Disease Information

GTO ID(s) GTC0228 | GTC0275 | GTC0185 | GTC1661
Disease NameAmyloid Neuropathy
Synonymscharcot-marie-tooth disease type 3, agenesis of the corpus callosum with peripheral neuropathy, charcot-marie-tooth disease type 1a, charcot-marie-tooth disease type 1f, charcot-marie-tooth disease type 1d, charcot-marie-tooth disease type 1c, charcot-marie-tooth disease type 1b, charcot-marie-tooth disease type 1e, charcot-marie-tooth disease type 2a1, charcot-marie-tooth disease type 2a2, charcot-marie-tooth disease type 2b1, charcot-marie-tooth disease type 2j, charcot-marie-tooth disease type 2i, charcot-marie-tooth disease type 2b, charcot-marie-tooth disease axonal type 2t, charcot-marie-tooth disease type 2r, charcot-marie-tooth disease axonal type 2f, charcot-marie-tooth disease type 2d, charcot-marie-tooth disease type 2e, charcot-marie-tooth disease axonal type 2h, charcot-marie-tooth disease axonal type 2k, charcot-marie-tooth disease type 2y, charcot-marie-tooth disease axonal type 2p, charcot-marie-tooth disease axonal type 2q, charcot-marie-tooth disease axonal type 2u, charcot-marie-tooth disease axonal type 2l, charcot-marie-tooth disease axonal type 2o, charcot-marie-tooth disease axonal type 2n, charcot-marie-tooth disease type 2b2, charcot-marie-tooth disease axonal type 2c, charcot-marie-tooth disease type 4c, charcot-marie-tooth disease type 4j, charcot-marie-tooth disease type 4a, charcot-marie-tooth disease type 4d, charcot-marie-tooth disease type 4k, charcot-marie-tooth disease type 4b2, charcot-marie-tooth disease type 4b1, charcot-marie-tooth disease type 4h, charcot-marie-tooth disease type 4f, charcot-marie-tooth disease type 4b3, charcot-marie-tooth disease type 4e, charcot-marie-tooth disease type 4g, charcot-marie-tooth disease dominant intermediate b, charcot-marie-tooth disease recessive intermediate c, charcot-marie-tooth disease dominant intermediate c, charcot-marie-tooth disease dominant intermediate d, charcot-marie-tooth disease dominant intermediate a, charcot-marie-tooth disease recessive intermediate d, charcot-marie-tooth disease recessive intermediate b, charcot-marie-tooth disease dominant intermediate e, charcot-marie-tooth disease dominant intermediate f, charcot-marie-tooth disease x-linked dominant 6, charcot-marie-tooth disease x-linked recessive 2, charcot-marie-tooth disease x-linked dominant 1, charcot-marie-tooth disease x-linked recessive 5, charcot-marie-tooth disease x-linked recessive 3, charcot-marie-tooth disease x-linked recessive 4, charcot-marie-tooth disease, motor peripheral neuropathy, charcot-marie-tooth disease, axonal, type 2t, d鑼卝鑼卹ine-sottas disease, hereditary motor and sensory neuropathy, roussy-levy syndrome, hypertrophic neuropathy of infancy, hereditary motor and sensory neuropathy, types i-iv, peroneal muscular atrophy (axonal type) (hypertrophic type), dejerine-sottas disease, hereditary, type vii, motor and sensory neuropathy, hereditary sensory and motor neuropathy, hereditary motor and sensory neuropathies, hereditary motor and sensory neuropathy type iii, hmsn3, cmt3, charcot-marie-tooth disease, type 3, hypertrophic neuropathy of dejerine-sottas, dejerine-sottas neuropathy, dejerine-sottas syndrome
DefinitionDO:A Charcot-Marie-Tooth disease that is characterized by motor and sensory peripheral neuropathies caused by demyelination.
Xref DO:0050540 | DO:0090003 | DO:0110148 | DO:0110149 | DO:0110150 | DO:0110151 | DO:0110152 | DO:0110153 | DO:0110154 | DO:0110155 | DO:0110156 | DO:0110157 | DO:0110158 | DO:0110159 | DO:0110160 | DO:0110161 | DO:0110163 | DO:0110164 | DO:0110165 | DO:0110166 | DO:0110167 | DO:0110168 | DO:0110169 | DO:0110170 | DO:0110173 | DO:0110174 | DO:0110175 | DO:0110177 | DO:0110179 | DO:0110182 | DO:0110183 | DO:0110184 | DO:0110185 | DO:0110186 | DO:0110187 | DO:0110190 | DO:0110191 | DO:0110192 | DO:0110193 | DO:0110194 | DO:0110195 | DO:0110196 | DO:0110197 | DO:0110198 | DO:0110199 | DO:0110200 | DO:0110202 | DO:0110203 | DO:0110204 | DO:0110205 | DO:0110206 | DO:0110207 | DO:0110208 | DO:0110209 | DO:0110210 | DO:0110211 | DO:0110212 | DO:10595 | DO:2477 | MIM:145900 | NCI:C133087 | EFO:0009162 | MONDO:0000902 | MONDO:0007307 | MONDO:0007308 | MONDO:0007309 | MONDO:0007311 | MONDO:0007790 | MONDO:0008961 | MONDO:0010479 | MONDO:0010549 | MONDO:0010550 | MONDO:0010551 | MONDO:0010689 | MONDO:0010699 | MONDO:0010949 | MONDO:0010995 | MONDO:0011066 | MONDO:0011085 | MONDO:0011091 | MONDO:0011113 | MONDO:0011475 | MONDO:0011527 | MONDO:0011534 | MONDO:0011569 | MONDO:0011570 | MONDO:0011633 | MONDO:0011674 | MONDO:0011675 | MONDO:0011687 | MONDO:0011889 | MONDO:0011890 | MONDO:0011894 | MONDO:0011901 | MONDO:0011902 | MONDO:0011903 | MONDO:0011909 | MONDO:0011916 | MONDO:0012012 | MONDO:0012096 | MONDO:0012231 | MONDO:0012250 | MONDO:0012640 | MONDO:0013212 | MONDO:0013338 | MONDO:0013644 | MONDO:0013753 | MONDO:0013758 | MONDO:0013959 | MONDO:0014012 | MONDO:0014074 | MONDO:0014117 | MONDO:0014154 | MONDO:0014208 | MONDO:0014467 | MONDO:0014566 | MONDO:0014733 | MONDO:0014735 | MONDO:0014866 | MSH:D015417 | OMIM:145900 | ORDO:64748
Disease GroupGenetic Disease

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