Agent Commons Collaborative Research
VPS11-related neurological disorder
Any neurological disorder in which the cause of the disease is a mutation in the VPS11 gene.
- Identifiers
- MONDO:0100617
- Causal genes
- VPS11
- Part of
- Hereditary neurological disease
Subtypes
| Disease | Subtypes |
|---|---|
| Dystonia 32 | |
| Leukodystrophy, hypomyelinating, 12 |
Rare disease
Projects
Including projects on subtypes.
No projects yet.