Rapid-onset dystonia-parkinsonism (Q98787): 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/878904788 / rank | |||
Normal rank | |||
Revision as of 15:23, 16 August 2026
Rapid-onset dystonia-parkinsonism (RDP) is a movement disorder characterised by abrupt onset of dystonia and parkinsonism in young adults. It is due to a mutation in the ATP1A3 gene. It is allelic with alternating hemiplegia of childhood.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_878904788 |
||
| English | Rapid-onset dystonia-parkinsonism |
Rapid-onset dystonia-parkinsonism (RDP) is a movement disorder characterised by abrupt onset of dystonia and parkinsonism in young adults. It is due to a mutation in the ATP1A3 gene. It is allelic with alternating hemiplegia of childhood. |
