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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,
Echinobase Genes : rsph1, ccdc39, dnai2, dnaaf5, dnaaf3, cfap298, rsph9, dnal1, zmynd10, drc1, armc4, spag1, ccdc103, dnah5, dnai1
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
ciliopathy (is_a)