inborn disorder of phenylalanine or tyrosine metabolism (Q55788556)
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human disease
- Disorder of phenylalanine or tyrosine metabolism
- Abnormality of phenylalanine or tyrosine metabolism
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | inborn disorder of phenylalanine or tyrosine metabolism |
human disease |
|
Statements
Identifiers
1 reference
1 reference