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Summary Literature (14)
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

Referenced OMIM:

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : spag1, dnah5, dnai2, ccdc103, cfap300, lrrc6, dnah11, zmynd10, ccno, hydin, armc4, dnal1, ccdc40, ccdc39, dnaaf6, [+]

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): X-linked recessive disease (is_a), ciliopathy (is_a)

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