Diseases

Renal Glycosuria

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.

National Library of MedicineMedical Subject Headings2026

Structured Summary

Abstract

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 Record

Classification

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MeSH Record

Synonyms

2 entry terms
  • Glycosuria, Renal
  • Renal Glucosuria

MeSH Record

Aspects Covered

34 allowable subheadings

Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.

MeSH Record

History Note

65

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AMA Style

References

  1. National Library of Medicine. Renal Glycosuria. Medical Subject Headings (MeSH). 2026. Unique ID D006030. http://id.nlm.nih.gov/mesh/2026/D006030
  2. Renal Glycosuria. In: Wikipedia. https://en.wikipedia.org/wiki/Renal_glycosuria
  3. Renal Glycosuria. In: Wikidata. https://www.wikidata.org/wiki/Q1207967