acyl-CoA dehydrogenase type-9 deficiency

acyl-CoA dehydrogenase type-9 deficiency

A hereditary condition (OMIM:611126) characterised by episodic liver dysfunction and otherwise mild disease, as well as cardiomyopathy and chronic neurologic dysfunction.
Molecular pathology
Defects in ACAD9 cause acyl-CoA dehydrogenase deficiency.