Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Chronic peptic ulcer of stomach |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic ischemic enteritis |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic liver disease |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Megaoesophagus in Chagas' disease |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic enamel dental caries |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic clonorchiasis |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Megacolon in Chagas' disease |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic dentine dental caries |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic left-sided ulcerative colitis |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic intestinal pseudo-obstruction |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Primary chronic pseudo-obstruction of gastrointestinal tract |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic sialadenitis |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
A form of chronic oral candidosis involving multiple oral sites with angular cheilitis, retrocommissural leukoplakia, median rhomboid glossitis and palatal lesions. |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic ulcerative stomatitis |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic erosive gastritis |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Periodontitis co-occurrent with cyclical neutropenia |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic non-specific colitis |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Recurrent rectal polyp |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic esophageal scar (disorder) |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic gingivitis |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic intestinal failure (CIF) is a chronic type of intestinal failure characterized by a nonfunctioning small bowel (that may be reversible or irreversible) where the body is unable to maintain energy and nutritional needs through absorption of food or nutrients via the intestinal tract (despite being metabolically stable) and which therefore necessitates long-term parenteral feeding. CIF may be the result of congenital digestive diseases (such as gastroschisis, atresia of small intestine), short bowel syndrome, intra-abdominal or pelvic cancer, or progressive and devastating gastrointestinal or systemic benign diseases (such as Crohn disease). |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic diarrhea |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
A paroxysmal dystonic movement disorder occurring in association with gastro-oesophageal reflux, and, in some cases, hiatal hernia. The prevalence is unknown. Onset usually occurs during infancy or early childhood. The dystonic movements are characterised by abnormal posturing of the head and neck (torticollis) and severe arching of the spine. The dystonic movements are clearly associated with gastro-oesophageal reflux but the pathophysiological mechanism is not clearly understood. |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Acute on chronic pancreatitis (disorder) |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic necrotizing ulcerative gingivitis (disorder) |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic non-specific multiple ulcers of small intestine (disorder) |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Recurrent ulcer of mouth (disorder) |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic idiopathic non-infectious enteritis of intestine |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Obstructed recurrent right femoral hernia with gangrene (disorder) |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Obstructed recurrent left femoral hernia with gangrene |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Anal furunculosis |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic desquamative gingivitis (disorder) |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic constipation |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic ischemic colitis |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic ischemic enterocolitis |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic vomiting |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic intussusception |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic follicular pharyngitis |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Obstruction without gangrene co-occurrent and due to recurrent left inguinal hernia |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Obstruction without gangrene co-occurrent and due to recurrent right inguinal hernia |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Obstructed recurrent left inguinal hernia with gangrene |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Obstructed recurrent right inguinal hernia with gangrene |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
A rare, genetic neuromuscular disease characterized by progressive external ocular, facial and pharyngeal muscle weakness, leading to variable degrees of ptosis, ophthalmoparesis, facial muscle atrophy, dysarthria and dysphagia, as well as distal muscle weakness and atrophy of lower and upper extremities. Respiratory muscle involvement is common, but sensorineural hearing loss, asymmetrical extremity weakness and severe proximal weakness are rare. |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic intestinal isosporiasis |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic granular pharyngitis |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
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. |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Oculopharyngeal muscular dystrophy (disorder) |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic atrophic candidiasis |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic peptic ulcer with hemorrhage AND with perforation but without obstruction |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic rejection of pancreas transplant (disorder) |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic duodenal ulcer with hemorrhage AND with perforation but without obstruction |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Recurrent cholangitis |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic thrombosis of mesenteric vein (disorder) |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic gastrointestinal tract vascular insufficiency (disorder) |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic plaque-like oral candidosis (disorder) |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Mitochondrial NeuroGastroIntestinal Encephalomyopathy (MNGIE) syndrome is characterized by the association of gastrointestinal dysmotility, peripheral neuropathy, chronic progressive external ophthalmoplegia and leukoencephalopathy. |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic partial afferent loop obstruction |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Recurrent infection caused by Clostridioides difficile (disorder) |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic inflammation of intestine caused by radiation (disorder) |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Behcet's syndrome, intestinal type |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Behçet's disease affecting oral mucosa (disorder) |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Familial actinic prurigo of lip (disorder) |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Lichen sclerosus of anus |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Oral lichen sclerosus (disorder) |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic radiation sickness |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Recurrent peritonsillar abscess |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Idiopathic paroxysmal sialorrhoea |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
maladie inflammatoire chronique idiopathique de l’intestin |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
A rare genetic skeletal muscle disease characterized by neonatal to childhood onset of slowly progressive muscle weakness and atrophy primarily affecting the lower limbs, joint contractures, kyphosis or lordosis of the spine, lateral tongue atrophy, and pes equinus. Progression to upper limb involvement, facial weakness, language impairment, intellectual disability, and behavioral abnormalities have been reported in addition. Muscle biopsy shows myopathic changes with increased fiber size variation, internalized nuclei, fiber atrophy, as well as rod structures and core targetoid defects. |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Juvenile arthritis in ulcerative colitis |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
A rare genetic hematologic and intestinal disease characterized by childhood onset of bleeding tendency with epistaxis, gum bleeding, gastrointestinal bleeding, hematuria, and menorrhagia due to impaired platelet aggregation and secretion, as well as recurrent gastrointestinal ulcer. Mildly reduced levels of coagulation factor XI have been reported in addition. |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
A rare genetic immune disease characterized by recurrent sinopulmonary infections and autoimmune enterocolopathy, manifesting as frequent episodes of intractable diarrhea with abdominal pain and fever, accompanied by eczematous rashes, due to deficits in components of innate and adaptive immunity. Immunologic abnormalities include IgG subclass deficiency, impaired antigen-induced lymphocyte proliferation, reduced cytokine production by CD8+ T lymphocytes, and decreased numbers of natural killer cells. |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
A rare genetic immune disease characterized by early onset of recurrent bacterial, viral, and fungal infections, chronic inflammatory bowel disease, gastritis, and inflammatory polyarthritis. Patients present with diarrhea, vomiting, hepatosplenomegaly, mouth ulcers, perianal abscesses, chronic lung disease with bronchiectasis, and failure to thrive. Occurrence of a skin rash associated with lymphocytic vasculitis has also been reported. Immunologic abnormalities include variable T-cell lymphopenia, decreased natural killer cells, and decreased B-cells with variable hypogammaglobulinemia. |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
A rare genetic gastroenterological disease characterised by the presence of multiple persistent, intractable ulcers of the small intestine, leading to chronic blood and protein loss. Signs and symptoms include abdominal pain, anaemia, fatigue, oedema, and diarrhoea. Morphologically, the condition manifests with multiple sharply demarcated shallow lesions with irregular circular or linear shape. |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
A rare genetic systemic or rheumatologic disease characterized by neonatal or infantile onset of enterocolitis (which resolves with age), periodic fever, and episodes of severe systemic inflammation, which may be precipitated by infections, stress, or fatigue. Signs and symptoms include splenomegaly, urticaria-like rashes, arthralgia, and myalgia. Associated laboratory findings are elevated inflammatory markers (such as ferritin, C-reactive protein), pancytopenia, and elevated transaminases. If left untreated, flares can progress to coagulopathy, organ failure, and death. |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic pseudo-obstruction of colon |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Relapsing pancreatic necrosis |
Is a |
False |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic antibiotic-refractory ileal pouchitis (disorder) |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic anal fissure |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic pancreatitis due to gallbladder calculus |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic gastric erosion (disorder) |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
A rare non-severe combined immunodeficiency characterised by tumour necrosis factor-dependent chronic mucocutaneous ulcerations and inflammatory bowel disease presenting during the first years of life. Ulcerations occur primarily in the oral, gastrointestinal, and vaginal mucosa. |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic primary epigastric pain syndrome |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Chronic primary orofacial pain |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|
Juvenile arthritis of inflammatory bowel disease |
Is a |
True |
Chronic digestive system disorder |
Inferred relationship |
Some |
|