Related MeSH Hierarchy (5)
Diseases [C] » Urogenital Diseases [C12] » Female Urogenital Diseases and Pregnancy Complications » Female Urogenital Diseases » Urologic Diseases » Kidney Diseases » Hyperoxaluria » Hyperoxaluria, Primary
Diseases [C] » Urogenital Diseases [C12] » Male Urogenital Diseases » Urologic Diseases » Kidney Diseases » Hyperoxaluria » Hyperoxaluria, Primary
Diseases [C] » Urogenital Diseases [C12] » Urologic Diseases » Kidney Diseases » Hyperoxaluria » Hyperoxaluria, Primary
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Metabolism, Inborn Errors » Carbohydrate Metabolism, Inborn Errors » Hyperoxaluria, Primary
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Carbohydrate Metabolism, Inborn Errors » Hyperoxaluria, Primary
Description
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. MeSH
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Approved Indicated Drugs (2)
Phase 3 Indicated Drugs (1)
Phase 2 Indicated Drugs (2)
Organization Involved with Phase 3 Indications (5)
Organization Involved with Phase 2 Indications (4)
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UMLS Data
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