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.
Also Known As:
Oxaluria, Primary; Hyperoxaluria, Primary; Primary Oxalosis; Primary Oxaluria; Hyperoxalurias, Primary; Oxaloses, Primary; Oxalosis, Primary; Oxalurias, Primary; Primary Hyperoxalurias; Primary Oxaloses; Primary Oxalurias