Complement factor h

Preferred Label : Complement factor h;

Symbol : CFH;

CISMeF acronym : CFH;

Type : Gene;

Alternative titles and symbols : H factor 1; Factor h; HF1; HF;

Included titles and symbols : Factor h-like 1; Complement factor h-like 1; FHL1; CFHL1;

Ensembl ID : ENSG00000000971;

Prefixed ID : *134370;

Details

Origin ID

134370;

UMLS CUI

C1538440;

Automatic exact mappings (from CISMeF team)
- CFH Gene [NCIt concept]
- CFH gene [LOINC component]
- CFH wt Allele [NCIt concept]
- CFHR1 wt Allele [NCIt concept]
- Complement Factor H [NCIt concept]
- Complement factor H [LOINC component]
- Factor H (substance) [SNOMED CT concept]
- Granzyme A [NCIt concept]
- Hafnium [NCIt concept]
- Heart failure [Bloc CIM-11]
- Hydrops fetalis [ORDO Disease]
- complement factor H [ORDO Gene]
- complement factor H [HGNC gene]
- complement factor H [MeSH concept]
- complement factor h [MeSH Descriptor]
- factor h [SNOMED Notion]
- familial hemophagocytic lymphohistiocytosis 1 [DO Concept]
HGNC gene
- complement factor H [HGNC gene]
NCIt concept(s)
- CFH Gene [NCIt concept]
- CFH wt Allele [NCIt concept]
- Complement Factor H [NCIt concept]
ORDO concept(s)
- complement factor H [ORDO Gene]
Phenotypes related
- Basal laminar drusen [OMIM Phenotype]
- Complement factor h deficiency [OMIM Phenotype]
- Hemolytic uremic syndrome, atypical, susceptibility to, 1 [OMIM Phenotype]
- Macular degeneration, age-related, 4 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CFH Gene [NCIt concept]
- CFH gene [LOINC component]
- complement factor H [HGNC gene]

Keyword's position in hierarchy(ies) :

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