CP Gene - CISMeF

Preferred Label : CP Gene;

NCIt synonyms : Ceruloplasmin (Ferroxidase) Gene;

NCIt related terms : CP;

CISMeF acronym : CP;

NCIt definition : This gene is a metalloprotein involved in copper binding in plasma.;

Détails

Origin ID

C104137;

UMLS CUI

C1439306;

Automatic exact mappings (from CISMeF team)
- Cerebral palsy [HPO term]
- Ceruloplasmin [OMIM gene]
- Cleft palate, isolated [OMIM Phenotype]
- centipoise (qualifier value) [SNOMED CT concept]
- cerebral palsy [MedlinePlus Topic]
- cerebral peduncle [UBERON concept]
- ceruloplasmin [ORDO Gene]
- choroid plexus [UBERON concept]
- cortical plate [UBERON concept]
- epilepsies, partial [MeSH Descriptor]
- pemphigoid, benign mucous membrane [MeSH Descriptor]
- tablets [MeSH Descriptor]
HGNC gene
- ceruloplasmin [HGNC gene]
OMIM relation
- Ceruloplasmin [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Ceruloplasmin [OMIM gene]
- ceruloplasmin [HGNC gene]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Reference Gene Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_encodes_gene_product
- Ceruloplasmin [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_mapped_to_disease
- Aceruloplasminemia [NCIt concept]
gene_plays_role_in_process
- Oxidation [NCIt concept]
- Oxidation/Reduction [NCIt concept]
genetic_biomarker_related_to
- Ceruloplasmin Measurement [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients