酶缺乏的英文

• azymia
• enzymatic defect
• enzymatic deficiencies

• "酶"英文翻译    enzyme; ferment
• "缺乏"英文翻译    be short of; lack; deficienc ...
• "asa合酶缺乏" 英文翻译 :    asa synthase deficiency
• "atp酶缺乏症" 英文翻译 :    atpase deficiency
• "c1酯酶缺乏" 英文翻译 :    c1 esterase deficiency
• "ump合酶缺乏" 英文翻译 :    ump synthase deficiency
• "二糖酶缺乏" 英文翻译 :    disaccharidase deficiency
• "黄递酶缺乏" 英文翻译 :    diaphorase deficiency
• "酶缺乏的" 英文翻译 :    enzymopenic; enzymoprivic
• "醛缩酶缺乏" 英文翻译 :    deficiency of aldolase
• "乳糖酶缺乏" 英文翻译 :    alactasia
• "脱碘酶缺乏" 英文翻译 :    deiodinase deficiency
• "胰酶缺乏症" 英文翻译 :    pancreatic enzyme deficiency
• "黄递酶缺乏症,黄递酶缺乏" 英文翻译 :    diaphorase deficiency
• "18-羟化酶缺乏" 英文翻译 :    18-hydroxylase deficiency
• "omp脱羧酶缺乏" 英文翻译 :    omp decarboxylase deficiency
• "α-羟化酶缺乏" 英文翻译 :    alpha-hydroxylase deficiency
• "表异构酶缺乏" 英文翻译 :    epimerase deficiency
• "肠肠激酶缺乏" 英文翻译 :    intestinal enterokinase deficiency
• "肠肠肽酶缺乏" 英文翻译 :    intestinal enteropeptidase deficiency
• "肠二糖酶缺乏" 英文翻译 :    intestinal disaccharidase deficiency
• "肠激酶缺乏症" 英文翻译 :    enterokinase deficiency
• "多羧酶缺乏症" 英文翻译 :    multiple carboxylase dificiency
• "肝脂酶缺乏症" 英文翻译 :    hepatic lipase deficiency
• "果糖激酶缺乏" 英文翻译 :    fructokinase deficiency

• Phenylketonuria is a condition in which phenylalanine to tyrosine conversion is diminished because the enzyme phenylalanine hydroxylaze is deficient .
  苯丙酮酸尿症是一种由于苯丙氨酸羟化酶缺乏，苯丙氨酸转变成酪氨酸的过程被削弱的病。
• Study of newborn umbilical blood screening of g6pd deficiency
  磷酸脱氢酶缺乏的研究
• Scid with adenosine deaminase deficiency scid
  并线苷酸去胺酶缺乏
• Hypophosphatasia is a rare inherited metabolic disease characterized by rickets with reduced plasma and tissue alkaline phosphatase activity
  摘要先天性磷酸酶缺乏症为一少见之代谢性疾病，其主要特徵为血清及组识之硷性磷酸酶下降以及佝偻症。
• Phenylketonuria ( pku ) is an inherited metabolic disease that results in mental retardation and other neurological problems when treatment is not started within the first few weeks of life . the disease arises from the deficiency of a single enzyme , phenylalanine hydroxylase , which converts the essential amino acid , phenylalanine , to another amino acid , tyrosine . failure of the conversion to take place results in a buildup of phenylalanine in the body that then damages the central nervous system
  苯丙酮尿症（ pku ）是一种智力发育不全的先天性疾病，患者由于肝赃内苯丙氨酸羟化酶缺乏，苯丙氨酸不能正常代谢为酪氨酸，从而导致苯丙氨酸在肌体组织内积累，引起脑损伤和累进性精神障碍，临床表现为智力低下,头发颜色转黄，尿有异臭味，重者似鼠臭。

• 酶缺乏的泰文