Kombinovaná porucha oxidativní fosforylace, typ 17
ORPHA:369913· ICD-10 E88.8· Combined oxidative phosphorylation defect type 17
- Prevalence
- <1 / 1 000 000
- Dědičnost
- Autosomal recessive
- Věk nástupu
- Infancy, Neonatal
ORPHA:369913· ICD-10 E88.8· Combined oxidative phosphorylation defect type 17