|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes/proteins associated with the disease Short chain Acyl CoA dehydrogenase deficiency from the curated CTD Gene-Disease Associations dataset.
|ACADS||acyl-CoA dehydrogenase, C-2 to C-3 short chain||2.88009|