Disease Info Card

Pseudohyperkalaemia

Information about Pseudohyperkalaemia: 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 Pseudohyperkalaemia

Most recent studies have shown that Pseudohyperkalaemia shares some biological mechanisms with acute-lymphocytic-leukemia, anemia, anemia-hemolytic, anemia-hemolytic-congenital, blood-coagulation-disorders, chronic-lymphocytic-leukemia, dehydration, edema, hemolysis-(disorder), hereditary-diseases, hereditary-spherocytosis, hereditary-stomatocytosis, leukemia, leukocytosis, lymphoid-leukemia, myeloproliferative-disease, stomatocytic-anemia, thrombocythemia-essential, thrombocytosis, xerocytosis.

Among the many pathways, these few ones have gauged particular interests from scientists studying Pseudohyperkalaemia, and have been seen in publications frequently: Blood Coagulation, Carbohydrate Transport, Cation Transport, Cell Development, Coagulation, Excretion, Gas Transport, Glucose Transport, Glutamate Homeostasis, Ion Transport, Localization, Platelet Activation, Platelet Aggregation, Renal Potassium Excretion, Secretion, Transport

Quite a number of genes have been found to play important roles in Pseudohyperkalaemia, such as ACE, ANK1, CD34, DHPS, EPB41, EPB42, GRIP1, LYN, POMC, PPBP, PTGFR, REN, SLC2A1, SLC4A1, SPTA1, SPTB, STOM, TUBA4A. 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.