autosomal dominant polycystic kidney disease

Summary

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

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: pkd2, pkd1, ganab

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0004691 - autosomal dominant polycystic kidney disease

MONDO:0004691 - autosomal dominant polycystic kidney disease

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), polycystic kidney disease (is_a)