Common Atrium

Overview of Common Atrium

Most recent studies have shown that Common Atrium shares some biological mechanisms with anomalous-pulmonary-venous-connection, atresia, atrial-septal-defects, atrioventricular-septal-defect-and-common-atrioventricular-junction, common-atrioventricular-canal, common-ventricle-disorder, congenital-heart-defects, coronary-vessel-anomalies, dextrocardia, double-outlet-right-ventricle, endocardial-cushion-defects, heart-diseases, heart-septal-defects, left-atrial-isomerisms, pulmonary-stenosis, scimitar-syndrome, situs-ambiguus, stenosis, transposition-of-great-vessels.

Among the many pathways, these few ones have gauged particular interests from scientists studying Common Atrium, and have been seen in publications frequently: Aging, Cardiac Chamber Formation, Dehiscence, Developmental Growth, Heart Development, Pathogenesis, Swimming, Transposition

Quite a number of genes have been found to play important roles in Common Atrium, such as AKT1, AMY2A, BLOC1S6, CA5A, DHCR7, EPB42, EVC, EVC2, FGF10, GDF1, MTSS1, PRH1, SDHA, SHF, SHH, TBX3. 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.

Common Atrium Related Genes

click to see detail information for each gene

Pathways Related to Common Atrium

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

Related Diseases