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Disease Info Card
Urea Cycle Disorders, Inborn
Information about Urea Cycle Disorders, Inborn: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Urea Cycle Disorders, Inborn
Most recent studies have shown that Urea Cycle Disorders, Inborn shares some biological mechanisms with argininosuccinic-aciduria, brain-edema, carbamoyl-phosphate-synthase-i-deficiency-disease, cerebral-edema, citrullinemia, comatose, edema, encephalopathies, hyperammonaemic-encephalopathy, hyperammonemia, hyperargininemia, inborn-errors-of-metabolism, liver-failure, metabolic-diseases, ornithine-carbamoyltransferase-deficiency, phenylketonurias, vomiting.
Among the many pathways, these few ones have gauged particular interests from scientists studying Urea Cycle Disorders, Inborn, and have been seen in publications frequently: Amino Acid Transport, Cell Activation, Cell Death, Cell Migration, Cell Proliferation, Coagulation, Cognition, Creatine Transport, Excretion, Fatty Acid Oxidation, Gluconeogenesis, Glycolysis, Glycosylation, Localization, Pathogenesis, Pyruvate Oxidation, Rna Splicing, Translation, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Urea Cycle Disorders, Inborn, such as ABCB11, ADSL, ARID4B, ARSH, ASL, ASS1, CFTR, LCT, LTA, NAGS, NOS1, NOS2, OTC, PAH, SEC14L2. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.