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Results 1 - 9 of 9 for "3-methylcrotonyl-coa"
  1. 3-methylcrotonyl-CoA carboxylase deficiency 
    3-methylcrotonyl-CoA carboxylase deficiency (also called MCC deficiency) is an inherited disorder in which the body is unable to process certain proteins. ...
    https://medlineplus.gov/...methylcrotonyl-coa-carboxylase-deficiency - Genetics
  2. MCCC1 gene 
    ... many proteins. This step converts a molecule called 3-methylcrotonyl-CoA to a molecule called 3-methylglutaconyl-CoA. Additional ... MCCC1 gene have been identified in people with 3-methylcrotonyl-CoA carboxylase deficiency (also called MCC deficiency). MCC deficiency ...
    https://medlineplus.gov/genetics/gene/mccc1 - Genetics
  3. MCCC2 gene 
    ... many proteins. This step converts a molecule called 3-methylcrotonyl-CoA to a molecule called 3-methylglutaconyl-CoA. Additional ... MCCC2 gene have been identified in people with 3-methylcrotonyl-CoA carboxylase deficiency (also called MCC deficiency). MCC deficiency ...
    https://medlineplus.gov/genetics/gene/mccc2 - Genetics
  4. IVD gene 
    ... a molecule called isovaleryl-CoA to another molecule, 3-methylcrotonyl-CoA. Additional chemical reactions convert 3-methylcrotonyl-CoA into molecules that are used for energy. Nearly ...
    https://medlineplus.gov/genetics/gene/ivd - Genetics
  5. CA5A gene 
    ... synthetase-1, pyruvate carboxylase, propionyl-CoA carboxylase, and 3-methylcrotonyl-CoA carboxylase. These enzymes help control the amount of ... gluconeogenesis) in the liver. Propionyl-CoA carboxylase and 3-methylcrotonyl-CoA carboxylase help break down certain protein building blocks ( ...
    https://medlineplus.gov/genetics/gene/ca5a - Genetics
  6. Amino Acid Metabolism Disorders (National Library of Medicine)  
    Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Your digestive system breaks ...
    https://medlineplus.gov/aminoacidmetabolismdisorders.html - Health Topics
  7. Genetic Brain Disorders (National Library of Medicine)  
    A genetic brain disorder is caused by a variation or a mutation in a gene. A variation is a different form of a gene. A mutation is a change in a gene. ...
    https://medlineplus.gov/geneticbraindisorders.html - Health Topics
  8. Newborn Screening (National Library of Medicine)  
    Your newborn infant has screening tests before leaving the hospital. There may be different tests depending on the state where you live. They include: Tests ...
    https://medlineplus.gov/newbornscreening.html - Health Topics
  9. Newborn Screening Tests for Your Baby (March of Dimes Foundation)  
    Newborn Screening/Specifics ... Newborn Screening ... March of Dimes Foundation
    https://www.marchofdimes.org/.../newborn-screening-tests-your-baby - External Health Links