Autosomal dominant nonsyndromic hearing loss 66

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the CD164 gene.

Also known as: CD164 autosomal dominant nonsyndromic deafness, DFNA66, autosomal dominant deafness 66, autosomal dominant nonsyndromic deafness 66, autosomal dominant nonsyndromic deafness caused by mutation in CD164, autosomal dominant nonsyndromic deafness type 66, deafness, autosomal dominant 66, deafness, autosomal dominant type 66

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 66 itself.