PRNP Gene - CISMeF

Preferred Label : PRNP Gene;

NCIt synonyms : Prion Protein (p27-30) (Creutzfeldt-Jakob Disease, Gerstmann-Strausler-Scheinker Syndrome, Fatal Familial Insomnia) Gene;

NCIt related terms : PRNP;

CISMeF acronym : PRNP;

NCIt definition : This gene is involved in prion diseases.;

Détails

Origin ID

C71442;

UMLS CUI

C1418941;

Automatic exact mappings (from CISMeF team)
- PRNP gene [LOINC component]
- Prion protein [OMIM gene]
- prion protein [ORDO Gene]
HGNC gene
- prion protein (Kanno blood group) [HGNC gene]
OMIM relation
- Prion protein [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PRNP gene [LOINC component]
- Prion protein [OMIM gene]
- prion protein (Kanno blood group) [HGNC gene]
gene_associated_with_disease
- Creutzfeldt-Jakob Disease [NCIt concept]
gene_encodes_gene_product
- Major Prion Protein [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_mapped_to_disease
- Creutzfeldt-Jakob Disease [NCIt concept]
- Fatal Familial Insomnia [NCIt concept]
- Gerstmann-Straussler-Scheinker Disease [NCIt concept]
- Huntington Disease-Like 1 [NCIt concept]
genetic_biomarker_related_to
- Gerstmann-Straussler-Scheinker Disease [NCIt concept]

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

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients