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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,
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MIM:613095 - polycystic kidney disease 2; pkd2 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee