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Results 1 - 8 of 8 for Citrullinemia type I
  1. Genetics Home Reference: Citrullinemia From the National Institutes of Health (National Library of Medicine)  
    ... gov Research studies OMIM Genetic disorder catalog Conditions > Citrullinemia On this page: Description Genetic changes Inheritance Diagnosis ... names Glossary definitions Reviewed June 2006 What is citrullinemia? Citrullinemia is an inherited disorder that causes ammonia ...
  2. Rare Diseases Clinical Research Network (Rare Diseases Clinical Research Network)  
    ... Deficiency Ornithine Transcarbamylase (OTC) Deficiency Argininosuccinate Synthetase Deficiency (Citrullinemia I) Citrin Deficiency (Citrullinemia II) Argininosuccinate Lyase Deficiency ( ...
  3. 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. ...
  4. ... aciduria Arginase deficiency Carbamyl phosphate synthetase (CPS) deficiency Citrullinemia N-acetyl glutamate synthetase deficiency (NAGS) Ornithine transcarbamylase ...
  5. National Urea Cycle Disorders Foundation (National Urea Cycle Disorders Foundation)  
    ... already available in most states for ASA lyase, citrullinemia and arginase deficiency, making it possible to identify ...
  6. 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 ...
  7. 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 ...
  8. ... depression, episodes of mania, and other abnormal moods); citrullinemia (condition that causes build-up of ammonia in ...