Kombinovaný deficit oxidativní fosforylace, typ 23
ORPHA:444013· ICD-10 E88.8· Combined oxidative phosphorylation defect type 23
- Prevalence
- <1 / 1 000 000
- Dědičnost
- Autosomal recessive
- Věk nástupu
- Childhood, Infancy, Neonatal
ORPHA:444013· ICD-10 E88.8· Combined oxidative phosphorylation defect type 23