| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Patent ductus arteriosus, bicuspid aortic valve, hand anomaly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Severe X-linked intellectual disability Gustavson type (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Severe X-linked intellectual disability Gustavson type (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Severe X-linked intellectual disability Gustavson type (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Perlman syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Perlman syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Ackerman syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Ackerman syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Ackerman syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Agnathia, holoprosencephaly, situs inversus syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Hypoplasia and coloboma of alar cartilage with telecanthus syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Hypoplasia and coloboma of alar cartilage with telecanthus syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Hypoplasia and coloboma of alar cartilage with telecanthus syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Auriculoocular anomaly and cleft lip syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Auriculoocular anomaly and cleft lip syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Auriculoocular anomaly and cleft lip syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Autism and facial port-wine stain syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| syndrome d'entéropathie et endocrinopathie auto-immunes-susceptibilité aux infections chroniques |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| syndrome d'entéropathie et endocrinopathie auto-immunes-susceptibilité aux infections chroniques |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
6 |
| Distal limb deficiency with micrognathia syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Distal limb deficiency with micrognathia syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Distal limb deficiency with micrognathia syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Distal trisomy 6p syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| syndrome d'utérus double-hémivagin-agénésie rénale |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| syndrome d'utérus double-hémivagin-agénésie rénale |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Duane anomaly, myopathy, scoliosis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Dyschondrosteosis and nephritis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Dyschondrosteosis and nephritis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Dysspondyloenchondromatosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Dystrophic epidermolysis bullosa nails only (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Dystrophic epidermolysis bullosa nails only (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Ectopia lentis, chorioretinal dystrophy, myopia syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Ectopia lentis, chorioretinal dystrophy, myopia syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Endothelial dystrophy, iris hypoplasia, congenital cataract, stromal thinning syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| syndrome de Meacham |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| syndrome de Meacham |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| syndrome de Meacham |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Macular coloboma, cleft palate, hallux valgus syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Macular coloboma, cleft palate, hallux valgus syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Macular coloboma, cleft palate, hallux valgus syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| X-linked congenital dyserythropoietic anemia with thrombocytopenia (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Thickened earlobe with conductive deafness syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Thickened earlobe with conductive deafness syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Toriello Carey syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Familial caudal dysgenesis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Familial caudal dysgenesis (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Optic disc dysplasia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Laryngo-onycho-cutaneous syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Laryngo-onycho-cutaneous syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Laryngo-onycho-cutaneous syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Pulmonary hypoplasia, agonadism, dextrocardia, diaphragmatic hernia syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Median cleft of upper lip, corpus callosum lipoma, cutaneous polyp syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Median cleft of upper lip, corpus callosum lipoma, cutaneous polyp syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Median cleft of upper lip, corpus callosum lipoma, cutaneous polyp syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Median cleft of upper lip, corpus callosum lipoma, cutaneous polyp syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
8 |
| Median cleft of upper lip, corpus callosum lipoma, cutaneous polyp syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
9 |
| Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| syndrome de kératodermie palmoplantaire-surdité |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| syndrome de kératodermie palmoplantaire-surdité |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Palmoplantar keratoderma Nagashima type (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Palmoplantar keratoderma Nagashima type (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
7 |
| Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Parastremmatic dwarfism (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Duane anomaly, myopathy, scoliosis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Symphalangism (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital diverticulum of small intestine (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Atresia of jejunum type IIIb (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Atresia of jejunum type IV (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Glycogen storage disease due to acid maltase deficiency, infantile onset |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Glycogen storage disease type II late onset (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital conduction defect |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Familial haemolytic uraemic syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital perineal groove (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital cyst of aryepiglottic fold (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital central hypothyroidism (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital hypothyroidism due to iodine deficiency (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital hypogonadotropic hypogonadism (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Congenital hypogonadotropic hypogonadism (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Congenital malformation of autonomic nervous system (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Hirschsprung's disease |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Long segment Hirschsprung's disease |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Short segment Hirschsprung's disease |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Total intestinal aganglionosis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Aganglionosis of Auerbach's plexus |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Mowat-Wilson syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |