Disease_Mapped_To_Gene
Fatty Acid Metabolism Disorder
Cellosaurus Disease Terminology
Cellosaurus Terminology
Rare Non-Neoplastic Disorder
ACADS Gene
Acyl-CoA Dehydrogenase, Short-Chain Deficiency
A genetic disorder characterized by deficiency of the enzyme short-chain acyl-coenzyme A dehydrogenase that metabolizes short-chain fatty acids. Signs and symptoms appear in infancy or childhood and may be triggered during fasting or illness. They include vomiting, hypoglycemia, lethargy, hypotonia and failure to thrive.
Acyl-CoA Dehydrogenase, Short-Chain Deficiency
Acyl-CoA Dehydrogenase, Short-Chain Deficiency
C0342783
C84539
Cellosaurus
Disease or Syndrome
SCAD
Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD)
Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency (SCAD)