coagulation factor VIII

Preferred Label : coagulation factor VIII;

Approved symbol HGNC : F8;

Name synonyms HGNC : hemophilia A; Factor VIIIF8B;

Alias symbols HGNC : HEMA; DXS1253E; FVIII;

Chromosome HGNC : Xq28;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000185010;

Details

Origin ID

HGNC:3546;

UMLS CUI

C1366370;

Automatic exact mappings (from CISMeF team)
- Coagulation Factor VIII [NCIt concept]
- Coagulation factor VIII [OMIM gene]
- Coagulation factor VIII [LOINC component]
- Coagulation factor VIII (substance) [SNOMED CT concept]
- Haemophilia A [MedDRA LLT]
- Hemophilia [PASCAL descriptor]
- Hemophilia [MedDRA LLT]
- Hemophilia [LOINC component]
- Hemophilia [NCIt concept]
- Hemophilia [ORDO Disease]
- Hemophilia (disorder) [SNOMED CT concept]
- Hemophilia - specialty (qualifier value) [SNOMED CT concept]
- Hemophilia A [PASCAL descriptor]
- Hemophilia A [MedDRA LLT]
- Hemophilia A [ORDO Disease]
- Hemophilia A [NCIt concept]
- Hemophilia a [OMIM Phenotype]
- Hereditary factor VIII deficiency [ICD-10 category]
- Hereditary factor VIII deficiency disease (disorder) [SNOMED CT concept]
- coagulation factor VIII [ORDO Gene]
- coagulation factor VIII [ATC Code]
- coagulation factor viii [SNOMED Notion]
- coagulation factor viii [EMDN type]
- factor VIII [MeSH Descriptor]
- factor VIII deficiency [DO Concept]
- hemophilia [MedlinePlus Topic]
- hemophilia A [MeSH Descriptor]
- hemophilia A [MeSH concept]
- hemophilia A [Blood Transfusion thesaurus concept]
NCIt concept
- F8 Gene [NCIt concept]
OMIM gene
- Coagulation factor VIII [OMIM gene]
Orphanet gene
- coagulation factor VIII [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Coagulation factor VIII [OMIM gene]
- F8 Gene [NCIt concept]
- F8 gene [LOINC component]
- Factor VIII-associated gene 2 [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients