autosomal dominant Wolfram syndrome (DOID:0080584)
Alliance: disease page
Alt IDs: OMIM:614296
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.