Deafness, Autosomal Dominant 50 (DFNA50)

Alias:

Autosomal Dominant Nonsyndromic Deafness 50

Dfna50

Autosomal Dominant Nonsyndromic Hearing Loss 50

Deafness, Autosomal Dominant, Type 50

Autosomal Dominant Deafness 50

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 50, also known as autosomal dominant nonsyndromic deafness 50, is related to posterior uveal melanoma and deafness, autosomal dominant 18. An important gene associated with Deafness, Autosomal Dominant 50 is MIR96 (MicroRNA 96). Related phenotypes are tinnitus and sensorineural hearing impairment

Related ID：

MALACARDS：DFN119

OMIM：613074