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Disease Ontology Browser
Wolfram syndrome 1 (DOID:0110629)
Alliance: disease page
Synonyms: diabetes mellitus AND insipidus with optic atrophy AND deafness; DIDMOAD; WFS1
Alt IDs: OMIM:222300, ICD10CM:E13.8
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.

Disease References using Mouse Models (10)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
01/31/2023
MGI 6.22
The Jackson Laboratory