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  • ...are genetic disorder characterized by a deficiency of the enzyme ornithine transcarbamylase. This enzyme plays a crucial role in the [[urea cycle]], which is the proce ...o denote a condition of the blood. In this case, it refers to an excess of ornithine in the blood.
    2 KB (237 words) - 04:43, 7 February 2024
  • There are six main types of urea cycle disorders, each caused by a deficiency in one of the six enzymes involved in the urea cycle. These include: * [[Carbamoyl phosphate synthetase I deficiency]] ({{IPA|kɑːrˈbæmoɪl ˈfɑːsfeɪt sɪnˈθiːtɪs aɪ dɪˈfɪʃənsi
    2 KB (271 words) - 22:05, 11 February 2024
  • ...dɪsˈɔːrdər}}) is a genetic disorder caused by a mutation that results in a deficiency of one of the six enzymes in the [[urea cycle]]. These enzymes are responsi * [[Ornithine transcarbamylase]]
    2 KB (251 words) - 22:20, 13 February 2024