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autosomal dominant nonsyndromic deafness 48 (DOID:0110571)
Alliance: disease page
Synonyms: autosomal dominant deafness 48; DFNA48
Alt IDs: OMIM:607841, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with progressive hearing loss and has_material_basis_in variation in the chromosome region 12q13-q14.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory