... acyl-CoA dehydrogenase (SBCAD) deficiency (also known as 2-methylbutyryl-CoA dehydrogenase deficiency) is a rare disorder in which the body ... 2-MBCD deficiency 2-MBG 2-methylbutyryl glycinuria 2-methylbutyryl-CoA dehydrogenase deficiency 2-methylbutyryl-coenzyme A dehydrogenase deficiency SBCADD Short/ ...

... deficiency</synonym><synonym >2M3HBA</synonym><synonym >3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency</synonym><synonym >3H2MBD deficiency</synonym><synonym >HSD10 deficiency</ ...

... see Short/branched chain acyl-CoA dehydrogenase deficiency 2-methylbutyryl-CoA dehydrogenase deficiency, see Short/branched chain acyl-CoA dehydrogenase deficiency ...

... name >2M3HBA</other_name><other_name >3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency</other_name><other_name >3H2MBD deficiency</other_name>< ...

... 3-hydroxybutyryl-CoA dehydrogenase deficiency 2M3HBA 3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency 3H2MBD deficiency HSD10 deficiency Hydroxyacyl-CoA dehydrogenase II ...

... a chemical reaction that converts a molecule called 2-methylbutyryl-CoA to another molecule, ... deficiency Researchers have identified more than 10 ACADSB gene ...

... 2-methyl-3-hydroxybutyryl-CoA dehydrogenase 3-hydroxy-2-methylbutyryl-CoA dehydrogenase 3-hydroxyacyl-CoA dehydrogenase II ABAD amyloid-beta ... Lehnert W, Sass JO, Sperl W, Wanders RJ. 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency is caused by mutations in the HADH2 gene. ...