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Results 1 - 8 of 8 for Primary "hyperoxaluria," type I
  1. Primary hyperoxaluria 
    ... differ in their severity and genetic cause. In primary hyperoxaluria type 1, kidney stones typically begin to appear anytime ... adulthood, and ESRD can develop at any age. Primary hyperoxaluria type 2 is similar to type 1, but ESRD ...
    https://medlineplus.gov/genetics/condition/primary-hyperoxaluria - Genetics
  2. Nedosiran Injection 
    ... children 9 years of age and older with primary hyperoxaluria type 1 (PH1; an inherited condition that leads to ...
    https://medlineplus.gov/druginfo/meds/a624010.html - Drugs and Supplements
  3. HOGA1 gene 
    ... the HOGA1 gene have been found to cause primary hyperoxaluria type 3. This condition is caused by the overproduction ... to an overproduction of oxalate in people with primary hyperoxaluria type 3. Some researchers think that the accumulation of ...
    https://medlineplus.gov/genetics/gene/hoga1 - Genetics
  4. GRHPR gene 
    ... the GRHPR gene have been found to cause primary hyperoxaluria type 2. This condition is caused by the overproduction ... the walls of blood vessels in people with primary hyperoxaluria type 2. More About This Health Condition D-glycerate ...
    https://medlineplus.gov/genetics/gene/grhpr - Genetics
  5. AGXT gene 
    ... the AGXT gene have been found to cause primary hyperoxaluria type 1. This condition is caused by the overproduction ... the walls of blood vessels in people with primary hyperoxaluria type 1. More About This Health Condition AGT AGT1 ...
    https://medlineplus.gov/genetics/gene/agxt - Genetics
  6. Understanding Hyperoxaluria (Oxalosis and Hyperoxaluria Foundation)  
    Kidney Stones/Specifics ... Kidney Stones ... Amino Acid Metabolism Disorders/Specifics ... Amino Acid Metabolism Disorders ... Oxalosis and Hyperoxaluria Foundation
    https://ohf.org/understanding-hyperoxaluria - External Health Links
  7. Where can I read more about the diseases and traits covered in my direct-to-consumer genetic testing report?: ... 
    ... called MCAD deficiency Maple syrup urine disease Mucolipidosis type IV ... Pyruvate kinase deficiency Rhizomelic chondrodysplasia punctata Sialic acid ...
    https://medlineplus.gov/.../dtcgenetictesting/dtcghrpages - Genetics
  8. Amino Acid Metabolism Disorders (National Library of Medicine)  
    Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Your digestive system breaks ...
    https://medlineplus.gov/aminoacidmetabolismdisorders.html - Health Topics