Autosomal recessive nonsyndromic hearing loss 53

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

Also known as: COL11A2 autosomal recessive nonsyndromic deafness, DFNB53, autosomal recessive deafness 53, autosomal recessive nonsyndromic deafness 53, autosomal recessive nonsyndromic deafness caused by mutation in COL11A2, autosomal recessive nonsyndromic deafness type 53, deafness, autosomal recessive 53, deafness, autosomal recessive type 53

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 53 itself.