Autosomal dominant nonsyndromic hearing loss 13

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the COL11A2 gene.

Also known as: COL11A2 autosomal dominant nonsyndromic deafness, DFNA13, autosomal dominant deafness 13, autosomal dominant nonsyndromic deafness 13, autosomal dominant nonsyndromic deafness caused by mutation in COL11A2, autosomal dominant nonsyndromic deafness type 13, deafness, autosomal dominant 13, deafness, autosomal dominant type 13

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 13 itself.