Autosomal dominant nonsyndromic hearing loss 22

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYO6 gene.

Also known as: DFNA22, MYO6 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 22, autosomal dominant nonsyndromic deafness 22, autosomal dominant nonsyndromic deafness caused by mutation in MYO6, autosomal dominant nonsyndromic deafness type 22, deafness, autosomal dominant 22, deafness, autosomal dominant 22, with hypertrophic cardiomyopathy

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