Autosomal dominant nonsyndromic hearing loss 9

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

Also known as: COCH autosomal dominant nonsyndromic deafness, DFNA9, autosomal dominant deafness 9, autosomal dominant nonsyndromic deafness 9, autosomal dominant nonsyndromic deafness caused by mutation in COCH, autosomal dominant nonsyndromic deafness type 9, deafness, autosomal dominant 9, deafness, autosomal dominant type 9

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