Autosomal recessive nonsyndromic hearing loss 12

MONDO:0011067

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the CDH23 gene on chromosome 10q22.

Also known as: autosomal recessive nonsyndromic hearing loss 12, DFNB12, autosomal recessive deafness 12, autosomal recessive nonsyndromic deafness 12, autosomal recessive nonsyndromic deafness type 12, deafness, autosomal recessive 12, deafness, autosomal recessive 12, modifier of, deafness, autosomal recessive type 12

60 clinical trials for this condition and its sub-types.

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