Autosomal dominant nonsyndromic hearing loss 6

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the WFS1 gene.

Also known as: DFNA14, DFNA38, DFNA6, WFS1 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 14, autosomal dominant deafness 38, autosomal dominant deafness 6, autosomal dominant nonsyndromic deafness 6

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