Kombinovaný deficit oxidativní fosforylace, typ 20
ORPHA:420728· ICD-10 E88.8· Combined oxidative phosphorylation defect type 20
- Prevalence
- <1 / 1 000 000
- Dědičnost
- Autosomal recessive
- Věk nástupu
- Infancy
ORPHA:420728· ICD-10 E88.8· Combined oxidative phosphorylation defect type 20