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Differential Diagnosis For Family history/Metabolic disease

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Family history/Metabolic disease
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Metabolic, Storage Disorders: Congenital erythropoetic porphyria; Metabolic disorders; Porphyria variegata; Porphyria, acute intermittent; Chylomicronemia syndrome; Xanthinuria; Coproporphyria erythrohepatica; Citrullinemia/Argininsuccinicaciduria; HyperArgininemia; Phenylketonuria/PKU; LCHAD/Long chain OH-CoA dehydrogenase def; MCAD/Medium chain OH-CoA Dehydrogenase def; Orotic aciduria, hereditary; VLCHAD/Very Long chain OH-CoA dehydrogenase def; Aminoaciduria; Fructose 1,6 diphosphatase deficiency; Fructose intolerance, hereditary; Fructosuria, essential; Galactosemia; Glutaric aciduria/Acidemia; Glutaric aciduria/type II; Hyperglycinuria; Hyperprolinemia; Lesch-Nyhan syndrome; Maple syrup urine disease; Pentosuria, essential
Biochemical Disorders: Hyperammonemia
Hereditary, Familial, Genetic Disorders: Hereditary disorder
Synonyms: DIS METAB, Disease Metabolic, Diseases Metabolic, Disorder metabolic, disorder metabolism, Disorder of metabolism, Disorder of metabolism (disorder), Family history, general metabolic disorder, Generalised metabolic disorder, Generalized metabolic disorder, Generalized metabolic disorder (disorder), MD Metabolic disorders, METAB DIS, Metabolic disease, Metabolic disease (disorder), Metabolic Diseases, Metabolic Disorder, metabolic disorder general, Metabolic disorder unspecified, Metabolic disorders, METABOLIC DISORDERS GENERAL, metabolism disorder, metabolism disorder general, Metabolism Disorders, Thesaurismoses, Thesaurismosis, Unspecified disorder of metabolism
External Links Related to Family history/Metabolic disease: Google; Wikipedia; Merck; Images; PubMed (National Library of Medicine); NGC (National Guideline Clearinghouse); Medscape (eMedicine); Harrison's Online (accessmedicine); NEJM (The New England Journal of Medicine)

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