Complement component 3

Preferred Label : Complement component 3;

Symbol : C3;

CISMeF acronym : C3;

Type : Gene;

Included titles and symbols : C3a; C3b; C3c; C3d; Acylation-stimulating protein; ASP;

Ensembl ID : ENSG00000125730;

Prefixed ID : *120700;

Détails

Origin ID

120700;

UMLS CUI

C1332656;

Automatic exact mappings (from CISMeF team)
- A1CF wt Allele [NCIt concept]
- ASIP wt Allele [NCIt concept]
- ASPED [MedDRA LLT]
- ASPM wt Allele [NCIt concept]
- ATG5 wt Allele [NCIt concept]
- Agouti-Signaling Protein [NCIt concept]
- Angel-shaped phalango-epiphyseal dysplasia [ORDO Disease]
- Aspartic Acid [NCIt concept]
- Aspartic Acid Measurement [NCIt concept]
- C3 Gene [NCIt concept]
- C3D Format [NCIt concept]
- Complement C3 [NCIt concept]
- Complement C3 Measurement [NCIt concept]
- Complement C3a DesArg Measurement [NCIt concept]
- Complement C3a Measurement [NCIt concept]
- Complement C3b Measurement [NCIt concept]
- Complement C3d [NCIt concept]
- Naja haje (organism) [SNOMED CT concept]
- aspartoacylase [ORDO Gene]
- assembly factor for spindle microtubules [ORDO Gene]
- central oculomotor nucleus [UBERON concept]
- complement C3 [ORDO Gene]
- complement C3 [MeSH Descriptor]
- complement C3 [HGNC gene]
- viperidae [MeSH Descriptor]
HGNC gene
- complement C3 [HGNC gene]
NCIt concept(s)
- Acylation Stimulating Protein [NCIt concept]
- C3 Gene [NCIt concept]
- C3 wt Allele [NCIt concept]
- C3a Anaphylatoxin [NCIt concept]
- Complement C3 [NCIt concept]
- Complement C3 Beta Chain [NCIt concept]
- Complement C3d [NCIt concept]
ORDO concept(s)
- complement C3 [ORDO Gene]
Phenotypes related
- Complement component 3 deficiency, autosomal recessive [OMIM Phenotype]
- Hemolytic uremic syndrome, atypical, susceptibility to, 5 [OMIM Phenotype]
- Macular degeneration, age-related, 9 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- C3 Gene [NCIt concept]
- complement C3 [HGNC gene]

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