Agent Commons Collaborative Research
Intestinal disorder
A non-neoplastic or neoplastic disorder that affects the small or large intestine.
- Identifiers
- MONDO:0005020
- Part of
- Digestive system disorder
- Also known as
- disease of intestine · disease or disorder of intestine · disease, intestinal · diseases, intestinal · disorder of intestine
Subtypes
Disease Rare Not rare Subtypes
- Intestinal neoplasm MONDO:0021118 141
- Large intestine disorder MONDO:0024634 104
- Small intestine disorder MONDO:0024635 56
- Intestinal motility disease MONDO:0021189 32
- Malabsorption syndrome MONDO:0020598 18
- Inflammatory bowel disease MONDO:0005265 14
- Intestinal obstruction MONDO:0004565 11
- Eosinophilic gastrointestinal disease MONDO:0018438 8
- Gastroenteritis MONDO:0002269 7
- Intestinal atresia MONDO:0001045 5
- Parasitic intestinal disorder MONDO:0024270 5
- Intestinal lymphangiectasia MONDO:0018178 2
- Trichohepatoenteric syndrome MONDO:0009105 2
- Glucose-galactose malabsorption MONDO:0011731 SLC5A1 1
- Hypertrophic pyloric stenosis MONDO:0001560 1
- Intestinal fistula MONDO:1040017 1
- Intestinal perforation MONDO:0006807 1
- Necrotizing enterocolitis MONDO:0005313 1
- Short bowel syndrome MONDO:0015183 1
- Volvulus of midgut MONDO:0008666 1
- 4-hydroxyphenylacetic aciduria MONDO:0022330
- NK-cell enteropathy MONDO:0016996
- Satoyoshi syndrome MONDO:0010922
- Whipple disease MONDO:0005116
- Abetalipoproteinemia MONDO:0008692 MTTP
- Aplasia cutis congenita-intestinal lymphangiectasia syndrome MONDO:0008808
- Chronic atrial and intestinal dysrhythmia MONDO:0014528 SGO1
- Chronic diarrhea with villous atrophy MONDO:0010786
- Chronic enteropathy associated with SLCO2A1 gene MONDO:0018766
- Chronic intestinal failure MONDO:0017418
- Congenital diarrhea 7 with exudative enteropathy MONDO:0014375 DGAT1
- Congenital enterocyte heparan sulfate deficiency MONDO:0015171
- Cryptogenic multifocal ulcerous stenosing enteritis MONDO:0018765
- Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder MONDO:0018794 PLA2G4A
- Intractable diarrhea-choanal atresia-eye anomalies syndrome MONDO:0015295
- Isolated mesenteric vein thrombosis MONDO:0035009
- Malakoplakia MONDO:0018913
- Primary desmosis coli MONDO:0034846
- Protein-losing enteropathy MONDO:0009174 CD55
- Refractory celiac disease MONDO:0018353
- Solitary rectal ulcer syndrome MONDO:0016208
Projects
Including projects on subtypes.
No projects yet.