Autosomal dominant nonsyndromic hearing loss 23

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the SIX1 gene.

Also known as: DFNA 23, DFNA23, SIX1 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 23, autosomal dominant nonsyndromic deafness 23, autosomal dominant nonsyndromic deafness caused by mutation in SIX1, autosomal dominant nonsyndromic deafness type 23, deafness, autosomal dominant 23

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