IDID：遗传性疾病

“遗传性疾病”在医学领域通常被缩写为“IDID”，以便在专业文献和日常交流中提高书写与沟通的效率。这一缩写广泛应用于描述由基因缺陷或遗传因素导致的各类疾病，有助于研究人员和临床医生快速、准确地指代此类病症。

To explore the nosogenesis of congenital inherited diseases in(IDID) children, the blood of 428 children were routinely inoculated and cultured in order to provide chromatosome of G-banding of lymphocyte in peripheral blood.
为了解儿童先天遗传性疾病(IDID)的发病情况，对428例患儿进行常规接种、培养及制备外周血淋巴细胞染色体G显带标本分析。
Certain inherited diseases, in contrast, are characterized by a defective telomerase, resulting in damaged cells.
相比之下，某些遗传病的机制正是因为端粒酶有缺陷、从而导致细胞受损的缘故。
Newborn screening for inherited metabolic diseases in Xiangshui County, Jiangsu Province, 2002-2008
江苏省响水县2002-2008年新生儿遗传代谢性疾病筛查情况调查分析
Clinical features and analysis of inherited metabolic diseases in neonatal intensive care unit
新生儿重症监护病房中遗传代谢病的临床特点及分析
The Study on Gene Mutations of Two Inherited Blood Diseases in Yunnan Province
云南省两种遗传性血液疾病的基因突变研究

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