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.
Year introduced: 1991(1987)
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Subheadings:
Tree Number(s): C12.050.351.968.419.313.500, C12.200.777.419.313.500, C12.950.419.313.500, C16.320.565.202.460, C18.452.648.202.460
MeSH Unique ID: D006960
Entry Terms:
- Hyperoxalurias, Primary
- Primary Hyperoxalurias
- Oxaluria, Primary
- Oxalurias, Primary
- Primary Oxalurias
- Primary Hyperoxaluria
- Primary Oxaluria
- Primary Oxalosis
- Oxaloses, Primary
- Oxalosis, Primary
- Primary Oxaloses