Mild hyperphenylalaninemia
MONDO:0019335Mild hyperphenylalaninemia (HPA) is a rare form of phenylketonuria, an inborn error of amino acid metabolism, characterized by mild symptoms of HPA.
Also known as: mHPA, mild HPA, non-PKU HPA
3 clinical trials for this condition and its sub-types, 3 tagged with Mild hyperphenylalaninemia itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Part of