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Condition report · Nutrition

Glucose-Galactose Malabsorption

A congenital monosaccharide transport defect caused by mutations in the SLC5A1 gene encoding the SGLT1 sodium-glucose cotransporter.

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The condition we analyse

Glucose-galactose Malabsorption

Autosomal recessive

Genes analysed

Also known as

carbohydrate intolerance of glucose galactose; Complex carbohydrate intolerance; GGM; glucose galactose malabsorption deficiency; SGLT1 deficiency

Includes 1 related subtype ↓
  • glucose intolerance
MONDO:0011731OMIM 606824Orphanet 35710MedGen 78647

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