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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 6 (DOID:0110584)
Synonyms: autosomal dominant deafness 6; autosomal dominant deafness 14; autosomal dominant deafness 38; DFNA6; DFNA14; DFNA38
Alt IDs: OMIM:600965, ICD10CM:H90.3, ORDO:90635
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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/14/2017
MGI 6.08
The Jackson Laboratory