核DNA异常所致线粒体氧化磷酸化障碍
ORPHA:2443· Mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies
- 患病率
- 1-9 / 100 000
- 遗传方式
- Autosomal recessive
- 发病年龄
- All ages
ORPHA:2443· Mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies