Human genes for autosomal recessive nonsyndromic deafness 12
Autosomal recessive nonsyndromic deafness 12 [DOID:0110467]
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.
Synonyms: autosomal recessive nonsyndromic deafness 12, DOID:0110467, autosomal recessive deafness 12, DFNB12