Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (9)
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


In Mondo Disease Ontology:
MONDO:0004691 - autosomal dominant polycystic kidney disease

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

Xenbase Genes : pkd2, pkd1, ganab

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