hypercholesterolemia due to arg3500 mutation of apo B-100

Preferred Label : hypercholesterolemia due to arg3500 mutation of apo B-100;

MeSH synonym : hypercholesterolemia, familial, due to ligand-defective apolipoprotein B;

Détails

Origin ID

C536083;

UMLS CUI

C2931106;

Automatic exact mappings (from CISMeF team)
- Familial defective apolipoprotein B-100 (disorder) [SNOMED CT concept]
- Hypercholesterolemia, familial, 2 [OMIM Phenotype]
MeSH term(s) associated for indexing
- hyperlipoproteinemia type ii [MeSH Descriptor]
Record concept(s)
- Hypercholesterolemia due to arg3500 mutation of Apo B-100 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Position du mot-clé dans l'(les) arborescence(s) :

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