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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 6 (DOID:0110584)
Alliance: disease page
Synonyms: autosomal dominant deafness 6; autosomal dominant deafness 14; autosomal dominant deafness 38; DFNA6; DFNA6/14/38; DFNA14; DFNA38
Alt IDs: OMIM:600965, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and low frequency progressive hearing loss and has_material_basis_in mutation in the WFS1 gene on chromosome 4p16.

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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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory