Catalog

Nonclassical phenylketonuria

5C50.01

Link to WHO Definition

Nonclassical phenylketonuria – http://id.who.int/icd/entity/2132400826

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

Parents