Autosomal dominant nonsyndromic hearing loss 3B

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the GJB6 gene.

Also known as: DFNA3B, GJB6 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 3B, autosomal dominant nonsyndromic deafness 3B, autosomal dominant nonsyndromic deafness caused by mutation in GJB6, autosomal dominant nonsyndromic deafness type 3B, deafness, autosomal dominant 3B, deafness, autosomal dominant 3b

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 3B itself.