Kombine oksidatif fosforilasyon defekti tip 26
ORPHA:477684· ICD-10 E88.8· Combined oxidative phosphorylation defect type 26
- Yaygınlık
- <1 / 1 000 000
- Kalıtım
- Autosomal recessive
- Başlangıç yaşı
- Childhood, Infancy
ORPHA:477684· ICD-10 E88.8· Combined oxidative phosphorylation defect type 26