Heterotaxy Syndrome

Overview of Heterotaxy Syndrome

Most recent studies have shown that Heterotaxy Syndrome shares some biological mechanisms with accessory-spleen, anomalous-pulmonary-venous-connection, atresia, cardiac-arrhythmia, common-ventricle-disorder, congenital-abnormality, congenital-absence-of-spleen, congenital-atresia-of-inferior-vena-cava, congenital-heart-defects, congenital-heart-disease, dextrocardia, heart-diseases, heart-septal-defects, hypoplastic-left-heart-syndrome, isomerism-right-atrial, regurgitation, scimitar-syndrome, situs-ambiguus, situs-inversus, stenosis.

Among the many pathways, these few ones have gauged particular interests from scientists studying Heterotaxy Syndrome, and have been seen in publications frequently: Axis Specification, Cardiac Conduction, Cell Adhesion, Coagulation, Forebrain Development, Gastrulation, Heart Looping, Limb Development, Localization, Pathogenesis, Transposition

Quite a number of genes have been found to play important roles in Heterotaxy Syndrome, such as ACVR2B, AMY2A, BLOC1S6, CFC1, CPB1, CRELD1, EPB42, GDF1, GLI1, GLI3, LEFTY2, MTHFR, NKX2-5, PITX2, PRH1, SHH, ZIC1, ZIC3. 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.

Heterotaxy Syndrome Related Genes

click to see detail information for each gene

Pathways Related to Heterotaxy Syndrome

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

Related Diseases