Glucose-galactose malabsorption

MONDO:0011731

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.

Also known as: SGLT1 deficiency, glucose-galactose malabsorption, Complex carbohydrate intolerance, GGM, carbohydrate intolerance of glucose galactose, glucose galactose malabsorption deficiency, glucose/galactose malabsorption, monosaccharide malabsorption

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