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Organic aciduria
Did you mean Organic acidemia?
- 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 ...
- Short/branched chain acyl-CoA dehydrogenase (SBCAD) deficiency (also known as 2-methylbutyryl-CoA dehydrogenase deficiency) is a rare disorder in which the body ...
- ... organic acids in the blood (organic acidemia), urine (organic aciduria), and tissues can be toxic and can cause ...
- ... organic acids in the blood (organic acidemia), urine (organic aciduria), and tissues can be toxic and can cause ...
- ... organic acids in the blood (organic acidemia), urine (organic aciduria), and tissues can be toxic and can cause ...
- ... disorders that run in families, such as glutaric aciduria and organic acidemias, Krabbe disease , maple syrup urine disease , and ...
- Lipid Metabolism Disorders/Specifics ... Lipid Metabolism Disorders ... Mitochondrial Diseases/Specifics ... Mitochondrial Diseases ... National Institute of Neurological ...
- Newborn Screening Tests for Your Baby (March of Dimes Foundation)Newborn Screening/Specifics ... Newborn Screening ... March of Dimes Foundation
- ... adipicaciduria GA II Glutaric acidemia, type 2 Glutaric aciduria, type 2 MAD MADD Multiple acyl-CoA dehydrogenase ...
- ... 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 ...