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Possible Causes For Acidosis, metabolic - Causes: Metabolic, Storage Disorders

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Acidosis, metabolic - Causes
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Metabolic, Storage Disorders: next: Biochemical Causes: Diabetic ketoacidosis/coma; Renal tubular disorders/metabolic; Primary lactic acidemia/children; Fanconi's syndrome, adult (acquired); Fanconi's Hereditary Renal Disease; Renal tubular acidosis type IV; Combined carboxylase/Biotinidase deficiency; Cytochrome C Oxidase Deficiency/COX Complex Defect; French-Canadian type COX mitochondrial defect; Hydroxybutyric acidemia; Ketotic hyperglycinemia, idiopathic; Methylmalonic acidemia/ketotic glycine; Propionicacidemia/ketotic glycinemia; Pyroglutamic acidemia; Pyruvate carboxylase enzyme deficiency/PCD; Pyruvate Dehydrogenase Complex Deficiency/PDCD; Infantile mitochondrial myopathy/Cox defect; Acyl-CoA Dehydrogenase/short chain def; Alphamethylacetoacetate accumulation; Beta-hydroxyisolvaleric acidemia; Carbamoyl phosphate synthetase defic; Hyperglycinemia, ketotic; LCHAD/Long chain OH-CoA dehydrogenase def; Proprionic acidemia/congenital; VLCHAD/Very Long chain OH-CoA dehydrogenase def; Cystinuria; Fructose intolerance, hereditary; Galactosemia; Glutaric aciduria/Acidemia; Glutaric aciduria/type II; Glycogen storage diseases; Hyperglycinuria; Phosphoenolpyruvate carboxykinase defic (PEPCK); Pipecolic acidemia; Von Gierke's disease/glycogenosis I; Renal tubular acidosis acquired

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