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 |