1) genetic disease
基因病
1.
However,as an abnormal behavior of human body,which is a very complex system,diseases result not only from genetic factors,but also from other internal and external factors,therefore,not all diseases are genetic diseases.
所以 ,并不能简单地将所有的疾病都归结为基因病。
2) monogenic disease
单基因病
1.
About human monogenic diseases,there are many kinds of inheritance patterns.
人类单基因病的遗传方式有常染色体显性遗传 ,常染色体隐性遗传 ;X伴性显性遗传 ,X伴性隐性遗传 ,Y伴性遗传 ;从性遗传和限性遗传等。
2.
In recent 20 years, with the endeavor of Chinese academician, great progresses have been made in the fields of mitochondrial genetic disease, prion infection and monogenic disease, especially in Wilson disease, Duchenne muscular dystrophy and hereditary ataxia.
近20年来,通过国内学者的共同努力,神经遗传病的研究取得了长足进步,特别是肝豆状核变性、假肥大型肌营养不良、遗传性共济失调等单基因病,以及线粒体遗传病和朊蛋白感染的研究成果最为显著。
3.
Objective: (1) To study the gene mutation in a pedigree with Dowling-Meara type epidermolysis bullosa simplex(DW-EBS) of monogenic disease.
目的 (1)寻找单基因病痒疹样亚型单纯型大疱性表皮松解症(DM-EBS)一家系的基因突变位点。
3) polygenic disease
多基因病
1.
(2) To study the relationship between paraoxonasel(PON1) and coronary heart disease(CHD) of polygenic disease.
(2)探讨对氧磷酶1(PON1)与多基因病冠心病(CHD)之间的相关性。
4) Gene-Virotherapy
基因-病毒
5) viral
基因.病毒
6) transgenic virus resistance
转基因病毒抗性
参考词条
补充资料：单基因病
单基因病
病名。亦称孟德尔遗传病。指某一基因发生异常(突变)时所致的一系列遗传性疾病的总称。简言之，即一个基因突变所致的疾病。单基因病按孟德尔简单遗传规律传递，故称孟德尔遗传病。单基因病按遗传方式可分为以下4种：常染色体显性遗传病、常染色体隐性遗传病、X连锁隐性遗传及X连锁显性遗传。详见各条。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。