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autosomal dominant polycystic kidney disease (DOID:898)
Alliance: disease page
Synonyms: Congenital biliary ectasias; POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1
Alt IDs: ICD10CM:Q61.3, ICD9CM:753.12, MESH:D007690, NCI:C75464, OMIM:PS173900, ORDO:730, UMLS_CUI:C0022680
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.

Disease References using Mouse Models (43)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/13/2019
MGI 6.13
The Jackson Laboratory