Organic Acidemia Association OAA

Description: Information, support and research about Organic Acidemia Disorders, Metabolic Disorders, Newborn Screening, Inborn Errors of Metabolism

Keywords: Propionic Acidemia, OAA, Organic Acidemia, Newborn Screening, Metabolic Disorders, Genetic Disorders, Inborn Errors of Metabolism, Cardiomyopathy, MMA, Methlymalonic Acidemia, MMA Research, Mut 0, Cobalamin C, IVA, Isovaleryl CoA Dehydrogenase Deficiency, Isovaleric Acidemia, 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, Type 1, Glutaryl CoA Dehydrogenase Deficiency Type I, Glutaric Acidemia Type I, ICBD, Isobutyryl-CoA Dehydrogenase Deficiency 3-Hydroxyisobutyric aciduria, L2HGA, L-2-Hydroxy- glutaricaciduria, MA, Malonyl-CoA Decarboxylase Deficiency aka Malonic Acidemia, BKT, Mitochondrial Acetoacetyl CoA Thiolase, 3-Keto hiolase, Ketone Utilization Disorder, MCD, holocarboxylase synthetase, Multiple carboxylase deficiency

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Pasupport.org

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