ONKI3 | Medical Subject Headings

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Lactose Intolerance

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Lactose Intolerance 18 coordinate concepts ∟ Carbohydrate-Deficient Glycoprotein Syndrome \| ∟ Fructose Metabolism, Inborn Errors \| ∟ Fucosidosis \| ∟ Galactosemias \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Glycogen Storage Disease \| ∟ Hyperoxaluria, Primary \| ∟ Mannosidase Deficiency Diseases \| ∟ Mucolipidoses \| ∟ Mucopolysaccharidoses \| ∟ Multiple Carboxylase Deficiency \| ∟ Pyruvate Metabolism, Inborn Errors \| ∟ Blind Loop Syndrome \| ∟ Celiac Disease \| ∟ Short Bowel Syndrome \| ∟ Sprue, Tropical \| ∟ Steatorrhea \| ∟ Whipple Disease Medical Subject Headings (MeSH) ∟ Digestive System Diseases ∟ Gastrointestinal Diseases ∟ Intestinal Diseases ∟ Malabsorption Syndromes ∟ Lactose Intolerance 18 coordinate concepts ∟ Carbohydrate-Deficient Glycoprotein Syndrome \| ∟ Fructose Metabolism, Inborn Errors \| ∟ Fucosidosis \| ∟ Galactosemias \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Glycogen Storage Disease \| ∟ Hyperoxaluria, Primary \| ∟ Mannosidase Deficiency Diseases \| ∟ Mucolipidoses \| ∟ Mucopolysaccharidoses \| ∟ Multiple Carboxylase Deficiency \| ∟ Pyruvate Metabolism, Inborn Errors \| ∟ Blind Loop Syndrome \| ∟ Celiac Disease \| ∟ Short Bowel Syndrome \| ∟ Sprue, Tropical \| ∟ Steatorrhea \| ∟ Whipple Disease Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Malabsorption Syndromes ∟ Lactose Intolerance 18 coordinate concepts ∟ Carbohydrate-Deficient Glycoprotein Syndrome \| ∟ Fructose Metabolism, Inborn Errors \| ∟ Fucosidosis \| ∟ Galactosemias \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Glycogen Storage Disease \| ∟ Hyperoxaluria, Primary \| ∟ Mannosidase Deficiency Diseases \| ∟ Mucolipidoses \| ∟ Mucopolysaccharidoses \| ∟ Multiple Carboxylase Deficiency \| ∟ Pyruvate Metabolism, Inborn Errors \| ∟ Blind Loop Syndrome \| ∟ Celiac Disease \| ∟ Short Bowel Syndrome \| ∟ Sprue, Tropical \| ∟ Steatorrhea \| ∟ Whipple Disease Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Lactose Intolerance 18 coordinate concepts ∟ Carbohydrate-Deficient Glycoprotein Syndrome \| ∟ Fructose Metabolism, Inborn Errors \| ∟ Fucosidosis \| ∟ Galactosemias \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Glycogen Storage Disease \| ∟ Hyperoxaluria, Primary \| ∟ Mannosidase Deficiency Diseases \| ∟ Mucolipidoses \| ∟ Mucopolysaccharidoses \| ∟ Multiple Carboxylase Deficiency \| ∟ Pyruvate Metabolism, Inborn Errors \| ∟ Blind Loop Syndrome \| ∟ Celiac Disease \| ∟ Short Bowel Syndrome \| ∟ Sprue, Tropical \| ∟ Steatorrhea \| ∟ Whipple Disease X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Lactose Intolerance Medical Subject Headings (MeSH) ∟ Digestive System Diseases ∟ Gastrointestinal Diseases ∟ Intestinal Diseases ∟ Malabsorption Syndromes ∟ Lactose Intolerance Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Malabsorption Syndromes ∟ Lactose Intolerance Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Carbohydrate Metabolism, Inborn Errors ∟ Lactose Intolerance Carbohydrate Metabolism, Inborn Errors > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Malabsorption Syndromes > Intestinal Diseases > Gastrointestinal Diseases > Digestive System Diseases > Medical Subject Headings (MeSH) Malabsorption Syndromes > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Carbohydrate Metabolism, Inborn Errors > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) X
historyNote*:	67(64) X
publicMeSHNote*:	67 X
Scope note:	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. X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1967-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Carbohydrate-Deficient Glycoprotein Syndrome \| Fructose Metabolism, Inborn Errors \| Fucosidosis \| Galactosemias \| Glucosephosphate Dehydrogenase Deficiency \| Glycogen Storage Disease \| Hyperoxaluria, Primary \| Mannosidase Deficiency Diseases \| Mucolipidoses \| Mucopolysaccharidoses \| Multiple Carboxylase Deficiency \| Pyruvate Metabolism, Inborn Errors \| Blind Loop Syndrome \| Celiac Disease \| Short Bowel Syndrome \| Sprue, Tropical \| Steatorrhea \| Whipple Disease X
URI:	X
Labels and equivalent concepts:	Laktoosi-intoleranssi (fi) Maitosokerin sietohäiriö (fi, replaced) Maitosokerin imeytymishäiriö (fi, replaced) Maitosokerivatsa (fi, replaced) Suolilaktaasin puutos (fi, replaced) Maitosokerihäiriö (fi, replaced) Laktoosin malabsorptio (fi, replaced) Laktaasin puute (fi, replaced) Hypolaktasia (fi, replaced) Laktaasin puutos (fi, replaced) Laktaasinpuute (fi, replaced) Laktoosin imeytymishäiriö (fi, replaced) Laktaasinpuutos (fi, replaced) Laktosintolerans (sv) Laktosmalabsorption (sv, replaced) Lactose Malabsorption (en, replaced) Intolerantia lactosi (la-FI, replaced) X
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