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Differential Diagnosis For DNATest specific/genetics laboratory/abnormality (Lab): Metabolic, Storage Disorders

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DNATest specific/genetics laboratory/abnormality (Lab)
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Metabolic, Storage Disorders: next: Congenital Causes: Diabetes mellitus/juvenile (Type I); Erythrohepatic protoporphyria; Porphyria, acute intermittent; Hemochromatosis; Tay-Sachs disease; Citrullinemia/Argininsuccinicaciduria; Combined carboxylase/Biotinidase deficiency; Methylmalonic acidemia/ketotic glycine; Phenylketonuria/PKU; Propionicacidemia/ketotic glycinemia; Acyl-CoA Dehydrogenase/short chain def; Carbamoyl phosphate synthetase defic; Hypertyrosinemia, persistent; LCHAD/Long chain OH-CoA dehydrogenase def; MCAD/Medium chain OH-CoA Dehydrogenase def; Ornithine Transcarbamylase (OTC) defic.; Tyrosinemia, hereditary; VLCHAD/Very Long chain OH-CoA dehydrogenase def; Wilsons Disease; Alkaptonuria/Ochronosis; Citrullinuria; Fructose intolerance, hereditary; Gaucher's disease; Maple syrup urine disease; Methyltetrahydofolate reductase defic

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