Autosomal dominant nonsyndromic hearing loss 56

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the TNC gene.

Also known as: DFNA56, TNC autosomal dominant nonsyndromic deafness, autosomal dominant deafness 56, autosomal dominant nonsyndromic deafness 56, autosomal dominant nonsyndromic deafness caused by mutation in TNC, autosomal dominant nonsyndromic deafness type 56, deafness, autosomal dominant 56, deafness, autosomal dominant type 56

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 56 itself.