Autosomal recessive nonsyndromic hearing loss 66

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the DCDC2 gene.

Also known as: DCDC2 autosomal recessive nonsyndromic deafness, DFNB66, autosomal recessive deafness 66, autosomal recessive nonsyndromic deafness 66, autosomal recessive nonsyndromic deafness caused by mutation in DCDC2, autosomal recessive nonsyndromic deafness type 66, deafness, autosomal recessive 66, deafness, autosomal recessive type 66

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