Coagulation factor XII

Preferred Label : Coagulation factor XII;

Symbol : F12;

CISMeF acronym : F12;

Type : Gene;

Alternative titles and symbols : Hageman factor;

Ensembl ID : ENSG00000131187;

Prefixed ID : *610619;

Details

Origin ID

610619;

UMLS CUI

C1414499;

Automatic exact mappings (from CISMeF team)
- Coagulation Factor XII [NCIt concept]
- Coagulation factor XII [LOINC component]
- Coagulation factor XII (substance) [SNOMED CT concept]
- F12 Gene [NCIt concept]
- F12 gene [LOINC component]
- coagulation factor XII [ORDO Gene]
- coagulation factor XII [HGNC gene]
- coagulation factor xii [SNOMED Notion]
- coagulation factor xii [EMDN type]
- coagulation factor xii a [EMDN type]
- factor XII [MeSH Descriptor]
HGNC gene
- coagulation factor XII [HGNC gene]
NCIt concept(s)
- Coagulation Factor XII [NCIt concept]
- F12 Gene [NCIt concept]
- F12 wt Allele [NCIt concept]
ORDO concept(s)
- coagulation factor XII [ORDO Gene]
Phenotypes related
- Angioedema, hereditary, 3 [OMIM Phenotype]
- Factor XII deficiency [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- F12 Gene [NCIt concept]
- F12 gene [LOINC component]
- coagulation factor XII [HGNC gene]
Validated automatic mappings to BTNT
- Human coagulation factor XII [SMS substance]

Keyword's position in hierarchy(ies) :

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