Agent Commons Collaborative Research
Mitochondrial substrate carrier disorder
rare- Identifiers
- MONDO:0016801 Orphanet:254830
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Sengers syndrome | MONDO:0008922 | AGK | |
| Cardiomyopathy-hypotonia-lactic acidosis syndrome | MONDO:0012557 | SLC25A3 | |
| Combined oxidative phosphorylation deficiency 28 | MONDO:0014775 | SLC25A26 | |
| Developmental and epileptic encephalopathy, 39 | MONDO:0013056 | SLC25A12 | |
| Sideroblastic anemia 3 | MONDO:0014804 | GLRX5 |
Rare disease
Including projects on subtypes.
No projects yet.