Succinyl-CoA:3-oxoacid CoA transferase deficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Succinyl-CoA:3-ketoacid CoA transferase deficiency (SCOTD) is a defect in ketone body utilization characterized by severe, potentially fatal intermittent episodes of ketoacidosis. (Orphanet Rare Disease Ontology, Orphanet_832)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C537527
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Genes

1 genes/proteins associated with the disease Succinyl-CoA:3-oxoacid CoA transferase deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
OXCT1 3-oxoacid CoA transferase 1 2.88009