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Results 1 - 7 of 7 for Homocystinuria due to CBS deficiency
  1. Genetics Home Reference: Homocystinuria From the National Institutes of Health (National Library of Medicine)  
    ... HOMOCYSTINURIA, cblD TYPE, VARIANT 1 Genetic Testing Registry: Homocystinuria due to CBS deficiency Genetic Testing Registry: Homocystinuria-Megaloblastic anemia ...
  2. Increased total urine amino acids may be due to: Alkaptonuria Canavan ... acidemia Rickets Tyrosinemia type 1 Tyrosinemia type 2 ...
  3. Genetics Home Reference: Methylmalonic acidemia From the National Institutes of Health (National Library of Medicine)  
    ... Methylmalonic acidemia Genetic Testing Registry: Methylmalonic acidemia with ... methylmalonyl-CoA mutase deficiency Genetic Testing Registry: Methylmalonyl- ...
  4. Homocysteine Test (American Association for Clinical Chemistry)  
    ... or a family member has been diagnosed with homocystinuria, then the patient should be tested for the ... Back to top Common Questions ...
  5. Heritable Disorders of Connective Tissue From the National Institutes of Health (National Institute of Arthritis and Musculoskeletal and Skin Diseases)  
    ... fluids. Heritable. Capable of being transmitted from parent to child through genes. Homocystinuria. A genetically transmitted disease in which an enzyme ...
  6. 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 ...
  7. 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 ...