Imerslund-Grasbeck syndrome

Preferred Label : Imerslund-Grasbeck syndrome;

MeSH note : Pernicious anemia, juvenile, due to selective intestinal malabsorption of vitamin b12, with proteinuria;

MeSH synonym : enterocyte intrinsic factor receptor, defect of; enterocyte cobalamin malabsorption; megaloblastic anemia 1;

Details

Origin ID

C538556;

UMLS CUI

C4551825;

Automatic exact mappings (from CISMeF team)
- Imerslund-grasbeck syndrome [OMIM phenotypic series]
- Vitamin B12 deficiency anaemia due to selective vitamin B12 malabsorption with proteinuria [ICD-10 Sub-category (who)]
- megaloblastic anemia [DO Concept]
CISMeF manual mappings
- Familial megaloblastic anemia (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Imerslund-Graesbeck syndrome [MedDRA LLT]
- Imerslund-Grasbeck syndrome [ICD-11 More detail]
- Imerslund-Gräsbeck syndrome [ORDO Disease]
- Imerslund-grasbeck syndrome 1 [OMIM Phenotype]
- Megaloblastic Anemia 1 [NCIt concept]
- Selective malabsorption of cyanocobalamin (disorder) [SNOMED CT concept]
- Vitamin B12 deficiency anaemia due to selective vitamin B12 malabsorption with proteinuria [ICD-11 More detail]
- Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria [ICD-10 Sub-category]
- familial megaloblastic anemia [SNOMED Notion]
MeSH term(s) associated for indexing
- anemia, megaloblastic [MeSH Descriptor]
- malabsorption syndromes [MeSH Descriptor]
- proteinuria [MeSH Descriptor]
- vitamin b 12 deficiency [MeSH Descriptor]
Record concept(s)
- Imerslund-Grasbeck syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Imerslund-Graesbeck syndrome [MedDRA LLT]
- Imerslund-Grasbeck syndrome [ICD-11 More detail]
- Imerslund-grasbeck syndrome 1 [OMIM Phenotype]
- Megaloblastic Anemia 1 [NCIt concept]
- Selective malabsorption of cyanocobalamin (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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