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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: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
auditory system disease (is_a)