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 |