QRSL1基因相关复合氧化磷酸化缺陷
ORPHA:570491· ICD-10 E88.8· QRSL1-related combined oxidative phosphorylation defect
- 患病率
- <1 / 1 000 000
- 遗传方式
- Autosomal recessive
- 发病年龄
- Antenatal, Infancy, Neonatal
ORPHA:570491· ICD-10 E88.8· QRSL1-related combined oxidative phosphorylation defect