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... > Urogenital Diseases > Female Urogenital Diseases and Pregnancy Complications > Female Urogenital Diseases > Urologic Diseases > Urination Disorders > Glycosuria > Glycosuria, Renal
... > Urogenital Diseases > Male Urogenital Diseases > Urologic Diseases > Urination Disorders > Glycosuria > Glycosuria, Renal
Nutritional and Metabolic Diseases > Metabolic Diseases > Glucose Metabolism Disorders > Glycosuria > Glycosuria, Renal
... > Urogenital Diseases > Female Urogenital Diseases and Pregnancy Complications > Female Urogenital Diseases > Urologic Diseases > Kidney Diseases > Renal Tubular Transport, Inborn Errors > Glycosuria, Renal
... > Urogenital Diseases > Male Urogenital Diseases > Urologic Diseases > Kidney Diseases > Renal Tubular Transport, Inborn Errors > Glycosuria, Renal
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Renal Tubular Transport, Inborn Errors > Glycosuria, Renal
Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Renal Tubular Transport, Inborn Errors > Glycosuria, Renal

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Glycosuria, Renal  

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Tipo

  • mesh:Descriptor

Definición

  • An autosomal inherited disorder due to defective reabsorption of GLUCOSE by the PROXIMAL RENAL TUBULES. The urinary loss of glucose can reach beyond 50 g/day. It is attributed to the mutations in the SODIUM-GLUCOSE TRANSPORTER 2 encoded by the SLC5A2 gene.

Concepto genérico

Etiquetas alternativas

  • Renal Glucosuria
  • Renal Glycosuria

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-T6C9TTLN-7

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