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Results 1 - 10 of 13 for Organic aciduria
Did you mean Organic acidemia?
  1. Holocarboxylase synthetase deficiency is an inherited disorder in which the body is unable to use the vitamin biotin effectively. This disorder is classified as a multiple ...
  2. Short/branched chain acyl-CoA dehydrogenase (SBCAD) deficiency (also known as 2-methylbutyryl-CoA dehydrogenase deficiency) is a rare disorder in which the body ...
  3. ... organic acids in the blood (organic acidemia), urine (organic aciduria), and tissues can be toxic and can cause ...
  4. ... organic acids in the blood (organic acidemia), urine (organic aciduria), and tissues can be toxic and can cause ...
  5. ... organic acids in the blood (organic acidemia), urine (organic aciduria), and tissues can be toxic and can cause ...
  6. ... disorders that run in families, such as glutaric aciduria and organic acidemias, Krabbe disease , maple syrup urine disease , and ...
  7. Barth Syndrome (BTHS) From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Lipid Metabolism Disorders/Specifics ... Lipid Metabolism Disorders ... Mitochondrial Diseases/Specifics ... Mitochondrial Diseases ... National Institute of Neurological ...
  8. Newborn Screening Tests for Your Baby (March of Dimes Foundation)  
    Newborn Screening/Specifics ... Newborn Screening ... March of Dimes Foundation
  9. ... adipicaciduria GA II Glutaric acidemia, type 2 Glutaric aciduria, type 2 MAD MADD Multiple acyl-CoA dehydrogenase ...
  10. ... processed normally, a buildup of chemical byproducts called organic acids can result in metabolic acidosis. A shortage ... A lyase deficiency 3-OH 3-CH3 glutaric aciduria 3-OH 3-methyl glutaric aciduria 3HMG Deficiency ...
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