Autosomal dominant nonsyndromic hearing loss 21

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 6p24.1-p22.3.

Also known as: DFNA21, autosomal dominant deafness 21, autosomal dominant nonsyndromic deafness 21, autosomal dominant nonsyndromic deafness type 21, deafness, autosomal dominant 21

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