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hereditary disease

美英

n.遗传病
网络遗传性疾病；遗传疾病；遗传性病

hereditary disease

英-汉网络释义

hereditary disease

遗传病

医学英语 ... Herbivore 草食性动物 Hereditary disease 遗传〔性疾〕病 Hereditary 遗传 ...

遗传性疾病

生物科学词汇（简体） ... hereditary 遗传的 hereditary disease 遗传病；遗传性疾病 heredity 遗传 ...

遗传疾病

遗传疾病(hereditary disease)涵盖的范围非常广, 它指的是因遗传物质或遗传因素的改变所造成的疾病, 有些会遗传给下一代或 …

遗传性病

... hereditary disease1. 遗传病 hereditary disease[ 医] 遗传性[疾]病 1.That's a hereditary disease. 那是一种遗传疾病。 ...

例句：

The bride and groom-to-be swore they were "of complete Aryan descent" and had "no hereditary disease to exclude their marriage . "

新娘和新郎宣誓他们是 “纯亚利安人种 ”，“没有不能结婚的遗传病。”

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

Ulcerative colitis (UC) is a complex , polygenetic hereditary disease and its pathogenesis is not fully known yet .

溃疡性结肠炎（UC ）为复杂的多基因遗传性疾病，其发病机制至今不明。

Conclusions DM is a hereditary disease. The main clinical features are muscle weakness and myotonia associated with multisystem lesions.

结论 DM 是一种以肌无力和肌强直为主要表现的多系统损害的遗传性疾病；

Perhaps the most thoroughly analyzed hereditary disease are those in which abnormal hemoglobin molecules are produced .

也许最详尽分析过的遗传性的疾病，乃是那些产生异常血红蛋白的遗传病。

Congenital fibrosis syndrome is a rare familial hereditary disease, characterized by fibrotic change of extraocular muscles.

先天性纤维化症候群是一少见的家族性遗传疾病。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease .

枫糖尿症属于常染色体隐性遗传病。

Craniomandibular osteopathy is a hereditary disease in West Highland White Terriers and also occurs in other terrier breeds.

前颚骨病是一种常见于西部高地白梗和其他梗类犬的一种遗传病。

Sara : That's right . And besides , our babies will be at lower risk for hereditary disease because we're an interracial couple .

莎拉：没错。此外，我们的孩子得遗传疾病的风险会比较低，因为我们是异国情侣。

Is leukaemia hereditary disease or contagion?

白血病是遗传病还是传染病？。

Cystic fibrosis is a hereditary disease.

囊性纤维性病是一种遗传性

Kallmann syndrome is a kind of hereditary disease caused by chromosome abnormality and presents as amenorrhea , sex infantilism, and anosmia .

Kallmannsyndrome 是一种染色体异常引起的遗传性疾病，表现为闭经、性幼稚，嗅觉丧失。

Make the diagnosis to congenitalness and the hereditary disease .

对先天性和遗传性疾病作出诊断。

are there any hereditary disease in the family ?

有没有家庭遗传性疾病？

hereditary disease

hereditary disease

遗传病

遗传性疾病

遗传疾病

遗传性病

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