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Tyrosinemia Pyruvate dehydrogenase deficiency Phenylketonuria Aceruloplasminemia Lysosomal acid lipase deficiency Glycogen storage disease Glycogen storage disease type iii Methylmalonic acidemia Tyrosinemia type i Glycogen storage disease type v Aminoacidopathy Congenital myasthenic syndrome Glycogen storage disease type i Glycogen storage disease type ii Gitelman syndrome Glycogenosis Metabolic disorder Focal cortical dysplasia Central diabetes insipidus Adrenal insufficiency Carnosinemia Myeloperoxidase deficiency Growth hormone deficiency Refsum disease Magnesium deficiency Adenosine deaminase deficiency Neuroferritinopathy Ketoacidemia Exocrine pancreatic insufficiency Menkes disease Pernicious anemia Aspartylglucosaminuria Renal tubular acidosis Citrullinemia Fucosidosis Bartter syndrome Iminoglycinuria Brain ischemia Mcardle's disease Sucrose intolerance Morquio syndrome Organic acidemia Hypophosphatemia T cell deficiency Afibrinogenemia Hypoadrenalism Sanfilippo syndrome Leigh syndrome Fanconi syndrome Inborn errors of metabolism Congenital adrenal hyperplasia Adrenoleukodystrophy Gaucher's disease Homocystinuria Hawkinsinuria Hypothyroidism Hyperkalemic periodic paralysis Cystinuria Alkaptonuria Fumarase deficiency Hunter syndrome Myopathy Cholinergic crisis Cerebellar hypoplasia Molybdenum cofactor deficiency Folate deficiency Hypomagnesemia Electrolyte imbalance Dyspraxia Hypochloremia Laron syndrome Liver failure Acute intermittent porphyria Mcleod syndrome Hydranencephaly Cystathioninuria Hypogammaglobulinemia Primary immunodeficiency Lactic acidosis Hypophosphatasia Cerebral hypoxia Protein toxicity Abetalipoproteinemia Biliary dyskinesia Fahr's syndrome Galactosemia Central pontine myelinolysis Metachromatic leukodystrophy Joubert syndrome Alexander disease Insulin resistance Severe combined immunodeficiency Fructose malabsorption Acdc Addison's disease Homocarnosinosis Opsoclonus myoclonus syndrome Osteomalacia Basal ganglia disease Lesch-nyhan syndrome

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