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Results 1 - 6 of 6 for Valine
  1. Isobutyryl-CoA dehydrogenase deficiency 
    ... helps break down a particular amino acid called valine.Most people with IBD deficiency are asymptomatic, which ... IBD enzyme, which is involved in breaking down valine. ACAD8 gene mutations reduce or eliminate the activity ...
    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. 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
  5. 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
  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