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Results 1 - 4 of 4 for Mitochondrial trifunctional protein deficiency
  1. ... gov Research studies OMIM Genetic disorder catalog Conditions > Mitochondrial trifunctional protein deficiency On this page: Description Genetic changes Inheritance Diagnosis ...
  2. 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 ...
  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. ... deficiency? Mutations in the HADHA gene cause LCHAD deficiency. The HADHA gene provides instructions for making part of an enzyme complex called mitochondrial trifunctional protein. This enzyme complex functions in mitochondria, the energy- ...