Succinyl-CoA:3-oxoacid CoA transferase deficiency
Synonyms: OXCT1 deficiency | SCOT deficiency | Succinyl-CoA acetoacetate transferase deficiency | Succinyl-CoA:3-ketoacid CoA transferase deficiency
A rare genetic disorder in ketone body utilization characterized by severe potentially fatal intermittent episodes of ketoacidosis.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version May 2024
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Succinyl-CoA:3-oxoacid CoA transferase deficiency?
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Clinical Trials
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