5C50.01 Nonclassical phenylketonuria

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

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.

synonyms

• Nonclassical phenylketonuria
• Atypical phenylketonuria
• Atypical PKU - [phenylketonuria]

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