apolipoprotein E, deficiency or defect of - CISMeF

" /> apolipoprotein E, deficiency or defect of - CISMeF

CISMeF

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Apolipoprotein E, deficiency or defect ofMeSH Supplementary Concept

Preferred Label : apolipoprotein E, deficiency or defect of;

Details

Origin ID

C566260;

UMLS CUI

C1862556;

Automatic exact mappings (from CISMeF team)
- Hyperlipoproteinemia, type III [OMIM Phenotype]
MeSH term(s) associated for indexing
- apolipoproteins e [MeSH Descriptor]
- lipid metabolism, inborn errors [MeSH Descriptor]
Record concept(s)
- apolipoprotein E, deficiency or defect of [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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22/05/2025

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