Autosomal dominant nonsyndromic hearing loss 31

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 6p21.3.

Also known as: DFNA31, autosomal dominant deafness 31, autosomal dominant nonsyndromic deafness 31, autosomal dominant nonsyndromic deafness type 31, deafness, autosomal dominant 31

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 31 itself.