Autosomal dominant nonsyndromic hearing loss 20

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the ACTG1 gene.

Also known as: ACTG1 autosomal dominant nonsyndromic deafness, DFNA20, DFNA26, autosomal dominant deafness 20, autosomal dominant nonsyndromic deafness 20, autosomal dominant nonsyndromic deafness caused by mutation in ACTG1, autosomal dominant nonsyndromic deafness type 20, deafness, autosomal dominant 20

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