Disease Info Card

Malabsorption Syndrome

Information about Malabsorption Syndrome: 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 Malabsorption Syndrome

Most recent studies have shown that Malabsorption Syndrome shares some biological mechanisms with anemia, atrophy, celiac-disease, chronic-diarrhea, crohn-disease, cystic-fibrosis, diabetes-mellitus, diarrhea, fibrosis, gastrointestinal-diseases, intestinal-diseases, lactose-intolerance, liver-diseases, malnutrition, nutrition-disorders, obesity, pain, short-bowel-syndrome, steatorrhea, vitamin-b-12-deficiency.

Among the many pathways, these few ones have gauged particular interests from scientists studying Malabsorption Syndrome, and have been seen in publications frequently: Acid Secretion, Aging, Bone Mineralization, Bone Resorption, Coagulation, Excretion, Fermentation, Gastric Acid Secretion, Gastric Emptying, Glucose Transport, Hypersensitivity, Immune Response, Inflammatory Response, Intestinal Absorption, Localization, Menopause, Pathogenesis, Pigmentation, Secretion, Transport

Quite a number of genes have been found to play important roles in Malabsorption Syndrome, such as ALB, BEST1, CCK, CFTR, DMD, F2, GCG, GLB1, GNAI1, INS, LCT, PTH, PTRH1, PYY, SLC46A1, SLC5A1, TGM2. 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.