Disease Browser
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Parent Node: Genetic Diseases, X-Linked (D040181) | Parent Node: Hypertrichosis (D006983) | ..Starting node ..Hypertrichosis congenital generalized X-linked (C538388)
| Child Nodes:
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Sister Nodes: | ..Acromegaloid facial appearance syndrome (C535655)
| ..Amaurosis hypertrichosis (C536604)
| ..Ambras syndrome (C536605)
| ..Barber Say syndrome (C537908)
| ..CAHMR syndrome (C537959)
| ..Cantu syndrome (C535572)
| ..Cervical hypertrichosis neuropathy (C537956)
| ..Cervical Hypertrichosis with Underlying Kyphoscoliosis (C566142)
| ..Congenital hypertrichosis lanuginosa (C538389)
| ..Facial Hypertrichosis (C565029)
| ..Fibromatosis, Gingival, with Hypertrichosis and Mental Retardation (C565331)
| ..Gorlin Chaudhry Moss syndrome (C537290)
| ..Hairy Ears (C562484)
| ..Hairy Ears, Y-Linked (C564029)
| ..Hairy elbows (C535618)
| ..Hairy nose tip (C535619)
| ..Hypertrichosis congenital generalized X-linked (C538388)
| ..Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia (C565016)
| ..Hypertrichosis, anterior cervical (C538390)
| ..Hypertrichosis, Congenital Anterior Cervical, with Peripheral Sensory and Motor Neuropathy (C565492)
| ..Hypertrichosis, hyperkeratosis, mental retardation, and distinctive facial features (C538391)
| ..Midphalangeal hair (C537471)
| ..Muller Barth Menger syndrome (C537370)
| ..Oliver-McFarlane syndrome (C536554)
| ..Ramon Syndrome (C535285)
| ..Schaap Taylor Baraitser syndrome (C536626)
| ..Wiedemann Grosse Dibbern syndrome (C536704)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 5510 |
Name: | Hypertrichosis congenital generalized X-linked |
Definition: | |
Alternative IDs: | OMIM:307150 |
ParentIDs: | MESH:D006983|MESH:D040181 |
TreeNumbers: | C16.320.322/C538388 |C17.800.329.875/C538388 |
Synonyms: | CGH |CHROMOSOME Xq27.1 INTERCHROMOSOMAL INSERTION SYNDROME |HCG |HTC2 |Hypertrichosis, Congenital Generalized |Macias-Flores Garcia-Cruz Rivera syndrome |
Slim Mappings: | Genetic disease (inborn)|Skin disease |
Reference: |
MedGen: C538388
MeSH: C538388
OMIM: 307150;
Genes: AF8T; | Phenotypes | | Disease Causing ClinVar Variants | |
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