Accessory Atrioventricular Bundle (disorder)

Overview of Accessory Atrioventricular Bundle (disorder)

Most recent studies have shown that Accessory Atrioventricular Bundle (disorder) shares some biological mechanisms with atrial-fibrillation, atrioventricular-block, bundle-branch-block, cardiac-arrhythmia, cardiac-fibrillation, ebstein-anomaly, heart-block, heart-diseases, paroxysmal-supraventricular-tachycardia, polyendocrinopathies-autoimmune, pre-excitation-syndromes, sudden-death, supraventricular-tachycardia, syncope, tachycardia-atrioventricular-nodal-reentry, tachycardia-paroxysmal, tachycardia-reciprocating, tachycardia-ventricular, ventricular-fibrillation, wolff-parkinson-white-syndrome.

Among the many pathways, these few ones have gauged particular interests from scientists studying Accessory Atrioventricular Bundle (disorder), and have been seen in publications frequently: Aging, Cardiac Conduction, Circadian Rhythm, Dedifferentiation, Dehiscence, Donor Selection, Heart Development, Localization, Pathogenesis, Reflex, Transposition

Quite a number of genes have been found to play important roles in Accessory Atrioventricular Bundle (disorder), such as AMY2A, BLOC1S6, CS, DCX, EBPL, ELK3, GJA1, GJC3, GNL3, IGKV1-5, KRAS, LIPH, MYL7, PGR, TMEM37, UBN1. 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.

Accessory Atrioventricular Bundle (disorder) Related Genes

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Pathways Related to Accessory Atrioventricular Bundle (disorder)

This information is being compiled and will come in a future update

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