Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Congenital atresia of colon |
Is a |
False |
Congenital atresia of intestinal tract |
Inferred relationship |
Some |
|
Congenital atresia of small intestine |
Is a |
True |
Congenital atresia of intestinal tract |
Inferred relationship |
Some |
|
Congenital atresia of rectum |
Is a |
False |
Congenital atresia of intestinal tract |
Inferred relationship |
Some |
|
atrésies gastro-intestinales multiples |
Is a |
False |
Congenital atresia of intestinal tract |
Inferred relationship |
Some |
|
Imperforate anus |
Is a |
False |
Congenital atresia of intestinal tract |
Inferred relationship |
Some |
|
Atresia of large intestine (disorder) |
Is a |
True |
Congenital atresia of intestinal tract |
Inferred relationship |
Some |
|
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. |
Is a |
True |
Congenital atresia of intestinal tract |
Inferred relationship |
Some |
|
Neonatal intestinal perforation co-occurrent and due to intestinal atresia (disorder) |
Due to |
True |
Congenital atresia of intestinal tract |
Inferred relationship |
Some |
3 |
Neonatal intestinal perforation co-occurrent and due to intestinal atresia (disorder) |
Is a |
True |
Congenital atresia of intestinal tract |
Inferred relationship |
Some |
|
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 |
Some |
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 |
Some |
|
A rare, potentially fatal, genetic, visceral malformation syndrome characterized by neonatal diabetes, hypoplastic or annular pancreas, duodenal and jejunal atresia, as well as gallbladder aplasia or hypoplasia. Patients typically present intrauterine growth restriction, failure to thrive, malnutrition, intestinal malrotation, malabsorption, conjugated hyperbilirubinemia, acholia and infections. Cardiac anomalies may also be associated. |
Is a |
True |
Congenital atresia of intestinal tract |
Inferred relationship |
Some |
|
Congenital atresia of intestine at multiple levels |
Is a |
True |
Congenital atresia of intestinal tract |
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 |
Congenital atresia of intestinal tract |
Inferred relationship |
Some |
|
Multiple intestinal atresia is a rare form of intestinal atresia characterized by the presence of numerous atresic segments in the small bowel (duodenum) or large bowel and leading to symptoms of intestinal obstruction: vomiting, abdominal bloating and inability to pass meconium in newborns. |
Is a |
True |
Congenital atresia of intestinal tract |
Inferred relationship |
Some |
|