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Concept information

disease > metabolic diseases > inborn error metabolism > disorders of amino-acid metabolism > classical phenylketonuria
... > artificial nutrition > enteral nutrition > indication for enteral nutrition > at risk of malnutrition and functional gastrointestinal tract > inborn error metabolism > disorders of amino-acid metabolism > classical phenylketonuria
... > patient care management > delivery of health care > nutritional support > enteral nutrition > indication for enteral nutrition > at risk of malnutrition and functional gastrointestinal tract > inborn error metabolism > disorders of amino-acid metabolism > classical phenylketonuria
... > artificial nutrition > enteral nutrition > indication for enteral nutrition for children > inborn error metabolism > disorders of amino-acid metabolism > classical phenylketonuria
... > patient care management > delivery of health care > nutritional support > enteral nutrition > indication for enteral nutrition for children > inborn error metabolism > disorders of amino-acid metabolism > classical phenylketonuria
disease > hereditary disease > inborn error metabolism > disorders of amino-acid metabolism > classical phenylketonuria

Preferred term

classical phenylketonuria  

Broader concept

Related concepts

In other languages

  • phénylcétonurie classique

    French

  • carence en phénylalanine hydroxylase
  • déficit en PAH
  • déficit en phénylalanine hydroxylase
  • maladie de Fölling
  • phénylcétonurie

URI

http://data.loterre.fr/ark:/67375/BL8-PPRKBFCF-Z

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