sucrose intolerance
Congenital sucrase-isomaltase deficiency (CSID) is a carbohydrate intolerance disorder characterised by malabsorption of oligosaccharides and disaccharides
Facts
9 properties- Instance of
- rare disease, class of disease[6]
- Subclass of
- disorder of carbohydrate absorption and transport, metabolic disease with intestinal involvement, congenital intestinal disease due to an enzymatic defect, carbohydrate metabolic disorder, autosomal recessive disease[7]
- Age of onset
- juvenile onset, adult onset, childhood onset, infantile onset[13][14][15][16]
- Has phenotype
- diarrhea, Infantile onset, abdominal pain, vomiting, nausea, constipation, flatulence, fecal incontinence, abdominal distention, colic, fatigue, failure to thrive[17][18][19][20][21][22][23][24][25][26][27][28]
- Health specialty
- endocrinology[11]
- ICD-9-CM
- 271.3[9]
- NCI Thesaurus ID
- C128190[10]
- Prevalence
- +0.0003[8]
🏷️ Also known as
en Sucrose-Isomaltose Malabsorption, Congenital
en sucrose intolerance
en Sucrose Intolerance, Congenital
en Sucrose isomaltose enzyme deficiency
en CISD
en congenital sucrase-isomaltase deficiency
en Congenital sucrase-isomaltose malabsorption
en Congenital sucrose intolerance
en congenital sucrose isomaltose malabsorption
en CSID
en Disaccharide intolerance
en Disaccharide Intolerance 1
en Si Deficiency
en sucrase-isomaltase deficiency
en SUCRASE-ISOMALTASE DEFICIENCY, CONGENITAL
en SUCRASE-ISOMALTASE DEFICIENCY, CONGENITAL; CSID
ar عدم تحمل السكروز
de Saccharoseintoleranz
de Zuckerunverträglichkeit
es Dcsi
🔖 Identifiers · 17
- Disease Ontology ID
- DOID:0111633
- DiseasesDB
- 29844
- Exact match
- www.orpha.net, purl.obolibrary.org, identifiers.org
- Freebase ID
- /m/026mk2c
- ICD-10 ID
- E74.3
- ICD-10-CM
- E74.3
- ICD-9 ID
- 271.3
- KEGG ID
- H00115
- MeSH descriptor ID
- C538139
- Microsoft Academic ID (discontinued)
- 2779567541
- Mondo ID
- MONDO_0022850
🔗 Connections
Health specialty 1
Instance of 1
← FactGrid item ID 1
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