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Organic aciduria
- 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 ...
- ... 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 ...
- ... leucine is not processed normally, chemical byproducts called organic acids can build up and make the blood ... into catalysis and the molecular basis for hydroxymethylglutaric aciduria. J Biol Chem. 2006 Mar 17;281(11): ...
- ... Glutaryl-CoA dehydrogenase deficiency: region-specific analysis of organic acids and acylcarnitines in post mortem brain predicts ...