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Summary Literature (11)
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,

Xenbase Genes : tgfbr1, pou3f4, tjp2, six1, met, lmx1a, tecta.2, esrrb, slc44a4, eya4, grhl2, gjb3, smpx, kitlg, ror1, [+]

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019497 - nonsyndromic genetic hearing loss

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): auditory system disease (is_a)