apolipoprotein E

Preferred Label : apolipoprotein E;

Approved symbol HGNC : APOE;

Chromosome HGNC : 19q13.32;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000130203;

Details

Origin ID

HGNC:613;

UMLS CUI

C1412481;

Automatic exact mappings (from CISMeF team)
- Apolipoprotein E [LOINC component]
- Apolipoprotein E [NCIt concept]
- Apolipoprotein E [MedDRA Preferred Term]
- Apolipoprotein E (substance) [SNOMED CT concept]
- Apolipoprotein E Measurement [NCIt concept]
- Apolipoprotein e [OMIM gene]
- apolipoprotein E [ORDO Gene]
- apolipoprotein e [SNOMED Notion]
- apolipoproteins E [MeSH concept]
- apolipoproteins e [MeSH Descriptor]
NCIt concept
- APOE Gene [NCIt concept]
OMIM gene
- Apolipoprotein e [OMIM gene]
Orphanet gene
- apolipoprotein E [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- APOE Gene [NCIt concept]
- APOE gene [LOINC component]
- Apolipoprotein E gene (substance) [SNOMED CT concept]
- Apolipoprotein e [OMIM gene]

Keyword's position in hierarchy(ies) :

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