Deafness, Autosomal Dominant 50 (DFNA50)

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