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.
Comprehensive, easy-to-understand information about this condition
Checking for content...
autosomal dominant nonsyndromic hearing loss 1
MONDO:0007424
autosomal dominant nonsyndromic hearing loss 2A
MONDO:0010817
autosomal dominant nonsyndromic hearing loss 4A
MONDO:0010915
autosomal dominant nonsyndromic hearing loss 6
MONDO:0010963
autosomal dominant nonsyndromic hearing loss 5
MONDO:0010973
autosomal dominant nonsyndromic hearing loss 10
MONDO:0011031