creutzfeldt-jakob disease

Preferred Label : creutzfeldt-jakob disease;

MedlinePlus synonym : vcjd; bovine spongiform encephalopathy; jakob-creutzfeldt disease; mad cow disease; prion diseases;

MedlinePlus acronym : CJD; BSE;

Details

Origin ID

T1242;

UMLS CUI

C0022336;

Automatic exact mappings (from CISMeF team)
- Bovine spongiform encephalopathy (disorder) [Inactive SNOMED CT concept]
- Breast Self-Examination [NCIt concept]
- CJD [MedDRA LLT]
- Creutzfeldt-Jakob disease [Blood Transfusion thesaurus concept]
- Human prion disease [ORDO Disease]
- Jacob-Creutzfeld disease [MedDRA LLT]
- Jakob-Creutzfeldt disease [ACR pathology]
- PRNP wt Allele [NCIt concept]
- Prion Disease Pathway [NCIt concept]
- Prion disease [MedDRA Preferred Term]
- Prion disease [PASCAL descriptor]
- Prion disease (disorder) [SNOMED CT concept]
- Spongiform encephalopathy (disorder) [SNOMED CT concept]
- Variant Creutzfeldt-Jakob Disease [ICD-11 Subcategory]
- Variant Creutzfeldt-Jakob disease [ORDO Disease]
- back scattered electrons [IUPAC Term]
- bovine spongiform encephalopathy [Blood Transfusion thesaurus concept]
- bovine spongiform encephalopathy [SNOMED Notion]
- encephalopathy, bovine spongiform [MeSH Descriptor]
- encephalopathy, bovine spongiform [MeSH concept]
- prion disease [DO Concept]
- prion disease [Blood Transfusion thesaurus concept]
- prion diseases [MeSH Descriptor]
- prion diseases [MeSH concept]
- prion protein [ORDO Gene]
- prion protein (Kanno blood group) [HGNC gene]
- variant Creutzfeldt-Jakob disease [DO Concept]
Currated CISMeF NLP mapping
- CREUTZFELDT-JAKOB DISEASE [WHO-ART Preferred Term]
- Creutzfeldt Jakob disease [Disease (Nov.)]
- Creutzfeldt-Jakob Disease [NCIt concept]
- Creutzfeldt-Jakob disease [ICD-10 Sub-category]
- Creutzfeldt-Jakob disease [ICD-10 Sub-category (who)]
- Creutzfeldt-Jakob disease [PASCAL descriptor]
- Creutzfeldt-Jakob disease [DO Concept]
- Creutzfeldt-Jakob disease [MedDRA Preferred Term]
- Creutzfeldt-Jakob syndrome [MeSH concept]
- Creutzfeldt-jakob disease [OMIM Phenotype]
- Genetic Creutzfeldt-Jakob disease [ICD-11 Subcategory]
- Jakob-Creutzfeldt disease [ICD-9 code]
- Jakob-Creutzfeldt disease [MedDRA LLT]
- Jakob-Creutzfeldt disease (disorder) [SNOMED CT concept]
- Spastic pseudosclerosis [OMIM Phenotype]
- Sporadic Creutzfeldt-Jakob disease [ORDO Disease]
- creutzfeldt-jakob syndrome [MeSH Descriptor]
- jakob-creutzfeldt disease [SNOMED Notion]
False automatic mappings
- Epidermolysis bullosa simplex [ORDO Disease]
MeSH descriptor(s)
- creutzfeldt-jakob syndrome [MeSH Descriptor]
- encephalopathy, bovine spongiform [MeSH Descriptor]
- prion diseases [MeSH Descriptor]
See also
- animal diseases and your health [MedlinePlus Topic]
- brain diseases [MedlinePlus Topic]
- degenerative nerve diseases [MedlinePlus Topic]
- food safety [MedlinePlus Topic]
See also inter- (CISMeF)
- Variant Creutzfeldt-Jakob Disease [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- CJ disease [MedDRA LLT]
- CJD [MedDRA LLT]
- CREUTZFELDT-JAKOB DISEASE [WHO-ART Preferred Term]
- Creutzfeld-Jacob disease [MedDRA LLT]
- Creutzfeld-Jakob disease [MedDRA LLT]
- Creutzfeldt-Jakob Disease [NCIt concept]
- Creutzfeldt-Jakob disease [MedDRA Preferred Term]
- Creutzfeldt-Jakob disease [ICD-10 Sub-category]
- Creutzfeldt-Jakob disease [DO Concept]
- Creutzfeldt-Jakob disease [ICD-10 Sub-category (who)]
- Creutzfeldt-Jakob syndrome [MeSH concept]
- Creutzfeldt-jakob disease [OMIM Phenotype]
- Genetic Creutzfeldt-Jakob disease [ICD-11 Subcategory]
- Jacob-Creutzfeld disease [MedDRA LLT]
- Jakob-Creutzfeldt disease [ICD-9 code]
- Jakob-Creutzfeldt disease [MedDRA LLT]
- Jakob-Creutzfeldt disease (disorder) [SNOMED CT concept]
- Sporadic Creutzfeldt-Jakob disease [ORDO Disease]
- creutzfeldt-jakob syndrome [MeSH Descriptor]
- jakob-creutzfeldt disease [SNOMED Notion]
- transmissible virus dementia [SNOMED Notion]
Validated automatic mappings to NTBT
- Transmissible Spongiform Encephalopathy [NCIt concept]

Keyword's position in hierarchy(ies) :

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