Autosomal dominant nonsyndromic hearing loss 25

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the SLC17A8 gene.

Also known as: DFNA25, SLC17A8 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 25, autosomal dominant nonsyndromic deafness 25, autosomal dominant nonsyndromic deafness caused by mutation in SLC17A8, autosomal dominant nonsyndromic deafness type 25, deafness, autosomal dominant 25, deafness, autosomal dominant type 25

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