Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of
Myopathy
Hypoglycemia
Intellectual Developmental Disorder, Autosomal Dominant 62
Hypertrophic Cardiomyopathy
Pericardial Effusion
Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of
Metabolic Dysfunction-Associated Steatotic Liver Disease
Myoglobinuria
Sudden Infant Death Syndrome