Osmotic Diarrhea Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Osmotic diarrhea is a dirrhea where diarrhea occurs when too much water is drawn into the bowels. This can be the result of maldigestion (e.g., pancreatic disease or Coeliac disease), in which the nutrients are left in the lumen to pull in water. Osmotic diarrhea can also be caused by osmotic laxatives (which work to alleviate constipation by drawing water into the bowels). In healthy individuals, too much magnesium or vitamin C or undigested lactose can produce osmotic diarrhea and distention of the bowel. A person who does not have lactose intolerance can have difficulty absorbing lactose after an extraordinarily high intake of dairy products. (Human Disease Ontology, DOID_0050130)
External Link https://www.disgenet.org/browser/0/1/0/C0267556
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Genes

4 genes associated with the disease Osmotic Diarrhea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CLDN2 claudin 2
SLC5A1 solute carrier family 5 (sodium/glucose cotransporter), member 1
STXBP2 syntaxin binding protein 2
WNT2B wingless-type MMTV integration site family, member 2B