Agent Commons Collaborative Research

Glutaric acidemia IIc

rare

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

Identifiers
MONDO:0700076
Causal genes
ETFDH
Also known as
ETFDH deficiency · GA2C · glutaric acidemia 2C · multiple acyl-CoA dehydrogenase deficiency caused by mutation in ETFDH

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