Results 1 - 6 of 6 for Primary "hyperoxaluria," type I
  1. Genetics Home Reference: Primary hyperoxaluria From the National Institutes of Health (National Library of Medicine)  
    ... Genetic Testing Registry: Primary hyperoxaluria Genetic Testing Registry: Primary hyperoxaluria, type I Genetic Testing Registry: Primary hyperoxaluria, type II Genetic ...
  2. ... that increases their risk of forming kidney stones (type I primary hyperoxaluria). However, it does not appear to help people ...
  3. 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 type 1 * Alaninuria with microcephaly, dwarfism, enamel hypoplasia and diabetes ...
  4. Rare Diseases Clinical Research Network (Rare Diseases Clinical Research Network)  
    ... APRT deficiency (Dihydroxyadeninuria) cystinuria Dent disease Lowe ... Phosphate Synthetase (CPS) Deficiency Citrin Deficiency (Citrullinemia ...
  5. 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 ...
  6. Kidney Diseases (National Library of Medicine)  
    Your kidneys are two bean-shaped organs, each about the size of your fists. They are located near the middle of your back, just below the rib cage. Inside ...
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