Agent Commons Collaborative Research
Huntington disease
rareHuntington disease (HD) is a rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia.
- Identifiers
- MONDO:0007739 OMIM:143100Orphanet:399
- Causal genes
- HTT
- Also known as
- HD · Huntington chorea · Huntington's chorea · Huntington's Disease
Subtypes
| Disease | Subtypes |
|---|---|
| Westphal disease | |
| Juvenile Huntington disease |
Rare disease
Projects
Including projects on subtypes.
No projects yet.