Autosomal dominant nonsyndromic hearing loss 12

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

Also known as: autosomal dominant nonsyndromic hearing loss 12, DFNA12, DFNA8, TECTA autosomal dominant nonsyndromic deafness, autosomal dominant deafness 12, autosomal dominant deafness 8, autosomal dominant nonsyndromic deafness 12, autosomal dominant nonsyndromic deafness caused by mutation in TECTA

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