Disease Browser
Parent Node: Hypopigmentation (D017496) ..Starting node Vitiligo (D014820) Child 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) Sister Nodes: ..Albinism (D000417) ..External Ophthalmoplegia, Synergistic Divergence, Jaw Winking, and Oculocutaneous Hypopigmentation (C566509) ..Hernandez Fragoso syndrome (C536062) ..HYPOMELANOSIS OF ITO (OMIM:300337) ..Leukonychia totalis (C535889) ..Raindrop Hypopigmentation (C566724) ..Vitiligo (D014820) ..Yemenite deaf-blind hypopigmentation syndrome (C536771) UMLS . MedGen , OMIM , CTD
Term ID: 11639 Name: Vitiligo Definition: A disorder consisting of areas of macular depigmentation, commonly on extensor aspects of extremities, on the face or neck, and in skin folds. Age of onset is often in young adulthood and the condition tends to progress gradually with lesions enlarging and extending until a quiescent state is reached. Alternative IDs: ParentIDs: MESH:D017496 TreeNumbers: C17.800.621.440.895 Synonyms: Slim Mappings: Skin disease Reference:
MedGen: D014820
MeSH: D014820 OMIM: 193200 ; Genes: Phenotypes Disease Causing ClinVar Variants
Vitiligo 
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