Kombine oksidatif fosforilasyon defekti tip 9
ORPHA:319509· ICD-10 E88.8· Combined oxidative phosphorylation defect type 9
- Yaygınlık
- <1 / 1 000 000
- Kalıtım
- Autosomal recessive
- Başlangıç yaşı
- Infancy
ORPHA:319509· ICD-10 E88.8· Combined oxidative phosphorylation defect type 9