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Acyl-CoA dehydrogenase 9 deficiency
What is Acyl-CoA dehydrogenase 9 deficiency?
A rare disorder characterized by neurological dysfunction, hepatic failure and cardiomyopathy due to a deficiency of complex I of the respiratory chain.
Other condition names
ACAD9 deficiency
Inheritance type
Autosomal recessive
Prevalence
Worldwide: Unknown
Age of Onset
Childhood
Infancy
Neonatal
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on
"https://www.orphadata.com"
. Data version 1.3.16 / 4.1.7.