Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Echinobase
Summary Literature (0)
DOID:2977 - primary hyperoxaluria

Disease Ontology Definition:A carbohydrate metabolic disorder characterized by impaired glyoxylate metabolism resulting in accumulation of oxalate throughout the body typically manifesting as kidney and bladder stones.

Synonyms:

Echinobase Genes : hoga1, agxt


MIM:
MIM:260000 - hyperoxaluria, primary, type ii; hp2
MIM:613616 - hyperoxaluria, primary, type iii; hp3

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): carbohydrate metabolic disorder (is_a), kidney disease (is_a)