Autoimmune disease, susceptibility to, 1

Preferred Label : Autoimmune disease, susceptibility to, 1;

Symbol : AIS1;

CISMeF acronym : AIS1; VAMAS2;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Vitiligo-associated multiple autoimmune disease susceptibility 2; VAMAS2; Autoimmune disease susceptibility locus, chromosome 1p-related;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the forkhead box D3 gene (FOXD3, 611539.0001);

Prefixed ID : #607836;

Details

Origin ID

607836;

UMLS CUI

C1842979;

Genes related to phenotype
- Forkhead box d3 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Hashimoto thyroiditis [HPO term]
- Vitiligo [HPO term]
ORDO concept(s)
- Vitiligo-associated autoimmune disease [ORDO Disease]
Semantic type(s)
- Finding [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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