Term Name:	autosomal dominant Wolfram syndrome
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.
Ontology:	Human Disease [DOID:0080584]   ( DOID:0080584 )