Acyl-CoA dehydrogenase 9 deficiency
ORPHA:99901· ICD-10 E71.3
Definition
A rare disorder characterized by neurological dysfunction, hepatic failure and cardiomyopathy due to a deficiency of complex I of the respiratory chain.
- Prevalence
- Unknown
- Inheritance
- Autosomal recessive
- Age of onset
- Childhood, Infancy, Neonatal