(Q5572341)

English

glucose-galactose malabsorption

Glucose-galactose malabsorption (GGM) is a very rare, potentially lethal, genetic metabolic disease characterized by impaired glucose-galactose absorption resulting in severe watery diarrhea and dehydration with onset inthe neonatal period

  • GLUCOSE/GALACTOSE MALABSORPTION
  • SGLT1 deficiency
  • GGM
  • GLUCOSE/GALACTOSE MALABSORPTION; GGM
  • glucose galactose malabsorption deficiency
  • garbohydrate intolerance of glucose galactose
  • complex carbohydrate intolerance
  • monosaccharide malabsorption

Statements

Identifiers

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5C61.0
Glucose-galactose malabsorption
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