phenylketonuria
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English[edit]
Etymology[edit]
From phenylketone + -uria.
Pronunciation[edit]
Noun[edit]
phenylketonuria (countable and uncountable, plural phenylketonurias)
- (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]
Coordinate terms[edit]
Translations[edit]
metabolic disorder
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