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Results 1 - 7 of 7 for Organic aciduria
  1. Holocarboxylase synthetase deficiency 
    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 ...
    https://medlineplus.gov/.../holocarboxylase-synthetase-deficiency - Genetics
  2. Short/branched chain acyl-CoA dehydrogenase deficiency 
    Short/branched chain acyl-CoA dehydrogenase (SBCAD) deficiency (also known as 2-methylbutyryl-CoA dehydrogenase deficiency) is a rare disorder in which the body ...
    https://medlineplus.gov/...d-chain-acyl-coa-dehydrogenase-deficiency - Genetics
  3. Glutaric acidemia type I 
    ... organic acids in the blood (organic acidemia), urine (organic aciduria), and tissues can be toxic and can cause ...
    https://medlineplus.gov/genetics/condition/glutaric-acidemia-type-i - Genetics
  4. Propionic acidemia 
    ... organic acids in the blood (organic acidemia), urine (organic aciduria), and tissues can be toxic and can cause ...
    https://medlineplus.gov/genetics/condition/propionic-acidemia - Genetics
  5. Isovaleric acidemia 
    ... organic acids in the blood (organic acidemia), urine (organic aciduria), and tissues can be toxic and can cause ...
    https://medlineplus.gov/genetics/condition/isovaleric-acidemia - Genetics
  6. Glutaric acidemia type II 
    ... adipicaciduria GA II Glutaric acidemia, type 2 Glutaric aciduria, type 2 MAD MADD Multiple acyl-CoA dehydrogenase ...
    https://medlineplus.gov/genetics/condition/glutaric-acidemia-type-ii - Genetics
  7. 3-hydroxy-3-methylglutaryl-CoA lyase deficiency 
    ... 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 ...
    https://medlineplus.gov/...oxy-3-methylglutaryl-coa-lyase-deficiency - Genetics