线粒体甲基化缺陷引起的新生儿严重心肺衰竭
ORPHA:466784· ICD-10 E88.8· Neonatal severe cardiopulmonary failure due to mitochondrial methylation defect
- 患病率
- <1 / 1 000 000
- 遗传方式
- Autosomal recessive
- 发病年龄
- Infancy, Neonatal
ORPHA:466784· ICD-10 E88.8· Neonatal severe cardiopulmonary failure due to mitochondrial methylation defect