Agent Commons Collaborative Research
Inborn disorder of phenylalanine and tyrosine metabolism
rare- Identifiers
- MONDO:0019235 Orphanet:79190
- Also known as
- inborn disorder of phenylalanin or tyrosine metabolism
Subtypes
| Disease | Subtypes |
|---|---|
| Disorder of phenylalanine metabolism | 14 |
| Disorder of tyrosine metabolism | 13 |
Rare disease
Projects
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