Peritonitis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A gastrointestinal system disease that involves inflammation of the peritoneum resulting from perforation of the gastrointestinal tract, which produces immediate chemical inflammation followed shortly by infection from intestinal organisms. Peritonitis can also result from appendicitis, diverticulitis, strangulating intestinal obstruction, pancreatitis, pelvic inflammatory disease, mesenteric ischemia, intraperitoneal blood, barium, or peritoneo-systemic shunts, drains, and dialysis catheters in the peritoneal cavity. The symptoms include abdominal pain and tenderness, fever, fluid in the abdomen, nausea, vomiting and low urine output. (Human Disease Ontology, DOID_8283)
External Link https://www.disgenet.org/browser/0/1/0/C0031154
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Genes

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

Symbol Name
BRCA1 breast cancer 1, early onset
C5 complement component 5
CFB complement factor B
F5 coagulation factor V (proaccelerin, labile factor)
FAS Fas cell surface death receptor
FASLG Fas ligand (TNF superfamily, member 6)
GSK3B glycogen synthase kinase 3 beta
IFNG interferon, gamma
JAK2 Janus kinase 2
MEFV Mediterranean fever
MVK mevalonate kinase
RIPK2 receptor-interacting serine-threonine kinase 2
TMEM67 transmembrane protein 67
TNF tumor necrosis factor
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A