Other disorders of intestinal carbohydrate absorption

Preferred Label : Other disorders of intestinal carbohydrate absorption;

ICD-10 exclusion note : lactose intolerance (E73.-);

Diag associé à un acte (%) : 53.7;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

E743;

UMLS CUI

C0348486;

Automatic exact mappings (from CISMeF team)
- Glucose-Galactose malabsorption [MeSH concept]
- Glucose-Galactose malabsorption [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Congenital Sucrase-Isomaltase Deficiency [NCIt concept]
- Congenital sucrase-isomaltase deficiency [ICD-11 Subcategory]
- Congenital sucrase-isomaltase deficiency [ORDO Disease]
- Disaccharidase deficiency (disorder) [SNOMED CT concept]
- Other disorders of intestinal carbohydrate absorption [ICD-11 More detail]
- Sucrase-isomaltase deficiency [MedDRA Preferred Term]
- Sucrase-isomaltase deficiency (disorder) [SNOMED CT concept]
- Sucrase-isomaltase deficiency, congenital [MeSH concept]
- congenital sucrase isomaltase deficiency [Disease (Nov.)]
- sucrase isomaltase deficiency [Disease (Nov.)]
- sucrase-isomaltase deficiency [SNOMED Notion]
- sucrase-isomaltase deficiency [TUV Concept]
- sucrase-isomaltase deficiency, congenital [MeSH Supplementary Concept]
ICD-10 exclusion(s)
- Lactose intolerance [ICD-10 category]
Orphanet concepts
- Chronic diarrhea due to glucoamylase deficiency [ORDO Disease]
- Congenital sucrase-isomaltase deficiency [ORDO Disease]
- Congenital sucrase-isomaltase deficiency with minimal starch tolerance [ORDO Disease]
- Congenital sucrase-isomaltase deficiency with starch and lactose intolerance [ORDO Disease]
- Congenital sucrase-isomaltase deficiency with starch intolerance [ORDO Disease]
- Congenital sucrase-isomaltase deficiency without starch intolerance [ORDO Disease]
- Congenital sucrase-isomaltase deficiency without sucrose intolerance [ORDO Disease]
- Glucose-galactose malabsorption [ORDO Disease]
- Trehalase deficiency [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Other disorders of intestinal carbohydrate absorption [ICD-11 More detail]
Validated automatic mappings to BTNT
- Acquired monosaccharide malabsorption [ICD-11 Subcategory]
- Congenital sucrase-isomaltase deficiency [ICD-11 Subcategory]
- Deficiency of beta-fructofuranosidase (disorder) [SNOMED CT concept]
- Fructose malabsorption [ICD-11 Sub-sub category]
- Glucose-galactose malabsorption [ICD-11 Subcategory]
- Maltase-glucoamylase deficiency [ICD-11 Subcategory]
- Sucrase-isomaltase deficiency, congenital [OMIM Phenotype]

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