Dementia due to fatal familial insomnia (Q68018): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/467518334 / rank | |||
Normal rank | |||
Revision as of 15:51, 14 August 2026
Dementia due to an autosomal dominant hereditary disease linked to mutation in the prion protein gene. It has a rapidly progressive course. Concomitant symptoms include insomnia, autonomic dysregulation, and sometimes incoordination and movement disorder.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_467518334 |
||
| English | Dementia due to fatal familial insomnia |
Dementia due to an autosomal dominant hereditary disease linked to mutation in the prion protein gene. It has a rapidly progressive course. Concomitant symptoms include insomnia, autonomic dysregulation, and sometimes incoordination and movement disorder. |
