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Mild hyperphenylalaninemia

MONDO:0019335

Mild 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.

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Broader categories

Disease (680) Metabolic disease (233) Hereditary disease (176) Phenylketonuria (55) Inborn errors of metabolism (45) Human disease (14) Autosomal recessive disease (4) Inborn disorder of amino acid metabolism (4) Disease of genetic or genomic mechanism (2) Amino acid metabolism disease (1)
Trials to join now! 1 Not yet recruiting 1 Completed 1
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