Primary hyperoxaluria type 3
MONDO:0013327Primary hyperoxaluria type 3 (PH3) is a disorder of glyoxylate metabolism that can be asymptomatic or characterized by oxalate nephrolithiasis.
Also known as: HOGA1 primary hyperoxaluria, primary hyperoxaluria caused by mutation in HOGA1, primary hyperoxaluria type III, HP3, PH III, hyperoxaluria, primary, type 3, hyperoxaluria, primary, type III
2 clinical trials for this condition and its sub-types.
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Disease
(680)
Metabolic disease
(233)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Human disease
(14)
Primary hyperoxaluria
(12)
Carbohydrate metabolism disease
(3)
Disease of genetic or genomic mechanism
(2)
Inborn carbohydrate metabolic disorder
(2)
Disease by developmental or physiological process
(0)