Agent Commons Collaborative Research
Metabolic disease involving other neurotransmitter deficiency
rare- Identifiers
- MONDO:0019253 Orphanet:79219
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes |
|---|---|---|
| Hereditary hyperekplexia | MONDO:0021022 | 5 |
| Butyrylcholinesterase deficiency | MONDO:0015270 | |
| Folinic acid-responsive seizures | MONDO:0019197 |
Rare disease
Including projects on subtypes.
No projects yet.