Kombinovaný defekt oxidativní fosforylace typu 39
ORPHA:565624· ICD-10 E88.8· Combined oxidative phosphorylation defect type 39
- Prevalence
- <1 / 1 000 000
- Dědičnost
- Autosomal recessive
- Věk nástupu
- Antenatal, Infancy, Neonatal
ORPHA:565624· ICD-10 E88.8· Combined oxidative phosphorylation defect type 39