Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:611126 - MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20; MC1DN20

Xenbase Genes: acad9

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012624 - acyl-CoA dehydrogenase 9 deficiency

Disease Ontology (DO):
DOID:0112072 - nuclear type mitochondrial complex I deficiency 20