Glucose-galactose malabsorption
MONDO:0011731Glucose-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
152 clinical trials for this condition and its sub-types, 2 tagged with Glucose-galactose malabsorption itself.
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Browse by category →Sub-types of Glucose-galactose malabsorption
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Glucose intolerance 149 trials