Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Neonatal intestinal perforation due to in utero intestinal volvulus (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Neonatal intestinal perforation co-occurrent and due to in utero intraluminal obstruction (disorder) |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
3 |
Neonatal intestinal perforation co-occurrent and due to in utero intraluminal obstruction (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
4 |
Chronic idiopathic non-infectious enteritis of intestine |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Neonatal perforation of intestine caused by drug (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
1 |
Infection of intestine caused by Vibrio (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
1 |
Diverticulitis of intestine (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
1 |
Diverticulosis of intestine |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
1 |
Acute intestinal ischemia due to obstruction of vasculature of intestine (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
4 |
Gastrointestinal hypersensitivity caused by food (disorder) |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
2 |
Closure of enterovesicovaginal fistula (procedure) |
Procedure site - Direct (attribute) |
True |
Intestinal structure |
Inferred relationship |
Some |
4 |
Intestinal angioedema caused by angiotensin-converting enzyme inhibitor (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
1 |
Intestinal anastomosis present |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Intestinal bypass present |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Left hemicolectomy with stoma |
Procedure site - Direct (attribute) |
False |
Intestinal structure |
Inferred relationship |
Some |
1 |
Right colectomy with stoma (procedure) |
Procedure site - Direct (attribute) |
False |
Intestinal structure |
Inferred relationship |
Some |
3 |
Partial resection of colon with stoma (procedure) |
Procedure site - Direct (attribute) |
False |
Intestinal structure |
Inferred relationship |
Some |
2 |
Neonatal candidiasis of intestine |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Nausea, vomiting and diarrhea |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Nervous diarrhea |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Raw-milk associated diarrhea |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Diarrhea due to diabetes mellitus |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Allergic diarrhea |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
3 |
Postcholecystectomy diarrhea |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Non-infective diarrhea |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Diarrhea caused by alcohol intake (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Dietetic diarrhea |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Inflammatory diarrhea |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Hemorrhagic diarrhea |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Diarrheic shellfish poisoning |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Diarrheal disorder |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Diarrhoea after gastrointestinal tract surgery |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
3 |
Post-vagotomy diarrhoea |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Psychogenic diarrhea |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Diarrhea and vomiting after gastrointestinal tract surgery |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
4 |
Antibiotic-associated diarrhea (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Acute diarrhea (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Brainerd diarrhea (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Diarrhea caused by drug |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Trichohepatoenteric syndrome |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Non-infective neonatal diarrhea (disorder) |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
|
Fetal intrauterine intestinal perforation co-occurrent and due to congenital stenosis of intestinal tract |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
3 |
Fetal intrauterine intestinal perforation co-occurrent and due to congenital stenosis of intestinal tract |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
4 |
Fetal intrauterine intestinal perforation co-occurrent and due to congenital atresia of intestinal tract (disorder) |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
3 |
Fetal intrauterine intestinal perforation co-occurrent and due to congenital atresia of intestinal tract (disorder) |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
4 |
Satoyoshi syndrome is a rare, multisystemic autoimmune disease mainly characterized by intermittent painful muscle spasms, alopecia (totalis or universalis in most cases) and long-lasting diarrhea that could lead to malnutrition, growth retardation, and amenorrhea. Secondary bone deformities and various endocrine anomalies may also be associated. Antinuclear antibodies are reported in many cases. |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Drug-induced constipation |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
1 |
Chronic idiopathic constipation |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
3 |
Obstipation |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Functional constipation |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Chronic constipation without overflow |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
3 |
Chronic constipation |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Constipation due to spasm of colon (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Constipation due to neurogenic bowel (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Therapeutic opioid induced constipation (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
1 |
MRI of intestine |
Procedure site - Direct (attribute) |
True |
Intestinal structure |
Inferred relationship |
Some |
1 |
Benign infantile seizures associated with mild gastroenteritis is a rare infantile epilepsy syndrome characterized by benign afebrile seizures in previously healthy infants and children (age range 1 month to 6 years) with mild acute gastroenteritis without any central nervous system infection, severe dehydration, or electrolyte imbalances. In most cases the seizures are tonic-clonic with focal origin on EEG, occur between day 1 and 6 following onset of acute gastroenteritis, cease within 24 hours and do not persist after the illness. |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
3 |
Diarrhea in pregnancy |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
1 |
Constipation alternates with diarrhea |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Chronic diarrhea |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Infectious diarrheal disease |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Intractable diarrhea-choanal atresia-eye anomalies syndrome is characterized by the association of intractable diarrhea of infancy with choanal atresia. Short stature, a prominent and broad nasal bridge, micrognathia, single palmar creases, chronic corneal inflammation, cytopenia, and abnormal hair texture were also reported. So far, the syndrome has been described in three children from the same family. The absence of intellectual deficit and immune deficiency allow this syndrome to be distinguished from other forms of intractable diarrhea of infancy described previously. |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
5 |
Chronic diarrhea of unknown origin |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Diarrhea co-occurrent and due to carcinoid syndrome (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
1 |
A very rare genetic gastroenterological disease characterized by severe malabsorptive diarrhea (requiring parenteral nutrition and disappearing at fasting) due to a lack of intestinal enteroendocrine cells. It is associated with early-onset (within the first weeks of life) dehydration, metabolic acidosis and diabetes mellitus (that can develop until late childhood). Patient may display various degrees of pancreatic insufficiency that does not explain diarrhea, as it is not reduced with pancreatic enzyme supplementation. Central hypogonadism (developing in the second decade), as well as an association with celiac disease have been reported. |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
1 |
A rare intestinal disease characterized by impaired absorption of starch and short polymers of glucose due to primary small intestinal glucoamylase deficiency. Patients present in infancy or early childhood with chronic diarrhea, abdominal distention, and bloating. Levels of pancreatic amylase are typically normal, and histopathological analysis shows normal morphology of the intestinal mucosa. |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
1 |
Chronic diarrhea of infants AND/OR young children |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Non-infective neonatal diarrhea (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Prototheca diarrhoea |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Traveler's diarrhea |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Epidemic diarrhea |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Chronic amoebiasis |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
1 |
Complete obstruction of intestine |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
1 |
Peutz-Jeghers polyps of small bowel |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
3 |
Peutz-Jeghers syndrome |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
2 |
Double incontinence |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
1 |
Childhood double incontinence (finding) |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
1 |
Acquired fructose intolerance |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
1 |
Infantile gastroenteritis |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
2 |
Nonbacterial gastroenteritis of infant |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
2 |
Refractory celiac disease is a rare intestinal disease characterized by persistent or recurrent symptoms and signs of confirmed celiac disease despite a long-term, strict, gluten-free diet, in the absence of other causes of villous atrophy or malignant complications and with or without presence of increased abnormal intraepithelial lymphocytes. |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
1 |
Familial omphalocele syndrome with facial dysmorphism is a rare genetic developmental defect during embryogenesis characterized by omphalocele associated with facial dysmorphism including flat face, short, upturned nose, long and wide philtrum and flattened maxillary arch and abnormalities of hands. |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
1 |
Isosporiasis co-occurrent with human immunodeficiency virus infection (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Chronic intestinal amoebiasis without abscess |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
1 |
Crohn disease of anal canal (disorder) |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
2 |
Inflammatory polyps co-occurrent and due to inflammatory bowel disease (disorder) |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
2 |
A rare immune dysregulation disease with immunodeficiency characterized by severe, progressive infantile onset inflammatory bowel disease with pancolitis, perianal disease (ulceration, fistulae), recurrent respiratory, genitourinary and cutaneous infections, arthritis and a high risk of B-cell lymphoma. |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
2 |
Chronic amoebiasis |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Bacterial dysentery |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Fetal intrauterine intestinal perforation co-occurrent and due to congenital atresia of intestinal tract (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Fetal intrauterine intestinal perforation co-occurrent and due to congenital atresia of intestinal tract (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
1 |
A rare syndromic intestinal malformation characterized by ulcer formation in the umbilical cord associated with congenital upper-intestinal atresia, typically presenting with intra-uterine hemorrhaging from the ulcer site and subsequent fetal bradycardia. |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
1 |
Neonatal intestinal perforation co-occurrent and due to intestinal atresia (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Neonatal intestinal perforation co-occurrent and due to intestinal atresia (disorder) |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
1 |
A rare multiple congenital anomaly syndrome characterized by flat face, hypertelorism, flat occiput, upward slanting palpebral fissures, cleft palate, micrognathia, short neck, and severe congenital heart defects. Malrotation of the intestine, bilateral clinodactyly, bilobed tongue, short fourth metatarsals and bifid thumbs may be additionally observed. |
Finding site |
True |
Intestinal structure |
Inferred relationship |
Some |
2 |
Cryptosporidial gastroenteritis |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
2 |
Intestinal obstruction co-occurrent and due to incisional hernia |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
1 |
Ultrasound scan of bowel (procedure) |
Procedure site - Direct (attribute) |
True |
Intestinal structure |
Inferred relationship |
Some |
1 |
Acquired pelvic enterocele |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
1 |
Fistula of enterostomy (disorder) |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
2 |
Neonatal inflammatory skin and bowel disease is a rare, life-threatening, autoinflammatory syndrome with immune deficiency disorder characterized by early-onset, life-long inflammation, affecting the skin and bowel, associated with recurrent infections. Patients present perioral and perianal psoriasiform erythema and papular eruption with pustules, failure to thrive associated with chronic malabsorptive diarrhea, intercurrent gastrointestinal infections and feeding troubles, as well as absent, short or broken hair and trichomegaly. Recurrent cutaneous and pulmonary infections lead to recurrent blepharitis, otitis externa and bronchiolitis. |
Finding site |
False |
Intestinal structure |
Inferred relationship |
Some |
1 |