Primary hyperoxaluria
MONDO:0002474A hereditary disorder characterized by excessive oxalate production, leading to hyperoxaluria.
Also known as: hyperoxaluria, primary, primary hyperoxaluria
16 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Broader categories
Disease
(680)
Metabolic disease
(233)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Human disease
(14)
Carbohydrate metabolism disease
(3)
Disease of genetic or genomic mechanism
(2)
Inborn carbohydrate metabolic disorder
(2)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)