Autosomal dominant nonsyndromic hearing loss 15

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the POU4F3 gene.

Also known as: DFNA15, POU4F3 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 15, autosomal dominant nonsyndromic deafness 15, autosomal dominant nonsyndromic deafness caused by mutation in POU4F3, autosomal dominant nonsyndromic deafness type 15, deafness, autosomal dominant 15, deafness, autosomal dominant type 15

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