RFVT3基因相关核黄素转运蛋白缺乏症
ORPHA:572550· ICD-10 G12.1· RFVT3-related riboflavin transporter deficiency
- 患病率
- <1 / 1 000 000
- 遗传方式
- Autosomal recessive
- 发病年龄
- Adolescent, Adult, Childhood, Infancy
ORPHA:572550· ICD-10 G12.1· RFVT3-related riboflavin transporter deficiency