Disease Info Card

Congenital Secretory Diarrhea, Chloride Type

Information about Congenital Secretory Diarrhea, Chloride Type: 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 Secretory Diarrhea, Chloride Type

Most recent studies have shown that Congenital Secretory Diarrhea, Chloride Type shares some biological mechanisms with adenoma, alkalosis, cystic-fibrosis, dehydration, diarrhea, diarrhea-watery, diastrophic-dysplasia, dysplasia, failure-to-thrive, fibrosis, hyperaldosteronism, hypochloraemia, inborn-errors-of-metabolism, infantile-diarrhea, kidney-failure, lymphoproliferative-disorder-of-the-skin, malabsorption-syndrome, metabolic-alkalosis, pathological-dilatation, polyhydramnios.

Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Secretory Diarrhea, Chloride Type, and have been seen in publications frequently: Anion Transport, Chloride Transport, Clathrin-mediated Endocytosis, Endocytosis, Excretion, Fertilization, Glomerular Filtration, Intestinal Absorption, Ion Transport, Oxalate Transport, Pathogenesis, Pinocytosis, Protein Phosphorylation, Secretion, Sperm Capacitation, Sperm Motility, Spermatogenesis, Sulfate Transport, Transport, Water Transport

Quite a number of genes have been found to play important roles in Congenital Secretory Diarrhea, Chloride Type, such as ATP8A2, CFTR, IL10, PTGDS, REN, SLC13A1, SLC26A1, SLC26A2, SLC26A3, SLC26A4, SLC26A5, SLC26A6, SLC26A8, SLC9A2, SLC9A3, YY1. 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.