Term Name:	autosomal recessive nonsyndromic deafness 59
Synonyms:	autosomal recessive deafness 59, DFNB59
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 DFNB59 gene on chromosome 2q31.
Ontology:	Human Disease [DOID:0110511]   ( DOID:0110511 )