Disease Info Card

Disorder Of Electrolytes

Information about Disorder Of Electrolytes: 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 Disorder Of Electrolytes

Most recent studies have shown that Disorder Of Electrolytes shares some biological mechanisms with acidosis, acute-kidney-injury, cardiac-arrhythmia, dehydration, diarrhea, edema, heart-diseases, heart-failure, hypernatremia, hypertensive-disease, hypocalcemia, inappropriate-adh-syndrome, kidney-diseases, kidney-failure, kidney-failure-acute, kidney-failure-chronic, malnutrition, neoplasms, vomiting, water-electrolyte-imbalance.

Among the many pathways, these few ones have gauged particular interests from scientists studying Disorder Of Electrolytes, and have been seen in publications frequently: Aging, Anaphylaxis, Coagulation, Diuresis, Excretion, Glomerular Filtration, Glucose Homeostasis, Hormone Secretion, Inflammatory Response, Localization, Natriuresis, Ovulation, Pathogenesis, Reflex, Secretion, Transport, Vasoconstriction, Vasopressin Secretion, Water Homeostasis, Water Transport

Quite a number of genes have been found to play important roles in Disorder Of Electrolytes, such as ACE, ALB, AQP2, AVP, AVPR2, CD55, EGFR, IFNAR1, INS, KCNJ10, MB, NLRP3, POMC, PTH, PTRH1, RAPGEF5, REN, TRPM6, VIP. 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.