Autosomal dominant nonsyndromic hearing loss 11

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYO7A gene.

Also known as: DFNA11, MYO7A autosomal dominant nonsyndromic deafness, autosomal dominant deafness 11, autosomal dominant nonsyndromic deafness 11, autosomal dominant nonsyndromic deafness caused by mutation in MYO7A, autosomal dominant nonsyndromic deafness type 11, deafness, autosomal dominant 11, deafness, autosomal dominant type 11

60 clinical trials for this condition and its sub-types.