal system disease that is characterized by painful inflammation and ulceration of the mucous membranes lining the digestive tract. DSA09735,GSE56481,GPL16686,743,Granulomatosis With Polyangiitis,C3495801,,GEO,Microarray,Homo sapiens,3|3,"DO:An autoimmune disease that is characterized by necrotizing granulomatous inflammation of the upper and lower respiratory tract, glomerulonephritis, vasculitis, and the presence of antineutrophil cytoplasmatic autoantibodies (ANCAs) in patient sera, and is located_in lung, located_in kidney, located_in skin resulting from an autoimmune attack by antineutrophil cytoplasmic antibodies against small and medium-size blood vessels." DSA09736,GSE56481,GPL16686,17,Granulomatosis With Polyangiitis,C3495801,,GEO,Microarray,Homo sapiens,3|3,"DO:An autoimmune disease that is characterized by necrotizing granulomatous inflammation of the upper and lower respiratory tract, glomerulonephritis, vasculitis, and the presence of antineutrophil cytoplasmatic autoantibodies (ANCAs) in patient sera, and is located_in lung, located_in kidney, located_in skin resulting from an autoimmune attack by antineutrophil cytoplasmic antibodies against small and medium-size blood vessels." DSA09737,GSE56481,GPL16686,233,Granulomatosis With Polyangiitis,C3495801,,GEO,Microarray,Homo sapiens,3|3,"DO:An autoimmune disease that is characterized by necrotizing granulomatous inflammation of the upper and lower respiratory tract, glomerulonephritis, vasculitis, and the presence of antineutrophil cytoplasmatic autoantibodies (ANCAs) in patient sera, and is located_in lung, located_in kidney, located_in skin resulting from an autoimmune attack by antineutrophil cytoplasmic antibodies against small and medium-size blood vessels." DSA09738,GSE56486,GPL10558,0,Ectodermal Dysplasia,C0013575,Skin,GEO,Microarray,Homo sapiens,4|2,"DO:An ectodermal dysplasia that is characterized by abnormalities of the hair, nails, and skin, with the teeth and sweat glands being unaffected and that has_material_basis_in heterozygous mutation in the GJB6 gene, which encodes connexin-30, on chromosome 13q12." DSA09739,GSE56495,GPL10558,0,Acute Myeloid Leukemia,C0023467,Whole blood,GEO,Microarray,Homo sapiens,8|4,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA09740,GSE56495,GPL10558,174,Chronic Myelogenous Leukemia,C0023473,Whole blood,GEO,Microarray,Homo sapiens,8|1,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA09741,GSE56495,GPL10558,571,Non-Hodgkins Lymphoma,C0024305,Whole blood,GEO,Microarray,Homo sapiens,8|1,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA09742,GSE56500,GPL5188,0,Amyotrophic Lateral Sclerosis,C0002736,,GEO,Microarray,Homo sapiens,6|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA09743,GSE56500,GPL5188,0,Amyotrophic Lateral Sclerosis,C0002736,,GEO,Microarray,Homo sapiens,6|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA09744,GSE56555,GPL18535,1000,C26-Tumor,,Tibialis anterior,GEO,Microarray,Mus musculus,4|4, DSA09745,GSE56555,GPL18535,1000,C26-Tumor,,Tibialis anterior,GEO,Microarray,Mus musculus,4|4, DSA09746,GSE56649,GPL570,1000,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,9|13,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA09747,GSE5667,GPL96,0,Atopic Dermatitis,C0011615,Skin,GEO,Microarray,Homo sapiens,4|2,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA09748,GSE5667,GPL96,0,Atopic Dermatitis,C0011615,Skin,GEO,Microarray,Homo sapiens,1|2,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA09749,GSE5667,GPL97,0,Atopic Dermatitis,C0011615,Skin,GEO,Microarray,Homo sapiens,4|2,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA09750,GSE5667,GPL97,0,Atopic Dermatitis,C0011615,Skin,GEO,Microarray,Homo sapiens,1|2,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA09751,GSE56741,GPL13667,1,Ullrich Congenital Muscular Dystrophy,C0410179,,GEO,Microarray,Homo sapiens,6|6,"DO:A congenital muscular dystrophy that is characterized by muscle weakness and respiratory depression and has_material_basis_in mutation in the COL6A1, COL6A2 and COL6A3 that produce components of type VI collagen." DSA09752,GSE56741,GPL13667,0,Ullrich Congenital Muscular Dystrophy,C0410179,,GEO,Microarray,Homo sapiens,5|6,"DO:A congenital muscular dystrophy that is characterized by muscle weakness and respiratory depression and has_material_basis_in mutation in the COL6A1, COL6A2 and COL6A3 that produce components of type VI collagen." DSA09753,GSE56766,GPL570,2,Chronic Obstructive Pulmonary Disease,C0024117,Whole blood,GEO,Microarray,Homo sapiens,24|49,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA09754,GSE56766,GPL570,141,Chronic Obstructive Pulmonary Disease,C0024117,Whole blood,GEO,Microarray,Homo sapiens,20|42,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA09755,GSE56766,GPL570,109,Chronic Obstructive Pulmonary Disease,C0024117,Whole blood,GEO,Microarray,Homo sapiens,18|46,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA09756,GSE56767,GPL570,0,Chronic Obstructive Pulmonary Disease,C0024117,Blood,GEO,Microarray,Homo sapiens,24|51,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA09757,GSE56767,GPL570,34,Chronic Obstructive Pulmonary Disease,C0024117,Blood,GEO,Microarray,Homo sapiens,24|49,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA09758,GSE56767,GPL570,0,Chronic Obstructive Pulmonary Disease,C0024117,Blood,GEO,Microarray,Homo sapiens,23|47,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA09759,GSE56808,GPL570,0,Primary Lateral Sclerosis,C1968845,Skin,GEO,Microarray,Homo sapiens,6|5,DO:A motor neuron disease characterized by painless but progressive weakness and stiffness of the muscles of the legs. DSA09760,GSE56808,GPL570,1,Sporadic Amyotrophic Lateral Sclerosis,C1862941,Skin,GEO,Microarray,Homo sapiens,6|6,DO:An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SOD1 gene on chromosome 21. The most common type of familial ALS. DSA09761,GSE56808,GPL570,0,Motor Neuron Disease,C0085084,Skin,GEO,Microarray,Homo sapiens,6|1,DO:An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SOD1 gene on chromosome 21. The most common type of familial ALS. DSA09762,GSE56885,GPL15207,106,Coronary Artery Disease,C1956346,,GEO,Microarray,Homo sapiens,2|4,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA09763,GSE56998,GPL5175,80,Idiopathic Cd4 Lymphocytopenia,C3809768,,GEO,Microarray,Homo sapiens,8|9,"MONDO:A rare primary immunodeficiency disorder characterized by persistent CD4 T-cell lymphopenia (less than 300 cells/B5L on multiple occasions) not associated with any other underlying primary or secondary immune deficiency. Patients typically present opportunistic infections (with cryptococcal, mycobacterial, candidal, varicella zoster virus infections and progressive multifocal leukoencephalopathy being the most prevalent), malignancies (mainly lymphoproliferative disorders), or autoimmune disorders. Some individuals are asymptomatic and incidentally diagnosed." DSA09764,GSE56998,GPL5175,0,Sarcoidosis,C0036202,,GEO,Microarray,Homo sapiens,8|8,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA09765,GSE13367,GPL570,0,Ulcerative Colitis,C0009324,Colon mucosa,GEO,Microarray,Homo sapiens,10|9,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA09766,GSE16334,GPL96,1000,Fanconi Anemia,C0015625,,GEO,Microarray,Homo sapiens,11|21,"DO:A congenital hypoplastic anemia characterized by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop hematological or solid tumors. It is a result of a genetic defect in a cluster of proteins responsible for DNA repair." DSA09767,GSE13071,GPL1261,1,"Arthritis, Collagen-Induced",C0971858,Knee joint,GEO,Microarray,Mus musculus,3|3,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA09768,GSE13071,GPL1261,1000,"Arthritis, Collagen-Induced",C0971858,Knee joint,GEO,Microarray,Mus musculus,3|3,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA09769,GSE57148,GPL11154,1000,Chronic Obstructive Pulmonary Disease,C0024117,Lung,GEO,RNA-Seq,Homo sapiens,64|98,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA09770,GSE13071,GPL1261,1000,"Arthritis, Collagen-Induced",C0971858,Knee joint,GEO,Microarray,Mus musculus,3|3,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA09771,GSE57178,GPL6244,1000,Chronic Idiopathic Urticaria,C0578870,Skin,GEO,Microarray,Homo sapiens,5|6,HPO:Urticaria characterized by spontaneously recurring hives for 6 weeks or longer. DSA09772,GSE57183,GPL10558,0,Fever,C0015967,Whole blood,GEO,Microarray,Homo sapiens,3|2,HPO:Body temperature elevated above the normal range. DSA09773,GSE57183,GPL10558,0,Kawasaki Disease,C0026691,Whole blood,GEO,Microarray,Homo sapiens,3|3,"DO:A lymphadenitis characterized by swelling of cervical lymph nodes in infants and young children and inflammation of medium-sized blood vessels located_in body, has_symptom fever, has_symptom congestion of ocular conjunctivae, has_symptom reddening of lips, has_symptom reddening of oral cavity, has_symptom protuberance of tongue papillae and has_symptom edema of extremities." DSA09774,GSE57183,GPL10558,0,Systemic Juvenile Idiopathic Arthritis,C1384600,Whole blood,GEO,Microarray,Homo sapiens,3|6,"EFO:Juvenile idiopathic arthritis (JIA), also known as juvenile rheumatoid arthritis (JRA), is the most common form of arthritis in children and adolescents. (Juvenile in this context refers to an onset before age 16, idiopathic refers to a condition with no defined cause, and arthritis is the inflammation of the synovium of a joint.) JIA is an autoimmune, non-infective, inflammatory joint disease of more than 6 weeks duration in children less than 16 years of age. The disease commonly occurs in children from the ages of 7 to 12, but it may occur in adolescents as old as 15 years of age, as well as in infants. It is a subset of arthritis seen in childhood, which may be transient and self-limited or chronic. It differs significantly from arthritis commonly seen in adults (osteoarthritis, rheumatoid arthritis), and other types of arthritis that can present in childhood which are chronic conditions (e.g. psoriatic arthritis and ankylosing spondylitis). Aetiopathology is similar to rheumatoid arthritis but with less marked cartilage erosion, and joint instability and absent rheumatoid factor. JIA affects approximately 1 in 1,000 children in any given year, with about 1 in 10,000 having a more severe form." DSA09775,GSE57188,GPL11533,0,"Carcinoma, Lewis Lung",C0243038,Hypothalamus,GEO,Microarray,Mus musculus,4|5,MSH:A carcinoma discovered by Dr. Margaret R. Lewis of the Wistar Institute in 1951. This tumor originated spontaneously as a carcinoma of the lung of a C57BL mouse. The tumor does not appear to be grossly hemorrhagic and the majority of the tumor tissue is a semifirm homogeneous mass. (From Cancer Chemother Rep 2 1972 Nov;(3)1:325) It is also called 3LL and LLC and is used as a transplantable malignancy. DSA09776,GSE57188,GPL11533,0,"Carcinoma, Lewis Lung",C0243038,Hypothalamus,GEO,Microarray,Mus musculus,4|7,MSH:A carcinoma discovered by Dr. Margaret R. Lewis of the Wistar Institute in 1951. This tumor originated spontaneously as a carcinoma of the lung of a C57BL mouse. The tumor does not appear to be grossly hemorrhagic and the majority of the tumor tissue is a semifirm homogeneous mass. (From Cancer Chemother Rep 2 1972 Nov;(3)1:325) It is also called 3LL and LLC and is used as a transplantable malignancy. DSA09777,GSE57188,GPL11533,0,"Carcinoma, Lewis Lung",C0243038,Hypothalamus,GEO,Microarray,Mus musculus,4|6,MSH:A carcinoma discovered by Dr. Margaret R. Lewis of the Wistar Institute in 1951. This tumor originated spontaneously as a carcinoma of the lung of a C57BL mouse. The tumor does not appear to be grossly hemorrhagic and the majority of the tumor tissue is a semifirm homogeneous mass. (From Cancer Chemother Rep 2 1972 Nov;(3)1:325) It is also called 3LL and LLC and is used as a transplantable malignancy. DSA09778,GSE57218,GPL6947,1000,Osteoarthritis,C0157946,Cartilage,GEO,Microarray,Homo sapiens,7|33,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA09779,GSE13071,GPL1261,1000,"Arthritis, Collagen-Induced",C0971858,Knee joint,GEO,Microarray,Mus musculus,3|3,"MSH:An experimental model of arthritis that is induced by injecting adjuvants. These adjuvants generally consists of a mixture of light paraffin oil, emulsifying agent, and infective agents or antigens, such as killed mycobacteria or bacterial lipopolysaccharides." DSA09780,GSE17363,GPL8938,1000,Chagas Cardiomyopathy,C0007930,Heart,GEO,Microarray,Mus musculus,4|4,"EFO:a form of cardiomyopathy that develops as a result of Chagas disease, an infection with the protozoan parasite Trypanosoma Cruzi" DSA09781,GSE17470,GPL2895,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Homo sapiens,4|7,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA09782,GSE13015,GPL6106,789,Sepsis,C0243026,Blood,GEO,Microarray,Homo sapiens,3|24,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA09783,GSE13015,GPL6106,226,Sepsis,C0243026,Blood,GEO,Microarray,Homo sapiens,3|24,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA09784,GSE57333,GPL6887,1000,T-Cell Acute Lymphoblastic Leukemia,C1961099,Thymus,GEO,Microarray,Mus musculus,5|22,DO:An acute lymphoblastic leukemia that is characterized by too many T-cell lymphoblasts found in the bone marrow and blood. DSA09785,GSE57338,GPL11532,1000,Heart Failure,C0018801,Heart left ventricle,GEO,Microarray,Homo sapiens,136|82,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA09786,GSE57338,GPL11532,1000,Heart Failure,C0018801,Heart left ventricle,GEO,Microarray,Homo sapiens,136|95,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA09787,GSE57344,GPL9052,1000,Heart Failure,C0018801,Heart left ventricle,GEO,RNA-Seq,Homo sapiens,2|1,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA09788,GSE57344,GPL9052,96,Heart Failure,C0018801,Heart left ventricle,GEO,RNA-Seq,Homo sapiens,2|2,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA09789,GSE57380,GPL17400,1000,Ovarian Clear Cell Adenocarcinoma,C1518693,Ovary,GEO,Microarray,Mus musculus,9|9,DO:A ovarian adenocarcinoma that derives_from epithelial cells which have clear cytoplasm. DSA09790,GSE57383,GPL13158,2,Psoriasis,C0033860,,GEO,Microarray,Homo sapiens,19|10,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09791,GSE57383,GPL13158,0,Psoriatic Arthritis,C0003872,,GEO,Microarray,Homo sapiens,19|12,DO:An arthritis that is characterized by joint inflammation that usually occurs in combination with psoriasis. DSA09792,GSE57383,GPL13158,40,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,19|9,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA09793,GSE57405,GPL13158,94,Rheumatoid Arthritis,C0003873,,GEO,Microarray,Homo sapiens,19|9,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA09794,GSE57405,GPL13158,1,Psoriasis,C0033860,,GEO,Microarray,Homo sapiens,19|10,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09795,GSE57405,GPL13158,0,Psoriatic Arthritis,C0003872,,GEO,Microarray,Homo sapiens,19|12,DO:An arthritis that is characterized by joint inflammation that usually occurs in combination with psoriasis. DSA09796,GSE57475,GPL6947,0,Parkinson's Disease,C0030567,Blood,GEO,Microarray,Homo sapiens,49|93,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA09797,GSE57555,GPL16699,2,Cholangiocarcinoma,C0206698,Liver,GEO,Microarray,Homo sapiens,11|11,DO:A bile duct carcinoma that derives_from epithelial cells of glandular origin. DSA09798,GSE57555,GPL16699,1,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,5|5,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA09799,GSE13276,GPL96,1,Glioblastoma Multiforme,C1621958,Brain,GEO,Microarray,Homo sapiens,3|7,"DO:A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes." DSA09800,GSE7278,GPL4987,56,Arthritis,C0003864,Cerebrum,GEO,Microarray,Mus musculus,5|5,DO:A bone disease that is located_in the joint. DSA09801,GSE57560,GPL16699,1,Interstitial Cystitis,C0282488,Bladder,GEO,Microarray,Homo sapiens,3|13,"DO:A chronic cystitis characterized by unpleasant sensation related to the bladder and lower urinary tract in the absence of identifiable causes and has_symptom pain, has_symptom pressure, has_symptom discomfort, has_symptom dysuria, and/or has_symptom urinary frequency." DSA09802,GSE57631,GPL15034,0,Pericementitis,C0031051,,GEO,Microarray,Homo sapiens,2|6,"MSH:Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology)" DSA09803,GSE57691,GPL10558,1000,Abdominal Aortic Aneurysm,C0162871,Aortic wall,GEO,Microarray,Homo sapiens,10|20,DO:An aortic aneurysm that is located_in the abdominal aorta. DSA09804,GSE57691,GPL10558,1000,Abdominal Aortic Aneurysm,C0162871,Aortic wall,GEO,Microarray,Homo sapiens,10|29,DO:An aortic aneurysm that is located_in the abdominal aorta. DSA09805,GSE57691,GPL10558,1000,Aortic Disease,C0003493,Aortic wall,GEO,Microarray,Homo sapiens,10|9,DO:An artery disease that is characterized by degeneration of the cells composing the aortic wall. DSA09806,GSE159556,GPL24676,1000,COVID-19,D8888888,Pancreatic islet,GEO,scRNA-Seq,Homo sapiens,2|2,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA09807,GSE159585,GPL20301,1000,Influenza A (H1N1),C2076600,Lung,GEO,RNA-Seq,Homo sapiens,14|7,"EFO:An influenza that results_in infection located_in respiratory tract of pigs and humans, has_material_basis_in Influenza C virus, or has_material_basis_in Influenza A virus subtypes (H1N1, H1N2, H3N1, H3N2, and H2N3), which are transmitted_by direct contact with infected pigs. The infection in humans has_symptom fever, has_symptom lethargy, has_symptom lack of appetite, has_symptom coughing, has_symptom runny nose, has_symptom sore throat, has_symptom nausea, has_symptom vomiting, and has_symptom diarrhea." DSA09808,GSE159585,GPL20301,1000,COVID-19,D8888888,Lung,GEO,RNA-Seq,Homo sapiens,14|7,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA09809,GSE4656,GPL1261,0,Type 2 Diabetes Mellitus,C0011847,Brown fat,GEO,Microarray,Mus musculus,3|4,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09810,GSE7142,GPL96,0,Precocious Puberty,C0034013,Hypothalamus,GEO,Microarray,Homo sapiens,3|1,"DO:A reproductive system disease characterized by increased extraglandular aromatization of steroids resulting in heterosexual precocity in males and isosexual precocity in females, and has_material_basis_in autosomal dominant inheritance of fusion of the aromatase gene (CYP19A1) with various partners, brought about by translocations and resulting in gain of function of the CYP19A1 gene." DSA09811,GSE159624,GPL18573,1000,Acute Myeloid Leukemia,C0023467,Bone marrow,GEO,scRNA-Seq,Homo sapiens,8|8,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA09812,GSE159631,GPL20301,285,Intracranial Aneurysm,C0007766,,GEO,RNA-Seq,Homo sapiens,3|3,EFO:Outpouching of BASILAR ARTERY at the base of the skull. The basilar artery is the most important artery in the posterior cerebral circulation. DSA09813,GSE159642,GPL16791,19,Spinal Muscular Atrophy,C0026847,Spinal cord,GEO,RNA-Seq,Homo sapiens,4|6,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA09814,GSE159642,GPL16791,51,Spinal Muscular Atrophy,C0026847,Diaphragm,GEO,RNA-Seq,Homo sapiens,3|5,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA09815,GSE159642,GPL16791,108,Spinal Muscular Atrophy,C0026847,Iliopsoas,GEO,RNA-Seq,Homo sapiens,3|4,DO:A motor neuron disease that is a degenerative neuromuscular disease characterized by lower motor neuron degeneration associated with progressive muscle weakness and atrophy. DSA09816,GSE159657,GPL24676,206,Acute Myocardial Infarction,C0155626,Plasma,GEO,RNA-Seq,Homo sapiens,10|10,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA09817,GSE159657,GPL24676,55,Coronary Artery Disease,C1956346,Plasma,GEO,RNA-Seq,Homo sapiens,10|8,DO:An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. DSA09818,GSE159676,GPL6244,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Homo sapiens,6|7,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA09819,GSE159676,GPL6244,1000,Primary Sclerosing Cholangitis,C0566602,Liver,GEO,Microarray,Homo sapiens,6|12,"DO:A sclerosing cholangitis characterized by fibroobliterative inflammation of the biliary tract, leading to cirrhosis and portal hypertension." DSA09820,GSE159676,GPL6244,1000,Primary Biliary Cirrhosis,C0008312,Liver,GEO,Microarray,Homo sapiens,6|3,DO:A liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts. DSA09821,GSE159676,GPL6244,707,Haemoperitoneum,C0019065,Liver,GEO,Microarray,Homo sapiens,6|1,HPO:Accumulation of blood in the peritoneal cavity owing to internal hemorrhage. DSA09822,GSE159676,GPL6244,1000,Autoimmune Hepatitis,C4721555,Liver,GEO,Microarray,Homo sapiens,6|3,DO:An autoimmune disease of gastrointestinal tract that results_in inflammation located_in liver caused by the body's immune system attacking the liver cells. DSA09823,GSE159676,GPL6244,572,Alcoholic Liver Disease,C0023896,Liver,GEO,Microarray,Homo sapiens,6|1,"EFO:A disorder caused by damage to the liver parenchyma due to alcohol consumption. It may present with an acute onset or follow a chronic course, leading to cirrhosis." DSA09824,GSE159699,GPL18573,1000,Alzheimer's Disease,C0002395,Brain,GEO,RNA-Seq,Homo sapiens,10|12,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA09825,GSE5108,GPL2895,1000,Endometriosis,C0014175,Uterus,GEO,Microarray,Homo sapiens,11|11,DO:A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body. DSA09826,GSE159771,GPL21626,3,Orbit (Eye Disorders),C0029182,Retina,GEO,RNA-Seq,Mus musculus,7|3,DO:An adnexa disease that is located_in the eye socket. DSA09827,GSE159771,GPL21626,30,Orbit (Eye Disorders),C0029182,Retina,GEO,RNA-Seq,Mus musculus,7|5,DO:An adnexa disease that is located_in the eye socket. DSA09828,GSE159812,GPL24676,1000,COVID-19,D8888888,Brain,GEO,snRNA-Seq,Homo sapiens,6|7,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA09829,GSE159812,GPL24676,1000,Influenza,C0021400,Brain,GEO,snRNA-Seq,Homo sapiens,6|1,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA09830,GSE4588,GPL570,27,Rheumatoid Arthritis,C0003873,Blood,GEO,Microarray,Homo sapiens,9|8,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA09831,GSE159812,GPL24676,1000,Influenza,C0021400,Brain,GEO,snRNA-Seq,Homo sapiens,13|1,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA09832,GSE159819,GPL24676,1000,Large Granular Lymphocytic Leukemia,C1955861,,GEO,RNA-Seq,Homo sapiens,6|10,MONDO:T-cell large granular lymphocyte leukemia (T-cell LGL leukemia) is a lymphoproliferative malignancy that arises from the mature T-cell (CD3+) lineage. DSA09833,GSE159859,GPL24676,1000,Pitt-Hopkins Syndrome,C1970431,,GEO,RNA-Seq,Homo sapiens,6|6,"DO:A syndrome characterized by intellectual disability and developmental delay, breathing problems, recurrent seizures, and distinctive facial features and that has_material_basis_in heterozygous de novo mutations in the TCF4 gene in chromosome 18q21." DSA09834,GSE159860,GPL24676,1000,Pitt-Hopkins Syndrome,C1970431,,GEO,RNA-Seq,Homo sapiens,4|1,"DO:A syndrome characterized by intellectual disability and developmental delay, breathing problems, recurrent seizures, and distinctive facial features and that has_material_basis_in heterozygous de novo mutations in the TCF4 gene in chromosome 18q21." DSA09835,GSE4588,GPL570,99,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,9|8,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA09836,GSE4588,GPL570,67,Rheumatoid Arthritis,C0003873,Blood,GEO,Microarray,Homo sapiens,9|7,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA09837,GSE159952,GPL24247,1000,"Carcinoma, Lewis Lung",C0243038,Tibialis anterior,GEO,RNA-Seq,Mus musculus,4|4,MSH:A carcinoma discovered by Dr. Margaret R. Lewis of the Wistar Institute in 1951. This tumor originated spontaneously as a carcinoma of the lung of a C57BL mouse. The tumor does not appear to be grossly hemorrhagic and the majority of the tumor tissue is a semifirm homogeneous mass. (From Cancer Chemother Rep 2 1972 Nov;(3)1:325) It is also called 3LL and LLC and is used as a transplantable malignancy. DSA09838,GSE4588,GPL570,54,Systemic Lupus Erythematosus,C0024141,Blood,GEO,Microarray,Homo sapiens,9|7,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA09839,GSE6112,GPL4475,0,Tuberculosis,C0041296,Blood,GEO,Microarray,Homo sapiens,5|11,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA09840,GSE160011,GPL19057,1000,Age Related Macular Degeneration,C0242383,,GEO,RNA-Seq,Mus musculus,12|7,DO:A degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision. DSA09841,GSE160100,GPL19057,1000,Breast Cancer,C0678222,Bone marrow,GEO,RNA-Seq,Mus musculus,2|3,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09842,GSE160145,GPL18573,28,Chronic Kidney Disease,C1561643,Heart,GEO,RNA-Seq,Homo sapiens,8|15,DO:A kidney failure that is characterized by the gradual loss of kidney function. DSA09843,GSE160145,GPL18573,1000,Hypertension,C0020538,Heart,GEO,RNA-Seq,Homo sapiens,8|10,DO:An artery disease characterized by chronic elevated blood pressure in the arteries. DSA09844,GSE160178,GPL16791,1000,Japanese Encephalitis,C0014057,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A viral infectious disease that results_in infection located_in brain, has_material_basis_in Japanese encephalitis virus, which is transmitted_by Culex tritaeniorhynchus mosquito bite. The infection has_symptom headache, has_symptom high fever, has_symptom neck stiffness, has_symptom stupor, has_symptom disorientation, has_symptom coma, has_symptom tremors, has_symptom convulsions, and has_symptom spastic paralysis." DSA09845,GSE6112,GPL4475,92,Tuberculosis,C0041296,Blood,GEO,Microarray,Homo sapiens,9|9,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA09846,GSE160185,GPL13912,50,Down Syndrome,C0013080,Hippocampus,GEO,Microarray,Mus musculus,4|4,DO:A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. DSA09847,GSE2400,GPL1800,0,Amyotrophic Lateral Sclerosis,C0002736,,GEO,Microarray,Mus musculus,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA09848,GSE1710,GPL284,129,Crohn's Disease,C0010346,Sigmoid colon,GEO,Microarray,Homo sapiens,11|10,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA09849,GSE1710,GPL284,87,Ulcerative Colitis,C0009324,Sigmoid colon,GEO,Microarray,Homo sapiens,11|10,DO:An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1. DSA09850,GSE160268,GPL24676,11,Vexas Syndrome,,Whole blood,GEO,RNA-Seq,Homo sapiens,4|9, DSA09851,GSE160268,GPL24676,0,Vexas Syndrome,,Blood,GEO,RNA-Seq,Homo sapiens,3|2, DSA09852,GSE160268,GPL24676,1000,Vexas Syndrome,,Blood,GEO,RNA-Seq,Homo sapiens,1|1, DSA09853,GSE160268,GPL24676,1000,Vexas Syndrome,,Blood,GEO,RNA-Seq,Homo sapiens,3|4, DSA09854,GSE160306,GPL20301,15,Diabetes,C0011847,Retina macula,GEO,RNA-Seq,Homo sapiens,10|10,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09855,GSE160306,GPL20301,1000,Diabetic Macular Edema,C0730285,Retina macula,GEO,RNA-Seq,Homo sapiens,10|1,"EFO:Characterized by build-up of fluid in and beneath the macula, affecting detailed central vision" DSA09856,GSE160306,GPL20301,43,Non-Proliferative Dr,,Retina macula,GEO,RNA-Seq,Homo sapiens,10|15, DSA09857,GSE160306,GPL20301,447,Proliferative Dr,,Retina macula,GEO,RNA-Seq,Homo sapiens,10|3, DSA09858,GSE160306,GPL20301,2,Diabetes,C0011847,Retina,GEO,RNA-Seq,Homo sapiens,10|10,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09859,GSE160306,GPL20301,1000,Diabetic Macular Edema,C0730285,Retina,GEO,RNA-Seq,Homo sapiens,10|1,"EFO:Characterized by build-up of fluid in and beneath the macula, affecting detailed central vision" DSA09860,GSE160306,GPL20301,111,Non-Proliferative Dr,,Retina,GEO,RNA-Seq,Homo sapiens,10|17, DSA09861,GSE160306,GPL20301,1000,Proliferative Dr,,Retina,GEO,RNA-Seq,Homo sapiens,10|2, DSA09862,GSE160322,GPL20301,1000,Pancreatic Cancer,C0235974,,GEO,RNA-Seq,Homo sapiens,1|1,DO:An endocrine gland cancer located_in the pancreas. DSA09863,GSE160322,GPL20301,1000,Pancreatic Cancer,C0235974,Pancreas,GEO,RNA-Seq,Homo sapiens,1|1,DO:An endocrine gland cancer located_in the pancreas. DSA09864,GSE160322,GPL20301,1000,Pancreatic Cancer,C0235974,Pancreas,GEO,RNA-Seq,Homo sapiens,1|1,DO:An endocrine gland cancer located_in the pancreas. DSA09865,GSE160322,GPL20301,1000,Pancreatic Cancer,C0235974,Pancreas,GEO,RNA-Seq,Homo sapiens,1|1,DO:An endocrine gland cancer located_in the pancreas. DSA09866,GSE160329,GPL20301,1000,Community Acquired Pneumonia,C0694549,,GEO,RNA-Seq,Homo sapiens,41|69,NCI:Pneumonia that is not acquired in a hospital or long-term care facility setting. DSA09867,GSE160329,GPL20301,61,Community Acquired Pneumonia,C0694549,,GEO,RNA-Seq,Homo sapiens,41|56,NCI:Pneumonia that is not acquired in a hospital or long-term care facility setting. DSA09868,GSE160351,GPL21697,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,1|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA09869,GSE160501,GPL18573,317,Atopic Dermatitis,C0011615,Skin,GEO,RNA-Seq,Homo sapiens,3|15,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA09870,GSE160501,GPL18573,1000,Atopic Dermatitis,C0011615,Dermis,GEO,RNA-Seq,Homo sapiens,3|9,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA09871,GSE160501,GPL18573,1000,Atopic Dermatitis,C0011615,Epidermis,GEO,RNA-Seq,Homo sapiens,3|9,DO:An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. DSA09872,GSE160517,GPL20301,1000,Severe Congenital Neutropenia,C1853118,Bone marrow,GEO,RNA-Seq,Homo sapiens,1|1,DO:A neutropenia characterized by a maturation arrest of granulopoiesis at the level or promyelocytes and early onset of severe bacterial infections. DSA09873,GSE16054,GPL570,0,Interstitial Lung Disease,C0206062,,GEO,Microarray,Homo sapiens,3|3,"DO:A lung disease that is characterized by inflammation and altered lung interstitium compromising pulmonary function and often has_symptom shortness of breath, dyspnea, and/or cough." DSA09874,GSE16054,GPL570,484,Interstitial Lung Disease,C0206062,,GEO,Microarray,Homo sapiens,3|3,"DO:A lung disease that is characterized by inflammation and altered lung interstitium compromising pulmonary function and often has_symptom shortness of breath, dyspnea, and/or cough." DSA09875,GSE160925,GPL18573,2,Crohn's Disease,C0010346,Terminal ileum,GEO,RNA-Seq,Homo sapiens,3|4,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA09876,GSE160925,GPL18573,2,Crohn's Disease,C0010346,Terminal ileum,GEO,RNA-Seq,Homo sapiens,5|8,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA09877,GSE160932,GPL23159,0,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,3|3,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09878,GSE160932,GPL23159,0,Psoriasis,C0033860,Skin,GEO,Microarray,Homo sapiens,3|3,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09879,GSE160936,GPL20301,0,Alzheimer's Disease,C0002395,Brain,GEO,RNA-Seq,Homo sapiens,12|12,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA09880,GSE160997,GPL11154,1000,Hypertrophic Cardiomyopathy,C0007194,Heart,GEO,RNA-Seq,Homo sapiens,2|18,DO:A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations. DSA09881,GSE161042,GPL18573,1000,Obesity,C0028754,,GEO,RNA-Seq,Homo sapiens,4|8,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA09882,GSE161045,GPL24676,75,Alzheimer's Disease,C0002395,Putamen,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA09883,GSE161045,GPL24676,84,Parkinson's Disease,C0030567,Putamen,GEO,RNA-Seq,Homo sapiens,3|3,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA09884,GSE161052,GPL21273,1000,Diabetic Cardiomyopathy,C0853897,Heart,GEO,RNA-Seq,Mus musculus,3|2,"MSH:Diabetes complications in which VENTRICULAR REMODELING in the absence of CORONARY ATHEROSCLEROSIS and hypertension results in cardiac dysfunctions, typically LEFT VENTRICULAR DYSFUNCTION. The changes also result in myocardial hypertrophy, myocardial necrosis and fibrosis, and collagen deposition due to impaired glucose tolerance." DSA09885,GSE161058,GPL23126,0,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,3|4,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA09886,GSE161058,GPL23126,0,Myelodysplastic Syndromes,C3463824,Bone marrow,GEO,Microarray,Homo sapiens,3|4,"DO:A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets." DSA09887,GSE161084,GPL21273,1000,Psoriasiform Dermatitis,C0033860,Skin,GEO,RNA-Seq,Mus musculus,3|3,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09888,GSE161199,GPL18573,18,Alzheimer's Disease,C0002395,Blood,GEO,RNA-Seq,Homo sapiens,6|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA09889,GSE161199,GPL18573,411,Parkinson's Disease,C0030567,Blood,GEO,RNA-Seq,Homo sapiens,6|5,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA09890,GSE16120,GPL887,1000,Prostate Carcinoma,C0600139,Prostate,GEO,Microarray,Homo sapiens,14|51,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA09891,GSE161225,GPL18573,1000,Maculopapular Lesion,C0423791,Skin,GEO,RNA-Seq,Homo sapiens,5|3,HPO:A skin rash that is characterized by diffuse cutaneous erythema with areas of skin elevation. It may evolve to vesicles or papules as part of a more severe clinical entity. Different degrees of angioedema with involvement of subcutaneous tissue may also appear. DSA09892,GSE161225,GPL18573,1000,Maculopapular Lesion,C0423791,Skin,GEO,RNA-Seq,Homo sapiens,5|7,HPO:A skin rash that is characterized by diffuse cutaneous erythema with areas of skin elevation. It may evolve to vesicles or papules as part of a more severe clinical entity. Different degrees of angioedema with involvement of subcutaneous tissue may also appear. DSA09893,GSE161350,GPL21273,879,Psoriasiform Dermatitis,C0033860,Dermis,GEO,RNA-Seq,Mus musculus,2|2,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09894,GSE2052,GPL1739,86,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,11|9,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA09895,GSE161355,GPL570,0,Type 2 Diabetes Mellitus,C0011847,Temporal cortex,GEO,Microarray,Homo sapiens,5|6,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09896,GSE161355,GPL570,0,Type 2 Diabetes Mellitus,C0011847,Temporal cortex,GEO,Microarray,Homo sapiens,5|6,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09897,GSE161355,GPL570,0,Type 2 Diabetes Mellitus,C0011847,Temporal cortex,GEO,Microarray,Homo sapiens,5|6,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09898,GSE161426,GPL18573,1000,Juvenile Idiopathic Arthritis,C3890205,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA09899,GSE161426,GPL18573,1000,Juvenile Idiopathic Arthritis,C3890205,,GEO,RNA-Seq,Homo sapiens,3|4,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA09900,GSE2052,GPL1739,176,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,Microarray,Homo sapiens,11|4,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA09901,GSE2355,GPL81,6,Heart Failure,C0018801,Heart,GEO,Microarray,Mus musculus,5|3,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA09902,GSE2355,GPL81,0,Cardiac Hypertrophy,C1383860,Heart,GEO,Microarray,Mus musculus,5|8,"EFO:an increase in size of the cardiac tissue, not due to increased cell number" DSA09903,GSE161648,GPL24247,1000,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,scRNA-Seq,Mus musculus,1|1,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA09904,GSE161648,GPL24247,411,Idiopathic Pulmonary Fibrosis,C1800706,Lung,GEO,scRNA-Seq,Mus musculus,1|1,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA09905,GSE161715,GPL16791,407,Von Willebrand Disease Type 3,C1264041,,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A von Willebrand's disease characterized by autosomal recessive inheritance of a severe quantitative defect or virtual absence of VWF in plasma, prolonged bleeding time, and more severe bleeding tendencies compared to the other types of von Willebrand disease that has_material_basis_in homozygous or compound heterozygous mutation in the VWF gene which maps to chromosome 12p13." DSA09906,GSE161731,GPL24676,430,COVID-19,D8888888,Whole blood,GEO,RNA-Seq,Homo sapiens,4|40,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA09907,GSE161731,GPL24676,858,Influenza,C0021400,Whole blood,GEO,RNA-Seq,Homo sapiens,4|9,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA09908,GSE161737,GPL24676,1000,Renal Fibrosis,C0151650,Kidney,GEO,RNA-Seq,Homo sapiens,2|3,HPO:Renal fibrosis is the consequence of an excessive accumulation of extracellular matrix that occurs in virtually every type of chronic kidney disease. DSA09909,GSE161751,GPL21103,195,Neurotic; Stress-Related And Somatoform Disorders,C0694453,,GEO,scRNA-Seq,Mus musculus,1|1, DSA09910,GSE161751,GPL21103,478,Neurotic; Stress-Related And Somatoform Disorders,C0694453,Pituitary gland,GEO,scRNA-Seq,Mus musculus,1|1, DSA09911,GSE161751,GPL21103,757,Neurotic; Stress-Related And Somatoform Disorders,C0694453,Adrenal gland,GEO,scRNA-Seq,Mus musculus,1|1, DSA09912,GSE161763,GPL17021,1000,Cbl-Related Disorder,C3150803,Brain,GEO,RNA-Seq,Mus musculus,3|3,"MONDO:CBL-related disorder is a genetic condition caused by pathogenic variants in the Cbl ubiquitin ligase gene, (CBL; HGNC:1541). Due to the proposed mechanism indicating the CBL gene's relationship to the RAS-MAPK pathway and the phenotypic presentation similar to that of the RASopathies, CBL-related disorder should be considered a RASopathy disorder. Though there is a wide spectrum of phenotypic variability, broadly, patients with CBL-related disorder have presented with developmental delay, intellectual disability, neurodevelopmental alterations, prenatal lymphatic anomalies, cardiac malformations as well as vascular anomalies particularly affecting the brain (e.g. Moya-moya arteriopathies), craniofacial features indicative of a RASopathy, hypotonia, feeding difficulties, edema of the legs, musculoskeletal and respiratory thorax abnormalities, ectodermal features including cafe-au-lait spots, immunological and hematological disorders and susceptibility to tumors diagnosed as juvenile myelomonocytic leukemia (JMML) that is usually self-remitting. Note tumor risk beyond JMML has not yet been thoroughly assessed. Due to the clinical presentation of a broad spectrum of these and other phenotypes in patients with variants in CBL, these conditions are currently defined by experts in reference to the causal gene, CBL." DSA09913,GSE2355,GPL82,27,Heart Failure,C0018801,Heart,GEO,Microarray,Mus musculus,5|3,DO:A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. DSA09914,GSE161777,GPL15520,29,COVID-19,D8888888,Peripheral blood,GEO,RNA-Seq,Homo sapiens,2|1,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA09915,GSE2355,GPL82,3,Cardiac Hypertrophy,C1383860,Heart,GEO,Microarray,Mus musculus,5|8,"EFO:an increase in size of the cardiac tissue, not due to increased cell number" DSA09916,GSE1377,GPL96,6,Kaposi Sarcoma,C0036220,,GEO,Microarray,Homo sapiens,2|2,"DO:A connective tissue cancer that derives_from lymphatic endothelium, and derives_from spindle cells, results_in_formation_of vascular channels that fill with blood cells, has_material_basis_in Human herpesvirus 8 (HHV8)." DSA09917,GSE1299,GPL8300,969,Lymphoma,C0024299,,GEO,Microarray,Homo sapiens,2|4,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA09918,GSE161777,GPL15520,0,COVID-19,D8888888,Peripheral blood,GEO,RNA-Seq,Homo sapiens,2|10,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA09919,GSE1299,GPL96,1000,Lymphoma,C0024299,,GEO,Microarray,Homo sapiens,2|4,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA09920,GSE1299,GPL97,773,Lymphoma,C0024299,,GEO,Microarray,Homo sapiens,2|4,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA09921,GSE775,GPL81,13,Myocardial Infarction,C0027051,Heart,GEO,Microarray,Mus musculus,4|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA09922,GSE775,GPL81,443,Myocardial Infarction,C0027051,Heart,GEO,Microarray,Mus musculus,4|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA09923,GSE775,GPL81,1000,Myocardial Infarction,C0027051,Heart,GEO,Microarray,Mus musculus,4|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA09924,GSE775,GPL81,1000,Myocardial Infarction,C0027051,Heart,GEO,Microarray,Mus musculus,4|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA09925,GSE775,GPL81,1000,Myocardial Infarction,C0027051,Heart,GEO,Microarray,Mus musculus,4|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA09926,GSE775,GPL81,2,Myocardial Infarction,C0027051,Heart,GEO,Microarray,Mus musculus,3|3,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA09927,GSE137108,GPL16686,1000,Chronic Mucocutaneous Candidiasis,C0006845,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|1,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA09928,GSE137108,GPL16686,1000,Chronic Mucocutaneous Candidiasis,C0006845,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|1,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA09929,GSE161785,GPL23159,1000,Head And Neck Cancer,C0018671,Blood,GEO,Microarray,Homo sapiens,5|5,"DO:An organ system cancer that arises in the head or neck region. This region includes the nasal cavity, sinuses, lips, mouth, salivary glands, throat, or larynx." DSA09930,GSE161827,GPL19057,15,Diabetes,C0011847,Heart,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09931,GSE161827,GPL19057,64,Diabetes,C0011847,Heart,GEO,RNA-Seq,Homo sapiens,4|4,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09932,GSE161829,GPL24676,328,Tuberculosis,C0041296,,GEO,RNA-Seq,Homo sapiens,9|2,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA09933,GSE161829,GPL24676,4,Tuberculosis,C0041296,,GEO,RNA-Seq,Homo sapiens,9|17,"MONDO:A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use." DSA09934,GSE161885,GPL21163,212,Diabetic Kidney Disease,C0011881,Kidney,GEO,Microarray,Mus musculus,2|2,"EFO:Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis." DSA09935,GSE161904,GPL13112,1000,Alzheimer's Disease,C0002395,Insular cortex,GEO,RNA-Seq,Mus musculus,15|15,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA09936,GSE161906,GPL16791,0,Psoriasis,C0033860,,GEO,RNA-Seq,Homo sapiens,8|3,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09937,GSE161906,GPL16791,2,Psoriasis,C0033860,,GEO,RNA-Seq,Homo sapiens,8|2,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09938,GSE161913,GPL21290,9,Large-Artery Atherosclerotic Stroke,,Blood,GEO,RNA-Seq,Homo sapiens,4|5, DSA09939,GSE161931,GPL24247,23,Diabetic Cardiomyopathy,C0853897,Heart,GEO,RNA-Seq,Mus musculus,5|5,"MSH:Diabetes complications in which VENTRICULAR REMODELING in the absence of CORONARY ATHEROSCLEROSIS and hypertension results in cardiac dysfunctions, typically LEFT VENTRICULAR DYSFUNCTION. The changes also result in myocardial hypertrophy, myocardial necrosis and fibrosis, and collagen deposition due to impaired glucose tolerance." DSA09940,GSE161945,GPL21103,145,Acute Pancreatitis,C0001339,Pancreas,GEO,RNA-Seq,Mus musculus,2|3,"DO:A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock." DSA09941,GSE161969,GPL20795,418,Pregnancy Loss; Recurrent; Susceptibility To; 2,C3280672,Decidua,GEO,RNA-Seq,Homo sapiens,3|4,EFO:Thrombin is a \ trypsin-like\ serine protease protein that in humans is encoded by the F2 gene. DSA09942,GSE161989,GPL11154,11,Type 2 Diabetes,C0011860,Subcutaneous adipose tissue,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA09943,GSE162012,GPL24676,368,Ciliopathy,C4551720,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer dynein arm defect and in about half of patients situs inversus and has_material_basis_in compound heterozygous mutation in the DNAI1 gene on chromosome 9p13. DSA09944,GSE162032,GPL18573,1000,Acute Lymphoblastic Leukemia,C0023449,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A acute leukemia that is characterized by over production of lymphoblasts. DSA09945,GSE137108,GPL16686,1000,Chronic Mucocutaneous Candidiasis,C0006845,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|1,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA09946,GSE137108,GPL16686,1000,Chronic Mucocutaneous Candidiasis,C0006845,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|1,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA09947,GSE137108,GPL16686,1000,Chronic Mucocutaneous Candidiasis,C0006845,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|1,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA09948,GSE162108,GPL20301,1000,Duchenne Muscular Dystrophy,C0013264,,GEO,RNA-Seq,Homo sapiens,1|1,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA09949,GSE162108,GPL20301,1000,Duchenne Muscular Dystrophy,C0013264,,GEO,RNA-Seq,Homo sapiens,1|1,DO:A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. DSA09950,GSE162113,GPL21290,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,6|6,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA09951,GSE162122,GPL24676,1000,Leiomyoma,C0042133,Myometrium,GEO,scRNA-Seq,Homo sapiens,5|4,DO:An uterine benign neoplasm derived from the smooth muscle layer of the uterus. DSA09952,GSE162183,GPL24676,1000,Psoriasis,C0033860,Skin,GEO,scRNA-Seq,Homo sapiens,3|3,DO:A skin disease that is characterized by patches of thick red skin and silvery scales. DSA09953,GSE162249,GPL13112,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,4|5,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA09954,GSE162249,GPL13112,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,4|6,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA09955,GSE162276,GPL13112,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,4|5,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA09956,GSE137108,GPL16686,1000,Chronic Mucocutaneous Candidiasis,C0006845,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|1,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA09957,GSE162306,GPL19057,1000,Joint Pain/Joint Inflammation,C4025256,Synovium,GEO,RNA-Seq,Mus musculus,3|1, DSA09958,GSE162349,GPL20301,1000,Huntington's Disease,C0020179,,GEO,RNA-Seq,Homo sapiens,16|23,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA09959,GSE162416,GPL10558,1000,Leprosy,C0023343,,GEO,Microarray,Homo sapiens,28|26,"DO:A primary bacterial infectious disease that results_in infection located_in superficial peripheral nerves, located_in skin, located_in mucous membranes of the upper respiratory tract, located_in anterior chamber of the eyes, or located_in testes, has_material_basis_in Mycobacterium leprae, which is transmitted_by aerosol spread from infected nasal secretions to exposed nasal and oral mucosa. The infection has_symptom skin lesions, has_symptom sensory loss, has_symptom motor loss and has_symptom eye damage." DSA09960,GSE162462,GPL18573,1000,Chronic Myeloid Leukemia,C0023473,Peripheral blood,GEO,RNA-Seq,Homo sapiens,1|2,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA09961,GSE162462,GPL18573,219,Chronic Myeloid Leukemia,C0023473,Peripheral blood,GEO,RNA-Seq,Homo sapiens,3|3,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA09962,GSE137108,GPL16686,1000,Chronic Mucocutaneous Candidiasis,C0006845,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|1,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA09963,GSE162462,GPL18573,110,Chronic Myeloid Leukemia,C0023473,Peripheral blood,GEO,RNA-Seq,Homo sapiens,5|5,DO:A myeloid leukemia that is characterized by over production of white blood cells. DSA09964,GSE162516,GPL21290,1000,Epstein-Barr Virus Infection,C0149678,Peripheral blood,GEO,RNA-Seq,Homo sapiens,1|1,"EFO:Infection with human herpesvirus 4 (HERPESVIRUS 4, HUMAN); which may facilitate the development of various lymphoproliferative disorders. These include BURKITT LYMPHOMA (African type), INFECTIOUS MONONUCLEOSIS, and oral hairy leukoplakia (LEUKOPLAKIA, HAIRY)." DSA09965,GSE162516,GPL21290,1000,Epstein-Barr Virus Infection,C0149678,Peripheral blood,GEO,RNA-Seq,Homo sapiens,1|1,"EFO:Infection with human herpesvirus 4 (HERPESVIRUS 4, HUMAN); which may facilitate the development of various lymphoproliferative disorders. These include BURKITT LYMPHOMA (African type), INFECTIOUS MONONUCLEOSIS, and oral hairy leukoplakia (LEUKOPLAKIA, HAIRY)." DSA09966,GSE162516,GPL21290,1000,Epstein-Barr Virus Infection,C0149678,Peripheral blood,GEO,RNA-Seq,Homo sapiens,1|1,"EFO:Infection with human herpesvirus 4 (HERPESVIRUS 4, HUMAN); which may facilitate the development of various lymphoproliferative disorders. These include BURKITT LYMPHOMA (African type), INFECTIOUS MONONUCLEOSIS, and oral hairy leukoplakia (LEUKOPLAKIA, HAIRY)." DSA09967,GSE162516,GPL21290,1000,Epstein-Barr Virus Infection,C0149678,Peripheral blood,GEO,RNA-Seq,Homo sapiens,1|1,"EFO:Infection with human herpesvirus 4 (HERPESVIRUS 4, HUMAN); which may facilitate the development of various lymphoproliferative disorders. These include BURKITT LYMPHOMA (African type), INFECTIOUS MONONUCLEOSIS, and oral hairy leukoplakia (LEUKOPLAKIA, HAIRY)." DSA09968,GSE162516,GPL21290,1000,Lymphoma,C0024299,Peripheral blood,GEO,RNA-Seq,Homo sapiens,1|1,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA09969,GSE162562,GPL24676,8,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,4|24,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA09970,GSE162562,GPL24676,69,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,4|30,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA09971,GSE162562,GPL24676,398,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,4|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA09972,GSE162615,GPL18573,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA09973,GSE162615,GPL18573,819,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA09974,GSE162615,GPL18573,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,3|3,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA09975,GSE162616,GPL24676,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,scRNA-Seq,Homo sapiens,3|3,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA09976,GSE162632,GPL24676,1000,Influenza,C0021400,,GEO,RNA-Seq,Homo sapiens,89|89,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA09977,GSE162632,GPL24676,2,Influenza,C0021400,,GEO,RNA-Seq,Homo sapiens,10|9,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA09978,GSE162632,GPL24676,1000,Influenza,C0021400,,GEO,RNA-Seq,Homo sapiens,10|10,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA09979,GSE162632,GPL24676,1000,Influenza,C0021400,,GEO,RNA-Seq,Homo sapiens,10|10,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA09980,GSE162632,GPL24676,1000,Influenza,C0021400,,GEO,RNA-Seq,Homo sapiens,10|7,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA09981,GSE162632,GPL24676,1000,Influenza,C0021400,,GEO,RNA-Seq,Homo sapiens,10|10,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA09982,GSE162632,GPL24676,1000,Influenza,C0021400,,GEO,RNA-Seq,Homo sapiens,10|8,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA09983,GSE162632,GPL24676,1000,Influenza,C0021400,,GEO,RNA-Seq,Homo sapiens,10|10,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA09984,GSE162632,GPL24676,1000,Influenza,C0021400,,GEO,RNA-Seq,Homo sapiens,10|10,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA09985,GSE162635,GPL570,1000,Chronic Obstructive Pulmonary Disease,C0024117,Bronchus,GEO,Microarray,Homo sapiens,20|185,"DO:An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both." DSA09986,GSE162669,GPL16791,1000,Lung Adenocarcinoma,C0152013,Lung,GEO,RNA-Seq,Homo sapiens,9|9,DO:A respiratory system cancer that is located_in the lung. DSA09987,GSE162688,GPL21626,209,Zika Virus Infection,C0276289,,GEO,RNA-Seq,Mus musculus,3|3,"DO:A viral infectious disease that has_material_basis_in Zika virus, which is transmitted_by Aedes aegypti mosquitoes and targets neural progenitor cells and neuronal cells in all stages of maturity and has_symptom fever, has_symptom rash, has_symptom headaches and has_symptom joint pain." DSA09988,GSE162689,GPL24014,333,Type 1 Diabetes,C0011854,Pancreas,GEO,RNA-Seq,Homo sapiens,8|7,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA09989,GSE162689,GPL24014,35,Type 1 Diabetes,C0011854,Pancreas,GEO,RNA-Seq,Homo sapiens,8|6,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA09990,GSE162689,GPL24014,27,Type 1 Diabetes,C0011854,Pancreas,GEO,RNA-Seq,Homo sapiens,8|7,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA09991,GSE162689,GPL24014,1000,Type 1 Diabetes,C0011854,Pancreas,GEO,RNA-Seq,Homo sapiens,8|7,DO:A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5. DSA09992,GSE162691,GPL24676,66,Osteoarthritis,C0157946,Adipose tissue,GEO,RNA-Seq,Homo sapiens,2|3,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA09993,GSE162691,GPL24676,1000,Osteoarthritis,C0157946,Fibrous tissue,GEO,RNA-Seq,Homo sapiens,3|1,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA09994,GSE162691,GPL24676,158,Osteoarthritis,C0157946,,GEO,RNA-Seq,Homo sapiens,3|3,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA09995,GSE162691,GPL24676,38,Osteoarthritis,C0157946,,GEO,RNA-Seq,Homo sapiens,2|2,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA09996,GSE162712,GPL18573,1000,Sarcoidosis,C0036202,Bronchus,GEO,RNA-Seq,Homo sapiens,3|3,DO:A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. DSA09997,GSE162746,GPL16791,1000,Aspergillosis,C0004030,,GEO,RNA-Seq,Homo sapiens,8|7,"DO:An opportunistic mycosis that involves a spectrum of diseases of humans and animals caused by members of the genus Aspergillus infecting lungs, brain, kidney, heart, bone, eyes, sinuses, skin and gastrointestinal tract. It is a serious illnesses in people with a weakened immune system." DSA09998,GSE162746,GPL16791,1000,Candidiasis,C0006840,,GEO,RNA-Seq,Homo sapiens,8|8,"DO:A candidiasis that involves fungal infection of the mucous membrane of the mouth by Candida species, which is characterized by thick white or cream-colored deposits on inflamed mucosal membranes." DSA09999,GSE162746,GPL16791,1000,Mucormycosis,C0026718,,GEO,RNA-Seq,Homo sapiens,8|8,"EFO:Any infection due to a fungus of the Zygomycota phylum. The disease typically involves the rhino-facial-cranial area, lungs, gastrointestinal tract, skin, or less commonly other organ systems. The infecting fungi have a predilection for invading vessels of the arterial system, causing embolization and subsequent necrosis of surrounding tissue." DSA10000,GSE162746,GPL16791,1000,Aspergillosis,C0004030,,GEO,RNA-Seq,Homo sapiens,8|8,"DO:An opportunistic mycosis that involves a spectrum of diseases of humans and animals caused by members of the genus Aspergillus infecting lungs, brain, kidney, heart, bone, eyes, sinuses, skin and gastrointestinal tract. It is a serious illnesses in people with a weakened immune system." DSA10001,GSE162746,GPL16791,1000,Candidiasis,C0006840,,GEO,RNA-Seq,Homo sapiens,8|8,"DO:A candidiasis that involves fungal infection of the mucous membrane of the mouth by Candida species, which is characterized by thick white or cream-colored deposits on inflamed mucosal membranes." DSA10002,GSE162746,GPL16791,1000,Mucormycosis,C0026718,,GEO,RNA-Seq,Homo sapiens,8|7,"EFO:Any infection due to a fungus of the Zygomycota phylum. The disease typically involves the rhino-facial-cranial area, lungs, gastrointestinal tract, skin, or less commonly other organ systems. The infecting fungi have a predilection for invading vessels of the arterial system, causing embolization and subsequent necrosis of surrounding tissue." DSA10003,GSE137108,GPL16686,1000,Chronic Mucocutaneous Candidiasis,C0006845,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|1,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA10004,GSE162828,GPL24676,1000,Systemic Lupus Erythematosus,C0024141,Peripheral blood,GEO,RNA-Seq,Homo sapiens,5|5,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA10005,GSE162873,GPL11154,1000,Alzheimer's Disease,C0002395,,GEO,RNA-Seq,Homo sapiens,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10006,GSE162892,GPL20301,1000,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA10007,GSE162892,GPL20301,1000,Amyotrophic Lateral Sclerosis,C0002736,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA10008,GSE137108,GPL16686,117,Chronic Mucocutaneous Candidiasis,C0006845,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA10009,GSE162960,GPL11154,1000,Rectal Cancer,C0007113,Liver,GEO,RNA-Seq,Homo sapiens,2|4,DO:A colorectal cancer that is located_in the rectum. DSA10010,GSE162960,GPL11154,1000,Rectal Cancer,C0007113,Liver,GEO,RNA-Seq,Homo sapiens,1|2,DO:A colorectal cancer that is located_in the rectum. DSA10011,GSE162992,GPL24247,1000,Sjogren's Syndrome,C1527336,Bone marrow,GEO,scRNA-Seq,Mus musculus,1|1,DO:An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. DSA10012,GSE163060,GPL21493,38,Obesity,C0028754,Heart,GEO,RNA-Seq,Mus musculus,6|6,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA10013,GSE163060,GPL21493,456,Obesity,C0028754,Adipose tissue,GEO,RNA-Seq,Mus musculus,5|6,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA10014,GSE163073,GPL18573,1000,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,1|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA10015,GSE163073,GPL18573,1000,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,1|6,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA10016,GSE163073,GPL18573,1000,Systemic Lupus Erythematosus,C0024141,,GEO,RNA-Seq,Homo sapiens,1|3,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA10017,GSE163090,GPL19057,1000,Macular Degeneration,C0024437,Choroid,GEO,RNA-Seq,Mus musculus,6|6,DO:A retinitis pigmentosa that has_material_basis_in mutation in the FSCN2 gene on chromosome 17q25. DSA10018,GSE163090,GPL18573,0,Macular Degeneration,C0024437,Choroid,GEO,RNA-Seq,Homo sapiens,4|3,DO:A retinitis pigmentosa that has_material_basis_in mutation in the FSCN2 gene on chromosome 17q25. DSA10019,GSE163121,GPL20301,1000,Systemic Lupus Erythematosus,C0024141,,GEO,scRNA-Seq,Homo sapiens,2|3,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA10020,GSE137108,GPL16686,1000,Chronic Mucocutaneous Candidiasis,C0006845,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA10021,GSE163122,GPL18573,0,Frontotemporal Dementia,C0338451,Frontal cortex,GEO,RNA-Seq,Homo sapiens,4|5,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA10022,GSE163122,GPL18573,4,Frontotemporal Dementia,C0338451,Frontal cortex,GEO,RNA-Seq,Homo sapiens,4|5,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA10023,GSE137108,GPL16686,102,Chronic Mucocutaneous Candidiasis,C0006845,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA10024,GSE163122,GPL18573,0,Frontotemporal Dementia,C0338451,Occipital cortex,GEO,RNA-Seq,Homo sapiens,4|5,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA10025,GSE163122,GPL18573,0,Frontotemporal Dementia,C0338451,Occipital cortex,GEO,RNA-Seq,Homo sapiens,4|5,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA10026,GSE137108,GPL16686,1000,Chronic Mucocutaneous Candidiasis,C0006845,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA10027,GSE163122,GPL18573,6,Frontotemporal Dementia,C0338451,Temporal cortex,GEO,RNA-Seq,Homo sapiens,4|5,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA10028,GSE163122,GPL18573,0,Frontotemporal Dementia,C0338451,Temporal cortex,GEO,RNA-Seq,Homo sapiens,4|5,"DO:A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31." DSA10029,GSE137108,GPL16686,119,Chronic Mucocutaneous Candidiasis,C0006845,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA10030,GSE137108,GPL16686,1000,Chronic Mucocutaneous Candidiasis,C0006845,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA10031,GSE137108,GPL16686,98,Chronic Mucocutaneous Candidiasis,C0006845,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA10032,GSE163129,GPL17021,1000,Myocardial Infarction,C0027051,Heart,GEO,scRNA-Seq,Mus musculus,1|1,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA10033,GSE163129,GPL17021,1000,Myocardial Infarction,C0027051,Heart,GEO,scRNA-Seq,Mus musculus,1|1,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA10034,GSE163129,GPL17021,1000,Myocardial Infarction,C0027051,Heart,GEO,scRNA-Seq,Mus musculus,1|1,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA10035,GSE163129,GPL17021,1000,Myocardial Infarction,C0027051,Heart,GEO,scRNA-Seq,Mus musculus,1|1,DO:A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia. DSA10036,GSE163151,GPL24676,1000,Viral Respiratory Tract Infection,C0877203,,GEO,RNA-Seq,Homo sapiens,31|3,"MONDO:A respiratory tract infection caused by a virus. Viruses represent the most common causes of upper and lower respiratory tract infections and include rhinoviruses, influenza viruses, parainfluenza viruses, and respiratory syncytial virus." DSA10037,GSE163151,GPL24676,1000,Viral Respiratory Tract Infection,C0877203,,GEO,RNA-Seq,Homo sapiens,31|3,"MONDO:A respiratory tract infection caused by a virus. Viruses represent the most common causes of upper and lower respiratory tract infections and include rhinoviruses, influenza viruses, parainfluenza viruses, and respiratory syncytial virus." DSA10038,GSE163151,GPL24676,1000,Viral Respiratory Tract Infection,C0877203,,GEO,RNA-Seq,Homo sapiens,31|3,"MONDO:A respiratory tract infection caused by a virus. Viruses represent the most common causes of upper and lower respiratory tract infections and include rhinoviruses, influenza viruses, parainfluenza viruses, and respiratory syncytial virus." DSA10039,GSE163151,GPL24676,1000,Viral Respiratory Tract Infection,C0877203,,GEO,RNA-Seq,Homo sapiens,31|3,"MONDO:A respiratory tract infection caused by a virus. Viruses represent the most common causes of upper and lower respiratory tract infections and include rhinoviruses, influenza viruses, parainfluenza viruses, and respiratory syncytial virus." DSA10040,GSE163151,GPL24676,1000,Viral Respiratory Tract Infection,C0877203,,GEO,RNA-Seq,Homo sapiens,31|3,"MONDO:A respiratory tract infection caused by a virus. Viruses represent the most common causes of upper and lower respiratory tract infections and include rhinoviruses, influenza viruses, parainfluenza viruses, and respiratory syncytial virus." DSA10041,GSE163151,GPL24676,237,Bacterial Sepsis,C0243026,Whole Blood,GEO,RNA-Seq,Homo sapiens,31|2,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA10042,GSE163151,GPL24676,1000,Bacterial Sepsis,C0243026,Whole Blood,GEO,RNA-Seq,Homo sapiens,31|1,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA10043,GSE163151,GPL24676,1000,Viral Respiratory Tract Infection,C0877203,,GEO,RNA-Seq,Homo sapiens,31|8,"MONDO:A respiratory tract infection caused by a virus. Viruses represent the most common causes of upper and lower respiratory tract infections and include rhinoviruses, influenza viruses, parainfluenza viruses, and respiratory syncytial virus." DSA10044,GSE163151,GPL24676,1000,Viral Respiratory Tract Infection,C0877203,,GEO,RNA-Seq,Homo sapiens,31|26,"MONDO:A respiratory tract infection caused by a virus. Viruses represent the most common causes of upper and lower respiratory tract infections and include rhinoviruses, influenza viruses, parainfluenza viruses, and respiratory syncytial virus." DSA10045,GSE163151,GPL24676,1000,Viral Respiratory Tract Infection,C0877203,,GEO,RNA-Seq,Homo sapiens,31|55,"MONDO:A respiratory tract infection caused by a virus. Viruses represent the most common causes of upper and lower respiratory tract infections and include rhinoviruses, influenza viruses, parainfluenza viruses, and respiratory syncytial virus." DSA10046,GSE163151,GPL24676,1000,Viral Respiratory Tract Infection,C0877203,,GEO,RNA-Seq,Homo sapiens,31|15,"MONDO:A respiratory tract infection caused by a virus. Viruses represent the most common causes of upper and lower respiratory tract infections and include rhinoviruses, influenza viruses, parainfluenza viruses, and respiratory syncytial virus." DSA10047,GSE163151,GPL24676,1000,Bacterial Sepsis,C0243026,Whole blood,GEO,RNA-Seq,Homo sapiens,31|2,DO:A bacterial infectious disease has_material_basis_in Bacteria. DSA10048,GSE163151,GPL24676,1000,Viral Respiratory Tract Infection,C0877203,,GEO,RNA-Seq,Homo sapiens,31|3,"MONDO:A respiratory tract infection caused by a virus. Viruses represent the most common causes of upper and lower respiratory tract infections and include rhinoviruses, influenza viruses, parainfluenza viruses, and respiratory syncytial virus." DSA10049,GSE163151,GPL24676,1000,Viral Respiratory Tract Infection,C0877203,,GEO,RNA-Seq,Homo sapiens,31|8,"MONDO:A respiratory tract infection caused by a virus. Viruses represent the most common causes of upper and lower respiratory tract infections and include rhinoviruses, influenza viruses, parainfluenza viruses, and respiratory syncytial virus." DSA10050,GSE163151,GPL24676,1000,Viral Respiratory Tract Infection,C0877203,,GEO,RNA-Seq,Homo sapiens,31|10,"MONDO:A respiratory tract infection caused by a virus. Viruses represent the most common causes of upper and lower respiratory tract infections and include rhinoviruses, influenza viruses, parainfluenza viruses, and respiratory syncytial virus." DSA10051,GSE163151,GPL24676,1000,COVID-19,D8888888,,GEO,RNA-Seq,Homo sapiens,31|145,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA10052,GSE163256,GPL18573,648,Cerebral Hemorrhage,C2937358,Blood,GEO,RNA-Seq,Homo sapiens,4|64,EFO:stroke subtype classified by the rupture of blood vessels in the lobar or nonlobar regions of the brain DSA10053,GSE163256,GPL18573,1000,Cerebral Hemorrhage,C2937358,,GEO,RNA-Seq,Homo sapiens,4|56,EFO:stroke subtype classified by the rupture of blood vessels in the lobar or nonlobar regions of the brain DSA10054,GSE163256,GPL18573,1000,Cerebral Hemorrhage,C2937358,,GEO,RNA-Seq,Homo sapiens,12|95,EFO:stroke subtype classified by the rupture of blood vessels in the lobar or nonlobar regions of the brain DSA10055,GSE163256,GPL18573,1000,Cerebral Hemorrhage,C2937358,,GEO,RNA-Seq,Homo sapiens,12|85,EFO:stroke subtype classified by the rupture of blood vessels in the lobar or nonlobar regions of the brain DSA10056,GSE163278,GPL16791,1000,Monoclonal Gammopathy of Undetermined Significance,C0026470,Bone marrow,GEO,scRNA-Seq,Homo sapiens,8|14,DO:A blood protein disease that is characterized by the presence of an abnormal protein called monoclonal protein in the blood. DSA10057,GSE163278,GPL16791,1000,Multiple Myeloma,C0026764,Bone marrow,GEO,scRNA-Seq,Homo sapiens,8|11,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA10058,GSE163290,GPL24247,0,Influenza,C0021400,,GEO,RNA-Seq,Mus musculus,1|4,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA10059,GSE163290,GPL24247,1000,Influenza,C0021400,,GEO,RNA-Seq,Mus musculus,1|4,"DO:A viral infectious disease that results in infection, located in respiratory tract, has_material_basis_in Influenzavirus A, has_material_basis_in Influenzavirus B, or has_material_basis_in Influenzavirus C, which are transmitted_by droplet spread of oronasal secretions during coughing, sneezing, or talking from an infected person. It is a highly contagious disease that affects birds and mammals and has_symptom chills, has_symptom fever, has_symptom sore throat, has_symptom runny nose, has_symptom muscle pains, has_symptom severe headache, has_symptom cough, and has_symptom weakness." DSA10060,GSE137108,GPL16686,1000,Chronic Mucocutaneous Candidiasis,C0006845,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp." DSA10061,GSE137108,GPL16686,1000,Loeys-Dietz Syndrome,C1836635,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A syndrome that is characterized by increased risk of aortic aneurysm and dissection, elongated limbs, hypertelorism, bifid uvula and easy skin bruising due to mutations in TGFB3 that results in connective tissue defects." DSA10062,GSE137108,GPL16686,1000,Loeys-Dietz Syndrome,C1836635,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A syndrome that is characterized by increased risk of aortic aneurysm and dissection, elongated limbs, hypertelorism, bifid uvula and easy skin bruising due to mutations in TGFB3 that results in connective tissue defects." DSA10063,GSE137108,GPL16686,1000,Loeys-Dietz Syndrome,C1836635,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A syndrome that is characterized by increased risk of aortic aneurysm and dissection, elongated limbs, hypertelorism, bifid uvula and easy skin bruising due to mutations in TGFB3 that results in connective tissue defects." DSA10064,GSE163405,GPL10558,0,Acquired Immunodeficiency Syndrome,C0001175,,GEO,Microarray,Homo sapiens,2|2,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA10065,GSE163405,GPL10558,50,Acquired Immunodeficiency Syndrome,C0001175,,GEO,Microarray,Homo sapiens,2|2,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA10066,GSE163405,GPL10558,0,Acquired Immunodeficiency Syndrome,C0001175,,GEO,Microarray,Homo sapiens,2|2,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA10067,GSE163426,GPL24676,1000,COVID-19,D8888888,Trachea,GEO,RNA-Seq,Homo sapiens,5|15,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA10068,GSE163498,GPL24676,1000,Leprosy,C0023343,Whole blood,GEO,RNA-Seq,Homo sapiens,19|3,"DO:A primary bacterial infectious disease that results_in infection located_in superficial peripheral nerves, located_in skin, located_in mucous membranes of the upper respiratory tract, located_in anterior chamber of the eyes, or located_in testes, has_material_basis_in Mycobacterium leprae, which is transmitted_by aerosol spread from infected nasal secretions to exposed nasal and oral mucosa. The infection has_symptom skin lesions, has_symptom sensory loss, has_symptom motor loss and has_symptom eye damage." DSA10069,GSE163498,GPL24676,2,Leprosy,C0023343,Whole blood,GEO,RNA-Seq,Homo sapiens,19|4,"DO:A primary bacterial infectious disease that results_in infection located_in superficial peripheral nerves, located_in skin, located_in mucous membranes of the upper respiratory tract, located_in anterior chamber of the eyes, or located_in testes, has_material_basis_in Mycobacterium leprae, which is transmitted_by aerosol spread from infected nasal secretions to exposed nasal and oral mucosa. The infection has_symptom skin lesions, has_symptom sensory loss, has_symptom motor loss and has_symptom eye damage." DSA10070,GSE163526,GPL13112,897,Alzheimer's Disease,C0002395,,GEO,RNA-Seq,Mus musculus,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10071,GSE163526,GPL13112,1000,Alzheimer's Disease,C0002395,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10072,GSE163526,GPL13112,1000,Alzheimer's Disease,C0002395,Cerebral cortex,GEO,RNA-Seq,Mus musculus,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10073,GSE163526,GPL13112,1000,Alzheimer's Disease,C0002395,Hippocampus,GEO,RNA-Seq,Mus musculus,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10074,GSE163526,GPL11154,1000,Alzheimer's Disease,C0002395,,GEO,RNA-Seq,Homo sapiens,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10075,GSE137108,GPL16686,1000,Loeys-Dietz Syndrome,C1836635,Skin fibroblasts,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A syndrome that is characterized by increased risk of aortic aneurysm and dissection, elongated limbs, hypertelorism, bifid uvula and easy skin bruising due to mutations in TGFB3 that results in connective tissue defects." DSA10076,GSE116752,GPL17021,1000,Attention Deficit Hyperactivity Disorder,C1263846,Striatum,GEO,RNA-Seq,Mus musculus,5|5,"DO:A specific developmental disorder that is characterized by co-existence of attentional problems and hyperactivity, with each behavior occurring infrequently alone and symptoms starting before seven years of age." DSA10077,GSE163572,GPL21103,111,Asthma,C0004096,Lung,GEO,scRNA-Seq,Mus musculus,1|2,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA10078,GSE171402,GPL17021,0,Pancreatic Tumor,C0030297,Visceral adipose tissue,GEO,RNA-Seq,Homo sapiens,5|5,DO:An endocrine gland cancer located_in the pancreas. DSA10079,GSE139505,GPL18573,1000,Cutaneous Squamous Cell Carcinoma,C0553723,Skin,GEO,RNA-Seq,Homo sapiens,7|9,DO:A skin carcinoma that has_material_basis_in squamous cells. DSA10080,GSE60837,GPL17021,1000,Colorectal Carcinoma,C0009402,,GEO,RNA-Seq,Mus musculus,3|5,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA10081,GSE60837,GPL17021,1000,Colorectal Carcinoma,C0009402,,GEO,RNA-Seq,Mus musculus,3|5,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA10082,GSE163634,GPL16791,1000,Acute Lymphoblastic Leukemia,C0023449,Peripheral blood,GEO,RNA-Seq,Homo sapiens,10|2,DO:A acute leukemia that is characterized by over production of lymphoblasts. DSA10083,GSE163634,GPL16791,1000,Acute Lymphoblastic Leukemia,C0023449,Peripheral blood,GEO,RNA-Seq,Homo sapiens,10|2,DO:A acute leukemia that is characterized by over production of lymphoblasts. DSA10084,GSE163634,GPL16791,1000,Acute Lymphoblastic Leukemia,C0023449,Peripheral blood,GEO,RNA-Seq,Homo sapiens,10|1,DO:A acute leukemia that is characterized by over production of lymphoblasts. DSA10085,GSE163650,GPL20301,1000,Syndromic Biliary Atresia,,Liver,GEO,scRNA-Seq,Homo sapiens,1|1, DSA10086,GSE163650,GPL20301,1000,Alagille Syndrome,C0085280,Liver,GEO,scRNA-Seq,Homo sapiens,1|1,DO:A liver disease that is characterized by an accumulation of bile in the liver resulting from a reducted number of liver small bile ducts. DSA10087,GSE163650,GPL20301,1000,Isolated Biliary Atresia,C0005411,Liver,GEO,scRNA-Seq,Homo sapiens,1|1,DO:A cholestasis characterized by blockage of the ducts that carry bile from the liver to the gallbladder. DSA10088,GSE163652,GPL19057,1000,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,RNA-Seq,Mus musculus,10|12,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA10089,GSE61141,GPL11154,0,Asthma,C0004096,Bronchia,GEO,RNA-Seq,Homo sapiens,6|6,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA10090,GSE61141,GPL11154,0,Asthma,C0004096,Bronchia,GEO,RNA-Seq,Homo sapiens,6|6,"DO:A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing." DSA10091,GSE111708,GPL21273,42,Schizophrenia,C0036341,Prefrontal cortex,GEO,RNA-Seq,Mus musculus,3|6,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA10092,GSE113919,GPL17021,1,Hyperglycemia,C0020456,Brain,GEO,RNA-Seq,Mus musculus,3|2,HPO:An increased concentration of glucose in the blood. DSA10093,GSE116288,GPL21103,341,Lymphoma,C0024299,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA10094,GSE163692,GPL23038,753,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Mus musculus,3|3,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA10095,GSE163707,GPL18573,473,Cytomegalovirus Infection,C0010823,,GEO,RNA-Seq,Homo sapiens,6|6,"EFO:Infection with CYTOMEGALOVIRUS, characterized by enlarged cells bearing intranuclear inclusions. Infection may be in almost any organ, but the salivary glands are the most common site in children, as are the lungs in adults." DSA10096,GSE163752,GPL19057,181,Ischemic Stroke,C0948008,Hemisphere,GEO,RNA-Seq,Mus musculus,6|6,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA10097,GSE163752,GPL19057,441,Ischemic Stroke,C0948008,Hemisphere,GEO,RNA-Seq,Mus musculus,6|6,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA10098,GSE163752,GPL19057,1000,Ischemic Stroke,C0948008,Hemisphere,GEO,RNA-Seq,Mus musculus,6|6,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA10099,GSE163752,GPL19057,1000,Ischemic Stroke,C0948008,Hemisphere,GEO,RNA-Seq,Mus musculus,6|6,DO:A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. DSA10100,GSE163770,GPL21103,1000,Visual Impairment,C3665347,Neural retina,GEO,RNA-Seq,Mus musculus,4|3,"HPO:Visual impairment (or vision impairment) is vision loss (of a person) to such a degree as to qualify as an additional support need through a significant limitation of visual capability resulting from either disease, trauma, or congenital or degenerative conditions that cannot be corrected by conventional means, such as refractive correction, medication, or surgery." DSA10101,GSE163877,GPL17303,33,Alzheimer's Disease,C0002395,Brain,GEO,RNA-Seq,Homo sapiens,3|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10102,GSE163908,GPL24676,935,Idiopathic Pulmonary Fibrosis,C1800706,,GEO,RNA-Seq,Homo sapiens,3|3,DO:A pulmonary fibrosis that is characterized by scarring of the lung. DSA10103,GSE163918,GPL21163,1000,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,Microarray,Mus musculus,3|3,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA10104,GSE163918,GPL21163,536,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,Microarray,Mus musculus,3|3,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA10105,GSE163943,GPL26963,0,Postoperative Delirium,C4721772,Blood,GEO,Microarray,Homo sapiens,4|4, DSA10106,GSE163973,GPL24676,1000,Skin Fibroma,C1333275,Dermis,GEO,scRNA-Seq,Homo sapiens,3|3,NCI:A benign neoplasm arising from the dermis. It is characterized by the presence of spindle-shaped fibroblasts. DSA10107,GSE164006,GPL21103,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,RNA-Seq,Mus musculus,4|4,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA10108,GSE164049,GPL21103,1000,Breast Metastasis,C0346993,Brain,GEO,RNA-Seq,Mus musculus,3|3,"NCI:The spread of a malignant neoplasm to the breast. This may be from a primary breast malignant neoplasm on the opposite side, or from a malignant neoplasm at a distant site." DSA10109,GSE164049,GPL21103,1000,Breast Metastasis,C0346993,Brain,GEO,RNA-Seq,Mus musculus,3|3,"NCI:The spread of a malignant neoplasm to the breast. This may be from a primary breast malignant neoplasm on the opposite side, or from a malignant neoplasm at a distant site." DSA10110,GSE164049,GPL21103,1000,Breast Metastasis,C0346993,Brain,GEO,RNA-Seq,Mus musculus,3|3,"NCI:The spread of a malignant neoplasm to the breast. This may be from a primary breast malignant neoplasm on the opposite side, or from a malignant neoplasm at a distant site." DSA10111,GSE164049,GPL21103,1000,Breast Metastasis,C0346993,Brain,GEO,RNA-Seq,Mus musculus,3|3,"NCI:The spread of a malignant neoplasm to the breast. This may be from a primary breast malignant neoplasm on the opposite side, or from a malignant neoplasm at a distant site." DSA10112,GSE164049,GPL21103,1000,Breast Metastasis,C0346993,Brain,GEO,RNA-Seq,Mus musculus,3|3,"NCI:The spread of a malignant neoplasm to the breast. This may be from a primary breast malignant neoplasm on the opposite side, or from a malignant neoplasm at a distant site." DSA10113,GSE164049,GPL21103,1000,Breast Metastasis,C0346993,Brain,GEO,RNA-Seq,Mus musculus,3|3,"NCI:The spread of a malignant neoplasm to the breast. This may be from a primary breast malignant neoplasm on the opposite side, or from a malignant neoplasm at a distant site." DSA10114,GSE164061,GPL23479,1000,Cardiomyopathy,C0878544,,GEO,RNA-Seq,Mus musculus,3|3,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA10115,GSE164062,GPL23479,1000,Cardiomyopathy,C0878544,,GEO,RNA-Seq,Mus musculus,3|3,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA10116,GSE164063,GPL23479,1000,Cardiomyopathy,C0878544,Embryo,GEO,RNA-Seq,Mus musculus,3|3,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA10117,GSE164064,GPL23479,1000,Cardiomyopathy,C0878544,,GEO,RNA-Seq,Mus musculus,3|3,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA10118,GSE164065,GPL23479,1000,Cardiomyopathy,C0878544,,GEO,RNA-Seq,Mus musculus,3|3,DO:A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. DSA10119,GSE164084,GPL21103,1000,Non-Alcoholic Fatty Liver Disease,C0400966,Liver,GEO,RNA-Seq,Mus musculus,3|3,DO:A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis. DSA10120,GSE116288,GPL21103,551,Lymphoma,C0024299,,GEO,RNA-Seq,Homo sapiens,3|6,DO:A hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs. DSA10121,GSE29006,GPL10999,0,Lung Cancer,C0684249,Lung,GEO,RNA-Seq,Homo sapiens,2|2,DO:A respiratory system cancer that is located_in the lung. DSA10122,GSE7510,GPL570,0,Acute Graft Versus Host Disease,C0856825,Peripheral blood,GEO,Microarray,Homo sapiens,2|2,"MONDO:A syndrome of immunologically mediated tissue damage that may occur following an allogeneic transplant, usually affecting the skin, liver, and GI tract. The onset is usually within one hundred days of transplantation or immunologic manipulation." DSA10123,GSE6054,GPL570,1,Familial Hypercholesterolemia,C0020445,,GEO,Microarray,Homo sapiens,13|6,DO:A familial hyperlipidemia characterized by very high levels of low-density lipoprotein (LDL) and early cardiovascular disease. DSA10124,GSE164120,GPL23126,8,Systemic-Onset Juvenile Idiopathic Arthritis,C0087031,Peripheral blood,GEO,Microarray,Homo sapiens,2|4,"MONDO:Systemic-onset juvenile idiopathic arthritis is marked by the severity of the extra-articular manifestations (fever, cutaneous eruptions) and by an equal sex ratio." DSA10125,GSE164140,GPL10333,89,Systemic Lupus Erythematosus,C0024141,Cortex,GEO,Microarray,Mus musculus,4|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA10126,GSE164140,GPL10333,1000,Systemic Lupus Erythematosus,C0024141,Cortex,GEO,Microarray,Mus musculus,4|4,"DO:A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart." DSA10127,GSE164191,GPL570,1000,Colorectal Carcinoma,C0009402,Peripheral blood,GEO,Microarray,Homo sapiens,62|59,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA10128,GSE164213,GPL16791,1000,Juvenile Idiopathic Arthritis,C3890205,Blood,GEO,RNA-Seq,Homo sapiens,10|12,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA10129,GSE164213,GPL16791,142,Juvenile Idiopathic Arthritis,C3890205,Blood,GEO,RNA-Seq,Homo sapiens,10|10,DO:A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. DSA10130,GSE6054,GPL570,24,Familial Hypercholesterolemia,C0020445,,GEO,Microarray,Homo sapiens,13|4,DO:A familial hyperlipidemia characterized by very high levels of low-density lipoprotein (LDL) and early cardiovascular disease. DSA10131,GSE164264,GPL23227,1000,Acquired Immunodeficiency Syndrome,C0001175,Blood,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA10132,GSE164264,GPL23227,1000,Acquired Immunodeficiency Syndrome,C0001175,Blood,GEO,RNA-Seq,Homo sapiens,2|2,"DO:A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands." DSA10133,GSE164266,GPL18573,89,Chronic Liver Disease,C0341439,Liver,GEO,RNA-Seq,Homo sapiens,5|5,"NCI:Hepatic necrosis, inflammation, or scarring due to any cause that persists for more than 6 months. Manifestations may include signs and symptoms of cholestasis, portal hypertension, and/or abnormal liver function tests." DSA10134,GSE164285,GPL16791,1000,Netherton Syndrome,C0265962,Skin,GEO,RNA-Seq,Homo sapiens,19|9,"DO:A skin disease that is characterized by chronic skin inflammation, trichorrhexis invaginata, atopic dermatitis and has_material_basis_in mutations in the SPINK5 gene resulting in reduced capacity to inhibit serine proteases expressed in the skin." DSA10135,GSE164285,GPL16791,1000,Netherton Syndrome,C0265962,Skin,GEO,RNA-Seq,Homo sapiens,19|9,"DO:A skin disease that is characterized by chronic skin inflammation, trichorrhexis invaginata, atopic dermatitis and has_material_basis_in mutations in the SPINK5 gene resulting in reduced capacity to inhibit serine proteases expressed in the skin." DSA10136,GSE164285,GPL16791,1000,Netherton Syndrome,C0265962,Skin,GEO,RNA-Seq,Homo sapiens,19|5,"DO:A skin disease that is characterized by chronic skin inflammation, trichorrhexis invaginata, atopic dermatitis and has_material_basis_in mutations in the SPINK5 gene resulting in reduced capacity to inhibit serine proteases expressed in the skin." DSA10137,GSE164285,GPL16791,1000,Netherton Syndrome,C0265962,Skin,GEO,RNA-Seq,Homo sapiens,19|4,"DO:A skin disease that is characterized by chronic skin inflammation, trichorrhexis invaginata, atopic dermatitis and has_material_basis_in mutations in the SPINK5 gene resulting in reduced capacity to inhibit serine proteases expressed in the skin." DSA10138,GSE164287,GPL18573,1000,Mycobacterium Tuberculosis,C1834752,,GEO,RNA-Seq,Homo sapiens,4|4, DSA10139,GSE164306,GPL19057,1000,Epilepsy,C0014544,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions." DSA10140,GSE164306,GPL19057,1000,Epilepsy,C0014544,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions." DSA10141,GSE164306,GPL19057,1000,Epilepsy,C0014544,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions." DSA10142,GSE164306,GPL19057,1000,Epilepsy,C0014544,Hippocampus,GEO,RNA-Seq,Mus musculus,4|4,"DO:A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions." DSA10143,GSE164332,GPL18573,3,COVID-19,D8888888,Frontal cortex,GEO,RNA-Seq,Homo sapiens,7|9,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA10144,GSE10950,GPL6104,1000,Colon Tumor,C0009375,Colon,GEO,Microarray,Homo sapiens,24|24,DO:A colorectal cancer that is located_in the colon. DSA10145,GSE164339,GPL19057,1000,Inflammatory Bowel Disease,C0021390,Intestine,GEO,RNA-Seq,Mus musculus,5|6,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA10146,GSE164339,GPL19057,1000,Inflammatory Bowel Disease,C0021390,Intestine,GEO,RNA-Seq,Mus musculus,6|6,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA10147,GSE164339,GPL19057,1000,Inflammatory Bowel Disease,C0021390,Intestine,GEO,RNA-Seq,Mus musculus,5|5,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA10148,GSE164339,GPL19057,1000,Inflammatory Bowel Disease,C0021390,Intestine,GEO,RNA-Seq,Mus musculus,5|6,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA10149,GSE164376,GPL24676,95,Schizophrenia,C0036341,,GEO,RNA-Seq,Homo sapiens,9|7,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA10150,GSE10953,GPL339,0,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,Microarray,Mus musculus,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA10151,GSE164397,GPL20301,579,Infantile Liver Failure,C3809522,Liver,GEO,RNA-Seq,Homo sapiens,2|22,MONDO:Any infantile liver failure in which the cause of the disease is a mutation in the LARS gene. DSA10152,GSE164461,GPL23479,51,Alzheimer's Disease,C0002395,Hippocampus,GEO,RNA-Seq,Mus musculus,7|8,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10153,GSE164461,GPL23479,514,Alzheimer's Disease,C0002395,Hippocampus,GEO,RNA-Seq,Mus musculus,7|7,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10154,GSE164461,GPL23479,5,Alzheimer's Disease,C0002395,Hippocampus,GEO,RNA-Seq,Mus musculus,6|6,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10155,GSE164461,GPL23479,1,Alzheimer's Disease,C0002395,Hippocampus,GEO,RNA-Seq,Mus musculus,7|7,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10156,GSE164485,GPL16791,39,COVID-19,D8888888,Brain,GEO,RNA-Seq,Homo sapiens,5|5,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA10157,GSE164485,GPL16791,14,COVID-19,D8888888,Brain,GEO,RNA-Seq,Homo sapiens,8|10,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA10158,GSE164489,GPL19057,1000,Retinal Diseases,C0035309,Retina,GEO,scRNA-Seq,Mus musculus,1|1,DO:An eye disease that is located_in the retina. DSA10159,GSE164493,GPL20301,1000,Pulmonary Arterial Hypertension,C2973725,,GEO,scRNA-Seq,Homo sapiens,4|3,"EFO:Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease)." DSA10160,GSE164517,GPL13112,1000,Atherosclerosis,C0004153,Liver,GEO,RNA-Seq,Mus musculus,3|4,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA10161,GSE164517,GPL13112,1000,Atherosclerosis,C0004153,Liver,GEO,RNA-Seq,Mus musculus,4|5,DO:An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. DSA10162,GSE164557,GPL24247,1000,Urinary Bladder Inflammation,C0010692,Bladder,GEO,scRNA-Seq,Mus musculus,2|2,DO:A bladder disease that is characterized by inflammation of the bladder. DSA10163,GSE164557,GPL24247,1000,Urinary Bladder Inflammation,C0010692,Bladder,GEO,scRNA-Seq,Mus musculus,2|2,DO:A bladder disease that is characterized by inflammation of the bladder. DSA10164,GSE164558,GPL23479,1000,Inflammatory Bowel Disease,C0021390,Colon,GEO,RNA-Seq,Mus musculus,3|3,DO:An intestinal disease characterized by inflammation located in all parts of digestive tract. DSA10165,GSE164618,GPL23479,9,Alzheimer's Disease,C0002395,Hippocampus,GEO,RNA-Seq,Mus musculus,11|11,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10166,GSE164618,GPL23479,20,Alzheimer's Disease,C0002395,Hippocampus,GEO,RNA-Seq,Mus musculus,10|11,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10167,GSE164618,GPL23479,92,Alzheimer's Disease,C0002395,Hippocampus,GEO,RNA-Seq,Mus musculus,10|11,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10168,GSE164618,GPL23479,85,Alzheimer's Disease,C0002395,Hippocampus,GEO,RNA-Seq,Mus musculus,10|11,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10169,GSE164760,GPL13667,130,Cirrhosis,C1623038,Liver,GEO,Microarray,Homo sapiens,6|8,"MSH:Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury." DSA10170,GSE164760,GPL13667,1000,Non-Alcoholic Steatohepatitis,C3241937,Liver,GEO,Microarray,Homo sapiens,6|74,MONDO:Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure. DSA10171,GSE164760,GPL13667,723,Non-Alcoholic Steatohepatitis;Hepatocellular Carcinoma,,Liver,GEO,Microarray,Homo sapiens,6|53, DSA10172,GSE164760,GPL13667,169,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,29|53,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA10173,GSE164798,GPL19057,1000,Alzheimer's Disease,C0002395,Brain,GEO,RNA-Seq,Mus musculus,4|2,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10174,GSE164798,GPL19057,11,Alzheimer's Disease,C0002395,Brain,GEO,RNA-Seq,Mus musculus,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10175,GSE164798,GPL19057,96,Alzheimer's Disease,C0002395,Brain,GEO,RNA-Seq,Mus musculus,3|4,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10176,GSE164799,GPL16791,1000,Cirrhosis,C1623038,Liver,GEO,RNA-Seq,Homo sapiens,5|4,"MSH:Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury." DSA10177,GSE164805,GPL26963,1000,COVID-19,D8888888,,GEO,Microarray,Homo sapiens,5|5,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA10178,GSE164805,GPL26963,1000,COVID-19,D8888888,,GEO,Microarray,Homo sapiens,5|5,"A Coronavirus infection that is characterized by fever, cough and shortness of breath and that has_material_basis_in SARS-CoV-2." DSA10179,GSE164825,GPL24247,1000,Myotonic Dystrophy,C0027126,Atria,GEO,RNA-Seq,Mus musculus,3|3,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA10180,GSE164825,GPL24247,1000,Myotonic Dystrophy,C0027126,Ventricle,GEO,RNA-Seq,Mus musculus,1|3,"DO:A myotonic disease that is characterized by progressive muscle wasting and weakness affecting the distal skeletal and smooth muscles of lower legs, hands, neck, and face along with myotonia and cataracts and has_material_basis_in the autosomal dominant inheritance of the DMPK gene containing an expansion of a CTG trinucleotide repeat in the non-coding region." DSA10181,GSE164871,GPL20301,1000,Crohn's Disease,C0010346,Colon,GEO,RNA-Seq,Homo sapiens,4|4,"DO:An inflammatory bowel disease characterized by inflammation located_in colon only, has_symptom diarrhea, has_symptom rectal bleeding, has_symptom skin lesions and has_symptom formation of ulcers, fistulas and abscesses around the anus." DSA10182,GSE44337,GPL1261,1000,Imyc B-Lymphoma,,,GEO,Microarray,Mus musculus,3|7, DSA10183,GSE44337,GPL570,1000,Diffuse Large B-Cell Lymphoma,C0079744,,GEO,Microarray,Homo sapiens,3|9,DO:A B-cell lymphoma that is a cancer of B cells presenting as an aggressive tumour which can arise in virtually any part of the body. DSA10184,GSE45267,GPL570,1000,Hepatocellular Carcinoma,C0334287,,GEO,Microarray,Homo sapiens,24|31,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA10185,GSE45267,GPL570,1000,Hepatocellular Carcinoma,C0334287,,GEO,Microarray,Homo sapiens,17|15,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA10186,GSE45516,GPL570,1000,Huntington's Disease,C0020179,,GEO,Microarray,Homo sapiens,3|6,"DO:A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13." DSA10187,GSE45827,GPL570,1000,Breast Cancer,C0678222,,GEO,Microarray,Homo sapiens,10|41,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA10188,GSE45827,GPL570,1000,Breast Cancer,C0678222,,GEO,Microarray,Homo sapiens,10|30,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA10189,GSE45827,GPL570,1000,Breast Cancer,C0678222,,GEO,Microarray,Homo sapiens,10|29,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA10190,GSE45827,GPL570,1000,Breast Cancer,C0678222,,GEO,Microarray,Homo sapiens,10|30,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA10191,GSE10953,GPL339,0,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,Microarray,Mus musculus,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA10192,GSE46687,GPL570,22,Turner Syndrome,C0041408,,GEO,Microarray,Homo sapiens,10|16,DO:A disorder of sexual development that is characterized by a progressive loss of germ cells on the developing gonads of an embryo. DSA10193,GSE46687,GPL570,1000,Turner Syndrome,C0041408,,GEO,Microarray,Homo sapiens,10|10,DO:A disorder of sexual development that is characterized by a progressive loss of germ cells on the developing gonads of an embryo. DSA10194,GSE48521,GPL570,0,Obesity,C0028754,,GEO,Microarray,Homo sapiens,8|8,"DO:An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness." DSA10195,GSE10953,GPL339,0,Amyotrophic Lateral Sclerosis,C0002736,Spinal cord,GEO,Microarray,Mus musculus,3|3,"DO:A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing." DSA10196,GSE50161,GPL570,1000,Brain Tumor,C0006118,Brain,GEO,Microarray,Homo sapiens,13|34,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA10197,GSE10913,GPL1261,436,Infertile,C0021359,Uterus,GEO,Microarray,Mus musculus,3|3,EFO:Inability to reproduce after a specified period of unprotected intercourse. Reproductive sterility is permanent infertility. DSA10198,GSE50161,GPL570,1000,Brain Tumor,C0006118,Brain,GEO,Microarray,Homo sapiens,13|15,DO:A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain. DSA10199,GSE10789,GPL3779,0,Adult T-Cell Leukemia,C0023493,,GEO,Microarray,Homo sapiens,3|3,"DO:A T-cell acute leukemia that results_in abnormal increase of lymphocytes, derives_from T-cells, has_material_basis_in Human T-lymphotropic virus 1 (HTLV-1), which is transmitted_by sexual contact, transmitted_by contaminated needles used by intravenous-drug users, and transmitted_by breast feeding. The infection results_in_formation_of skin lesions." DSA10200,GSE10774,GPL6569,803,Head And Neck Squamous Cell Carcinoma,C1168401,,GEO,Microarray,Homo sapiens,4|10,"DO:A head and neck carcinoma that has_material_basis_in squamous cells that line the moist, mucosal surfaces inside the head and neck." DSA10201,GSE17114,GPL570,0,Behcet's Disease,C0004943,,GEO,Microarray,Homo sapiens,14|15,"DO:A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis." DSA10202,GSE10500,GPL8300,911,Rheumatoid Arthritis,C0003873,Synovial fluid,GEO,Microarray,Homo sapiens,3|5,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA10203,GSE17679,GPL570,1000,Ewing Sarcoma,C0553580,,GEO,Microarray,Homo sapiens,18|44,"DO:A connective tissue cancer that has_material_basis_in neural crest cells derives_from undeveloped, undifferentiated neuroectoderm." DSA10204,GSE18309,GPL570,0,Alzheimer's Disease,C0002395,,GEO,Microarray,Homo sapiens,3|3,"DO:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21." DSA10205,GSE18309,GPL570,0,Cognitive Impairment,C0338656,,GEO,Microarray,Homo sapiens,3|3,"HPO:Abnormal cognition with deficits in thinking, reasoning, or remembering." DSA10206,GSE18462,GPL570,0,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,4|2,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA10207,GSE18462,GPL570,0,Colorectal Carcinoma,C0009402,Liver,GEO,Microarray,Homo sapiens,2|2,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA10208,GSE18520,GPL570,1000,Papillary Serous Ovarian Adenocarcinomas,,,GEO,Microarray,Homo sapiens,10|53, DSA10209,GSE8507,GPL570,1000,Hyper-Ige Syndrome,C3887645,,GEO,Microarray,Homo sapiens,17|17,DO:A hyper IgE syndrome that has_material_basis_in heterozygous mutation in the STAT3 gene on chromosome 17q21. DSA10210,GSE8507,GPL570,1000,Hyper-Ige Syndrome,C3887645,,GEO,Microarray,Homo sapiens,18|18,DO:A hyper IgE syndrome that has_material_basis_in heterozygous mutation in the STAT3 gene on chromosome 17q21. DSA10211,GSE8507,GPL570,1000,Hyper-Ige Syndrome,C3887645,,GEO,Microarray,Homo sapiens,18|18,DO:A hyper IgE syndrome that has_material_basis_in heterozygous mutation in the STAT3 gene on chromosome 17q21. DSA10212,GSE19650,GPL570,1000,Intraductal Papillary Adenocarcinoma,C0334372,Pancreas,GEO,Microarray,Homo sapiens,7|12,NCI:Breast ductal carcinoma in situ characterized by the presence of filiform arborizing fibrovascular cores lined by neoplastic ductal epithelium. (WHO 2019) DSA10213,GSE19650,GPL570,44,Intraductal Papillary Adenocarcinoma,C0334372,Pancreas,GEO,Microarray,Homo sapiens,12|3,NCI:Breast ductal carcinoma in situ characterized by the presence of filiform arborizing fibrovascular cores lined by neoplastic ductal epithelium. (WHO 2019) DSA10214,GSE5839,GPL96,0,Multiple Sclerosis,C0026769,Brain,GEO,Microarray,Homo sapiens,1|3,DO:A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. DSA10215,GSE19728,GPL570,0,Astrocytoma,C0004114,,GEO,Microarray,Homo sapiens,4|2,"DO:A malignant glioma that is has_material_basis_in astrocyte cells, a type of star-shaped glial cell, located in the brain and spinal cord." DSA10216,GSE19728,GPL570,1000,Astrocytoma,C0004114,,GEO,Microarray,Homo sapiens,4|5,"DO:A malignant glioma that is has_material_basis_in astrocyte cells, a type of star-shaped glial cell, located in the brain and spinal cord." DSA10217,GSE19728,GPL570,1000,Astrocytoma,C0004114,,GEO,Microarray,Homo sapiens,4|5,"DO:A malignant glioma that is has_material_basis_in astrocyte cells, a type of star-shaped glial cell, located in the brain and spinal cord." DSA10218,GSE19728,GPL570,1000,Astrocytoma,C0004114,,GEO,Microarray,Homo sapiens,4|4,"DO:A malignant glioma that is has_material_basis_in astrocyte cells, a type of star-shaped glial cell, located in the brain and spinal cord." DSA10219,GSE19750,GPL570,1000,Adrenocortical Carcinoma,C0206686,,GEO,Microarray,Homo sapiens,4|44,DO:An adrenal cortex cancer that forms in the outer layer of tissue of the adrenal gland and that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA10220,GSE19776,GPL570,933,Adrenocortical Carcinoma,C1859973,,GEO,Microarray,Homo sapiens,4|44,DO:An adrenal cortex cancer that forms in the outer layer of tissue of the adrenal gland and that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA10221,GSE10072,GPL96,618,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Homo sapiens,4|8,DO:A respiratory system cancer that is located_in the lung. DSA10222,GSE19826,GPL570,0,Gastric Cancer,C0699791,Stomach,GEO,Microarray,Homo sapiens,3|2,DO:A gastrointestinal system cancer that is located_in the stomach. DSA10223,GSE19826,GPL570,0,Gastric Cancer,C0699791,Stomach,GEO,Microarray,Homo sapiens,3|3,DO:A gastrointestinal system cancer that is located_in the stomach. DSA10224,GSE19826,GPL570,1,Gastric Cancer,C0699791,Stomach,GEO,Microarray,Homo sapiens,3|3,DO:A gastrointestinal system cancer that is located_in the stomach. DSA10225,GSE19826,GPL570,0,Gastric Cancer,C0699791,Stomach,GEO,Microarray,Homo sapiens,3|3,DO:A gastrointestinal system cancer that is located_in the stomach. DSA10226,GSE19882,GPL570,0,Diffuse Large B-Cell Lymphoma,C0079744,,GEO,Microarray,Homo sapiens,2|2,DO:A B-cell lymphoma that is a cancer of B cells presenting as an aggressive tumour which can arise in virtually any part of the body. DSA10227,GSE19882,GPL570,0,Peripheral T-Cell Lymphoma,C0079774,,GEO,Microarray,Homo sapiens,2|1,DO:A mature T-cell and NK-cell lymphoma includes a group of T-cell lymphomas that develop away from the thymus. DSA10228,GSE19963,GPL570,2,Hyperplastic Polyposis Syndrome,C4296896,Colon,GEO,Microarray,Homo sapiens,2|2,"MONDO:Hyperplastic polyposis syndrome is a rare, genetic intestinal disease characterized by the presence of multiple (usually large) hyperplastic/serrated colorectal polyps, usually with a pancolonic distribution. Histology reveals hyperplastic polyps, sessile serrated adenomas (most common), traditional serrated adenomas or mixed polyps. It is associated with an increased personal and familial (first-degree relatives) risk of colorectal cancer." DSA10229,GSE19963,GPL570,9,Hyperplastic Polyposis Syndrome,C4296896,Colon,GEO,Microarray,Homo sapiens,2|2,"MONDO:Hyperplastic polyposis syndrome is a rare, genetic intestinal disease characterized by the presence of multiple (usually large) hyperplastic/serrated colorectal polyps, usually with a pancolonic distribution. Histology reveals hyperplastic polyps, sessile serrated adenomas (most common), traditional serrated adenomas or mixed polyps. It is associated with an increased personal and familial (first-degree relatives) risk of colorectal cancer." DSA10230,GSE20141,GPL570,0,Parkinson's Disease,C0030567,Substantia nigra,GEO,Microarray,Homo sapiens,8|10,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA10231,GSE20146,GPL570,0,Parkinson's Disease,C0030567,Brain,GEO,Microarray,Homo sapiens,9|10,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA10232,GSE20153,GPL570,0,Parkinson's Disease,C0030567,,GEO,Microarray,Homo sapiens,8|8,DO:An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31. DSA10233,GSE21138,GPL570,0,Schizophrenia,C0036341,,GEO,Microarray,Homo sapiens,29|30,DO:A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness. DSA10234,GSE21354,GPL570,1000,Diffuse Astrocytoma,C0280785,,GEO,Microarray,Homo sapiens,4|5,"DO:A malignant glioma that is has_material_basis_in astrocyte cells, a type of star-shaped glial cell, located in the brain and spinal cord." DSA10235,GSE21354,GPL570,1000,Ependymoma,C0014474,,GEO,Microarray,Homo sapiens,4|4,"EFO:A well-differentiated (WHO grade II), diffusely infiltrating neuroglial tumor, typically located in the cerebral hemispheres. It is composed predominantly of cells which morphologically resemble oligodendroglia. The neoplastic cells have rounded homogeneous nuclei and, on paraffin sections, a swollen, clear cytoplasm ('honeycomb' appearance). (Adapted from WHO)" DSA10236,GSE21354,GPL570,1000,Oligodendroglioma,C0028945,,GEO,Microarray,Homo sapiens,4|5,"EFO:A well-differentiated (WHO grade II), diffusely infiltrating neuroglial tumor, typically located in the cerebral hemispheres. It is composed predominantly of cells which morphologically resemble oligodendroglia. The neoplastic cells have rounded homogeneous nuclei and, on paraffin sections, a swollen, clear cytoplasm ('honeycomb' appearance). (Adapted from WHO)" DSA10237,GSE21411,GPL570,124,Interstitial Lung Disease,C0206062,Lung,GEO,Microarray,Homo sapiens,6|23,"DO:A lung disease that is characterized by inflammation and altered lung interstitium compromising pulmonary function and often has_symptom shortness of breath, dyspnea, and/or cough." DSA10238,GSE22242,GPL570,0,Colorectal Carcinoma,C0009402,,GEO,Microarray,Homo sapiens,1|4,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA10239,GSE22356,GPL570,1000,Scleroderma,C0011644,,GEO,Microarray,Homo sapiens,10|10,"DO:A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies." DSA10240,GSE22356,GPL570,0,Scleroderma;Pulmonary Hypertension,,,GEO,Microarray,Homo sapiens,10|10, DSA10241,GSE22356,GPL570,0,Pulmonary Hypertension,C0020542,,GEO,Microarray,Homo sapiens,10|8,"DO:A hypertension characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein or pulmonary capillaries." DSA10242,GSE22840,GPL570,1000,Infiltrating Ductal Carcinoma,C1134719,Breast,GEO,Microarray,Homo sapiens,4|14,DO:A breast ductal carcinoma that is characterized by infiltration into the fibrous or fatty tissue of the breast outside of the duct where it originated. DSA10243,GSE22840,GPL570,0,Infiltrating Ductal Carcinoma,C1134719,Breast,GEO,Microarray,Homo sapiens,14|2,DO:A breast ductal carcinoma that is characterized by infiltration into the fibrous or fatty tissue of the breast outside of the duct where it originated. DSA10244,GSE23066,GPL570,0,Non-Small Cell Lung Cancer,C0007131,,GEO,Microarray,Homo sapiens,5|4,DO:A respiratory system cancer that is located_in the lung. DSA10245,GSE23604,GPL570,1000,Cutaneous T Cell Lymphoma,C0079773,,GEO,Microarray,Homo sapiens,5|6,DO:A non-Hodgkin's lymphoma that has_material_basis_in a mutation of T cells. DSA10246,GSE10072,GPL96,1000,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Homo sapiens,11|13,DO:A respiratory system cancer that is located_in the lung. DSA10247,GSE25427,GPL570,0,Epithelial Ovarian Cancer,C0677886,Ovary,GEO,Microarray,Homo sapiens,21|13,DO:A female reproductive organ cancer that is located_in the ovary. DSA10248,GSE25429,GPL570,0,Epithelial Ovarian Cancer,C0677886,Ovary,GEO,Microarray,Homo sapiens,21|13,DO:A female reproductive organ cancer that is located_in the ovary. DSA10249,GSE25462,GPL570,0,Type 2 Diabetes,C0011860,Skeletal muscle,GEO,Microarray,Homo sapiens,13|10,"DO:A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin." DSA10250,GSE25487,GPL570,1000,Breast Cancer,C0678222,,GEO,Microarray,Homo sapiens,9|10,DO:A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA10251,GSE137511,GPL17586,1000,Colorectal Carcinoma,C0009402,Colon,GEO,Microarray,Homo sapiens,4|4,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA10252,GSE10072,GPL96,1000,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Homo sapiens,12|16,DO:A respiratory system cancer that is located_in the lung. DSA10253,GSE143025,GPL16570,1000,Multiple Myeloma,C0026764,,GEO,Microarray,Mus musculus,3|3,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA10254,GSE10072,GPL96,1000,Lung Tumor,C0242379,Lung,GEO,Microarray,Homo sapiens,49|58,DO:A lung cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells and is located_in the lungs and has_symptom cough and has_symptom chest discomfort or pain and has_symptom weight loss and has_symptom hemoptysis. DSA10255,GSE10760,GPL96,175,Facioscapulohumeral Dystrophy,C0238288,Muscle,GEO,Microarray,Homo sapiens,60|38,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA10256,GSE10760,GPL97,107,Facioscapulohumeral Dystrophy,C0238288,Muscle,GEO,Microarray,Homo sapiens,60|38,DO:A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. DSA10257,GSE10072,GPL96,1000,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Homo sapiens,18|16,DO:A respiratory system cancer that is located_in the lung. DSA10258,GSE10072,GPL96,632,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Homo sapiens,4|3,DO:A respiratory system cancer that is located_in the lung. DSA10259,GSE12021,GPL97,31,Rheumatoid Arthritis,C0003873,Synovium,GEO,Microarray,Homo sapiens,4|12,DO:An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint. DSA10260,GSE12021,GPL97,20,Osteoarthritis,C0157946,Synovium,GEO,Microarray,Homo sapiens,4|10,DO:An arthritis that has_material_basis_in worn out cartilage located_in joint. DSA10261,GSE13591,GPL96,11,Monoclonal Gammopathy of Undetermined Significance,C0026470,,GEO,Microarray,Homo sapiens,5|11,DO:A blood protein disease that is characterized by the presence of an abnormal protein called monoclonal protein in the blood. DSA10262,GSE13591,GPL96,311,Multiple Myeloma,C0026764,,GEO,Microarray,Homo sapiens,5|133,DO:A myeloid neoplasm that is located_in the plasma cells in bone marrow. DSA10263,GSE13591,GPL96,1000,Plasma Cell Leukemia,C0023484,,GEO,Microarray,Homo sapiens,5|9,DO:A plasma cell neoplasm that is characterized by the presence of a circulating clonal plasma cell count that exceeds 2x10^9/L or is 20% of the leukocyte differential count. DSA10264,GSE14323,GPL571,1000,Hepatocellular Carcinoma,C0334287,Liver,GEO,Microarray,Homo sapiens,19|38,"DO:A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers." DSA10265,GSE14323,GPL571,1000,Cirrhosis,C1623038,Liver,GEO,Microarray,Homo sapiens,19|41,"MSH:Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury." DSA10266,GSE15641,GPL96,1000,Clear Cell Renal Cell Carcinoma,C0007134,Kidney,GEO,Microarray,Homo sapiens,23|32,DO:A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney. DSA10267,GSE15641,GPL96,1000,Papillary Renal Cell Carcinoma,C1306837,Kidney,GEO,Microarray,Homo sapiens,23|11,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA10268,GSE15641,GPL96,1000,Transitional Cell Tumor,C0334265,Kidney,GEO,Microarray,Homo sapiens,23|8,DO:A carcinoma that derives_from transitional epithelial cells. DSA10269,GSE15641,GPL96,1000,Chromophobe Renal Cell Carcinoma,C1266042,Kidney,GEO,Microarray,Homo sapiens,23|6,"DO:A renal cell carcinoma that has_material_basis_in chromophobe cell that appear pale when viewed under microscope, but that are larger and display different features than clear cells." DSA10270,GSE15641,GPL96,1000,Kidney Oncocytoma,C0346255,Kidney,GEO,Microarray,Homo sapiens,23|12,"EFO:A benign tumor of the kidney, characterized by the presence of large cells with abundant eosinophilic granular cytoplasm. The majority of these tumors are discovered incidentally, during work-up of other conditions." DSA10271,GSE16873,GPL96,0,Simple Ductal Hyperplasia,,Breast,GEO,Microarray,Homo sapiens,12|4, DSA10272,GSE16873,GPL96,5,Atypical Ductal Hyperplasia,C1332347,Breast,GEO,Microarray,Homo sapiens,12|12,EFO:Atypical ductal hyperplasia is an atypical proliferative lesion that falls in between the continuum from normal hyperplasia to low grade ductal carcinoma in situ. DSA10273,GSE16873,GPL96,72,Ductal Carcinoma In Situ,C0007124,Breast,GEO,Microarray,Homo sapiens,12|12,"EFO:A malignant tumor arising from epithelial cells. Carcinomas that arise from glandular epithelium are called adenocarcinomas, those that arise from squamous epithelium are called squamous cell carcinomas, and those that arise from transitional epithelium are called transitional cell carcinomas. Morphologically, the malignant epithelial cells may display abnormal mitotic figures, anaplasia, and necrosis. Carcinomas are graded by the degree of cellular differentiation as well, moderately, or poorly differentiated. Carcinomas invade the surrounding tissues and tend to metastasize to other anatomic sites. Lung carcinoma, skin carcinoma, breast carcinoma, colon carcinoma, and prostate carcinoma are the most frequently seen carcinomas." DSA10274,GSE18155,GPL96,1000,Malignant Germ Cell Tumor,C4048549,,GEO,Microarray,Homo sapiens,3|17,DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from germ cells. DSA10275,GSE18155,GPL96,1000,Malignant Germ Cell Tumor,C4048549,,GEO,Microarray,Homo sapiens,4|8,DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from germ cells. DSA10276,GSE18155,GPL96,1000,Seminoma,C0036631,Testis,GEO,Microarray,Homo sapiens,4|12,DO:A germinoma that has_material_basis_in cells that make sperm and eggs. DSA10277,GSE23400,GPL96,1000,Esophageal Squamous Cell Carcinoma,C0279626,Esophagus,GEO,Microarray,Homo sapiens,53|53,DO:An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus. DSA10278,GSE23400,GPL97,1000,Esophageal Squamous Cell Carcinoma,C0279626,Esophagus,GEO,Microarray,Homo sapiens,51|51,DO:An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus. DSA10279,GSE27155,GPL96,244,Follicular Thyroid Carcinoma,C0206682,Thyroid,GEO,Microarray,Homo sapiens,4|13,DO:A differentiated thyroid gland carcinoma that has_material_basis_in follicular cells. DSA10280,GSE27155,GPL96,184,Follicular Thyroid Adenoma,C0151468,Thyroid,GEO,Microarray,Homo sapiens,4|10,DO:An endocrine organ benign neoplasm that is located_in the thyroid and derives_from glandular epithelial cells. DSA10281,GSE27155,GPL96,1000,Thyroid Oncocytic Adenoma,C1336750,Thyroid,GEO,Microarray,Homo sapiens,4|7,HPO:A kind of thyroid adenoma characterized by the presence of oxyphil cells. DSA10282,GSE27155,GPL96,569,Thyroid Oncocytic Carcinoma,C0749424,Thyroid,GEO,Microarray,Homo sapiens,4|8,"DO:A thyroid gland follicular carcinoma that is characterized by the presence of large cells with eosinophilic granular cytoplasm and pleomorphic nuclei with prominent, eosinophilic nucleoli." DSA10283,GSE27155,GPL96,1000,Papillary Thyroid Carcinoma,C0238463,Thyroid,GEO,Microarray,Homo sapiens,4|51,"DO:An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue." DSA10284,GSE27155,GPL96,1000,Anaplastic Thyroid Carcinoma,C0238461,Thyroid,GEO,Microarray,Homo sapiens,4|2,DO:A thyroid gland carcinoma that is composed of undifferentiated cells. DSA10285,GSE27155,GPL96,1000,Anaplastic Thyroid Carcinoma,C0238461,Thyroid,GEO,Microarray,Homo sapiens,4|2,DO:A thyroid gland carcinoma that is composed of undifferentiated cells. DSA10286,GSE27155,GPL96,1000,Medullary Thyroid Carcinoma,C0238462,Thyroid,GEO,Microarray,Homo sapiens,4|2,DO:A thyroid gland carcinoma that has_material_basis_in parafollicular cells. DSA10287,GSE29272,GPL96,1000,Cancer of The Gastric Cardia,C1333763,Stomach,GEO,Microarray,Homo sapiens,134|72,MONDO:A carcinoma that arises from epithelial cells of the cardia of stomach. DSA10288,GSE29272,GPL96,1000,Cancer of The Gastric Cardia,C1333763,Stomach,GEO,Microarray,Homo sapiens,134|62,MONDO:A carcinoma that arises from epithelial cells of the cardia of stomach. DSA10289,GSE31547,GPL96,1000,Lung Adenocarcinoma,C0152013,Lung,GEO,Microarray,Homo sapiens,20|30,DO:A respiratory system cancer that is located_in the lung. DSA10290,GSE32269,GPL96,1000,Prostate Cancer,C0600139,Prostate,GEO,Microarray,Homo sapiens,4|51,DO:A prostate cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. DSA10291,GSE37023,GPL96,1000,Gastric Tumor,C0038356,Stomach,GEO,Microarray,Homo sapiens,39|112,DO:A gastrointestinal system cancer that is located_in the stomach. DSA10292,GSE37023,GPL97,1000,Gastric Tumor,C0038356,Stomach,GEO,Microarray,Homo sapiens,36|29,DO:A gastrointestinal system cancer that is located_in the stomach. DSA10293,GSE41258,GPL96,1000,Colorectal Carcinoma,C0009402,Colorectum,GEO,Microarray,Homo sapiens,54|186,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA10294,GSE41258,GPL96,1000,Colorectal Carcinoma,C0009402,Liver,GEO,Microarray,Homo sapiens,13|47,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA10295,GSE41258,GPL96,1000,Colorectal Carcinoma,C0009402,Lung,GEO,Microarray,Homo sapiens,7|20,DO:A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa. DSA10296,GSE43176,GPL96,552,Acute Myeloid Leukemia,C0023467,,GEO,Microarray,Homo sapiens,4|104,DO:A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. DSA10297,GSE43290,GPL96,1000,Meningioma,C0025286,Meninges,GEO,Microarray,Homo sapiens,4|47,DO:A central nervous system cancer that are manifested in the central nervous system and arise from the arachnoid cap cells of the arachnoid villi in the meninges. DSA10298,GSE46517,GPL96,1000,Melanoma,C0025202,,GEO,Microarray,Homo sapiens,7|31,"DO:A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from melanocytes which are found in skin, the bowel and the eye." DSA10299,GSE6008,GPL96,1000,Ovarian Tumor,C1140680,Ovary,GEO,Microarray,Homo sapiens,4|8,DO:A female reproductive organ cancer that is located_in the ovary. DSA10300,GSE6008,GPL96,1000,Ovarian Tumor,C1140680,Ovary,GEO,Microarray,Homo sapiens,4|37,DO:A female reproductive organ cancer that is located_in the ovary. DSA10301,GSE6008,GPL96,1000,Ovarian Tumor,C1140680,Ovary,GEO,Microarray,Homo sapiens,4|13,DO:A female reproductive organ cancer that is located_in the ovary. DSA10302,GSE6008,GPL96,1000,Ovarian Tumor,C1140680,Ovary,GEO,Microarray,Homo sapiens,4|41,DO:A female reproductive organ cancer that is located_in the ovary. DSA10303,GSE6280,GPL96,758,Kidney Tumor,C0022665,Kidney,GEO,Microarray,Homo sapiens,6|14,DO:A urinary system cancer that is located_in the kidney. DSA10304,GSE6280,GPL97,337,Kidney Tumor,C0022665,Kidney,GEO,Microarray,Homo sapiens,6|14,DO:A urinary system cancer that is located_in the kidney. DSA10305,GSE6344,GPL96,1000,Clear Cell Ependymoma,C1384403,Kidney,GEO,Microarray,Homo sapiens,5|5,"EFO:A WHO grade II, slow growing tumor of children and young adults, usually located intraventricularly. It is the most common ependymal neoplasm. It often causes clinical symptoms by blocking cerebrospinal fluid pathways. Key histological features include perivascular pseudorosettes and ependymal rosettes. (WHO)" DSA10306,GSE6344,GPL96,1000,Clear Cell Ependymoma,C1384403,Kidney,GEO,Microarray,Homo sapiens,5|5,"EFO:A WHO grade II, slow growing tumor of children and young adults, usually located intraventricularly. It is the most common ependymal neoplasm. It often causes clinical symptoms by blocking cerebrospinal fluid pathways. Key histological features include perivascular pseudorosettes and ependymal rosettes. (WHO)"