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DOID:898 - autosomal dominant polycystic kidney disease
Disease Ontology Definition:An autosomal dominant disease characterized by the presence of multiple cysts located_in the kidney resulting from ciliopathy that disrupts the function of primary cilium.
Synonyms: Congenital biliary ectasias, POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1,
Echinobase Genes : pkd2
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a)