coagulation factor IX

Preferred Label : coagulation factor IX;

Approved symbol HGNC : F9;

Name synonyms HGNC : hemophilia B; Christmas disease; plasma thromboplastic component; Factor IX;

Alias symbols HGNC : FIX;

Chromosome HGNC : Xq27.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000101981;

Details

Origin ID

HGNC:3551;

UMLS CUI

C1366464;

Automatic exact mappings (from CISMeF team)
- Coagulation Factor IX [NCIt concept]
- Coagulation factor IX [LOINC component]
- Coagulation factor IX (substance) [SNOMED CT concept]
- Factor IX [PASCAL descriptor]
- Factor IX [LOINC component]
- Factor IX Measurement [NCIt concept]
- Haemophilia B [ICD-11 Subcategory]
- Hemophilia B [PASCAL descriptor]
- Hemophilia B [ORDO Disease]
- Hemophilia B [NCIt concept]
- Hemophilia B [MedDRA LLT]
- Hemophilia b [OMIM Phenotype]
- Hereditary factor IX deficiency [ICD-10 category]
- Hereditary factor IX deficiency disease (disorder) [SNOMED CT concept]
- coagulation factor IX [ORDO Gene]
- coagulation factor IX [ATC Code]
- coagulation factor ix [SNOMED Notion]
- coagulation factor ix [EMDN type]
- factor IX [MeSH Descriptor]
- factor IX [MeSH concept]
- factor IX [Blood Transfusion thesaurus concept]
- hemophilia [MedlinePlus Topic]
- hemophilia B [MeSH Descriptor]
- hemophilia B [MeSH concept]
- hemophilia B [DO Concept]
- hemophilia B [Blood Transfusion thesaurus concept]
Currated CISMeF NLP mapping
- Coagulation factor ix [OMIM gene]
- F9 Gene [NCIt concept]
NCIt concept
- F9 Gene [NCIt concept]
OMIM gene
- Coagulation factor ix [OMIM gene]
Orphanet gene
- coagulation factor IX [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Coagulation factor ix [OMIM gene]
- F9 Gene [NCIt concept]
- F9 gene [LOINC component]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients