Autosomal dominant nonsyndromic hearing loss 49

An autosomal dominant nonsyndromic deafness that is characterized by moderate loss for low and mid frequencies and mild loss for high frequencies and has material basis in variation in the chromosome region 1q21-q23.

Also known as: DFNA49, autosomal dominant deafness 49, autosomal dominant nonsyndromic deafness 49, autosomal dominant nonsyndromic deafness type 49, deafness, autosomal dominant 49

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 49 itself.