Short chain Acyl CoA dehydrogenase deficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Short-chain acyl-CoA dehydrogenase (SCAD) deficiency is a very rare inborn error of mitochondrial fatty acid oxidation characterized by variable manifestations ranging from asymptomatic individuals (in most cases) to those with failure to thrive, hypotonia, seizures, developmental delay and progressive myopathy. (Orphanet Rare Disease Ontology, Orphanet_26792)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C537596
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Genes

1 genes/proteins associated with the disease Short chain Acyl CoA dehydrogenase deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ACADS acyl-CoA dehydrogenase, C-2 to C-3 short chain 2.88009