Ceruloplasmin - CISMeF

Preferred Label : Ceruloplasmin;

Symbol : CP;

CISMeF acronym : CP;

Type : Gene;

Alternative titles and symbols : FERROXIDASE;

Ensembl ID : ENSG00000047457;

Prefixed ID : *117700;

Details

Origin ID

117700;

UMLS CUI

C1439306;

Automatic exact mappings (from CISMeF team)
- CP Gene [NCIt concept]
- Centipoise [NCIt concept]
- Cerebral palsy [HPO term]
- Ceruloplasmin [LOINC component]
- Ceruloplasmin [MedDRA Preferred Term]
- Ceruloplasmin [NCIt concept]
- Ceruloplasmin Measurement [NCIt concept]
- Ferroxidase (substance) [SNOMED CT concept]
- Propionibacterium acnes [NCIt concept]
- centipoise (qualifier value) [SNOMED CT concept]
- cerebral palsy [MedlinePlus Topic]
- cerebral peduncle [UBERON concept]
- ceruloplasmin [ORDO Gene]
- ceruloplasmin [MeSH concept]
- ceruloplasmin [Substance BNPC]
- ceruloplasmin [MeSH Descriptor]
- ceruloplasmin [HGNC gene]
- ceruloplasmin [EMDN type]
- choroid plexus [UBERON concept]
- cortical plate [UBERON concept]
- epilepsies, partial [MeSH Descriptor]
- ferroxidase [SNOMED Notion]
- pemphigoid, benign mucous membrane [MeSH Descriptor]
- platelet concentrate [Blood Transfusion thesaurus concept]
- tablets [MeSH Descriptor]
False automatic mappings
- Chlorambucil/Prednisone Regimen [NCIt concept]
- Clipperton Island [NCIt concept]
HGNC gene
- ceruloplasmin [HGNC gene]
NCIt concept(s)
- CP Gene [NCIt concept]
- CP wt Allele [NCIt concept]
- Ceruloplasmin [NCIt concept]
ORDO concept(s)
- ceruloplasmin [ORDO Gene]
Phenotypes related
- Aceruloplasminemia [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CP Gene [NCIt concept]
- ceruloplasmin [HGNC gene]

Keyword's position in hierarchy(ies) :

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