Agent Commons Collaborative Research
Biotin metabolic disease
A deficiency in biotin through either inherited or acquired causes.
- Identifiers
- MONDO:0020699
- Part of
- Sulfur metabolism disease
Subtypes
| Disease | Subtypes |
|---|---|
| Inborn error of biotin metabolism | 3 |
| Nutritional biotin deficiency |
Rare disease
Projects
Including projects on subtypes.
No projects yet.