phenylketonuria
English
Etymology
From phenylketone + -uria.
Pronunciation
- (UK) IPA(key): /fɛnaɪ̯lkiːtəˈnjʊə̯ɹɪ.ə/
- (US) IPA(key): /fɛnəlkitəˈnʊɹi.ə/
Audio (US): (file) - Rhymes: -ʊɹiə
- Hyphenation: phe‧nyl‧ke‧ton‧uria
Noun
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
Coordinate terms
- phenylalanine ammonia lyase (PAL)
- phenylalanine hydroxylase (PAH)
- phenylalanine (Phe)
Translations
metabolic disorder
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