Coagulation factor II

Preferred Label : Coagulation factor II;

Symbol : F2;

CISMeF acronym : F2;

Type : Gene;

Alternative titles and symbols : Factor II; THROMBIN; PROTHROMBIN;

Ensembl ID : ENSG00000180210;

Prefixed ID : *176930;

Details

Origin ID

176930;

UMLS CUI

C1414504;

Automatic exact mappings (from CISMeF team)
- Coagulation factor II (substance) [SNOMED CT concept]
- F2 Gene [NCIt concept]
- F2 gene [LOINC component]
- International Unit [NCIt concept]
- NDC F2 (International Unit) [NCIt concept]
- Prothrombin [NCIt concept]
- Prothrombin [MedDRA LLT]
- Prothrombin [NCIt concept]
- Prothrombin [LOINC component]
- Prothrombin Measurement [NCIt concept]
- Thrombin [NCIt concept]
- Thrombin [ICD-11 Extension code]
- Thrombin [MedDRA LLT]
- Thrombin [ICHI extension code]
- Thrombin [LOINC part]
- Thrombin (substance) [SNOMED CT concept]
- Thrombin Alfa [NCIt concept]
- coagulation factor II, thrombin [HGNC gene]
- coagulation factor II, thrombin [ORDO Gene]
- coagulation factor ii [SNOMED Notion]
- prothrombin [MeSH Descriptor]
- prothrombin [MeSH concept]
- prothrombin [Blood Transfusion thesaurus concept]
- thrombin [SNOMED Notion]
- thrombin [MeSH concept]
- thrombin [ATC Code]
- thrombin [Substance BNPC]
- thrombin [MeSH Descriptor]
- thrombin [ATC Code]
- thrombin [Blood Transfusion thesaurus concept]
HGNC gene
- coagulation factor II, thrombin [HGNC gene]
NCIt concept(s)
- Des-Gamma Carboxyprothrombin [NCIt concept]
- F2 Gene [NCIt concept]
- F2 wt Allele [NCIt concept]
- Prothrombin [NCIt concept]
ORDO concept(s)
- coagulation factor II, thrombin [ORDO Gene]
Phenotypes related
- Pregnancy loss, recurrent, susceptibility to, 2 [OMIM Phenotype]
- Prothrombin deficiency, congenital [OMIM Phenotype]
- Stroke, ischemic [OMIM Phenotype]
- Thrombophilia due to thrombin defect [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- F2 Gene [NCIt concept]
- F2 gene [LOINC component]
- coagulation factor II, thrombin [HGNC gene]

Keyword's position in hierarchy(ies) :

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