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Echinobase
Summary Literature (0)
DOID:0110629 - Wolfram syndrome 1

Disease Ontology 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.

Synonyms: WFS1,

Echinobase Genes :


OMIM:
OMIM:222300 - wolfram syndrome 1; wfs1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Wolfram syndrome (is_a)