Deafness, Autosomal Dominant 85 (DFNA85)

Alias:

Dfna85

Hearing Loss, Autosomal Dominant 85

Deafness, Autosomal Dominant, 85

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 85, is also known as dfna85. An important gene associated with Deafness, Autosomal Dominant 85 is USP48 (Ubiquitin Specific Peptidase 48). Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and cochlear nerve hypoplasia

Related ID：

MALACARDS：DFN400

OMIM：620227

MESH：D006319