Benign hereditary chorea is an autosomal dominant disorder of early onset characterised by non progressive choreic movements with normal cognitive function occasionally associated with hypothyroidism and respiratory problems.
良性遗传性舞蹈症是一种早发的常染色体显性遗传性疾病，以非进展性的舞蹈样运动为特点，偶尔伴有甲状腺机能减退和呼吸系统疾病，但认知功能正常。
Objectives Epidermodysplasia verruciformis is an autosomal recessive hereditary skin disorder, in which there is widespread infection with specific types of human papillomavirus. More than 30 HPV types, including 3, 5, 8-10, 12, 14, 15, 17, 19-21, 23-26, 37, 38 and 47 have been identified in EV and EV tumors.
目的 疣状表皮发育不良是一种由特殊的HPV引起的常染色体隐性遗传性皮肤病，目前已发现有30多种类型的HPV与EV有关，包括HPV3，5，8-10，12，14，15，17，19-21，23-26，37，38和47。
Objectives Epidermodysplasia verruciformis is an autosomal recessive hereditary skin disorder, in which there is widespread infection with specific types of human papillomavirus.
目的 疣状表皮发育不良是一种由特殊的HPV引起的常染色体隐性遗传性皮肤病，目前已发现有30多种类型的HPV与EV有关，包括HPV3，5，8-10，12，14，15，17，19-21，23-26，37，38和47。本研究的主要目的是，用PCR扩增我科最近10年EV和EV肿瘤石蜡标本中的HPVsDNA，并进行分型。
Or also possibly due to a syndrome, known as Familial Mediterranean Fever which is a hereditary inflammatory disorder that affects groups of people originating from around the Mediterranean Sea.
或者是因为名为家族性地中海热病的综合症，这是一种感染来自地中海区域的人群的一种遗传性发热病。
The same risk does not however occur as men get older. Because KS is not passed on but occurs by accident, it is said to be congenital, which means that it is not inherited, that is, it is not an hereditary disorder. This means that the parents of a boy who has Klinefelter's syndrome need not be anxious about having more children as the likelihood of having another KS boy is minimal.
相同的风险不发生，但由於男性老年人，由於堪萨斯州是不获通过，但发生意外，这是说是先天性，这意味著它是没有继承，即是，这是不是一个遗传性障碍，这意味著父母的一名男童谁已克氏综合徵不必担心有更多的儿童的可能性后，堪萨斯州的另一名男童是微乎其微。
At present, mang hereditary disease and acquired disease are concerned with the functional disorder of UPP.
目前发现的许多遗传性和获得性疾病的发生都与此系统功能失调有关。
Coarctation of the aorta is a rare hereditary disorder that is one of the most common causes of hypertension in children.
主动脉缩窄是一种并不多见的遗传性疾患，但却是儿童高血压的主要病因之一。
Conclusion Schizophrenia was a polygenic hereditary disorder.
结论精神分裂症是一种多基因遗传疾病。
Hemophilia: Hereditary Bleeding disorder caused by deficiency of a coagulation factor.
血友病：一种遗传性出血性疾病，因先天性缺乏某种凝血因子而引起。
Dr. Marion, who said he had no specific knowledge of the brothers, added that the disorder they reportedly have is hereditary and that the mental deterioration happens gradually.
马里恩博士说他对兄弟俩的情况还并不完全了解，此外他还补充说，他们患有的病变是遗传性的，而且大脑智力在逐渐衰变。
This characteristic is caused by a hereditary disorder called myotonia congenita.
这种情形是由一种称做「先天性肌强直症」的遗传性疾病所引起。
According to these results, the oppositional defiant disorder (ODD) which was relevant with hereditary factor belonged to polygenic inheritance. The biological mechanism and the social psychological stress factor to ODD has been carried on systematic analysis, which contribute to exploring the mechanism of ODD.
对儿童对立违抗性障碍（ODD）的生物学机制及社会心理应激因素进行了系统的分析，对进一步探讨ODD的发病机制有所启示。
Result: ATD is an uncommon autosomal recessive hereditary disorder of osteochondrodysplasia.
结果：①ATD是一种少见的常染色体隐性遗传性骨软骨发育不良疾病。
Hereditary Hemochromatosis is the most common genetic disorder of persons of northern European extraction.
遗传性血色病是最常见的遗传性疾病的人的北欧提取。
The hereditary long QT syndrome (LQTS) is a cardiac disorder characterized by prolongation of the QT interval on electrocardiograms (ECGs), syncope and sudden death.
遗传性长QT综合征（LQTS）是一种常染色体遗传性心脏病。特征性表现为心电图上QTc延长，及尖端扭转型室性心动过速（TdP）导致的晕厥和猝死。
Marie Unna hereditary hypotrichosis is an autosomal dominant hair loss disorder, with the affected individuals usually born with little or no hair, and coarse twisted hair growth on the scalp in early childhood.
国际上将MUHH基因座定位于人染色体8p21区域，但对此区域中与毛发周期密切相关的Hairless基因编码区进行突变筛查时都没有发现任何致病性突变。