Kombine oksidatif fosforilasyon defekti tip 7
ORPHA:254930· ICD-10 E88.8· Combined oxidative phosphorylation defect type 7
- Yaygınlık
- <1 / 1 000 000
- Kalıtım
- Autosomal recessive
- Başlangıç yaşı
- Childhood, Infancy
ORPHA:254930· ICD-10 E88.8· Combined oxidative phosphorylation defect type 7