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... > Urogenital Diseases > Female Urogenital Diseases and Pregnancy Complications > Female Urogenital Diseases > Urologic Diseases > Kidney Diseases > Hyperoxaluria > Hyperoxaluria, Primary
... > Urogenital Diseases > Male Urogenital Diseases > Urologic Diseases > Kidney Diseases > Hyperoxaluria > Hyperoxaluria, Primary
Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Hyperoxaluria, Primary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Hyperoxaluria, Primary

Preferred term

Hyperoxaluria, Primary  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

  • Oxaluria, Primary
  • Oxalurias, Primary
  • Primary Hyperoxaluria
  • Primary Oxaluria
  • Primary Oxalurias

Scope note

  • 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.

History note

  • 91(87); was see under HYPEROXALURIA 1987-90

In other languages

URI

http://www.yso.fi/onto/mesh/D006960

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