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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Alopecia (D000505)
Parent Node: Nails, Malformed (D009264)
Parent Node: Vitiligo (D014820)
..Starting node ..Alopecia universalis onychodystrophy vitiligo (C537056)
Child Nodes:
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)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	460
Name:	Alopecia universalis onychodystrophy vitiligo
Definition:
Alternative IDs:
ParentIDs:	MESH:D000505\|MESH:D009264\|MESH:D014820
TreeNumbers:	C17.800.329.937.122/C537056 \|C17.800.621.440.895/C537056 \|C23.300.035/C537056 \|C23.300.820/C537056
Synonyms:	Alopecia universalis, onychodystrophy, and total vitiligo
Slim Mappings:	Pathology (anatomical condition)\|Skin disease
Reference:	MedGen: C537056 MeSH: C537056 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants