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 |
|
Renal tubulopathy with encephalopathy and liver failure syndrome (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Some |
|