Disease Info Card

Deficiency Of Amp Pyrophorylase

Information about Deficiency Of Amp Pyrophorylase: 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 Deficiency Of Amp Pyrophorylase

Most recent studies have shown that Deficiency Of Amp Pyrophorylase shares some biological mechanisms with enzymopathy, gout, hereditary-diseases, inborn-errors-of-metabolism, kidney-calculi, kidney-diseases, kidney-failure, kidney-failure-acute, kidney-failure-chronic, lesch-nyhan-syndrome, lithiasis, neoplasms, nephritis, nephritis-interstitial, nephrolithiasis, pain, renal-insufficiency, ureteral-calculi, urinary-tract-infection, urolithiasis.

Among the many pathways, these few ones have gauged particular interests from scientists studying Deficiency Of Amp Pyrophorylase, and have been seen in publications frequently: Adenine Salvage, Cell Cycle, Chemotaxis, Dna Repair, Excretion, Fibroblast Activation, Gene Conversion, Germination, Glomerular Filtration, Killer Activity, Lymphocyte Differentiation, Meiosis, Mismatch Repair, Mitotic Recombination, Nucleoside Transport, Pathogenesis, Spermatogenesis, Sporulation, Transport, Xanthine Oxidation

Quite a number of genes have been found to play important roles in Deficiency Of Amp Pyrophorylase, such as ADA, ADK, APRT, DAP, DCK, DNPEP, DOCK11, GALNS, HPRT1, IAPP, MRC1, MTAP, OTC, PNP, QPCT, RAPGEF5, XDH. 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.