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Disease Info Card
Right Aortic Arch (disorder)
Information about Right Aortic Arch (disorder): 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 Right Aortic Arch (disorder)
Most recent studies have shown that Right Aortic Arch (disorder) shares some biological mechanisms with aberrant-subclavian-artery, aneurysm, aortic-arch-syndromes, aortic-coarctation, atresia, congenital-abnormality, congenital-heart-defects, congenital-heart-disease, deglutition-disorders, diverticulum, heart-diseases, heart-septal-defects, kommerells-diverticulum, patent-ductus-arteriosus, stenosis, tetralogy-of-fallot, vascular-ring, ventricular-septal-defects.
Among the many pathways, these few ones have gauged particular interests from scientists studying Right Aortic Arch (disorder), and have been seen in publications frequently: Aging, Artery Development, Cell Development, Cell Migration, Diuresis, Glucose Homeostasis, Heart Development, Localization, Neural Crest Cell Development, Neural Crest Cell Migration, Ovulation, Parturition, Pathogenesis, Peristalsis, Reflex, Transposition
Quite a number of genes have been found to play important roles in Right Aortic Arch (disorder), such as AMY2A, ARSA, BLOC1S6, CAT, CRAT, EPB42, FEZF2, FGF8, GLYAT, INVS, LPA, NKX2-5, PRH1, SS18L1, TBX1, TF, ZBTB8OS. 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.