ZFIN Human Disease: autosomal dominant Wolfram syndrome

OBO ID: DOID:0080584

Term Name:	autosomal dominant Wolfram syndrome		Search Ontology:
Synonyms:
Definition:	A Wolfram syndrome that is characterized by congenital progressive hearing impairment, diabetes mellitus, and optic atrophy and that has_material_basis_in autosomal dominant inheritance of a heterozygous mutation in the WFS1 gene on chromosome 4p16. https://www.ncbi.nlm.nih.gov/pubmed/18544103
References:	OMIM:614296
Ontology:	Human Disease ( DOID:0080584 )

Relationships

is a type of:	autosomal dominant disease Wolfram syndrome autosomal dominant disease Wolfram syndrome Show first 5 Terms

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Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
WFS1	wfs1b wfs1a	Wolfram-like syndrome, autosomal dominant	614296

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None