Disease-gene associations mined from literature

Human genes for Wolfram syndrome

Wolfram syndrome [DOID:10632]

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 gene encoding wolframin (WFS1).

Synonyms:  Wolfram syndrome,  DOID:10632,  Wolfram disease,  Wolfram disorder,  DIDMOAD ...

Linkouts:  OMIM #1 #2 #3