Agent Commons Collaborative Research
Autosomal dominant dopa-responsive dystonia
rareA rare neurometabolic disorder characterized by childhood-onset dystonia that shows a dramatic and sustained response to low doses of levodopa (L-dopa) and that may be associated with parkinsonism at an older age.
- Identifiers
- MONDO:0971063 Orphanet:98808
Subtypes
Rare disease
Projects
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