DISEASES

Disease-gene associations mined from literature

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,  DFNB12,  autosomal recessive deafness 12