Deafness, Autosomal Dominant 58 (DFNA58)

Deafness, Autosomal Dominant 58, also known as autosomal dominant nonsyndromic deafness 58, is related to autosomal dominant nonsyndromic deafness and contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a. An important gene associated with Deafness, Autosomal Dominant 58 is DFNA58 (Deafness, Autosomal Dominant 58), and among its related pathways/superpathways is Sensory processing of sound. Related phenotypes are tinnitus and hearing impairment