| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Congenital chalasia of esophagus (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Congenital diverticulitis of small intestine (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Hyperinsulinism due to uncoupling protein 2 deficiency (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Median nodule of upper lip (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Paraganglioma and gastric stromal sarcoma syndrome (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Deafness, small bowel diverticulosis, neuropathy syndrome (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Schmitt Gillenwater Kelly syndrome |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Odontoma dysphagia syndrome (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Chronic diarrhea due to glucoamylase deficiency (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Autosomal dominant hyperinsulinism due to sulfonylurea receptor 1 deficiency (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Hyperinsulinism due to hepatocyte nuclear factor 4-alpha deficiency (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Hyperinsulinism due to deficiency of glucokinase (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Hyperinsulinism and hyperammonemia syndrome (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Mottled teeth, congenital |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Hutchinson's teeth |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Mitochondrial DNA depletion syndrome hepatocerebrorenal form |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Heart defect, tongue hamartoma, polysyndactyly syndrome (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Autosomal recessive hyperinsulinism due to sulfonylurea receptor 1 deficiency (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Autosomal recessive hyperinsulinism due to Kir6.2 deficiency |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Navajo neurohepatopathy |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Aberrant retroesophageal subclavian artery causing dysphagia lusoria (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Congenital teratoma of nasopharynx (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Moon's molar teeth |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Mulberry molar teeth |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Hereditary hemorrhagic telangiectasia of gingiva |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Hypohidrosis, electrolyte imbalance, lacrimal gland dysfunction, ichthyosis, xerostomia syndrome (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Juvenile polyposis syndrome with hereditary haemorrhagic telangiectasia |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Anterior maxillary protrusion, strabismus, intellectual disability syndrome (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Digenic haemochromatosis |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth syndrome (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Congenital arteriovenous malformation of duodenum and jejunum (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|
| Congenital malposition of tongue (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|