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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,
Echinobase Genes : pcdh15, pou4f3, tbc1d24, myo7a, otof, kars1, whrn, pnpt1, six1, msrb3
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)