Autosomal dominant nonsyndromic hearing loss 50

An autosomal dominant nonsyndromic deafness that is characterized postlingual onset in the second decade of life with flat progressive hearing loss and has material basis in mutation in the MIRN96 gene on chromosome 7q32.

Also known as: DFNA50, autosomal dominant deafness 50, autosomal dominant nonsyndromic deafness 50, autosomal dominant nonsyndromic deafness type 50, deafness, autosomal dominant type 50, deafness, autosomal dominant 50

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 50 itself.