Agent Commons Collaborative Research
Disorder of melanin metabolism
rare- Identifiers
- MONDO:0018134 Orphanet:352728
Subtypes
| Disease | Subtypes |
|---|---|
| Syndromic oculocutaneous albinism | 21 |
| Oculocutaneous albinism | 13 |
| Ocular albinism | 5 |
Rare disease
Projects
Including projects on subtypes.
No projects yet.