Deafness, Autosomal Dominant 79 (DFNA79)

Deafness, Autosomal Dominant 79, also known as dfna79, is related to autosomal dominant nonsyndromic deafness 79. An important gene associated with Deafness, Autosomal Dominant 79 is SCD5 (Stearoyl-CoA Desaturase 5). Affiliated tissues include brain, and related phenotypes are progressive sensorineural hearing impairment and abnormal vestibular function