hereditary disease

Jin: You never know. That's a hereditary disease. I wouldn't want my nephews to get it.

阿敬: 天有不测风云. 那是一种遗传疾病. 我可不想让我的外甥有这种病.

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That's a hereditary disease.

那是一种遗传疾病.

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Is leukaemia hereditary disease? Can be you cured? What disease is there?

白血病是遗传病 吗 ?能治愈 么 ?有什么病症?

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Primary congenital glaucoma ( PCG ) is a blind leading hereditary disease.

原发性先天性青光眼 ( primarycongenital glauco-ma,PCG ) 是一种遗传性致盲眼病.

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Is this disease hereditary?

这种病遗传 吗 ?

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Is leukaemia hereditary disease or contagion?

白血病是遗传病还是传染病?

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Does dominance hereditary disease have those ? Recessive have those again ?

像红绿色盲, 白化病,血友病都是隐性遗传病,六指就是显性的.

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Retinitis pigmentosa is one hereditary disease that cause blind eyes and have relatively high incidence disease.

视网膜色素变性是一种遗传性致盲性眼病,发病率较高,危害性较大.

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High risk hereditary disease families were studied by using genetic analytic methods.

用遗传分析方法对150户遗传病高危家庭进行了分析。

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Glucose-6-phosphate dehydrogenase ( G6PD) is the key enzyme of Pentose Phosphate Pathway, G6PD deficiency is common hereditary disease.

G6PD是磷酸戊糖旁路代谢的限速酶，也是重要的看家酶.G6PD缺乏症是人类常见的遗传性疾病。

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The investigation on hereditary disease and congenital malformation, on the children below eleven years old and living in the surrounding area of the nuclear test site and control area is reported.

本文报告了在新疆核试验场周围地区和对照区居住10年以上家庭的11岁以下儿童的19种遗传性疾病及先天性畸形的调查结果。

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It is said that cholera is a rare hereditary disease.

据说,舞蹈症是一种具有家庭遗传性的罕见病症.

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PM can cause many complications including amblyopia, glaucoma, cataract, vitreous opacification, Detachment of retina etc, and become a kind of severe hereditary ocular disease that can lead to blinding.

可伴有弱视、青光眼、白内障、玻璃体混浊、视网膜脱离等多种并发症，是导致低视力及盲的重要遗传眼病之一。

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Clinical disease severity and axonal dysfunction in hereditary motor and sensory neuropathy Ia

I a型遗传性运动感觉神经病的临床严重程度和轴突功能障碍

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α-Thalassemia major is a hereditary disease with a syndrome of hemolytic anemia, often caused bv the complete or partial deletion of a-globin genes.

α-地中海贫血是由于α-珠蛋白基因全部和部分缺失所致的一种遗传性溶血性贫血综合征。

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A rat with retinal hereditary disease similar to congenital stationary night blindness patient's ERG

类似先天性静止性夜盲症视觉电生理异常大鼠1例

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The retinitis pigmentosa ( RP ) is an hereditary disease which causes visual deficiency leading to blindness.

视网膜 色素 变性 是一种具有遗传性的致盲性眼病.

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[ Background and objective] Charcot-Marie-Tooth ( CMT) disease, also known as hereditary motor and sensory neuropathies ( HMSN), is genetically heterogeneous and characterized by slowly progressive distal muscle wasting and weakness with sensory loss.

[背景与目的]腓骨肌萎缩症（Charcot-Marie-Tooth，CMT）亦称为遗传性运动感觉神经病，具有明显的遗传异质性，临床主要特征是四肢远端进行性的肌无力、肌萎缩以及感觉障碍。

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It is a recessive hereditary disease of autosome to be deaf and dumb. It was analysed through heredity that reducing or preventing consanguineous marriage can reduce the deaf-mute's birth rate.

聋哑是常染色体隐性遗传病，通过遗传分析发现，减少或防止近亲结婚可以降低聋哑人的出生。

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