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.
Segen's Medical Dictionary. © 2012 Farlex, Inc. All rights reserved.
Full browser ?