Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Noninfectious inflammation of intestine (disorder) |
Is a |
True |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
Infectious enteritis of intestine |
Is a |
True |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
Granuloma of intestine |
Is a |
True |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
Chronic proliferative enteritis of intestine |
Is a |
True |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
Necrotizing inflammation of intestine (disorder) |
Is a |
True |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
Gastroenteritis |
Is a |
True |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
Inflammatory fibroid polyposis of intestine |
Is a |
True |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
Inflammation of large intestine |
Is a |
True |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
Hemorrhagic enteritis of intestine |
Is a |
True |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
Fibrinous enteritis of intestine |
Is a |
True |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
Behcet's syndrome, intestinal type |
Is a |
True |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
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. |
Is a |
True |
Inflammation of intestine (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 |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
Diverticulitis of intestine (disorder) |
Is a |
True |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
Crohn's disease of intestine (disorder) |
Is a |
True |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
Idiopathic diffuse ulcerative nongranulomatous inflammation of intestine (disorder) |
Is a |
True |
Inflammation of intestine (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 |
True |
Inflammation of intestine (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 |
True |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
Enteritis of intestine presumed infectious |
Is a |
True |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
Inflammation of small intestine (disorder) |
Is a |
True |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
Eosinophilic inflammation of intestine (disorder) |
Is a |
True |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
A rare genetic disease characterized by multiple intestinal atresia in association with combined immunodeficiency and inflammatory bowel disease. Clinical features include widespread atresia extending from the stomach to the rectum, homogenous calcifications in the abdominal cavity, hepatic cholestasis, cirrhosis, and chronic liver failure, hypoplastic thymus, and increased susceptibility to mainly bacteria and viruses. The immunological phenotype consists of profound generalized T-cell lymphopenia and milder natural killer cell and B-cell lymphopenia, as well as low serum levels of IgG, IgA, and IgM, with elevated serum IgE. The disease is mostly fatal in infancy or childhood. |
Is a |
True |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|
A rare genetic gastroenterological disease characterized by severe, refractory intestinal inflammation with mucosal erosions and ulcerations potentially involving the small and large intestine. Epithelioid granulomas are typically absent. Patients present with severe diarrhea, abdominal pain, vomiting, rectal bleeding, and weight loss. |
Is a |
True |
Inflammation of intestine (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 |
Inflammation of intestine (disorder) |
Inferred relationship |
Some |
|