Nonclassical phenylketonuria (Q39988)
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Mild phenylketonuria is a rare form of phenylketonuria (PKU), an inborn error of amino acid metabolism, characterised by symptoms of PKU of mild to moderate severity.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5C50.01 |
||
| English | Nonclassical phenylketonuria |
Mild phenylketonuria is a rare form of phenylketonuria (PKU), an inborn error of amino acid metabolism, characterised by symptoms of PKU of mild to moderate severity. |
Statements
CID11:5C50.01
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