| disease_description | ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 4,Myoglobinuria,Metabolic Syndrome X,Generalized glycogen storage disease of infants,Kidney Failure, Acute,CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL,Myopathy,Obesity,melanoma,Malignant neoplasm of prostate,Glycogen storage disease type II,Encephalopathies,CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET,Lipoidosis,Prostate carcinoma,Left Ventricular Hypertrophy,Brain Diseases, Metabolic,Hypoglycemia,Myalgia,CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE,Lipid Metabolism Disorders,Encephalitis,Multiple Acyl Coenzyme A Dehydrogenase Deficiency,Kidney Failure, Chronic,Influenza,Glycogen Storage Disease Type V,Brain Edema,Cardiomyopathy, Dilated,Acute encephalopathy,Cardiomyopathies,Mitochondrial Diseases,Rhabdomyolysis,Carnitine palmitoyl transferase 2 deficiency |