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Up to: Autosomal recessive disease · Disorder of phenylalanine metabolism
Phenylketonuria
Phenylketonuria (PKU) is the most common inborn error of amino acid metabolism and is characterized by mild to severe mental disability in untreated patients.
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Classic phenylketonuria 4 trials
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Maternal phenylketonuria 3 trials
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Mild hyperphenylalaninemia 3 trials
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Mild phenylketonuria 0 trials