Hunter syndrome, known more formally as mucopolysaccharidosis type II or MPS II, is an extremely rare inherited enzyme disorder that occurs almost exclusively in males.

亨特氏综合症是二型粘多糖沉积病(MPS II)，是一种极其罕见的遗传性酶紊乱疾病，发病者基本只有男性。

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AIM: To study the relationship of the polymorphism of angiotensin converting enzyme (ACE) gene and hypertensive disorder complicating pregnancy (HDCP).

前言：目的：探讨妊娠期高血压疾病(H DCP)与血管紧张素转换酶(ace)基因多态性的关系。

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Gaucher disease is an inherited disorder that is caused by a deficiency in an enzyme called glucocerebrosidase.

戈谢病是一种遗传性疾病，是由缺乏一种名为葡萄糖脑苷脂酶的酶引起的。

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