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Results 1 - 6 of 6 for Valine
  1. Isobutyryl-CoA dehydrogenase deficiency 
    ... deficiency have problems breaking down the amino acid valine. Most people with IBD deficiency are asymptomatic, which ... the IBD enzyme is involved in breaking down valine. Specifically, this enzyme functions in the third step ...
    https://medlineplus.gov/.../isobutyryl-coa-dehydrogenase-deficiency - Genetics
  2. Maple syrup urine disease 
    ... breaking down the amino acids leucine, isoleucine, and valine, which are present in many kinds of food, ... preventing the normal breakdown of leucine, isoleucine, and valine. As a result, these amino acids and their ...
    https://medlineplus.gov/genetics/condition/maple-syrup-urine-disease - Genetics
  3. Wilson disease 
    ... block (amino acid) methionine or the amino acid valine. Among people who have variants in the ATP7B gene, it appears that having methionine instead of valine at position 129 of the prion protein is ...
    https://medlineplus.gov/genetics/condition/wilson-disease - Genetics
  4. Familial paroxysmal nonkinesigenic dyskinesia 
    ... Bird TD, Raskind WH. Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic ...
    https://medlineplus.gov/...lial-paroxysmal-nonkinesigenic-dyskinesia - Genetics
  5. Short/branched chain acyl-CoA dehydrogenase deficiency 
    ... for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolism. Am J Hum Genet. 2000 Nov;67( ...
    https://medlineplus.gov/...d-chain-acyl-coa-dehydrogenase-deficiency - Genetics
  6. Dihydrolipoamide dehydrogenase deficiency 
    ... found in protein-rich foods: leucine, isoleucine, and valine. Breakdown of these amino acids produces molecules that ...
    https://medlineplus.gov/...dihydrolipoamide-dehydrogenase-deficiency - Genetics