glutaric aciduria inborn mitochondrial metabolism disorder multiple acyl-CoA dehydrogenase deficiency https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/4691 https://github.com/monarch-initiative/mondo/issues/9097 https://www.malacards.org/card/multiple_acyl_coa_dehydrogenase_deficiency ICD10CM:E71.313 multiple acyl-CoA dehydrogenase deficiency Also known as glutaric acidemia II. Referenced from Glutaric aciduria, type I (231670). DOID:0060358 A disorder of fatty acid and amino acid oxidation, caused by mutations in ETFDH, ETFA, or ETFB, and is a clinically heterogeneous disorder ranging from a severe neonatal presentation with metabolic acidosis, cardiomyopathy and liver disease, to a mild childhood/adult disease with episodic metabolic decompensation, muscle weakness, and respiratory failure. NORD:1192 Etfdh deficiency MAD deficiency NCIT:C84907 MADD glutaric acidemia type II MEDGEN:75696 glutaric acidemia IIA OMIM:231680 Glutaric Aciduria Type II glutaric acidemia IIC glutaric acidemia IIB Orphanet:26791 Etfa deficiency Etfb deficiency multiple acyl Coenzyme A dehydrogenase deficiency NANDO:2200502 GARD:0006523 glutaric aciduria type 2 EMA MONDO:0009282 glutaric acidemia type 2 icd11.foundation:977130875 glutaric aciduria, type 2 UMLS:C0268596 electron transfer flavoprotein deficiency glutaric acidemia 2C NANDO:1200801 glutaric acidemia 2B glutaric acidemia 2A acyl-CoA dehydrogenase deficiency familial hypertrophic cardiomyopathy