Autosomal dominant nonsyndromic hearing loss 16

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 2q23-q24.3.

Also known as: DFNA16, autosomal dominant deafness 16, autosomal dominant nonsyndromic deafness 16, autosomal dominant nonsyndromic deafness type 16, deafness, autosomal dominant 16

60 clinical trials for this condition and its sub-types.