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Summary Literature (0)
DOID:0111672 - primary hyperoxaluria type 3

Disease Ontology Definition:A primary hyperoxaluria characterized by recurring calcium oxalate stones that has_material_basis_in homozygous or compound heterozygous mutation in the HOGA1 gene on chromosome 10q24.2.

Synonyms: HP3, PH III, primary hyperoxaluria type III

Xenbase Genes : hoga1



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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): primary hyperoxaluria (is_a)