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Results 1 - 5 of 5 for Citrullinemia type II
  1. Genetics Home Reference: Citrullinemia From the National Institutes of Health (National Library of Medicine)  
    ... First Test: Citrullinemia, Type I Baby's First Test: Citrullinemia, Type II Gene Review: Citrin Deficiency Gene Review: Citrullinemia Type ... Testing Registry: Citrullinemia type I Genetic Testing Registry: Citrullinemia type II Genetic Testing Registry: Neonatal intrahepatic cholestasis caused by ...
  2. 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 ...
  3. Rare Diseases Clinical Research Network (Rare Diseases Clinical Research Network)  
    ... Opitz Syndrome Sjögren-Larsson Syndrome Niemann-Pick Disease Type ... Deficiency (Argininosuccinic Aciduria) Arginase Deficiency ( Hyperargininemia) ...
  4. 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. ...
  5. 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 ...