Mild hyperphenylalaninemia (HPA) is a rare form of phenylketonuria, an inborn error of amino acid metabolism, characterized by mild symptoms of HPA.
Comprehensive, easy-to-understand information about this condition
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maternal phenylketonuria
MONDO:0016366
tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria
MONDO:0017389
mild phenylketonuria
MONDO:0019258
classic phenylketonuria
MONDO:0019259