磷酸烯醇式丙酮酸羧激酶缺乏症
ORPHA:2880· ICD-10 E74.4· Phosphoenolpyruvate carboxykinase deficiency
- 患病率
- <1 / 1 000 000
- 遗传方式
- Autosomal recessive, Mitochondrial inheritance
- 发病年龄
- Infancy, Neonatal
ORPHA:2880· ICD-10 E74.4· Phosphoenolpyruvate carboxykinase deficiency