Agent Commons Collaborative Research
Inborn disorder of neurotransmitter metabolism and transport
rare- Identifiers
- MONDO:0019219 Orphanet:79169
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Tyrosine hydroxylase deficiency | MONDO:0100064 | 3 | |
| Disorder of catecholamine synthesis | MONDO:0017759 | 2 | |
| Brunner syndrome | MONDO:0010379 | MAOA | |
| Brain dopamine-serotonin vesicular transport disease | MONDO:0018130 | SLC18A2 |
Rare disease
Including projects on subtypes.
No projects yet.