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Results 1 - 4 of 4 for "Methylcrotonyl-CoA" carboxylase deficiency
  1. ... Genetic testing OMIM Genetic disorder catalog Conditions > 3-methylcrotonyl-CoA carboxylase deficiency (often shortened to 3-MCC deficiency ) On this ... October 2008 What is 3-MCC deficiency? 3-methylcrotonyl-CoA carboxylase deficiency (also known as 3-MCC deficiency) is an ...
  2. 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. ...
  3. Metabolic Disorders (National Library of Medicine)  
    Metabolism is the process your body uses to get or make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive ...
  4. 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 ...