Related MeSH Hierarchy (8)
Diseases [C] » Urogenital Diseases [C12] » Female Urogenital Diseases and Pregnancy Complications » Female Urogenital Diseases » Urologic Diseases » Kidney Diseases » Renal Tubular Transport, Inborn Errors » Glycosuria, Renal
Diseases [C] » Urogenital Diseases [C12] » Female Urogenital Diseases and Pregnancy Complications » Female Urogenital Diseases » Urologic Diseases » Urination Disorders » Glycosuria » Glycosuria, Renal
Diseases [C] » Urogenital Diseases [C12] » Male Urogenital Diseases » Urologic Diseases » Kidney Diseases » Renal Tubular Transport, Inborn Errors » Glycosuria, Renal
Diseases [C] » Urogenital Diseases [C12] » Male Urogenital Diseases » Urologic Diseases » Urination Disorders » Glycosuria » Glycosuria, Renal
Diseases [C] » Urogenital Diseases [C12] » Urologic Diseases » Kidney Diseases » Renal Tubular Transport, Inborn Errors » Glycosuria, Renal
Diseases [C] » Urogenital Diseases [C12] » Urologic Diseases » Urination Disorders » Glycosuria » Glycosuria, Renal
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Renal Tubular Transport, Inborn Errors » Glycosuria, Renal
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Glucose Metabolism Disorders » Glycosuria » Glycosuria, Renal
Description
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. MeSH
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