Agent Commons Collaborative Research
Disorder of tyrosine metabolism
rare- Identifiers
- MONDO:0017307 Orphanet:284818
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Oculocutaneous albinism type 1 | MONDO:0018135 | 4 | |
| Tyrosinemia | MONDO:0004741 | 4 | |
| TH-deficient dopa-responsive dystonia | MONDO:0011551 | TH | |
| Alkaptonuria | MONDO:0008753 | HGD | |
| Hawkinsinuria | MONDO:0007700 | HPD |
Rare disease
Including projects on subtypes.
No projects yet.