apolipoprotein E, deficiency or defect of - CISMeF

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

CISMeF

chu

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) :

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
01/05/2025

© Rouen University Hospital. Any partial or total use of this material must mention the source.