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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: Hypopigmentation (D017496)
..Starting node ..Raindrop Hypopigmentation (C566724)
Child Nodes:
Sister Nodes:
..Albinism (D000417) 30
..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) 11
..Yemenite deaf-blind hypopigmentation syndrome (C536771)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

9590

Name:

Raindrop Hypopigmentation

Definition:

Alternative IDs:

ParentIDs:

MESH:D017496

TreeNumbers:

C17.800.621.440/C566724

Synonyms:

Slim Mappings:

Skin disease

Reference:

MedGen: C566724
MeSH: C566724
OMIM: 179500;

Genes:

Phenotypes

1	HP:0000006	Autosomal dominant inheritance
2	HP:0001010	Hypopigmentation of the skin

Disease Causing ClinVar Variants