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Concept information

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Hyperoxaluria, Primary
Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Hyperoxaluria, Primary
... > 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

Terme préférentiel

Hyperoxaluria, Primary  

Type

  • mesh:Descriptor

Définition

  • 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.

Concept générique

Concepts associés

Synonyme(s)

  • Oxaluria, Primary
  • Primary Hyperoxaluria
  • Primary Oxaluria

Qualificatif(s) autorisé(s)

Traductions

URI

http://data.loterre.fr/ark:/67375/JVR-L0K97STQ-5

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RDF/XML TURTLE JSON-LD Date de création 18/04/1986, dernière modification le 30/06/2021