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
|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)