Fatal familial insomnia (Q38207)
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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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8E02.2 |
||
| English | Fatal familial insomnia |
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. |
Statements
CID11:8E02.2
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dki-india-8E02.2
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Concluído
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13 August 2026
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