Mild phenylketonuria

MONDO:0019258

Mild phenylketonuria is a rare form of phenylketouria (PKU), an inborn error of amino acid metabolism, characterized by symptoms of PKU of mild to moderate severity.

Also known as: mPKU, mild PKU, variant PKU, variant phenylketonuria

0 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)

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