Term Name:	autosomal recessive nonsyndromic deafness 39
Synonyms:	autosomal recessive deafness 39, DFNB39
Definition:	An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has_material_basis_in mutation in the HGF gene on chromosome 7q21.
Ontology:	Human Disease [DOID:0110497]   ( DOID:0110497 )