Apolipoprotein e

Preferred Label : Apolipoprotein e;

Symbol : APOE;

CISMeF acronym : APOE;

Type : Gene;

Ensembl ID : ENSG00000130203;

Prefixed ID : *107741;

Details

Origin ID

107741;

UMLS CUI

C1412481;

Automatic exact mappings (from CISMeF team)
- APOE Gene [NCIt concept]
- APOE gene [LOINC component]
- Apolipoprotein A [NCIt concept]
- Apolipoprotein E Measurement [NCIt concept]
- Apolipoprotein(a) [NCIt concept]
- apolipoprotein E [HGNC gene]
Currated CISMeF NLP mapping
- Apolipoprotein E [LOINC component]
- Apolipoprotein E [MedDRA Preferred Term]
- Apolipoprotein E [NCIt concept]
- Apolipoprotein E (substance) [SNOMED CT concept]
- apolipoprotein E [ORDO Gene]
- apolipoprotein e [SNOMED Notion]
- apolipoproteins E [MeSH concept]
- apolipoproteins e [MeSH Descriptor]
False automatic mappings
- clusterin [MeSH Descriptor]
HGNC gene
- apolipoprotein E [HGNC gene]
NCIt concept(s)
- APOE Gene [NCIt concept]
- APOE wt Allele [NCIt concept]
- APOE*2 Allele [NCIt concept]
- APOE*4 Allele [NCIt concept]
- Apolipoprotein E [NCIt concept]
- Apolipoprotein E4 [NCIt concept]
ORDO concept(s)
- apolipoprotein E [ORDO Gene]
Phenotypes related
- Alzheimer disease 2 [OMIM Phenotype]
- Alzheimer disease 3 [OMIM Phenotype]
- Hyperlipoproteinemia, type III [OMIM Phenotype]
- Lipoprotein glomerulopathy [OMIM Phenotype]
- Macular degeneration, age-related, 1 [OMIM Phenotype]
- Sea-blue histiocyte disease [OMIM Phenotype]
See also inter- (CISMeF)
- APOE*2 Allele [NCIt concept]
- APOE*4 Allele [NCIt concept]
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 [HGNC gene]

Keyword's position in hierarchy(ies) :

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