Glutaric acidemia IIa

MONDO:0700073

Any multiple acyl-CoA dehydrogenase deficiency in which the cause of the disease is a mutation in the ETFA gene.

Also known as: ETFA deficiency, GA2A, glutaric acidemia 2A, multiple acyl-CoA dehydrogenase deficiency caused by mutation in ETFA

21 clinical trials for this condition and its sub-types, 0 tagged with Glutaric acidemia IIa itself.

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