Complement factor I

Preferred Label : Complement factor I;

Symbol : CFI;

CISMeF acronym : CFI;

Type : Gene;

Alternative titles and symbols : Complement component I; Factor I; C3b inactivator; FI;

Ensembl ID : ENSG00000205403;

Prefixed ID : *217030;

Details

Origin ID

217030;

UMLS CUI

C1442484;

Automatic exact mappings (from CISMeF team)
- 2-oxoglutarate carboxylase activity [GO term]
- Chemotaxis factor inhibitor (substance) [SNOMED CT concept]
- Complement factor I [LOINC component]
- Complement factor I [SNOMED Notion]
- Factor I (substance) [SNOMED CT concept]
- Fibrinogen [LOINC component]
- Flexibility Index [NCIt concept]
- chemotactic factor inactivator [MeSH Supplementary Concept]
- complement C3b [MeSH Descriptor]
- complement C3b inactivator proteins [MeSH Descriptor]
- complement factor I [ORDO Gene]
- complement factor I [MeSH Descriptor]
- complement factor I [HGNC gene]
- complement factor I [MeSH concept]
- fibrinogen [MeSH Descriptor]
- inactivated C3b [MeSH concept]
False automatic mappings
- Finland [NCIt concept]
HGNC gene
- complement factor I [HGNC gene]
NCIt concept(s)
- CFI Gene [NCIt concept]
- CFI wt Allele [NCIt concept]
- Complement Factor I [NCIt concept]
ORDO concept(s)
- complement factor I [ORDO Gene]
Phenotypes related
- Complement factor I deficiency [OMIM Phenotype]
- Hemolytic uremic syndrome, atypical, susceptibility to, 3 [OMIM Phenotype]
- Macular degeneration, age-related, 13 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CFI Gene [NCIt concept]
- complement factor I [HGNC gene]

Keyword's position in hierarchy(ies) :

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