8E02.2 Fatal familial insomnia
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
A disease of the brain, caused by inheritance of mutation(s) of normal prion protein genes. This disease is characterised by severe insomnia and autonomic system dysfunction, and is fatal. Confirmation is by pathological examination of the brain and genetic testing.
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
- Fatal familial insomnia
- FFI - [fatal familial insomnia]
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