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DOID:9562 - primary ciliary dyskinesia
Disease Ontology Definition:A ciliopathy that is characterized by impaired function of the cilia lining the respiratory tract (lower and upper, sinuses, Eustachian tube, middle ear) and fallopian tube.
Synonyms: ciliary motility disorder, immotile ciliary syndrome,
Xenbase Genes
:
spag1,
foxj1,
dnah5,
dnai2,
odad3,
foxj1.2,
dnah1,
ccdc103,
cfap300,
dnaaf11,
dnah11,
dnaaf4,
gas2l2,
zmynd10,
gas8,
| MONDO:0016575 - primary ciliary dyskinesia |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
ciliopathy (is_a)