See phenylketonuria in All languages combined, or Wiktionary
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"A metabolic disorder in which individuals lack the liver enzyme phenylalanine hydroxylase (PAH) which is needed to metabolize the amino acid phenylalanine."
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"(medicine) A metabolic disorder in which individuals lack the liver enzyme phenylalanine hydroxylase (PAH) which is needed to metabolize the amino acid phenylalanine."
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"sense": "metabolic disorder",
"word": "苯丙酮尿癥"
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{
"code": "cmn",
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"roman": "běnbǐngtóngniàozhèng",
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{
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"A metabolic disorder in which individuals lack the liver enzyme phenylalanine hydroxylase (PAH) which is needed to metabolize the amino acid phenylalanine."
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"code": "cmn",
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"sense": "metabolic disorder",
"word": "苯丙酮尿癥"
},
{
"code": "cmn",
"lang": "Chinese Mandarin",
"roman": "běnbǐngtóngniàozhèng",
"sense": "metabolic disorder",
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"code": "cmn",
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"word": "苯酮尿症"
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"word": "fenilcetonúria"
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"code": "tr",
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"sense": "metabolic disorder",
"word": "fenilketonüri"
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"word": "phenylketonuria"
}
Download raw JSONL data for phenylketonuria meaning in English (3.4kB)
This page is a part of the kaikki.org machine-readable English dictionary. This dictionary is based on structured data extracted on 2024-11-06 from the enwiktionary dump dated 2024-10-02 using wiktextract (fbeafe8 and 7f03c9b). The data shown on this site has been post-processed and various details (e.g., extra categories) removed, some information disambiguated, and additional data merged from other sources. See the raw data download page for the unprocessed wiktextract data.
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