Huntington Disease Like 2 C1847987
A rare progressive brain disorder that resembles Huntington disease with movement abnormalities and cognitive decline. Caused by a genetic mutation distinct from Huntington disease. Treatment focuses on symptom management.
Key facts at a glance
- ICD-10
- G43.909
- ICD-11
- 8A00.0
- Body system
- neurologic
- Severity
- severe
- Chronic
- true
Medication Comparisons
Compare medications used to treat Huntington Disease Like 2 C1847987. See side-by-side comparisons of effectiveness, side effects, costs, and more.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy