Disease Browser
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Parent Node: Intellectual Disability (D008607) | Parent Node: Skin Diseases, Genetic (D012873) | Parent Node: Vitiligo (D014820) | ..Starting node ..Vitiligo, Progressive, with Mental Retardation and Urethral Duplication (C564739)
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Sister Nodes: | ..Alopecia universalis onychodystrophy vitiligo (C537056)
| ..AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:607836)
| ..AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 2 (OMIM:608391)
| ..AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 3 (OMIM:608392)
| ..AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 4 (OMIM:609400)
| ..Deafness, Congenital, with Vitiligo and Achalasia (C565642)
| ..Schrander-Stumpel Theunissen Hulsmans syndrome (C536639)
| ..Spastic paraplegia 23 (C536859)
| ..Vitiligo, Progressive, with Mental Retardation and Urethral Duplication (C564739)
| ..VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (OMIM:606579)
| ..VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 (OMIM:193200)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 11642 |
Name: | Vitiligo, Progressive, with Mental Retardation and Urethral Duplication |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D008607|MESH:D012873|MESH:D014820 |
TreeNumbers: | C10.597.606.643/C564739 |C16.320.850/C564739 |C17.800.621.440.895/C564739 |C17.800.827/C564739 |C23.888.592.604.646/C564739 |F03.550.600/C564739 |
Synonyms: | |
Slim Mappings: | Genetic disease (inborn)|Mental disorder|Nervous system disease|Signs and symptoms|Skin disease |
Reference: |
MedGen: C564739
MeSH: C564739
OMIM: 277465;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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