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Glutaric acidemia IIc(GA2C)

MedGen UID:
479786
Concept ID:
C3278156
Disease or Syndrome
Synonym: ETFDH deficiency
 
Monarch Initiative: MONDO:0700076
OMIM®: 231675; 231680

Definition

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

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