Autosomal recessive nonsyndromic hearing loss 32

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in variation in the chromosome region 1p22.1-p13.3.

Also known as: CDC14A autosomal recessive nonsyndromic deafness, DFNB105, DFNB32, autosomal recessive deafness 105, autosomal recessive deafness 32, autosomal recessive nonsyndromic deafness 105, autosomal recessive nonsyndromic deafness 32, autosomal recessive nonsyndromic deafness caused by mutation in CDC14A

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 32 itself.