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:
Ontology: Human Disease   (DOID:0080584)
OTHER autosomal dominant Wolfram syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
WFS1 Wolfram-like syndrome, autosomal dominant 614296
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None