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Summary Literature (0)
MIM:611126 - MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20; MC1DN20

Xenbase Genes: acad9

Human Disease Resource: OMIM

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