Any multiple acyl-CoA dehydrogenase deficiency in which the cause of the disease is a mutation in the ETFDH gene.
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multiple acyl-CoA dehydrogenase deficiency, severe neonatal type
MONDO:0018332
multiple acyl-CoA dehydrogenase deficiency, mild type
MONDO:0018333
glutaric acidemia IIa
MONDO:0700073
glutaric acidemia IIb
MONDO:0700074