Autosomal recessive nonsyndromic hearing loss 12
Autosomal recessive nonsyndromic hearing loss 12
Definition
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 — per MONDO