DOID:0110497 - autosomal recessive nonsyndromic deafness 39
Disease Ontology 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.
Synonyms: DFNB39, autosomal recessive deafness 39
|OMIM:608265 - DEAFNESS, AUTOSOMAL RECESSIVE 39; DFNB39|
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes : hgf
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD