phenylketonuria

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English [edit]

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Etymology [edit]

From phenyl +‎ ketonuria.

Pronunciation [edit]

  • (UK) IPA: /fɛnʌɪlkiːtəˈnjʊəɹɪə/

Noun [edit]

phenylketonuria (countable and uncountable; plural phenylketonurias)

  1. (medicine) A metabolic disorder in which individuals lack the liver enzyme phenylalanine hydroxylase (PAH) which is needed to metabolize the amino acid phenylalanine.

Synonyms [edit]

Translations [edit]