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DOID:0110861 - autosomal recessive 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 recessive fashion.
Synonyms: Arpkd, Pkhd1, Polycystic Kidney Disease, Infantile, Type I, Polycystic Kidney and Hepatic Disease 1,
Xenbase Genes : pkhd1, dzip1l
MONDO:0009889 - autosomal recessive polycystic kidney disease |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee