Seizure Disorder,Acyl-Coa Dehydrogenase Deficiency,2-Methylbutyryl-Coa Dehydrogenase Deficiency,Propionic Acidemia,Isovaleric Acidemia,Acyl-Coa Dehydrogenase, Short-Chain, Deficiency Of

Developmental And Epileptic Encephalopathy 44,Nephronophthisis,Mitochondrial Trifunctional Protein Deficiency,Benign Secondary Hypertension,Benign Renovascular Hypertension,Nephronophthisis 3

Cerebral Creatine Deficiency Syndrome 3,Methylmalonic Acidemia,Multiple Acyl-Coa Dehydrogenase Deficiency,Propionic Acidemia,Isovaleric Acidemia,Metabolic Acidosis,Maple Syrup Urine Disease,Glycerol Kinase Deficiency,Organic Acidemia,3-Methylglutaconic Aciduria, Type Iii

Immunodeficiency 48,Encephalopathy, Ethylmalonic,Glutaric Acidemia I,Multiple Acyl-Coa Dehydrogenase Deficiency,Isobutyryl-Coa Dehydrogenase Deficiency,3-Methylcrotonyl-Coa Carboxylase Deficiency,Acyl-Coa Dehydrogenase, Short-Chain, Deficiency Of

Dystonia 9,Myoglobinuria,Myopathy,Citrullinemia, Classic,Pericardial Effusion,Rare Cardiomyopathy,Hypertrophic Cardiomyopathy,Complement Component 2 Deficiency,Hypoglycemia,Dilated Cardiomyopathy,Mitochondrial Trifunctional Protein Deficiency,Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency,Chanarin-Dorfman Syndrome,Acyl-Coa Dehydrogenase Deficiency,Respiratory Failure,3-Hydroxyacyl-Coa Dehydrogenase Deficiency,Multiple Acyl-Coa Dehydrogenase Deficiency,Encephalopathy, Progressive, Early-Onset, With Episodic Rhabdomyolysis,Propionic Acidemia,Isovaleric Acidemia,3-Methylcrotonyl-Coa Carboxylase Deficiency,Vitamin B12 Deficiency,Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency Of,Acyl-Coa Dehydrogenase, Short-Chain, Deficiency Of,Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency Of,Carnitine Palmitoyltransferase I Deficiency,Carnitine-Acylcarnitine Translocase Deficiency,Carnitine Deficiency, Systemic Primary,Carnitine Palmitoyltransferase Ii Deficiency, Infantile

Myopathy,Diabetes Mellitus,Riboflavin Deficiency,Spinocerebellar Ataxia, Autosomal Recessive 3,X-Linked Cerebellar Ataxia,Mitochondrial Trifunctional Protein Deficiency,Malignant Hyperthermia,Encephalopathy, Ethylmalonic,Infantile Hypotonia,Prader-Willi Syndrome,Multiple Acyl-Coa Dehydrogenase Deficiency,Short-Rib Thoracic Dysplasia 2 With Or Without Polydactyly,Isovaleric Acidemia,3-Methylcrotonyl-Coa Carboxylase Deficiency,Spinocerebellar Ataxia, X-Linked 1,Spinocerebellar Ataxia, X-Linked 2,Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency Of,Acyl-Coa Dehydrogenase, Short-Chain, Deficiency Of,Organic Acidemia,Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency Of,Mitochondrial Complex I Deficiency, Nuclear Type 1,Short-Rib Thoracic Dysplasia 1 With Or Without Polydactyly,Carnitine Palmitoyltransferase I Deficiency,Fazio-Londe Disease,Carnitine Deficiency, Systemic Primary

Congenital Hydrocephalus,Fatty Liver Disease,Fasting Hypoglycemia,Hypoglycemia,Sudden Infant Death Syndrome,Alcoholic Cardiomyopathy,Mitochondrial Trifunctional Protein Deficiency,Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency,Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency,Hydrocephalus, Congenital, 2, With Or Without Brain Or Eye Anomalies,Multiple Carboxylase Deficiency,Acyl-Coa Dehydrogenase Deficiency,Encephalopathy,Reye Syndrome,Methylmalonic Acidemia,Galactosemia I,3-Hydroxyacyl-Coa Dehydrogenase Deficiency,Multiple Acyl-Coa Dehydrogenase Deficiency,Congenital Hypothyroidism,Arrhythmogenic Right Ventricular Cardiomyopathy,Maple Syrup Urine Disease,Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency Of,Acyl-Coa Dehydrogenase, Short-Chain, Deficiency Of,Organic Acidemia,Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency Of,Argininemia,Carnitine Palmitoyltransferase I Deficiency,Carnitine Deficiency, Systemic Primary,Carnitine Palmitoyltransferase Ii Deficiency, Infantile,Phenylketonuria

Amino Acid Metabolic Disorder,Movement Disease,Dystonia,Athetosis,Glutaric Acidemia I,Multiple Acyl-Coa Dehydrogenase Deficiency,L-2-Hydroxyglutaric Aciduria,2-Hydroxyglutaric Aciduria,Spastic Cerebral Palsy,3-Methylcrotonyl-Coa Carboxylase Deficiency,Organic Acidemia,Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency Of,Leber Congenital Amaurosis 1,2-Aminoadipic 2-Oxoadipic Aciduria,Taqi Polymorphism,Carnitine Deficiency, Systemic Primary,D-2-Hydroxyglutaric Aciduria 1