sucrose intolerance
Sign in to saveAlso known as sucrase-isomaltase deficiency, congenital sucrase-isomaltase deficiency, CISD, Disaccharide intolerance, SUCRASE-ISOMALTASE DEFICIENCY, CONGENITAL; CSID, Congenital sucrase-isomaltose malabsorption, Si Deficiency, Sucrose Intolerance, Congenital
Congenital sucrase-isomaltase deficiency (CSID) is a carbohydrate intolerance disorder characterised by malabsorption of oligosaccharides and disaccharides
In the Vinony graph
Vinony's link graph records 67 inbound references to sucrose intolerance, and connects out to inguinal hernia, human digestive system and large intestine.
Vinony files it under Inborn errors of carbohydrate metabolism and Sensitivities.
Vinony links it to 7 Wikipedia language editions.
Research
761 papers- Artificial sweeteners induce glucose intolerance by altering the gut microbiota.Nature · 2014
- Hereditary fructose intolerance: A comprehensive review.World journal of clinical pediatrics · 2022
- Sucrose intolerance in adults with common functional gastrointestinal symptoms.Proceedings (Baylor University. Medical Center) · 2022
- SUCROSE INTOLERANCE: AN ENZYMATIC DEFECT.Nutrition reviews · 1965
- [Food intolerance].Endocrinologia y nutricion : organo de la Sociedad Espanola de Endocrinologia y Nutricion · 2009
via PubMed
Wikidata facts
Show 4 more facts
- health specialty
- endocrinology
- NCI Thesaurus ID
- C128190
- ICD-9-CM
- 271.3
- exact match
- identifiers.org/doid/DOID:0111633
via Wikidata · CC0
Connections
inguinal hernia
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human digestive system
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large intestine
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gastroenteritis
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hernia
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gastrointestinal tract
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colitis
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ascending cholangitis
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enzyme
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metabolism
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diarrhea
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small intestine
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glucose
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hemorrhoid
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anxiety
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digital object identifier
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mutation
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dysentery
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hepatitis
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liver cirrhosis
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