Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Congenital atresia of colon |
Is a |
False |
Congenital atresia of intestinal tract |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital atresia of small intestine |
Is a |
True |
Congenital atresia of intestinal tract |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital atresia of rectum |
Is a |
False |
Congenital atresia of intestinal tract |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Multiple intestinale Atresie |
Is a |
False |
Congenital atresia of intestinal tract |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Imperforate anus |
Is a |
False |
Congenital atresia of intestinal tract |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital atresia of large intestine |
Is a |
True |
Congenital atresia of intestinal tract |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ulceration of umbilical cord and atresia of intestine syndrome (disorder) |
Is a |
True |
Congenital atresia of intestinal tract |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal intestinal perforation co-occurrent and due to intestinal atresia (disorder) |
Due to |
True |
Congenital atresia of intestinal tract |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Neonatal intestinal perforation co-occurrent and due to intestinal atresia (disorder) |
Is a |
True |
Congenital atresia of intestinal tract |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fetal intrauterine intestinal perforation co-occurrent and due to congenital atresia of intestinal tract (disorder) |
Due to |
True |
Congenital atresia of intestinal tract |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Fetal intrauterine intestinal perforation co-occurrent and due to congenital atresia of intestinal tract (disorder) |
Is a |
True |
Congenital atresia of intestinal tract |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypoplasia of pancreas, intestinal atresia, hypoplasia of gallbladder syndrome (disorder) |
Is a |
True |
Congenital atresia of intestinal tract |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital atresia of intestine at multiple levels |
Is a |
True |
Congenital atresia of intestinal tract |
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 |
Congenital atresia of intestinal tract |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|