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autosomal dominant nonsyndromic deafness 50 (DOID:0110576)
Alliance: disease page
Synonyms: autosomal dominant deafness 50; DFNA50
Alt IDs: OMIM:613074, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized postlingual onset in the second decade of life with flat progressive hearing loss and has_material_basis_in mutation in the MIRN96 gene on chromosome 7q32.

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