Autosomal dominant nonsyndromic hearing loss 36

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the TMC1 gene.

Also known as: DFNA36, TMC1 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 36, autosomal dominant nonsyndromic deafness 36, autosomal dominant nonsyndromic deafness caused by mutation in TMC1, autosomal dominant nonsyndromic deafness type 36, deafness, autosomal dominant 36, deafness, autosomal dominant type 36

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 36 itself.