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autosomal dominant nonsyndromic deafness 44 (DOID:0110569)
Alliance: disease page
Synonyms: autosomal dominant deafness 44; DFNA44
Alt IDs: OMIM:607453, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized postlingual onset with low to mild frequency progressive hearing loss and has_material_basis_in mutation in the CCDC50 gene on chromosome 3q28.


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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
12/05/2017
MGI 6.11
The Jackson Laboratory