Gilbert's syndrome
Third-person singular simple present indicative form of latticize
Third-person singular simple present indicative form of autoscroll
A hereditary condition characterized by hyperbilirubinemia due to reduced activity of the enzyme glucuronyltransferase.
plural of Carew
定期的な血液検査の結果、彼女はグルクロン酸抱合酵素の活性低下による高ビリルビン血症を特徴とする遺伝性の疾患、ジルベール症候群と診断されました。
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