Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria

Preferred Label : Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria;

Inclusion CIM-10 : Megaloblastic hereditary anemia; Imerslund (Gräsbeck) syndrome;

Diag associé à un acte (%) : 65.6;

CMA : 2;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D511;

UMLS CUI

C0494218;

Currated CISMeF NLP mapping
- Imerslund-Grasbeck syndrome [MeSH Supplementary Concept]
- Imerslund-Gräsbeck syndrome [ORDO Disease]
- Imerslund-grasbeck syndrome 1 [OMIM Phenotype]
- Vitamin B12 deficiency anaemia due to selective vitamin B12 malabsorption with proteinuria [ICD-11 More detail]
Orphanet concepts
- Constitutional megaloblastic anemia due to vitamin B12 metabolism disorder [ORDO Disease]
- Imerslund-Gräsbeck syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Vitamin B12 deficiency anaemia due to selective vitamin B12 malabsorption with proteinuria [ICD-11 More detail]

Keyword's position in hierarchy(ies) :

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