| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Polydactyly myopia syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Preaxial polydactyly, colobomata, intellectual disability syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Preaxial polydactyly, colobomata, intellectual disability syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Spastic paraplegia, nephritis, deafness syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
7 |
| Spastic paraplegia, nephritis, deafness syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
9 |
| Microcephalus, digital anomaly, intellectual disability syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Microcephalus, digital anomaly, intellectual disability syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| syndrome de Dandy-Walker-polydactylie postaxiale |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| syndrome de Dandy-Walker-polydactylie postaxiale |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Skeletal dysplasia brachydactyly syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Skeletal dysplasia brachydactyly syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Van den Bosch syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Van den Bosch syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Van den Bosch syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Congenital disorder of glycosylation type 1w (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital disorder of glycosylation type 1x |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Hypogonadotropic hypogonadism retinitis pigmentosa syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Hypogonadotropic hypogonadism retinitis pigmentosa syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Hypogonadotropic hypogonadism retinitis pigmentosa syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| Congenital disorder of glycosylation type 1y |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Aniridia, renal agenesis, psychomotor retardation syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Aniridia, renal agenesis, psychomotor retardation syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Thumb stiffness, brachydactyly, intellectual disability syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Thumb stiffness, brachydactyly, intellectual disability syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Anomalous origin of right subclavian artery |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
11 |
| Acrocephalopolysyndactyly type IV (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Acrocephalopolysyndactyly type IV (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| syndrome de microduplication 16p11.2p12.2 |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| 17q12 microdeletion syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| 17q12 microdeletion syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| 20q13.33 microdeletion syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| 20q13.33 microdeletion syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Distal 16p11.2 microdeletion syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Distal 16p11.2 microdeletion syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Megalocornea with intellectual disability syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital epulis of newborn |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital gingival granular cell tumor |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| anomalie congénitale de la trachée |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital absence of upper limb |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Diplomyelia |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Vestigial remnants of canal of Cloquet |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Myeloschisis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Microstomia |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Late-infantile neuronal ceroid lipofuscinosis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Uterus cordiformis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| tophus goutteux d'une oreille |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| 20q partial trisomy (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Situs ambiguus |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Achondrogenesis, type IB |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Abdominal heart |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital anomaly of large intestine |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Aarskog syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Spastic paraplegia, nephritis, deafness syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
6 |
| Excessively long umbilical cord |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Retinal dystrophy in systemic lipidosis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Russell-Silver syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| insuffisance congénitale de la valve pulmonaire |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital stricture of bile duct |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital transposition of stomach |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| syndrome de Coffin-Lowry |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital phlebectasia |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Origin of innominate artery from left side of aortic arch |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Isolated hereditary congenital facial paralysis (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Atrophia bulborum hereditaria |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Facial asymmetry |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Adenylosuccinate lyase deficiency |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Biotin-(propionyl-CoA-carboxylase) ligase deficiency |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| syndrome de Dandy-Walker-polydactylie postaxiale |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
9 |
| Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital disorder of glycosylation type 1q (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Microcephalus, lymphedema, chorioretinopathy syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| hypoalphalipoprotéinémie familiale |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| XY type gonadal dysgenesis with associated anomalies syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| XY type gonadal dysgenesis with associated anomalies syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| XY type gonadal dysgenesis with associated anomalies syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Summitt syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Summitt syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Double kidney AND/OR pelvis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Female Kallman's syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Central nervous system malformation in fetus affecting obstetrical care |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital pyloric membrane |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Omphalocele with obstruction |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Corectopia |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Frontonasal dysplasia with alopecia and genital anomaly syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Dementia with Down syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Deletion of part of long arm of chromosome 17 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Deletion of part of long arm of chromosome 17 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Congenital cyst of orbit (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Congenital dislocation of knee with genu recurvatum |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Endocardial cushion defect |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Citrullinemia |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital duplication of uterus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|