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Concept information

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Lactose Intolerance
Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Lactose Intolerance
Digestive System Diseases > Gastrointestinal Diseases > Intestinal Diseases > Malabsorption Syndromes > Lactose Intolerance
Nutritional and Metabolic Diseases > Metabolic Diseases > Malabsorption Syndromes > Lactose Intolerance

Terme préférentiel

Lactose Intolerance  

Type

  • mesh:Descriptor

Définition

  • The condition resulting from the absence or deficiency of LACTASE in the MUCOSA cells of the GASTROINTESTINAL TRACT, and the inability to break down LACTOSE in milk for ABSORPTION. Bacterial fermentation of the unabsorbed lactose leads to symptoms that range from a mild indigestion (DYSPEPSIA) to severe DIARRHEA. Lactose intolerance may be an inborn error or acquired.

Concept générique

Concepts associés

Synonyme(s)

  • Alactasia
  • Dairy Product Intolerance
  • Hypolactasia
  • Lactose Malabsorption
  • Milk Sugar Intolerance

Qualificatif(s) autorisé(s)

Traductions

URI

http://data.loterre.fr/ark:/67375/JVR-W0P3QR5V-R

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RDF/XML TURTLE JSON-LD Date de création 01/01/1999, dernière modification le 08/07/2013