Disease Info Card

Congenital Digestive System Anomalies

Information about Congenital Digestive System Anomalies: 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 Congenital Digestive System Anomalies

Most recent studies have shown that Congenital Digestive System Anomalies shares some biological mechanisms with anorectal-anomaly, anus-imperforate, atresia, cardiovascular-abnormalities, congenital-abnormality, congenital-heart-defects, constipation, diaphragmatic-hernia, esophageal-atresia, fetal-diseases, gastrointestinal-diseases, hernia, hirschsprung-disease, intestinal-atresia, intestinal-obstruction, pathologic-fistula, respiratory-system-abnormalities, stenosis, urogenital-abnormalities, vomiting.

Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Digestive System Anomalies, and have been seen in publications frequently: Aging, Cell Adhesion, Cell Proliferation, Defecation, Enteric Nervous System Development, Excretion, Gastric Emptying, Gastrulation, Innervation, Localization, Micturition, Midgut Development, Notochord Development, Pathogenesis, Peristalsis, Reflex, Segmentation, System Development, Transport, Transposition

Quite a number of genes have been found to play important roles in Congenital Digestive System Anomalies, such as ACD, ACHE, AFP, BMP4, CAT, ELSPBP1, FGF10, GDNF, GNAI1, HLA-DQA1, HTT, MNX1, NOD2, RET, SHH, SLC7A5, TAPBP, TEF, VIP. 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.