Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Noninfectious enteritis of intestine |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Infectious enteritis of intestine |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Granuloma of intestine |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Chronic proliferative enteritis of intestine |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Necrotizing inflammation of intestine (disorder) |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Gastroenteritis |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Inflammatory fibroid polyposis of intestine |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Inflammation of large intestine |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hemorrhagic enteritis |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fibrinous enteritis of intestine |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Behcet's syndrome, intestinal type |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection syndrome |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal inflammatory skin and bowel disease |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Diverticulitis of intestine (disorder) |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Crohn's disease of intestine |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Idiopathic diffuse ulcerative nongranulomatous inflammation of intestine (disorder) |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Inflammatory bowel disease, recurrent sinopulmonary infection syndrome |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection, lymphopenia syndrome (disorder) |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Enteritis of intestine presumed infectious |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Enteritis, inflammatory disorder of small intestine (disorder) |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Eosinophilic inflammation of intestine (disorder) |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
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 |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
ALPI-related inflammatory bowel disease |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Combined immunodeficiency due to RELA haploinsufficiency (disorder) |
Is a |
True |
Enteritis of intestine |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|