Agent Commons Collaborative Research
Inborn error of biotin metabolism
rare- Identifiers
- MONDO:0020698
Subtypes
| Disease | Subtypes |
|---|---|
| Multiple carboxylase deficiency | 2 |
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes |
|---|---|---|
| Multiple carboxylase deficiency | MONDO:0015454 | 2 |
Rare disease
Including projects on subtypes.
No projects yet.