Autosomal dominant nonsyndromic hearing loss 44

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the CCDC50 gene.

Also known as: CCDC50 autosomal dominant nonsyndromic deafness, DFNA44, autosomal dominant deafness 44, autosomal dominant nonsyndromic deafness 44, autosomal dominant nonsyndromic deafness caused by mutation in CCDC50, autosomal dominant nonsyndromic deafness type 44, deafness, autosomal dominant 44, deafness, autosomal dominant type 44

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 44 itself.