Term Name:	Wolfram syndrome 1
Synonyms:	diabetes mellitus AND insipidus with optic atrophy AND deafness, WFS1
Definition:	An autosomal recessive disease that is characterized by diabetes mellitus, optic atrophy, and deafness as well as various other possible disorders and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the WFS1 gene on chromosome 4p16.1.
Ontology:	Human Disease [DOID:0110629]   ( DOID:0110629 )