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Results 1 - 2 of 2 for Inborn organic aciduria
  1. Short/branched chain acyl-CoA dehydrogenase deficiency 
    Short/branched chain acyl-CoA dehydrogenase (SBCAD) deficiency (also known as 2-methylbutyryl-CoA dehydrogenase deficiency) is a rare disorder in which the body ...
    https://medlineplus.gov/...d-chain-acyl-coa-dehydrogenase-deficiency - Genetics
  2. Hereditary urea cycle abnormality 
    ... ammonia in the body. These diseases include: Argininosuccinic aciduria Arginase deficiency Carbamyl phosphate synthetase (CPS) deficiency Citrullinemia ...
    https://medlineplus.gov/ency/article/000372.htm - Medical Encyclopedia