MONDO_0008722 (short chain acyl-CoA dehydrogenase deficiency) can be described as follows. 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. Also known as: ACADS deficiency, SCAD, SCAD deficiency, SCADD, Short Chain Acyl CoA Dehydrogenase Deficiency, acyl-CoA dehydrogenase, short-chain deficiency, short-chain acyl-CoA dehydrogenase deficiency (SCAD), short-chain acyl-Coenzyme A dehydrogenase deficiency (SCAD).