8E02.0 Genetic Creutzfeldt-Jakob disease
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
A disease of the brain, that is associated with a prion. This disease is characterised by neurological deficits, and is fatal. Confirmation is by pathological examination of the brain.
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has manifestation - multiple selections are allowed
synonyms
- Genetic Creutzfeldt-Jakob disease
- CJD - [Creutzfeldt-Jakob disease]
- Creutzfeldt-Jakob
- Creutzfeldt-Jakob disease
- JCD - [Jakob-Creutzfeldt disease]
- Genetic prion disease due to prion gene mutations
- Dementia due to Creutzfeldt-Jakob disease
- transmissible virus dementia
- Creutzfeldt-Jakob disease encephalopathy
- Subacute spongiform encephalopathy
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