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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:0002474 - primary hyperoxaluria |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee