Primary Hyperoxaluria

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

Urogenital Diseases: 126
- Urologic Diseases: 799
  - Kidney Diseases: 12250
    - Hyperoxaluria: 1448
      - Primary Hyperoxaluria: 700
- Female Urogenital Diseases and Pregnancy Complications
  - Female Urogenital Diseases
    - Urologic Diseases: 799
      - Kidney Diseases: 12250
        Hyperoxaluria: 1448
        Primary Hyperoxaluria: 700
- Male Urogenital Diseases
  - Urologic Diseases: 799
    - Kidney Diseases: 12250
      - Hyperoxaluria: 1448
        Primary Hyperoxaluria: 700
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Carbohydrate Metabolism
      - Primary Hyperoxaluria: 700
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Carbohydrate Metabolism
      - Primary Hyperoxaluria: 700

S El Kabbaj Selected Research

S El Kabbaj Research Topics

Disease

Drug/Important Bio-Agent (IBA)