Complement component 2

Preferred Label : Complement component 2;

Symbol : C2;

CISMeF acronym : C2;

Type : Gene;

Ensembl ID : ENSG00000166278;

Prefixed ID : *613927;

Details

Origin ID

613927;

UMLS CUI

C1412938;

Automatic exact mappings (from CISMeF team)
- C2 Gene [NCIt concept]
- Complement C2 [NCIt concept]
- Complement C2 [LOINC component]
- Complement component C2 (substance) [SNOMED CT concept]
- MATCH Arm EAY131-C2 [NCIt concept]
- complement C2 [ORDO Gene]
- complement C2 [MeSH Descriptor]
- complement C2 [HGNC gene]
HGNC gene
- complement C2 [HGNC gene]
NCIt concept(s)
- C2 Gene [NCIt concept]
- C2 wt Allele [NCIt concept]
- Complement C2 [NCIt concept]
ORDO concept(s)
- complement C2 [ORDO Gene]
Phenotypes related
- Complement component 2 deficiency [OMIM Phenotype]
- Macular degeneration, age-related, 14 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- C2 Gene [NCIt concept]
- complement C2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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