Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Congenital anomaly of lower alimentary tract |
Is a |
False |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital anomaly of small intestine |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital fistula of intestinal tract |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital redundant colon (disorder) |
Is a |
False |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital diverticulum of intestinal tract |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital hypoplasia of intestinal tract |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital malposition of intestinal tract |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital fecaliths causing obstruction (disorder) |
Is a |
False |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital anomaly of large intestine |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital duplication of intestine |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Ectopic intestinal mucosa |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Gastroschisis |
Is a |
False |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital absence of intestinal tract |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital atresia of intestinal tract |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital dilatation of intestinal tract |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital stenosis of intestinal tract |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital intestinal adhesions |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital fecal fistula |
Is a |
False |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Andre tarmanomalier |
Is a |
False |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
[X]Other specified congenital malformations of intestine |
Is a |
False |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
[X]Congenital malformation of intestine, unspecified |
Is a |
False |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
andre tarmanomalier, ikke nærmere specificeret |
Is a |
False |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Neuronal intestinal dysplasia |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Generalized congenital intestinal dysmotility (disorder) |
Is a |
False |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital omphalocele |
Is a |
False |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital arteriovenous malformation of small intestine (disorder) |
Is a |
False |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital redundant colon (disorder) |
Is a |
False |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital malrotation of intestine |
Is a |
False |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Immature ganglionosis of large intestine (disorder) |
Is a |
False |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
A rare, severe, genetic, intestinal disease characterized by congenital absence of heparan sulfate from small intestine epithelium manifesting with secretory diarrhea and massive enteric protein loss. Patients present intolerance to enteral feeds during the first few weeks to months of life. Apart from absence of heparan sulfate from the basolateral surface of small intestine enterocytes, small bowel biopsy is otherwise normal. |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Peutz-Jeghers syndrome |
Is a |
False |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Familial omphalocele syndrome with facial dysmorphism is a rare genetic developmental defect during embryogenesis characterized by omphalocele associated with facial dysmorphism including flat face, short, upturned nose, long and wide philtrum and flattened maxillary arch and abnormalities of hands. |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Oculogastrointestinal muscular dystrophy is an extremely rare autosomal recessively inherited neuromuscular disease characterized by ocular manifestations such as ptosis and diplopia followed by chronic diarrhea, malnutrition and intestinal pseudo-obstruction. |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by developmental delay, neuropathic visceral dysmotility (resulting in neurogenic megacystis and sometimes chronic intestinal pseudo-obstruction syndrome), intracerebral calcifications, and dysmorphic facial features (including broad forehead, downslanted palpebral fissures, strabismus, protruding and low-set ears, and retrognathia). Microcephaly and renal abnormalities have also been reported. |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Cowden syndrome |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital diverticulosis |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital neurogenic ileus syndrome |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
Congenital fecaliths |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|
A rare intestinal disease characterized by congenital partial or complete lack of the collagen mesh network in the intestinal wall, resulting in hypoperistalsis or aperistalsis. The enteric nervous system is normal or near-normal in the affected areas, although hypo- and dysganglionosis may be found in some proximal segments of the colon and/or small bowel. Patients present with chronic intractable slow transit constipation. |
Is a |
True |
Congenital anomaly of intestinal tract |
Inferred relationship |
Some |
|