DOID:0050563 - nonsyndromic deafness
Disease Ontology Definition:An auditory system disease that is associated with permanent hearing loss caused by damage to structures in the inner ear and/or the middle ear, which is not associated with other signs and symptoms.
Synonyms: nonsyndromic hearing loss, nonsyndromic hereditary hearing loss
|MONDO:0019497 - nonsyndromic genetic deafness|
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes : tgfbr1, pou3f4, tjp2, six1, met, lmx1a, tecta.2, esrrb, slc44a4, eya4, grhl2, gjb3, smpx, kitlg, ror1,
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): auditory system disease (is_a)