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glucose-galactose malabsorption

См. также в других словарях:

  • Glucose-galactose malabsorption — Classification and external resources ICD 10 E74.3 ICD 9 271.3 …   Wikipedia

  • glucose-galactose malabsorption — an autosomal recessive disorder caused by mutation in the SLC5A1 (SGLT1) gene (locus: 22q13.1), which encodes the intestinal sodium/glucose cotransporter, resulting in defective intestinal glucose and galactose transport. It is characterized by… …   Medical dictionary

  • Galactose-1-phosphate uridylyltransferase deficiency — Classification and external resources Galactose ICD 10 E …   Wikipedia

  • Fructose malabsorption — Classification and external resources Fructose ICD 10 E …   Wikipedia

  • Natrium/Glucose-Cotransporter 1 — Masse/Länge Primärstruktur 664 Aminosäuren …   Deutsch Wikipedia

  • Sodium-glucose transport proteins — solute carrier family 5 (sodium/glucose cotransporter), member 1 Identifiers Symbol SLC5A1 Alt. symbols SGLT1 Entrez …   Wikipedia

  • malabsorption — Imperfect, inadequate, or otherwise disordered gastrointestinal absorption. congenital selective glucose and galactose m. an inherited disorder in which d glucose and d galactose accumulate in the intestinal lumen and exert an osmotic …   Medical dictionary

  • GGM — glucose galactose malabsorption …   Medical dictionary

  • GGM — • glucose galactose malabsorption …   Dictionary of medical acronyms & abbreviations

  • SLC5A1 — Solute carrier family 5 (sodium/glucose cotransporter), member 1, also known as SLC5A1, is a human gene.cite web | title = Entrez Gene: SLC5A1 solute carrier family 5 (sodium/glucose cotransporter), member 1| url =… …   Wikipedia

  • Galactosemia — Classification and external resources Galactose ICD 10 E …   Wikipedia

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