Glutaric acidemia IIc

MONDO:0700076

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

Also known as: ETFDH deficiency, GA2C, glutaric acidemia 2C, multiple acyl-CoA dehydrogenase deficiency caused by mutation in ETFDH

265 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by