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