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 |