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Disease Info Card
Cortisol 11-beta-ketoreductase Deficiency
Information about Cortisol 11-beta-ketoreductase Deficiency: 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 Cortisol 11-beta-ketoreductase Deficiency
Most recent studies have shown that Cortisol 11-beta-ketoreductase Deficiency shares some biological mechanisms with adrenal-hyperplasia, alkalosis, congenital-adrenal-hyperplasia, conn-syndrome, cushing-syndrome, essential-hypertension, hereditary-diseases, hyperaldosteronism, hypernatremia, hyperplasia, hypertensive-disease, inborn-errors-of-metabolism, kidney-diseases, kidney-failure-chronic, liddle-syndrome, mineralocorticoid-excess-syndrome-apparent, pseudohypoaldosteronism.
Among the many pathways, these few ones have gauged particular interests from scientists studying Cortisol 11-beta-ketoreductase Deficiency, and have been seen in publications frequently: Aldosterone Secretion, Catecholamine Secretion, Corticotropin Secretion, Cortisol Secretion, Diuresis, Excretion, Glycosylation, Localization, Menstruation, Metaphase, Natriuresis, Pathogenesis, Regulation Of Blood Pressure, Response To Water Deprivation, Secretion, Transepithelial Transport, Transport, Vasoconstriction, Water Homeostasis, Water Transport
Quite a number of genes have been found to play important roles in Cortisol 11-beta-ketoreductase Deficiency, such as ACE, AGT, AMY2A, BLOC1S6, CHST3, CRAT, CYP11B1, CYP11B2, EDN1, GSR, HSD11B1, HSD11B2, NR3C1, NR3C2, POMC, REN, S100A6. 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.