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- Tuberous sclerosis (TSC) is a common autosomal dominant disease. 结节性硬化症是一种临床较常见的显性遗传病。
- Benign familial pemphigus （HHD） is a rare autosomal dominant disease caused by mutations in the ATP2C1gene encoding a novel Ca2+ pump. 家族性良性天疱疮是一种少见的常染色体显性遗传性疾病，由ATP2C1基因突变所致。
- Familial hypertrophic cardiomyopathy (FHC) is an autosomal dominant disease characterized by left ventricular hypertrophy, myofibrillar disarray, and sudden cardiac death. a心肌肥大症（FHC）是一种体染色体显性遗传的疾病，主要症状为左心室肥大、心肌排列不整，甚至导致猝死。
- autosome dominant disease 常染色体显性遗传疾病
- an autosomal dominant disease characterized by elongated bones (especially of limbs and digits) and abnormalities of the eyes and circulatory system 一种常染色体显性疾病
- an autosomal dominant disease characterized by elongated bones (especially of limbs and digits) and abnormalities of the eyes and circulatory system. 一种常染色体显性疾病。
- Pedigree analysis reveals that it is consistent with autosome dominant inheritance. 用家系法分析, 符合常染色体显性遗传。
- The Alzheimer in this ancestry appears as autosomal dominant genetic disease. 阿尔茨海默病在本家系中显示为常染色体显性遗传。
- This disorder is inherited as an autosomal dominant trait. 本病作为常染色体显性传递。
- With pedigree analysis, the genetic mode of the disease in the family are autosomal dominant inheritance. 据系谱分析,该疾病符合常染色体显性遗传方式。
- Neurofibromatosis is an autosomal dominant genetic disease, which also named as Von Recklinghausen disease before. 神经纤维瘤病，以前又称von Recknn沙ausen病，属常染色体显性遗传病。
- Peutz-Jeghers, also known as Hereditary Intestinal Polyposis Syndrome, is an autosomal dominant genetic disease. 什么是'黑斑息肉综合征-多生长在肠道'?
- According to genetic analysis, this disease is caused by autosomal dominant inheritance. 经过遗传分析，认为该畸形属常染色体显性遗传。
- Conclusion The congenital teeth agenesis maily is autosomal dominant inheritant disease. 结论先天缺牙家系多为常染色体显性遗传；
- autosome dominant inheritance(AD) 常染色体显性遗传
- Dentinogenesis imperfecta type I(DGI-I) is an autosomal dominant dental disease with abnormal dentin production and mineralization. 我国科学家成功地克隆了遗传性乳光牙本质I型病的基因，为遗传性乳光牙I型病的诊断带来希望。
- HHT is an autosomal dominant disordercharacterized by vascular dysplasia. HHT是常染色体显性遗传性血管发育异常的一种疾病。
- Hereditary angioedema (HAE) is an autosomal dominant genetic disease caused by synthesis defect or dysfunction of C1 esterase inhibitor. 遗传性血管性水肿是一种由于C1酯酶抑制剂的合成障碍或功能缺陷所致的常染色体显性遗传病。
- It is obviously autosomal dominant inheritance according to the pedigree. 由于第一代病例仅为右眼虹膜缺损，故较支持中胚层迷走发育的理论。
- This malformation may occur in association with autosomal dominant or recessive polycystic kidney disease of varying severity. 此种疾病常与体细胞显性遗传或隐性遗传的多发性肾脏囊肿疾病合并出现。
