sucrase-isomaltase deficiency, congenital

Preferred Label : sucrase-isomaltase deficiency, congenital;

Obsolete resource : false;

MeSH synonym : sucrose-isomaltase malabsorption, congenital; sucrose intolerance congenital; congenital sucrose-isomaltase malabsorption; disaccharide intolerance, 1; Sucrase-Isomaltase deficiency; sucrose intolerance, congenital; Sucrose-Isomaltose malabsorption, congenital; disaccharide intolerance I; congenital Sucrase-Isomaltase deficiency; congenital sucrose intolerance; congenital Sucrose-Isomaltose malabsorption; si deficiency;

Details

Origin ID

C538139;

UMLS CUI

C1283620;

Automatic exact mappings (from CISMeF team)
- Congenital sucrase-isomaltase deficiency without sucrose intolerance [ORDO Disease]
CISMeF manual mappings
- Deficiency of isomaltase (disorder) [SNOMED CT 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-10 Sub-category]
- Sucrase-isomaltase deficiency [MedDRA Preferred Term]
- Sucrase-isomaltase deficiency (disorder) [SNOMED CT concept]
- Sucrase-isomaltase deficiency, congenital [OMIM Phenotype]
- congenital sucrase isomaltase deficiency [Disease (Nov.)]
- congenital sucrase-isomaltase deficiency [DO Concept]
- sucrase isomaltase deficiency [Disease (Nov.)]
- sucrase-isomaltase deficiency [SNOMED Notion]
- sucrase-isomaltase deficiency [TUV Concept]
DO Cross reference
- congenital sucrase-isomaltase deficiency [DO Concept]
MeSH term(s) associated for indexing
- carbohydrate metabolism, inborn errors [MeSH Descriptor]
- sucrase-isomaltase complex [MeSH Descriptor]
ORDO relation(s)
- Congenital sucrase-isomaltase deficiency [ORDO Disease]
Record concept(s)
- Sucrase-isomaltase deficiency, congenital [MeSH concept]
See also (suggested by CISMeF)
- sucrose [MeSH Descriptor]
See also inter- (CISMeF)
- Deficiency of beta-fructofuranosidase (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Sucrase-Isomaltase Deficiency [NCIt concept]
- Congenital sucrase-isomaltase deficiency [ORDO Disease]
- Deficiency of isomaltase (disorder) [SNOMED CT concept]
- Sucrase-isomaltase deficiency [MedDRA Preferred Term]
- Sucrase-isomaltase deficiency (disorder) [SNOMED CT concept]
- Sucrase-isomaltase deficiency, congenital [OMIM Phenotype]
- congenital sucrase isomaltase deficiency [Disease (Nov.)]
- congenital sucrase-isomaltase deficiency [DO Concept]
- sucrase isomaltase deficiency [Disease (Nov.)]
- sucrase-isomaltase deficiency [SNOMED Notion]
- sucrase-isomaltase deficiency [TUV Concept]
Validated automatic mappings to NTBT
- sucrase isomaltase deficiency [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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