Succinyl-CoA:3-oxoacid CoA transferase deficiency (Q7632698)
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Succinyl-CoA:3-ketoacid CoA transferase deficiency (SCOTD) is a defect in ketone body utilization characterized by severe, potentially fatal intermittent episodes of ketoacidosis
- Succinyl-Coa:Acetoacetate Transferase Deficiency
- Ketoacidosis Due to Scot Deficiency
- Succinyl-CoA acetoacetate transferase deficiency
- OXCT1 deficiency
- Scot Deficiency
- SUCCINYL-CoA:3-OXOACID-CoA TRANSFERASE DEFICIENCY
- SCOTD
- SUCCINYL-CoA:3-OXOACID-CoA TRANSFERASE DEFICIENCY; SCOTD
- Succinyl-Coa:3-Ketoacid Coa-Transferase Deficiency
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Succinyl-CoA:3-oxoacid CoA transferase deficiency |
Succinyl-CoA:3-ketoacid CoA transferase deficiency (SCOTD) is a defect in ketone body utilization characterized by severe, potentially fatal intermittent episodes of ketoacidosis |
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Statements
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Identifiers
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Sitelinks
Wikipedia(2 entries)
- dewiki SCOT-Mangel
- enwiki Succinyl-CoA:3-oxoacid CoA transferase deficiency