综合征是 - 翻译成英语

• syndrome is

在 中文 中使用 综合征是 的示例及其翻译为 英语

利马综合征是斯德哥尔摩综合症的完全相反。
The Lima Syndrome is the inverse of Stockholm Syndrome..

基本上代谢综合征是胰岛素抵抗的子集;
Metabolic syndrome is essentially a subset of insulin resistance;

这种综合征是由在STK11基因突变引起的。
This syndrome is caused by mutations in the gene STK11.

MPSIS，Scheie综合征是最轻微的MPSI型。
Scheie syndrome(MPS 1-S) is the mildest type of MPS.

该综合征是由STK11（LKB1）基因突变引起的。
This syndrome is caused by mutations in the STK11(LKB1) gene.

不安腿综合征是一种也称为Willis-Ekbom病的病症。
Restless leg syndrome is also known as Willis-Ekbom disease.

克里格勒-纳贾尔综合征是列出的最严重的遗传性疾病;
Crigler-Najjar syndrome is the most serious inherited condition listed;

Q37缺失综合征是一种疾病，可以影响身体的许多部分。
Q37 deletion syndrome is a chromosome disease that can affect many parts of the body.

这种综合征是由基因中的REQL4的异常变化引起的。
This syndrome is caused by abnormal changes in the REQL4 gene.

这种综合征是由基因中的REQL4的异常变化引起的。
This syndrome is usually caused by abnormal changes in the REQL4 gene.

Rett综合征是一种罕见的非遗传性基因的神经系统疾病。
Rett syndrome is a rare non-inherited genetic neurological disorder.

类癌瘤综合征是在类癌瘤患者中偶尔见到的一组症状。
Carcinoid syndrome is a cluster of symptoms sometimes seen in people with carcinoid tumors.

Borjeson-Forssman-Lehmann综合征是一种罕见的由PHF6突变引起的X连锁疾病。
Borjeson-Forssman-Lehmann syndrome(BFLS) is a rare X-linked disease caused by PHF6 mutations.

茹贝尔综合征是影响一个80,000人一种罕见的遗传性疾病。
Joubert syndrome is a rare genetic disease affecting one in 80,000 individuals.

CorneliadeLange综合征是一种发展性疾病，会影响身体的许多部位。
Cornelia de Lange syndrome(CdLS) is a developmental disorder that can affect many parts of the body.

类癌综合征是一个集群的症状，有时可见于类癌肿瘤患者。
Carcinoid syndrome is a cluster of symptoms sometimes seen in people with carcinoid tumors.

急性冠脉综合征是一种适用于心脏病发作以及静息时胸痛的术语。
Acute coronary syndrome is a term applied to heart attacks as well as chest pain during rest.

SturgeWeber综合征是一种罕见的神经系统和皮肤疾病，可导致发育异常。
Sturge Weber Syndrome is a rare neurological and skin disorder that causes developmental anomalies.

Joubert综合征是一种罕见的遗传性疾病，影响80,000人中的一人。
Joubert syndrome is a rare genetic disease affecting 1 in 80,000 individuals.

Joubert综合征是一种罕见的遗传性疾病，影响80,000人中的一人。
Joubert syndrome is a relatively rare genetic disease affecting 1 in 80,000 individuals.