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Results 1 - 4 of 4 for Primary "hyperoxaluria," type II
  1. Genetics Home Reference: Primary hyperoxaluria From the National Institutes of Health (National Library of Medicine)  
    ... Registry: Primary hyperoxaluria, type I Genetic Testing Registry: Primary hyperoxaluria, type II Genetic Testing Registry: Primary hyperoxaluria, type III You ...
  2. What Is Hyperoxaluria and Oxalosis? (Oxalosis and Hyperoxaluria Foundation)  
    ... other major organs. Primary Hyperoxaluria Type I and Type II Primary Hyperoxaluria (PH) is a rare genetic (inherited) disorder that is present at birth. Primary hyperoxaluria comes in many forms, of which only two, Type I and Type II are well characterized. Type I and Type II ...
  3. Rare Diseases Clinical Research Network (Rare Diseases Clinical Research Network)  
    ... web site ] [ Study Information ] [+] Rare Kidney Stone Consortium ... Lyase Deficiency (Argininosuccinic Aciduria) Arginase Deficiency ( Hyperargininemia) ...
  4. 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 ...