Term Name:	autosomal recessive nonsyndromic deafness 12
Synonyms:	autosomal recessive deafness 12, DFNB12
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.
Ontology:	Human Disease [DOID:0110467]   ( DOID:0110467 )