Complement component 1, s subcomponent

Preferred Label : Complement component 1, s subcomponent;

Symbol : C1S;

CISMeF acronym : C1S;

Type : Gene;

Alternative titles and symbols : Complement component c1s;

Ensembl ID : ENSG00000182326;

Prefixed ID : *120580;

Details

Origin ID

120580;

UMLS CUI

C1412937;

Automatic exact mappings (from CISMeF team)
- Complement C1s [LOINC component]
- Complement C1s Subcomponent [NCIt concept]
- Complement component C1 (substance) [SNOMED CT concept]
- Complement component C1s (substance) [SNOMED CT concept]
- complement C1s [ORDO Gene]
- complement C1s [HGNC gene]
- complement component c1s [SNOMED Notion]
HGNC gene
- complement C1s [HGNC gene]
NCIt concept(s)
- C1S Gene [NCIt concept]
- C1S wt Allele [NCIt concept]
- Complement C1s Subcomponent [NCIt concept]
ORDO concept(s)
- complement C1s [ORDO Gene]
Phenotypes related
- Complement component c1s deficiency [OMIM Phenotype]
- Ehlers-danlos syndrome, periodontal type, 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- C1S Gene [NCIt concept]
- complement C1s [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients