Fatal familial insomnia (Q38207): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| (One intermediate revision by the same user not shown) | |||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Linked ICD 10 | |||||||||||||||
| Property / Linked ICD 10: A81.9 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 02:56, 13 August 2026
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
0 references
dki-india-8E02.2
0 references
Concluído
0 references
13 August 2026
0 references
