Variant Creutzfeldt-Jakob Disease

ICD-11 code : 8E01.2;

Preferred Label : Variant Creutzfeldt-Jakob Disease;

ICD-11 definition : A disease of the brain, that is suspected to be caused by a prion associated with Bovine Spongiform Encephalopathy. This disease is characterized by a long incubation period, psychiatric symptoms followed by neurological deficits, and is fatal. Transmission may be by ingestion of food (with a bovine origin) contaminated with infected brain or spinal cord from an infected cow, or blood transfusion. Confirmation is by pathological examination of the brain.;

ICD-11 synonym : vCJD - [Variant Creutzfeldt-Jakob Disease]; vCJD;

Details

Origin ID

378572696;

Automatic exact mappings (from CISMeF team)
- Creutzfeldt-jakob disease [OMIM Phenotype]
- creutzfeldt-jakob disease [MedlinePlus Topic]
- creutzfeldt-jakob syndrome [MeSH Descriptor]
Currated CISMeF NLP mapping
- Creutzfeldt-Jakob disease variant [Blood Transfusion thesaurus concept]
- Variant Creutzfeldt-Jakob Disease [NCIt concept]
- Variant Creutzfeldt-Jakob disease [ICD-9 code]
- Variant Creutzfeldt-Jakob disease [MedDRA Preferred Term]
- Variant Creutzfeldt-Jakob disease [ORDO Disease]
- Variant Creutzfeldt-Jakob disease (disorder) [SNOMED CT concept]
- new variant Creutzfeldt-Jakob disease [MeSH concept]
- variant Creutzfeldt Jakob disease [Disease (Nov.)]
- variant Creutzfeldt-Jakob disease [DO Concept]
ICD-10 Mapping
- Atypical virus infection of central nervous system, unspecified [ICD-10 Sub-category]

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