Prion protein - CISMeF

Preferred Label : Prion protein;

Symbol : PRNP;

CISMeF acronym : PRNP;

Type : Gene;

Alternative titles and symbols : Prion-related protein; PRP; PRIP;

Ensembl ID : ENSG00000171867;

Prefixed ID : *176640;

Details

Origin ID

176640;

UMLS CUI

C1418941;

Automatic exact mappings (from CISMeF team)
- ABCB6 wt Allele [NCIt concept]
- Atypical adult pityriasis rubra pilaris (disorder) [SNOMED CT concept]
- CARD14 wt Allele [NCIt concept]
- Major Prion Protein [NCIt concept]
- NCOA6 wt Allele [NCIt concept]
- Nuclear Receptor Coactivator 6 [NCIt concept]
- PRNP Gene [NCIt concept]
- PRNP gene [LOINC component]
- PRNP wt Allele [NCIt concept]
- Panretinal photocoagulation (procedure) [SNOMED CT concept]
- Pityriasis rubra pilaris [ICD-11 Category]
- Platelet-rich Plasma [NCIt concept]
- Prion (organism) [SNOMED CT concept]
- Prion Proteins [MeSH Descriptor]
- Prion Proteins [MeSH concept]
- Therapeutic Autologous Platelet-rich Plasma [NCIt concept]
- nucleus prepositus [UBERON concept]
- prion protein [ORDO Gene]
- prion protein (Kanno blood group) [HGNC gene]
HGNC gene
- prion protein (Kanno blood group) [HGNC gene]
NCIt concept(s)
- Major Prion Protein [NCIt concept]
- PRNP Gene [NCIt concept]
- PRNP wt Allele [NCIt concept]
ORDO concept(s)
- prion protein [ORDO Gene]
Phenotypes related
- Creutzfeldt-jakob disease [OMIM Phenotype]
- Fatal familial insomnia [OMIM Phenotype]
- Gerstmann-straussler disease [OMIM Phenotype]
- Huntington disease-like 1 [OMIM Phenotype]
- Kuru, susceptibility to [OMIM Phenotype]
- Spongiform encephalopathy with neuropsychiatric features [OMIM Phenotype]
See also inter- (CISMeF)
- Prion protein [LOINC component]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PRNP Gene [NCIt concept]
- PRNP gene [LOINC component]
- prion protein (Kanno blood group) [HGNC gene]

Keyword's position in hierarchy(ies) :

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