Disease Info Card

Complete Atrioventricular Block

Information about Complete Atrioventricular Block: 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 Complete Atrioventricular Block

Most recent studies have shown that Complete Atrioventricular Block shares some biological mechanisms with atrial-fibrillation, atrioventricular-block, bradycardia, bundle-branch-block, cardiac-arrhythmia, cardiac-fibrillation, cardiomyopathies, congenital-complete-heart-block, congenital-heart-defects, heart-block, heart-diseases, heart-failure, heart-septal-defects, infarction, myocardial-infarction, right-bundle-branch-block, stenosis, syncope, tachycardia-ventricular, ventricular-septal-defects.

Among the many pathways, these few ones have gauged particular interests from scientists studying Complete Atrioventricular Block, and have been seen in publications frequently: Aging, Cardiac Conduction, Cell Death, Coagulation, Dehiscence, Excretion, Hypersensitivity, Immune Response, Inflammatory Response, Innervation, Localization, Pathogenesis, Pigmentation, Reflex, Regeneration, Secretion, Sensitization, Transposition, Vasoconstriction, Vasodilation

Quite a number of genes have been found to play important roles in Complete Atrioventricular Block, such as CALCR, CALR, DCX, GNL3, KRAS, KRT5, LIPH, PGR, PRB1, REST, SLC6A8, SSB, TMEM37, TRIM21. 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.