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Summary Literature (3)
DOID:0110859 - polycystic kidney disease 2


Disease Ontology Definition:A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD2 gene on chromosome 4q22.1.

Synonyms: Apkd2, Pkd2, Polycystic Kidney Disease, Adult, Type II

Xenbase Genes : pkd2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013131 - polycystic kidney disease 2

OMIM:
OMIM:613095 - POLYCYSTIC KIDNEY DISEASE 2 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE; PKD2

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant polycystic kidney disease (is_a)