Phenylketonuria

From BugSigDB


Phenylketonuria (PKU) is the most common inborn error of amino acid metabolism and is characterized by mild to severe mental disability in untreated patients.
Aliases
  • Folling disease
  • Folling's disease
  • Folling's syndrome
  • Følling's disease
  • HPA, non-PKU mild
  • hyperphenylalaninemia, non-PKU mild
  • imbecilitus phenylpyruvica
  • oligophrenia Phenylpyruvica
  • oligophrenia phenylpyruvica
  • PAH deficiency
  • Pah deficiency
  • pah deficiency
  • Phenylalanine hydroxylase deficiency
  • phenylalanine hydroxylase deficiency
  • phenylalaninemia
  • phenylketonuria
  • phenylketonuria
  • phenylketonuria, maternal
  • phenylpyruvic oligophrenia
  • PKU