Autosomal dominant nonsyndromic hearing loss 18

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 3q22.

Also known as: DFNA18, autosomal dominant deafness 18, autosomal dominant nonsyndromic deafness 18, autosomal dominant nonsyndromic deafness type 18, deafness, autosomal dominant 18

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