| GTO ID(s) | GTC0249 |
| Disease Name | Esophagus Sarcoma |
| Synonyms | cutis aplasia, aplasia cutis congenita, congenital absence of skin, absence of part of skin at birth, aplasia cutis congenita (disease), ectodermal dysplasia, hidrotic ectodermal dysplasia, anhydrotic ectodermal dysplasias, acc, aplasia cutis congenita, nonsyndromic, congenital defect of skull and scalp |
| Definition | HPO:A developmental defect resulting in the congenital absence of skin in multiple or solitary non-inflammatory, well-demarcated, oval or circular ulcers with a diameter of about 1 to 2 cm. Aplasia cutis congenita most commonly occurs on the scalp, but may present in the face, trunk, or limbs. |
| Xref | NCI:C5341 | NCI:C98822 | HPO:HP:0001057 | MONDO:0007145 | MSH:D004476 | OMIM:107600 | ORDO:1114 | UMLS_CUI:C1333466 |
| Disease Group | Cancer |