lactase deficiency, congenital

Preferred Label : lactase deficiency, congenital;

Obsolete resource : false;

MeSH synonym : alactasia, congenital; disaccharide intolerance II;

Details

Origin ID

C562600;

UMLS CUI

C0268179;

Currated CISMeF NLP mapping
- Congenital lactase deficiency [ICD-10 Sub-category]
- Congenital lactase deficiency [ICD-11 Sub-sub category]
- Congenital lactase deficiency [MedDRA Preferred Term]
- Congenital lactase deficiency [ICD-10 Sub-category (who)]
- Congenital lactase deficiency [ORDO Disease]
- Congenital lactase deficiency (disorder) [SNOMED CT concept]
- Lactase deficiency, congenital [OMIM Phenotype]
- congenital lactase deficiency [Disease (Nov.)]
- congenital lactase deficiency [DO Concept]
- congenital lactase deficiency [SNOMED Notion]
DO Cross reference
- congenital lactase deficiency [DO Concept]
MeSH term(s) associated for indexing
- carbohydrate metabolism, inborn errors [MeSH Descriptor]
- lactase [MeSH Descriptor]
Record concept(s)
- lactase deficiency, congenital [MeSH concept]
See also (suggested by CISMeF)
- lactose [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital lactase deficiency [ICD-10 Sub-category (who)]
- Congenital lactase deficiency [ORDO Disease]
- Congenital lactase deficiency [ICD-10 Sub-category]
- Congenital lactase deficiency [ICD-11 Sub-sub category]
- Congenital lactase deficiency [MedDRA Preferred Term]
- Congenital lactase deficiency (disorder) [SNOMED CT concept]
- Lactase deficiency, congenital [OMIM Phenotype]
- congenital lactase deficiency [SNOMED Notion]
- congenital lactase deficiency [Disease (Nov.)]
- congenital lactase deficiency [DO Concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients