体染色体隐性遗传 autosomal recessive inheritance
体染色体隐性遗传模式 Autosomal recessive inheritance pattern
体染色体隐性耳聋 autosomal recessive deafness
体染色体隐性耳聋36 autosomal recessive deafness
枫糖尿症是支链氨基酸代谢异常的体染色体隐性遗传疾病。
Maple syrup urine disease (MSUD), or branched-chain ketoaciduria, is an autosomal recessive disorder of branched-chain amino acid metabolism.
该病属常染色体隐性遗传，与X-染色体关联，所以，母亲是基因携带者的男性表现为发病。
The disease is autosomal-recessive and linked to the X-chromosome, so that men whose mothers are carriers of the gene manifest the disease.
目前根据遗传方式分为1型（常染色体显性）和2型（常染色体隐性） ，每一型根据不同基因缺陷又分为许多亚型。
The limb-girdle muscular dystrophies are divided into two types according to inheritance pattern, type 1 is autosomal dominant and type 2 is autosomal recessive.
应用推荐