Autosomal dominant nonsyndromic hearing loss 51

An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the fourth decade of life with high frequency progressive hearing loss and has material basis in a 269-kb duplication of chromosome 9q21.11 involving the TJP2 and FAM189A2 genes.

Also known as: chromosome 9q21.11 duplication syndrome, DFNA51, autosomal dominant deafness 51, autosomal dominant nonsyndromic deafness 51, autosomal dominant nonsyndromic deafness type 51, chromosome 9Q21.11 Duplication syndrome, deafness, autosomal dominant 51, deafness, autosomal dominant type 51

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 51 itself.