glucose-galactose malabsorption (Q5572341)
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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
| Language | Label | Description | Also known as |
|---|---|---|---|
| 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 |
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