autosomal

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

摘要牙本成不良是一种体染色体显遗传的中胚层缺陷。

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

先天小球是一种先天发育异常疾病,遗传方式有常染色体显遗传、常染色体隐遗传和X连锁隐遗传。

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

手掌小鱼际区真实花纹可能属于常染色体显遗传。

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

皮肤白化病是由于黑色素合成相关基因突变导致、皮肤、毛发黑色素沉着减少或缺乏引起的一类常染色体隐遗传疾病的总称。