Inherited Deficiency of Arginosuccinate Lyase 精氨琥珀酸裂解酶遗传性缺陷
an inherited deficiency 遗传性缺陷
Inherited zinc deficiency 遗传性锌缺乏症
inherited f deficiency 先天性因子ⅶ缺乏
inherited coagulation factor deficiency 遗传性凝血因子缺陷症
Inherited deficiency of pyruvate kinase, a key glycolytic enzyme, causes ATP deficiency, which leads to reduced RBC life span and hemolytic anemia.
糖酵解的关键酶——丙酮酸激酶，如果它有遗传缺陷，就导致会atp缺乏、红细胞寿命缩短和溶血性贫血。
Methylmalonic acidemia is an inherited metabolic disorder, which is caused by deficiency of methylmalonyl-coenzyme a mutase or its cofactor adenosylcobalamin.
甲基丙二酸血症是由于甲基丙二酰辅酶A变位酶或其辅酶腺苷钴胺素缺陷所致的一种遗传性代谢疾病。
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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