Coagulation factor ix

Preferred Label : Coagulation factor ix;

Symbol : F9;

CISMeF acronym : F9;

Type : Gene;

Alternative titles and symbols : Factor ix; Plasma thromboplastin component; PTC;

Ensembl ID : ENSG00000101981;

Prefixed ID : *300746;

Details

Origin ID

300746;

UMLS CUI

C1366464;

Automatic exact mappings (from CISMeF team)
- CCDC6 wt Allele [NCIt concept]
- Coagulation Factor IX [NCIt concept]
- Coagulation Factor V [NCIt concept]
- Coagulation factor IX [LOINC component]
- Coagulation factor IX (substance) [SNOMED CT concept]
- F9 wt Allele [NCIt concept]
- Factor IX [PASCAL descriptor]
- Factor IX [LOINC component]
- Factor IX Measurement [NCIt concept]
- PTCH1 wt Allele [NCIt concept]
- Peptichemio [NCIt concept]
- Percutaneous Transhepatic Cholangiography [NCIt concept]
- Protein Patched Homolog 1 [NCIt concept]
- RET wt Allele [NCIt concept]
- Thyroid Gland Papillary Carcinoma [NCIt concept]
- coagulation factor IX [ORDO Gene]
- coagulation factor IX [ATC Code]
- coagulation factor ix [SNOMED Notion]
- coagulation factor ix [EMDN type]
- coiled-coil domain containing 6 [ORDO Gene]
- factor IX [MeSH Descriptor]
- factor IX [MeSH concept]
- factor IX [Blood Transfusion thesaurus concept]
- ret proto-oncogene [ORDO Gene]
Currated CISMeF NLP mapping
- F9 Gene [NCIt concept]
- F9 gene [LOINC component]
- coagulation factor IX [HGNC gene]
HGNC gene
- coagulation factor IX [HGNC gene]
NCIt concept(s)
- Coagulation Factor IX [NCIt concept]
- F9 Gene [NCIt concept]
- F9 wt Allele [NCIt concept]
ORDO concept(s)
- coagulation factor IX [ORDO Gene]
Phenotypes related
- Hemophilia b [OMIM Phenotype]
- Thrombophilia, X-linked, due to factor ix defect [OMIM Phenotype]
- Warfarin sensitivity, X-linked [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- F9 Gene [NCIt concept]
- F9 gene [LOINC component]
- coagulation factor IX [HGNC gene]

Keyword's position in hierarchy(ies) :

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