Coagulation factor V

Preferred Label : Coagulation factor V;

Symbol : F5;

CISMeF acronym : F5;

Type : Gene;

Alternative titles and symbols : Activated protein C cofactor; Protein C cofactor; Apc cofactor; Labile factor; PCCF;

Included titles and symbols : Factor V leiden;

Ensembl ID : ENSG00000198734;

Prefixed ID : *612309;

Details

Origin ID

612309;

UMLS CUI

C1414509;

Automatic exact mappings (from CISMeF team)
- Coagulation Factor V [NCIt concept]
- Coagulation factor V [LOINC component]
- Coagulation factor V (substance) [SNOMED CT concept]
- F5 Gene [NCIt concept]
- F5 gene [LOINC component]
- F5 wt Allele [NCIt concept]
- Factor V Leiden [NCIt concept]
- Factor V Leiden Measurement [NCIt concept]
- Factor V Measurement [NCIt concept]
- Protein C cofactor [LOINC component]
- coagulation factor V [ORDO Gene]
- coagulation factor V [HGNC gene]
- coagulation factor v [SNOMED Notion]
- coagulation factor v [EMDN type]
- factor V Leiden [MeSH concept]
- factor V leiden [MeSH Supplementary Concept]
- factor v [MeSH Descriptor]
- proaccelerin [Blood Transfusion thesaurus concept]
HGNC gene
- coagulation factor V [HGNC gene]
NCIt concept(s)
- Coagulation Factor V [NCIt concept]
- F5 Gene [NCIt concept]
- F5 wt Allele [NCIt concept]
ORDO concept(s)
- coagulation factor V [ORDO Gene]
Phenotypes related
- Budd-chiari syndrome [OMIM Phenotype]
- Factor V deficiency [OMIM Phenotype]
- Pregnancy loss, recurrent, susceptibility to, 1 [OMIM Phenotype]
- Stroke, ischemic [OMIM Phenotype]
- Thrombophilia due to activated protein C resistance [OMIM Phenotype]
See also inter- (CISMeF)
- Coagulation factor V [SMS substance]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- F5 Gene [NCIt concept]
- F5 gene [LOINC component]
- coagulation factor V [HGNC gene]

Keyword's position in hierarchy(ies) :

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