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. Rare Diseases Clinical Research Network (Rare Diseases Clinical Research Network)  
    ... APRT deficiency (Dihydroxyadeninuria) cystinuria Dent disease Lowe Syndrome primary ... Synthase (NAGS) Deficiency Ornithine Transcarbamylase (OTC) ...
  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. Rare Diseases and Related Terms From the National Institutes of Health (Office of Rare Diseases)  
    ... island eye disease * Alanine-glyoxylate aminotransferase deficiency - See Primary hyperoxaluria ... ALG2-CDG (CDG-Ii) * ALG2-CDG (CDG-Ii) * ALG2-CDG (CDG-Ii) - ...
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