Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常隐性传病。

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显性传。

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

先天性小球是一种先天发育异常性科疾病,传方式有常显性传、常隐性传和X连锁隐性传。

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素合成相关基因突变、皮肤、毛发黑素沉着减少或缺乏引起的一类常隐形传疾病的总称。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常染色体隐性传病。

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性传。

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

先天性小眼球是种先天发育异常性眼科疾病,传方式有常染色体显性传、常染色体隐性传和X连锁隐性传。

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

眼皮肤白化病是由于黑色素合成相关基因突变导致眼、皮肤、毛发黑色素沉着减少或缺乏引类常染色体隐形传疾病总称。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于体隐性传病。

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体显性传。

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

先天性小球是一种先天发育异性科疾病,传方式有体显性传、体隐性传和X连锁隐性传。

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

肤白化病是由于黑素合成相关基因突变导、肤、毛发黑素沉着减少或缺乏引起的一类体隐形传疾病的总称。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常染隐性传病。

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性传。

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常性眼科疾病,传方式有常染性传、常染隐性传和X连锁隐性传。

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

眼皮肤白化病是由于黑素合成相关基因突变导致眼、皮肤、毛黑素沉着减少或缺乏引起的一类常染隐形传疾病的总称。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿常染色体隐性传病。

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常染色体显性传。

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育异常性眼科疾病,传方式有常染色体显性传、常染色体隐性传和X连锁隐性传。

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

眼皮白化病是由黑色素合成相关基因突变导致眼、皮、黑色素沉着减少或缺乏引起的一类常染色体隐形传疾病的总称。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常隐病。

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显。

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

先天小眼球是一种先天发育异常眼科疾病,方式有常显、常隐和X连锁隐。

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的一类常隐形疾病的总称。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症常染色体隐性传病。

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常染色体显性传。

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常性眼科疾病,传方式有常染色体显性传、常染色体隐性传和X连锁隐性传。

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

眼化病是由黑色素合成相关基因突变导致眼、、毛发黑色素沉着减少或缺乏引起的一类常染色体隐形传疾病的总称。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常染色体隐性传病。

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性传。

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

先天性小眼球是种先天发育异常性眼科疾病,传方式有常染色体显性传、常染色体隐性传和X连锁隐性传。

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

眼皮肤白化病是由于黑色素合成相关基因突变导致眼、皮肤、毛发黑色素沉着减少或缺乏引起常染色体隐形传疾病总称。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

症属于常染体隐性传病。

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体显性传。

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常性眼科疾病,传方式有常染体显性传、常染体隐性传和X连锁隐性传。

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

眼皮肤白化病是由于合成相关基因突变导致眼、皮肤、毛发沉着减少或缺乏引起的一类常染体隐形传疾病的总称。