autosomal recessive nonsyndromic deafness 39

Summary

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: autosomal recessive deafness 39, DFNB39

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: hgf

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012003 - autosomal recessive nonsyndromic hearing loss 39

MONDO:0012003 - autosomal recessive nonsyndromic hearing loss 39

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive nonsyndromic deafness (is_a)