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Glucose-galactose malabsorption

rare

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.

Identifiers
MONDO:0011731 OMIM:606824Orphanet:35710
Causal genes
SLC5A1
Part of
Congenital diarrheaGlucose transport disorderIntestinal disorder
Also known as
carbohydrate intolerance of glucose galactose · Complex carbohydrate intolerance · GGM · glucose galactose malabsorption deficiency · glucose/galactose malabsorption

Subtypes

All diseases Rare only
Disease Subtypes
Glucose intolerance

Rare disease

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