apolipoprotein A2

Preferred Label : apolipoprotein A2;

Approved symbol HGNC : APOA2;

Chromosome HGNC : 1q23.3;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000158874;

Details

Origin ID

HGNC:601;

UMLS CUI

C1412469;

Automatic exact mappings (from CISMeF team)
- Apolipoprotein A-II [NCIt concept]
- Apolipoprotein a-II [OMIM Phenotype]
- apolipoprotein A2 [ORDO Gene]
- apolipoprotein a-ii [MeSH Descriptor]
Currated CISMeF NLP mapping
- APOA2 Gene [NCIt concept]
- APOA2 gene [LOINC component]
NCIt concept
- APOA2 Gene [NCIt concept]
Orphanet gene
- apolipoprotein A2 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- APOA2 Gene [NCIt concept]
- APOA2 gene [LOINC component]
- Apolipoprotein a-II [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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