DOID:0110526 - autosomal recessive nonsyndromic deafness 79
Disease Ontology 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 TPRN gene on chromosome 9q34.
Synonyms: DFNB79, autosomal recessive deafness 79
Xenbase Genes : tprn
|MONDO:0013215 - autosomal recessive nonsyndromic hearing loss 79|
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee