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Results 1 - 4 of 4 for Inborn disorder of pyrimidine metabolism
  1. Beta-ureidopropionase deficiency 
    Beta-ureidopropionase deficiency is a disorder that causes excessive amounts of molecules called N-carbamyl-beta-aminoisobutyric acid and N-carbamyl-beta- ...
    https://medlineplus.gov/.../beta-ureidopropionase-deficiency - Genetics
  2. Dihydropyrimidinase deficiency 
    Dihydropyrimidinase deficiency is a disorder that can cause neurological and gastrointestinal problems in some affected individuals. Other people with dihydropyrimidinase ...
    https://medlineplus.gov/.../condition/dihydropyrimidinase-deficiency - Genetics
  3. Dihydropyrimidine dehydrogenase deficiency 
    Dihydropyrimidine dehydrogenase deficiency is a disorder characterized by a wide range of severity, with neurological problems in some individuals and no signs or symptoms ...
    https://medlineplus.gov/...ihydropyrimidine-dehydrogenase-deficiency - Genetics
  4. Lesch-Nyhan syndrome 
    Harris JC. Disorders of purine and pyrimidine metabolism. In: Kliegman RM, St. Geme JW, Blum NJ, Shah SS, Tasker RC, Wilson KM, eds. Nelson Textbook of Pediatrics . ...
    https://medlineplus.gov/ency/article/001655.htm - Medical Encyclopedia