complement factor H

Preferred Label : complement factor H;

Approved symbol HGNC : CFH;

Name synonyms HGNC : age-related maculopathy susceptibility 1; beta-1H; H factor 2 (complement);

Alias symbols HGNC : ARMS1; ARMD4; HUS; FHL1;

Chromosome HGNC : 1q31.3;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000000971;

Details

Origin ID

HGNC:4883;

UMLS CUI

C1538440;

Automatic exact mappings (from CISMeF team)
- Complement Factor H [NCIt concept]
- Complement factor H [LOINC component]
- Complement factor h [OMIM gene]
- Factor H (substance) [SNOMED CT concept]
- Four-and-a-half lim domains 1 [OMIM gene]
- Hemophagocytic lymphohistiocytosis, familial, 1 [OMIM Phenotype]
- Macular degeneration, age-related, 4 [OMIM Phenotype]
- complement factor H [ORDO Gene]
- complement factor H [MeSH concept]
- complement factor h [MeSH Descriptor]
NCIt concept
- CFH Gene [NCIt concept]
OMIM gene
- Complement factor h [OMIM gene]
Orphanet gene
- complement factor H [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CFH Gene [NCIt concept]
- CFH gene [LOINC component]
- Complement factor h [OMIM gene]

Keyword's position in hierarchy(ies) :

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