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Hyperoxaluria, Primary

A genetic disorder characterized by excretion of large amounts of OXALATES in urine; NEPHROLITHIASIS; NEPHROCALCINOSIS; early onset of RENAL FAILURE; and often a generalized deposit of CALCIUM OXALATE. There are subtypes classified by the enzyme defects in glyoxylate metabolism.

Drugs by status

Approved for this indication (2)

Phase 2 trials (2)

Phase 1 trials (1)

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