Genetic Creutzfeldt-Jakob disease

ICD-11 code : 8E02.0;

Preferred Label : Genetic Creutzfeldt-Jakob disease;

ICD-11 definition : A disease of the brain, that is associated with a prion. This disease is characterized by neurological deficits, and is fatal. Confirmation is by pathological examination of the brain.;

ICD-11 synonym : Jakob-Creutzfeldt disease; JCD - [Jakob-Creutzfeldt disease]; CJD - [Creutzfeldt-Jakob disease]; Creutzfeldt-Jakob disease; Creutzfeldt-Jakob;

ICD-11 acronym : JCD; CJD;

Details

Origin ID

607607042;

UMLS CUI

C0022336;

Automatic exact mappings (from CISMeF team)
- CJD [MedDRA LLT]
- Creutzfeldt-Jakob disease [Blood Transfusion thesaurus concept]
- PRNP wt Allele [NCIt concept]
- prion protein [ORDO Gene]
- prion protein (Kanno blood group) [HGNC gene]
Currated CISMeF NLP mapping
- CREUTZFELDT-JAKOB DISEASE [WHO-ART Preferred Term]
- Creutzfeldt-Jakob Disease [NCIt concept]
- Creutzfeldt-Jakob disease [PASCAL descriptor]
- Creutzfeldt-Jakob disease [MedDRA Preferred Term]
- Creutzfeldt-Jakob disease [ICD-10 Sub-category]
- Creutzfeldt-Jakob disease [DO Concept]
- Creutzfeldt-Jakob syndrome [MeSH concept]
- Creutzfeldt-jakob disease [OMIM Phenotype]
- 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 disease [MedlinePlus Topic]
- creutzfeldt-jakob syndrome [MeSH Descriptor]
- jakob-creutzfeldt disease [SNOMED Notion]
ICD-10 Mapping
- Creutzfeldt-Jakob disease [ICD-10 Sub-category]
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 [DO Concept]
- Creutzfeldt-Jakob disease [ICD-10 Sub-category]
- Creutzfeldt-Jakob disease [MedDRA Preferred Term]
- Creutzfeldt-Jakob syndrome [MeSH concept]
- Creutzfeldt-jakob disease [OMIM Phenotype]
- 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 disease [MedlinePlus Topic]
- creutzfeldt-jakob syndrome [MeSH Descriptor]
- jakob-creutzfeldt disease [SNOMED Notion]
- transmissible virus dementia [SNOMED Notion]

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