| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Steatocystoma multiplex with natal tooth syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Microcephalus cleft palate syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Lethal omphalocele with cleft palate syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Uveal coloboma with cleft lip and palate and intellectual disability syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Congenital bile acid synthesis defect type 3 (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Cleft lip and cleft palate with intestinal malrotation and cardiopathy syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Cleft palate with short stature and vertebral anomaly syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Schmitt Gillenwater Kelly syndrome |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Haim Munk syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Multiple endocrine neoplasia, type 1 |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Exercise-induced hyperinsulinism (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Autosomal dominant hyperinsulinism due to Kir6.2 deficiency (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Autosomal dominant hyperinsulinism due to sulfonylurea receptor 1 deficiency (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Hyperinsulinism due to hepatocyte nuclear factor 4-alpha deficiency (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Hyperinsulinism due to deficiency of glucokinase (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Hyperinsulinism and hyperammonemia syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Partial agenesis of pancreas (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Acro-dermato-ungual-lacrimal-tooth syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Cystic fibrosis with gastritis and megaloblastic anemia syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Contracture with ectodermal dysplasia and orofacial cleft syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Cutaneous photosensitivity and lethal colitis syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Deafness, enamel hypoplasia, nail defect syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Goldberg Shprintzen megacolon syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Hirschsprung disease with deafness and polydactyly syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Hirschsprung disease with type D brachydactyly syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Hirschsprung disease with nail hypoplasia and dysmorphism (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Hyperinsulinism due to insulin receptor deficiency (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Hyperinsulinism due to uncoupling protein 2 deficiency (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Bilateral microtia with deafness and cleft palate syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Joubert syndrome with congenital hepatic fibrosis (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Chronic atrial and intestinal dysrhythmia (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Hypertelorism with microtia and facial clefting syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Kapur Toriello syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Median nodule of upper lip (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Oculopalatocerebral syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Odonto-tricho-ungual-digito-palmar syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Odontoleukodystrophy (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Bamforth Lazarus syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Oculogastrointestinal muscular dystrophy (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Ackerman syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Macular coloboma, cleft palate, hallux valgus syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Paraganglioma and gastric stromal sarcoma syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Familial hypercholanemia (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Macrostomia, preauricular tag, external ophthalmoplegia syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Microbrachycephaly, ptosis, cleft lip syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Native American myopathy |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Steroid dehydrogenase deficiency and dental anomaly syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Retinohepatoendocrinologic syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Glycogen phosphorylase kinase deficiency |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Weaver Williams syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Cleft lip retinopathy syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Deafness, vitiligo, achalasia syndrome |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Stimmler syndrome |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Skeletal dysplasia with wormian bone, multiple fractures, dentinogenesis imperfecta syndrome |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Intestinal obstruction in newborn due to guanylate cyclase 2C deficiency |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Deafness, small bowel diverticulosis, neuropathy syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| XY type gonadal dysgenesis with associated anomalies syndrome (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Ectodermal dysplasia trichoodontoonychial type (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Chronic diarrhea with villous atrophy syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Hereditary coproporphyria |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Hypogonadism, diabetes mellitus, alopecia, mental retardation and electrocardiographic abnormalities |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Cleft palate, large ears, small head syndrome |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Oculopharyngodistal myopathy (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Oro-facial digital syndrome type 9 (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Joubert syndrome with orofaciodigital defect (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Oro-facial digital syndrome type 5 (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Oro-facial digital syndrome type 8 (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Oro-facial digital syndrome type 1 (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Oro-facial digital syndrome type 14 |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Renal hepatic pancreatic dysplasia (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Focal palmoplantar and gingival keratoderma |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Trichoodontoonychial dysplasia |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| X-linked cleft palate and ankyloglossia |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Otopalatodigital syndrome |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Congenital deafness with labyrinthine aplasia, microtia and microdontia |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Choanal atresia with radial ray hypoplasia |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Familial omphalocele syndrome with facial dysmorphism (disorder) |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Dentin dysplasia with sclerotic bone syndrome |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Poikiloderma, alopecia, retrognathism, cleft palate syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Pilodental dysplasia, refractive errors syndrome (disorder) |
Is a |
False |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|
| Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection syndrome |
Is a |
True |
Digestive system hereditary disorder (disorder) |
Inferred relationship |
Some |
|