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	(MHBD) 2-Methyl-3-Hydroxybutyrl CoA Dehydrogenase deficiency
	(2MBCD) 2-Methylbutyryl-CoA Dehydrogenase Deficiency
	(HMG) 3-hydroxy-3 -methylglutaryl-CoA lyase deficiency
	(3-MCC) 3-methylcrotonyl- CoA carboxylase deficiency
	(MGA) 3-Methylglutaconic acidemia or 3-Methylglutaconyl-CoA Hydratase Deficiency
	5-oxoprolinemia
	(D2-HGA) D-2 Hydroxyglutaric Aciduria
	(GA-I) Glutaryl CoA Dehydrogenase Deficiency Type I aka Glutaric Acidemia Type I
	(ICBD) Isobutyryl-CoA Dehydrogenase Deficiency 3-Hydroxyisobutyric aciduria
	(IVA) Isovaleryl CoA Dehydrogenase Deficiency aka Isovaleric Acidemia
	(L2HGA) L-2-Hydroxy- glutaricaciduria
	(MA) Malonyl-CoA Decarboxylase Deficiency aka Malonic Acidemia
	(MMA) Methlymalonic Acidemia
	(BKT) Mitochondrial Acetoacetyl CoA Thiolase- (3-Ketothiolase)
	(MCD, holocarboxylase synthetase) Multiple carboxylase deficiency
	(PA) Propionyl CoA Carboxylase Deficiency aka Propionic Acidemia
	(HIBCH) 3-Hydroxyisobutyryl-CoA Hydrolase Deficiency

The Association publishes the Organic Acidemia Association Newsletter, which includes updates, editorials and letters from and for affected families three times a year for a suggested donation of $25 (in the US) or $35 (outside of US) members with $5 for a copy of the roster. Back copies of the newsletter are available on request.

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