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RFVT2基因相关核黄素转运蛋白缺乏症

ORPHA:572543· ICD-10 G12.1· RFVT2-related riboflavin transporter deficiency

患病率
<1 / 1 000 000
遗传方式
Autosomal recessive
发病年龄
Childhood, Infancy
ICD-10 G12.1 →