8A02.11 Dystonia-plus
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
This is a group of heterogenous syndromes present with dystonia – a disorder of involuntary muscle contractions – along with other clinical features, but not in tandem with a neurodegenerative disease. Examples include myoclonus dystonia and dopa responsive dystonia.
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
- Dystonia-plus
- Myoclonus-dystonia
- Dopa-responsive dystonia
- Segawa syndrome
- DYT5
- DRD - [dopa-responsive dystonia]
- Autosomal dominant dopa-responsive dystonia
- Hereditary progressive dystonia with marked diurnal fluctuation
- Autosomal dominant Segawa syndrome
- DYT5a
- HPD - [ hereditary progressive dystonia] with marked diurnal fluctuation
- Autosomal dominant DRD - [dopa-responsive dystonia]
- Autosomal recessive dopa-responsive dystonia
- Autosomal recessive Segawa syndrome
- Autosomal recessive DRD - [dopa-responsive dystonia]
- Tyrosine hydroxylase deficiency
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