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Disease Info Card
Conotruncal Heart Malformations (disorder)
Information about Conotruncal Heart Malformations (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 Conotruncal Heart Malformations (disorder)
Most recent studies have shown that Conotruncal Heart Malformations (disorder) shares some biological mechanisms with 22q11-deletion-syndrome, atresia, cleft-palate, congenital-abnormality, congenital-atresia-of-pulmonary-valve, congenital-heart-defects, congenital-heart-disease, congenital-hypoplasia-of-thymus, crest-syndrome, cytogenetic-abnormality, digeorge-syndrome, heart-diseases, hypocalcemia, hypoparathyroidism, hypoplasia, mental-disorders, tetralogy-of-fallot, transposition-of-great-vessels, truncus-arteriosus-persistent.
Among the many pathways, these few ones have gauged particular interests from scientists studying Conotruncal Heart Malformations (disorder), and have been seen in publications frequently: Cell Differentiation, Cell Migration, Cell Proliferation, Citrate Transport, Limb Development, Localization, Meiosis, Metaphase, Neural Crest Cell Differentiation, Neural Crest Cell Migration, Outflow Tract Morphogenesis, Pathogenesis, Secretion, Transport, Transposition
Quite a number of genes have been found to play important roles in Conotruncal Heart Malformations (disorder), such as CD4, COMT, DGCR6, GLB1, GSC2, HIC2, ITGA2B, ITGB3, MTHFR, NAT1, PRODH, PTH, SLC25A1, SLC38A3, SS18L1, TBX1, TYMS. 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.