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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.
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Phase 3 trials (2)
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Organization Involved with Phase 3 Indications (5)
Organization Involved with Phase 2 Indications (4)