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Summary Literature (8)
DOID:898 - autosomal dominant polycystic kidney disease


Disease Ontology Definition:A polycystic kidney disease characterized by the presence of multiple cysts located_in the kidney resulting from ciliopathy that disrupts the function of primary cilium, inherited in an autosomal dominant fashion.

Synonyms: Congenital biliary ectasias, POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1

Referenced OMIM:

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

Xenbase Genes : pkd2, pkd1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant disease (is_a)


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Version: 4.15.0
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