| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Ectopic artery (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Autosomal recessive cutis laxa type 2A (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Autosomal recessive cutis laxa type 2A (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Posterior fossa arachnoid cyst (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Atrioventricular septal defect with atrioventricular valve regurgitation through right anterosuperior inferior mural commissure (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Atrioventricular septal defect with atrioventricular valve regurgitation through right anterosuperior superior bridging leaflet commissure (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Atrioventricular septal defect with atrioventricular valve regurgitation through right inferior bridging leaflet inferior mural commissure (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital cystic disease of liver |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Atrioventricular septal defect with atrioventricular valve regurgitation through left septal commissure (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Atrioventricular septal defect with atrioventricular valve regurgitation through left superior bridging leaflet lateral mural commissure (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Atrioventricular septal defect with atrioventricular valve regurgitation through right septal commissure (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital vesicoureterorenal reflux, bilateral |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Atrioventricular septal defect with atrioventricular valve regurgitation through left inferior bridging leaflet lateral mural commissure (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Atrioventricular septal defect with atrioventricular valve regurgitation (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Multiple congenital anomalies, hypotonia, seizures syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Multiple congenital anomalies, hypotonia, seizures syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Multiple congenital anomalies, hypotonia, seizures syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Muscle eye brain disease with bilateral multicystic leukodystrophy |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Muscle eye brain disease with bilateral multicystic leukodystrophy |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Cobblestone lissencephaly without muscular or ocular involvement (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Autosomal recessive spastic paraplegia type 24 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Autosomal dominant spastic paraplegia type 8 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Lissencephaly with cerebellar hypoplasia type E |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Hypertrophic Meckel's diverticulum |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Pachyonychia congenita syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Obesity due to leptin receptor gene deficiency |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Obesity due to leptin receptor gene deficiency |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| cavité et fistule d'une fente branchiale |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Fistula of branchial cleft |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Aneurysm osteoarthritis syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Aneurysm osteoarthritis syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Fordyce's disease (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Fordyce spots of lips (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Bilateral multicystic renal dysplasia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Lethal arthrogryposis co-occurrent with anterior horn cell disease (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Distal arthrogryposis type 4 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Lethal congenital contracture syndrome type 2 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Congenital anomaly of right optic disc |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital anomaly of bilateral optic discs (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital anomaly of bilateral optic discs (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Congenital anomaly of left optic disc (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| fistule congénitale du cou |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Arthrogryposis and ectodermal dysplasia syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| Arthrogryposis and ectodermal dysplasia syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Arthrogryposis and ectodermal dysplasia syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Arthrogryposis and ectodermal dysplasia syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Congenital systemic arteriovenous fistula |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Microphthalmos of right eye |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Microphthalmos of left eye |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital pit of optic disc (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital pit of optic disc of left eye (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital pit of optic disc of right eye |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital anterior subcapsular polar cataract (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Major aortopulmonary collateral artery |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Congenital posterior subcapsular polar cataract (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital blepharophimosis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Congenital blepharophimosis of lower eyelid (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Bilateral congenital aniridia of eyes |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Bilateral congenital aniridia of eyes |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Bilateral infantile esotropia of eyes |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Bilateral infantile esotropia of eyes |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Microcephalus with brachydactyly and kyphoscoliosis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Accessory tarsal bone of left foot (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital muscular dystrophy type 1A |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Distal arthrogryposis type 6 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Neurogenic arthrogryposis multiplex congenita (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| syndrome des ptérygiums multiples autosomique dominant |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Segmental progressive overgrowth syndrome with fibroadipose hyperplasia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital and developmental myasthenia |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| 21q22.11q22.12 microdeletion syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| 21q22.11q22.12 microdeletion syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| 21q22.11q22.12 microdeletion syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Monosomy 22 syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Muenke syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Osteopathia striata, pigmentary dermopathy, white forelock syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Oligodontia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Oligodontia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Bifid nose (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Solitary infantile myofibromatosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| myofibromatose infantile |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Aggressive systemic infantile myofibromatosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Multicentric infantile myofibromatosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital nuclear cataract of bilateral eyes (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Congenital nuclear cataract of bilateral eyes (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital posterior subcapsular polar cataract of left eye (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital posterior subcapsular polar cataract of bilateral eyes (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Congenital posterior subcapsular polar cataract of bilateral eyes (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital posterior subcapsular polar cataract of right eye (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Amyotonia congenita |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Amyotonia congenita |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital subaortic diverticulum (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital ectopia of lacrimal punctum (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital rhabdomyomatous mesenchymal hamartoma |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital diffuse lipomatosis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| scoliose posturale congénitale |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Encephalocraniocutaneous lipomatosis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Congenital hydrocele of canal of Nuck (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |