Complement component 9

Preferred Label : Complement component 9;

Symbol : C9;

CISMeF acronym : C9;

Type : Gene;

Ensembl ID : ENSG00000113600;

Prefixed ID : *120940;

Details

Origin ID

120940;

UMLS CUI

C1413029;

Automatic exact mappings (from CISMeF team)
- AKR1C1 wt Allele [NCIt concept]
- Active C5b6789 (substance) [SNOMED CT concept]
- Complement C9 [LOINC component]
- Complement Component C9 [NCIt concept]
- complement C9 [ORDO Gene]
- complement C9 [MeSH Descriptor]
- complement C9 [HGNC gene]
HGNC gene
- complement C9 [HGNC gene]
NCIt concept(s)
- C9 Gene [NCIt concept]
- C9 wt Allele [NCIt concept]
- Complement Component C9 [NCIt concept]
ORDO concept(s)
- complement C9 [ORDO Gene]
Phenotypes related
- Complement component 9 deficiency [OMIM Phenotype]
- Macular degeneration, age-related, 15 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- C9 Gene [NCIt concept]
- complement C9 [HGNC gene]

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