autosomal

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育异性眼科疾病,方式有显性、隐性和X连锁隐性。

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

摘要牙本质形成不良是一种显性中胚层缺陷。

Conclusion: The genetics of the true pattern in human palmar hypothenar area may belong to autosomal dominant inheritance.

结论：手掌小鱼际区真实花纹可能属于显性。

Conclusion: Homocystinuria is a rare autosomal-recessive disorder with multiple systemic complications.Progressive myopia and ectopia lentis are common presenting signs in such patients.

结论：高胱胺酸尿症为一少见之隐性疾病，可导致多样全身并发症，其中最以渐进性近视及水晶异位呈现。

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑素合成相关基因突变导致眼、皮肤、毛发黑素沉着减少或缺乏引起一类隐形疾病总称。

Gitelman's syndrome (GS) is a rare autosomal recessive renal tubular disorder characterized by hypokalemia, metabolic alkalosis, hypomagnesemia, and hypocalciuria.

摘要吉特曼症候群是一种少见性肾小管疾病，于1966年由吉特曼等人提出，其方式大多属于自隐性。