Dent Disease

X-linked recessive NEPHROLITHIASIS characterized by HYPERCALCIURIA; HYPOPHOSPHATEMIA; NEPHROCALCINOSIS; and PROTEINURIA. It is associated with mutations in the voltage-gated chloride channel, CLC-5 (Dent Disease I). Another group of mutations associated with this disease is in phosphatidylinositol 4,5-bisphosphate-5-phosphatase gene.

Also Known As:

Dents Disease; Disease, Dent; Disease, Dent's; Disease, Dents; Dent's Disease

Urogenital Diseases: 126
- Urologic Diseases: 799
  - Kidney Diseases: 12250
    - Inborn Errors Renal Tubular Transport
      - Dent Disease: 195
- Female Urogenital Diseases and Pregnancy Complications
  - Female Urogenital Diseases
    - Urologic Diseases: 799
      - Kidney Diseases: 12250
        Inborn Errors Renal Tubular Transport
        Dent Disease: 195
- Male Urogenital Diseases
  - Urologic Diseases: 799
    - Kidney Diseases: 12250
      - Inborn Errors Renal Tubular Transport
        Dent Disease: 195
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - X-Linked Genetic Diseases: 42
    - Dent Disease: 195
  - Inborn Errors Renal Tubular Transport
    - Dent Disease: 195

Winnie Luong Selected Research

Winnie Luong Research Topics

Disease

Drug/Important Bio-Agent (IBA)