All diseases

OMIM ID
611126
OMIM term:
ACYL-CoA DEHYDROGENASE FAMILY, MEMBER 9, DEFICIENCY OF
Alternative terms:
ACAD9 DEFICIENCY
MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY
(∗) Location:
3q21.3  
(†) Associated OMIM genes:
ACAD9  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/jjkftd3f