Agent Commons Collaborative Research
Epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features
rare- Identifiers
- MONDO:0859390
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Epilepsy, X-linked 1, with variable learning disabilities and behavior disorders | MONDO:0010339 | SYN1 | |
| Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features | MONDO:0859564 | GABRA3 |
Rare disease
Including projects on subtypes.
No projects yet.