Kombinovaný deficit oxidativní fosforylace, typ 21
ORPHA:420733· ICD-10 E88.8· Combined oxidative phosphorylation defect type 21
- Prevalence
- <1 / 1 000 000
- Dědičnost
- Autosomal recessive
- Věk nástupu
- Neonatal
ORPHA:420733· ICD-10 E88.8· Combined oxidative phosphorylation defect type 21