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

枫糖尿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。

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

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.

眼皮肤白化病是由于黑色合成相关基因突变导致眼、皮肤、毛发黑色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性眼科疾病,传方式有染色体显性传、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.

眼白化病是由黑色素合成相关基因突变导致眼、、发黑色素沉着减少或缺乏引起的一类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。

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

小眼球是一种发育异常眼科疾病,方式有常染色体显、常染色体隐和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的一类常染色体隐形疾病的总称。

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.

手掌小鱼际区纹可能属常染色体显性传。

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.

眼皮肤白化病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。

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。

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,方式有常染色体显性、常染色体隐性和X连锁隐性。

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

眼皮肤白化是由于黑色素合成因突变导致眼、皮肤、毛发黑色素沉着减少或缺乏引起的一类常染色体隐形疾的总称。

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.

眼皮肤白化病是由于黑色素关基因突变导致眼、皮肤、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.

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.

眼皮肤白化病是由于黑色合成相关基因突变导致眼、皮肤、毛发黑色减少或缺乏引起的一类常染色体隐形传疾病的总称。