| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Congenital tracheoesophageal fistula with esophageal stenosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital tracheoesophageal fistula with esophageal stenosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Carpotarsal osteochondromatosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Faciocardiorenal syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Faciocardiorenal syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Auriculoocular anomaly and cleft lip syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Aniridia, renal agenesis, psychomotor retardation syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Precocious osteodysplasty (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Steinfeld syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Arachnoid / ependymal cyst |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Heart-hand syndrome type 2 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Anencephalus and similar anomalies |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Laryngeal cleft type III |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Thymic aplasia or dysplasia with immunodeficiency |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Multiple intracardiac shunts |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Double aortic valve |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cryptophthalmos syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Craniolenticulosutural dysplasia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Craniolenticulosutural dysplasia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Craniolenticulosutural dysplasia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Osteogenesis imperfecta type IIA |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| 14q11.2 microdeletion syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| 14q11.2 microdeletion syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Microspherophakia with metaphyseal dysplasia syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Microspherophakia with metaphyseal dysplasia syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Ulnar dimelia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Right descending aorta |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Atrioventricular septal defect with ventricular component under superior bridging leaflet without chordal attachment to ventricular septal crest (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Endocardial fibroelastosis of left atrium (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Segmental neurofibromatosis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| albinoïdisme |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Incomplete bilateral cleft palate (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Craniosynostosis with facial dysmorphism and brachydactyly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Craniosynostosis with facial dysmorphism and brachydactyly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Craniosynostosis with facial dysmorphism and brachydactyly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Townes syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Epidermolysis bullosa simplex with hypodontia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Talipomanus |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Mixed sclerosing bone dysplasia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cleidocranial dysostosis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Cleidocranial dysostosis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cleidocranial dysostosis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Cleidocranial dysostosis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Retrocaval ureter |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Chondrodysplasia punctata |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cataract glaucoma syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| X-linked distal arthrogryposis multiplex congenita (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Nemaline myopathy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Hydatid cyst of Morgagni - male |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| tache de naissance (trouble) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Incomplete ossification of maxilla |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Sparse hair with short stature and skin anomaly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Sparse hair with short stature and skin anomaly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Siegler Brewer Carey syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Spondylodysplasia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Spina bifida with stenosis of aqueduct of Sylvius |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Ectodermal dysplasia with hair-tooth defects |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Sialic acid storage disease, severe infantile type |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Epidermolysis bullosa |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Stimmler syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Stimmler syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Osteopathia striata |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| False tendon - heart |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Double cardiac valve orifice |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Netherton's syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital arteriovenous fistula thrombosis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Craniopagus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Retrosternal thyroid gland |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Synophrys |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Crouzon syndrome with acanthosis nigricans (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Crouzon syndrome with acanthosis nigricans (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Cataract, congenital heart disease, neural tube defect syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Cataract, congenital heart disease, neural tube defect syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cataract, congenital heart disease, neural tube defect syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Cataract, congenital heart disease, neural tube defect syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Multiple epiphyseal dysplasia Beighton type (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Odontomicronychial ectodermal dysplasia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cherubism with gingival fibromatosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| dolichocôlon |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Triangular alopecia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Defect of skull ossification |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Accessory sternebral ossification site |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Accessory sternebral ossification site |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Uhl's disease |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Uterus bicameratus vetularum |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Preaxial polydactyly, colobomata, intellectual disability syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Osteochondrodysplasia with osteopetrosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Spherophakia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| syndrome de Beckwith-Wiedemann |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Ehlers-Danlos syndrome classic type (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Chondrodysplasia punctata, X-linked dominant type (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| dysplasie fronto-métaphysaire |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Amaurosis hypertrichosis syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |