Acyl-CoA dehydrogenase 9 deficiency

A rare disorder leading to a deficiency of complex I of the respiratory chain and is characterized by neurological dysfunction, hepatic failure and cardiomyopathy.

Also known as: ACAD9 deficiency, acyl-CoA dehydrogenase 9 deficiency, mitochondrial complex I deficiency due to ACAD9 deficiency, mitochondrial complex I deficiency, nuclear type 20

0 clinical trials for this condition and its sub-types, 0 tagged with Acyl-CoA dehydrogenase 9 deficiency itself.