| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| scaphocéphalie familiale type McGillivray |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| scaphocéphalie familiale type McGillivray |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Autosomal dominant osteopetrosis type 2 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital coxa valga |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Congenital coloboma of iris (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital coxa vara |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Junctional epidermolysis bullosa non-Herlitz type (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Hereditary hypotrichosis with recurrent skin vesicles syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Congenital absence of sternum |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Periodic hyperlysinaemia |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Periodic hyperlysinaemia with hyperammonaemia |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Mesio-occlusion of teeth |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Supernumerary roots |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital trigger thumb of right hand (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital trigger thumb of left hand (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Polysyndactyly and cardiac malformation syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Polysyndactyly and cardiac malformation syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Permanent neonatal diabetes mellitus with cerebellar agenesis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Permanent neonatal diabetes mellitus with cerebellar agenesis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
6 |
| Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Congenital disorder of glycosylation type 1e (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital disorder of glycosylation type 1j (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cryptomicrotia brachydactyly syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Cryptomicrotia brachydactyly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Crisponi syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| Crisponi syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Crisponi syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Craniomicromelic syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Craniomicromelic syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Craniomicromelic syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Craniometadiaphyseal dysplasia wormian bone type (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Craniolenticulosutural dysplasia (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Craniolenticulosutural dysplasia (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Craniolenticulosutural dysplasia (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| raccourcissement congénital du ligament costo-coracoïde |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Bowed tibia, radial anomaly, osteopenia, fracture syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Cheirospondyloenchondromatosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Combined immunodeficiency due to CD3gamma deficiency (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Immunodeficiency by defective expression of human leukocyte antigen class 1 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Neutropenia, monocytopenia, deafness syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Persistent fetal uterus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital articular rigidity with myopathy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital eventration of left crus of diaphragm |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Crowding of teeth |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Sex chromosome aneuploidy (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Reticular dysgenesis with congenital aleucocytosis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Congenital anomaly of scapula |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital anomaly of humerus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital anomaly of radius |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital anomaly of ulna (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital anomaly of femur |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital anomaly of fibula |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital anomaly of tibia |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital anomaly of calcaneus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital anomaly of tarsal bone |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital anomaly of metatarsal bone |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| syndrome d'hémangiome périnéal, malformations génitales externes, lipomyéloméningocèle, anomalies vésicorénales, imperforation anale, acrochordon |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| syndrome d'hémangiome périnéal, malformations génitales externes, lipomyéloméningocèle, anomalies vésicorénales, imperforation anale, acrochordon |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Temple Baraitser syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Temple Baraitser syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Temple Baraitser syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Atelosteogenesis type 1 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Atelosteogenesis type 3 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Atrial septal defect, atrioventricular conduction defect syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Atrial septal defect, atrioventricular conduction defect syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Auricular abnormality, cleft lip, ocular abnormality syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Auricular abnormality, cleft lip, ocular abnormality syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Auricular abnormality, cleft lip, ocular abnormality syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Congenital anomaly of carpal bone |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Omodysplasia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital anomaly of metacarpal bone |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Autosomal dominant omodysplasia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Autosomal recessive omodysplasia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital anomaly of rib |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| 5-amino-4-imidazole carboxamide ribosiduria (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| 5-amino-4-imidazole carboxamide ribosiduria (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Combined immunodeficiency due to partial recombination-activating gene 1 deficiency (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Defect of purinergic receptor p2y G protein-coupled 12 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Paraplegia, brachydactyly, cone-shaped epiphysis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Paraplegia, brachydactyly, cone-shaped epiphysis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Paraplegia, brachydactyly, cone-shaped epiphysis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Mucolipidosis type IV (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Congenital anomaly of external female genitalia |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Acquired atresia of pulmonary valve |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Gynandromorphism syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Group chromosomal alteration |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Chromosomal alterations of group A |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Chromosomal alterations of group B |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Chromosomal alterations of group C and X |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Chromosomal alterations of group D |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Chromosomal alterations of group E |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Chromosomal alterations of group F |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Chromosomal alterations of group G and Y |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital anomaly of lower respiratory system |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Accessory structure of lower respiratory tract |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital atresia of cardiac valve |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Glycogen storage disease type IX (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |