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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:

Xenbase Genes : agxt, grhpr.1, hoga1, grhpr.2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0002474 - primary hyperoxaluria


Other Model Organisms: AGR, 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)