autosomal recessive nonsyndromic deafness 12 (DOID:0110467)
Alliance: disease page
Synonyms: autosomal recessive deafness 12; DFNB12
Alt IDs: OMIM:601386, ICD10CM:H90.3
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.