线粒体DNA耗竭综合征，脑肌病伴甲基丙二酸尿症型
ORPHA:1933· ICD-10 G71.3· Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria
- 患病率
- <1 / 1 000 000
- 遗传方式
- Mitochondrial inheritance
- 发病年龄
- Infancy
ORPHA:1933· ICD-10 G71.3· Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria