| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Low set ears |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Double aortic arch with left arch dominant and atresia of right arch (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Autosomal recessive spastic paraplegia type 43 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Mosaic trisomy 4 syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Distal 17p13.3 microdeletion syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Oro-facial digital syndrome type 11 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Cleft soft palate with bilateral cleft lip and bilateral cleft of alveolar process of maxilla (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Pachygyria, intellectual disability, epilepsy syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Branchiootic syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Oculopharyngodistal myopathy (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Oculopharyngodistal myopathy (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Oculopharyngodistal myopathy (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| syndrome de Larsen-like de type B3GAT3 (beta-1,3 glucuronyltransferase 3) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| syndrome de Larsen-like de type B3GAT3 (beta-1,3 glucuronyltransferase 3) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| syndrome de Larsen-like de type B3GAT3 (beta-1,3 glucuronyltransferase 3) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Chondroectodermal dysplasia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Chondroectodermal dysplasia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Isolated agammaglobulinaemia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Autosomal dominant spastic paraplegia type 37 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Autosomal dominant spastic paraplegia type 37 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Facial dysmorphism, cleft palate, loose skin syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Facial dysmorphism, cleft palate, loose skin syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Craniofaciofrontodigital syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Craniofaciofrontodigital syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Short stature, wormian bones, dextrocardia syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Multiple epiphyseal dysplasia with severe proximal femoral dysplasia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Multiple epiphyseal dysplasia with severe proximal femoral dysplasia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cleft soft palate with left cleft lip and cleft of left alveolar process of maxilla (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Craniodigital syndrome and intellectual disability syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Dislocation of hip and facial dysmorphism syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Malan overgrowth syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Spina bifida and hypospadias syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| Spina bifida and hypospadias syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Spina bifida and hypospadias syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Spina bifida and hypospadias syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Spina bifida and hypospadias syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| KLHL9-related early-onset distal myopathy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Symbrachydactyly of digit of hand (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Spondyloperipheral dysplasia with short ulna syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Mosaic trisomy 14 syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Intellectual disability, brachydactyly, Pierre Robin syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Oro-facial digital syndrome type 14 |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Oro-facial digital syndrome type 14 |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Oro-facial digital syndrome type 14 |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Oro-facial digital syndrome type 14 |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Oro-facial digital syndrome type 14 |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| Larsen-like osseous dysplasia, short stature syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Double aortic arch with left arch dominant (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Autosomal recessive spastic paraplegia type 35 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Right aortic arch |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Intellectual disability, polydactyly, uncombable hair syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Intellectual disability, polydactyly, uncombable hair syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Oro-facial digital syndrome type 8 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Cleft hard and soft palate with bilateral cleft lip and bilateral cleft of alveolar process of maxilla (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Cleft soft palate with right cleft lip and cleft of right alveolar process of maxilla |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Velofacioskeletal syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Striate palmoplantar keratoderma (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Right cleft lip (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Colobomatous microphthalmia, rhizomelic dysplasia syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Colobomatous microphthalmia, rhizomelic dysplasia syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| syndrome de cardiopathie, blépharophimosis, anomalie du radius, anomalie anale |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| syndrome de cardiopathie, blépharophimosis, anomalie du radius, anomalie anale |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| syndrome de cardiopathie, blépharophimosis, anomalie du radius, anomalie anale |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Familial hyperprolactinemia |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Myosclerosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| 17q12 microduplication syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Primary laryngeal lymphangioma |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Agenesis of corpus callosum and abnormal genitalia syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Multiple pterygium syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Wooly hair with palmoplantar keratoderma syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Wooly hair with palmoplantar keratoderma syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Left cleft lip |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Autosomal recessive myogenic arthrogryposis multiplex congenita (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Autosomal recessive myogenic arthrogryposis multiplex congenita (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Autosomal recessive myogenic arthrogryposis multiplex congenita (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Autosomal recessive spastic paraplegia type 15 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Intellectual disability, myopathy, short stature, endocrine defect syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Spondyloepimetaphyseal dysplasia anauxetic type (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| syndrome de déficience intellectuelle-obésité-malformations cérébrales-dysmorphie faciale |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| syndrome de déficience intellectuelle-obésité-malformations cérébrales-dysmorphie faciale |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Oro-facial digital syndrome type 10 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Double aortic arch with right arch dominant and atresia of left arch and left ligament to diverticulum (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| X-linked lethal multiple pterygium syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Verloove Vanhorick Brubakk syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Verloove Vanhorick Brubakk syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Wiedemann Steiner syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Wiedemann Steiner syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Microcephalus, complex motor and sensory axonal neuropathy syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| syndrome de pectus excavatum-macrocéphalie-dysplasie unguéale |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| syndrome de pectus excavatum-macrocéphalie-dysplasie unguéale |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| syndrome de pectus excavatum-macrocéphalie-dysplasie unguéale |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Oculomaxillofacial dysostosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |