autosomal recessive nonsyndromic deafness 39 (DOID:0110497)
Alliance: disease page
Synonyms: autosomal recessive deafness 39; DFNB39
Alt IDs: OMIM:608265, ICD10CM:H90.3
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.