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Disease Ontology Browser
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 Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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12/10/2024
MGI 6.24 		The Jackson Laboratory