Human genes for autosomal dominant Wolfram syndrome
Autosomal dominant Wolfram syndrome [DOID:0080584]
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.
Synonyms: autosomal dominant Wolfram syndrome, autosomal dominant Wolfram disease, autosomal dominant Wolfram disorder, autosomal dominant Wolfram syndromes, DOID:0080584