|OBO ID: DOID:0080584|
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|Term Name:||autosomal dominant Wolfram syndrome||Search Ontology:|
|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|
|Ontology:||Human Disease (DOID:0080584)|
|is a type of:||