| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Hydrolethalus syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Congenital dilatation of aortic root (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital trigger finger and trigger thumb (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Deafness, enamel hypoplasia, nail defect syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Congenital malformation of tongue, mouth and pharynx |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital absence of pelvis and lower limb |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Aplasia of fibula and ectrodactyly syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Aplasia of fibula and ectrodactyly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Aplasia of fibula and ectrodactyly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Hydrocephalus with endocardial fibroelastosis and cataract syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Hydrocephalus with endocardial fibroelastosis and cataract syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Hydrocephalus with endocardial fibroelastosis and cataract syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| dermato-ostéolyse type Kirghize |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| dermato-ostéolyse type Kirghize |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| dermato-ostéolyse type Kirghize |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| Alpha-2-antitrypsin deficiency |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Siegler Brewer Carey syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| ectropion congénital (trouble) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Cleft palate with cleft lip |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cheilognathoschisis (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Cheilognathoprosoposchisis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Oromandibular-limb hypogenesis spectrum |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Bilateral incomplete cleft palate with cleft lip |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Central complete cleft palate with cleft lip |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Central incomplete cleft palate with cleft lip |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cleft hard palate with cleft lip, bilateral |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Cheilopalatoschisis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Bilateral incomplete cleft lip and bilateral incomplete cleft of alveolar process of maxilla (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Complete cleft hard and soft palate |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cleft upper lip, upper jaw AND palate |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cheilognathouranoschisis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cheilognathopalatoschisis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Component of oligomeric golgi complex 7 congenital disorder of glycosylation (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Component of oligomeric golgi complex 8 congenital disorder of glycosylation (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Coloboma of macula with brachydactyly type B syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Coloboma of macula with brachydactyly type B syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Coloboma of macula with brachydactyly type B syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Global developmental delay, osteopenia, ectodermal defect syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Global developmental delay, osteopenia, ectodermal defect syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Glossopalatine ankylosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Glossopalatine ankylosis (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Glossopalatine ankylosis (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Glossopalatine ankylosis (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Goldberg Shprintzen megacolon syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
8 |
| Goldberg Shprintzen megacolon syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
9 |
| Goldberg Shprintzen megacolon syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
10 |
| Goldberg Shprintzen megacolon syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
11 |
| Hereditary sensory and autonomic neuropathy with spastic paraplegia (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| syndrome léthal d'hydrocéphalie, malformation cardiaque, hyperdensité osseuse |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| syndrome léthal d'hydrocéphalie, malformation cardiaque, hyperdensité osseuse |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| syndrome léthal d'hydrocéphalie, malformation cardiaque, hyperdensité osseuse |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Blepharoptosis, myopia, ectopia lentis syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Blepharoptosis, myopia, ectopia lentis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Bifid nose, anorectal anomaly, renal anomaly syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| syndrome de malformations cérébrales-cardiopathie congénitale-polydactylie postaxiale |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| syndrome de malformations cérébrales-cardiopathie congénitale-polydactylie postaxiale |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| syndrome de malformations cérébrales-cardiopathie congénitale-polydactylie postaxiale |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| syndrome de malformations cérébrales-cardiopathie congénitale-polydactylie postaxiale |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Branchiogenic deafness syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Intellectual disability, epilepsy, bulbous nose syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| dysplasie ectodermique hidrotique type Halal |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| dysplasie ectodermique hidrotique type Halal |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| dysplasie ectodermique hidrotique type Halal |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| dysplasie ectodermique hidrotique type Halal |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Hirschsprung disease with deafness and polydactyly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
8 |
| Hirschsprung disease with deafness and polydactyly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
9 |
| syndrome de maladie de Hirschsprung-brachydactylie type D |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| syndrome de maladie de Hirschsprung-brachydactylie type D |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
8 |
| Hirschsprung disease with nail hypoplasia and dysmorphism (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
8 |
| Hirschsprung disease with nail hypoplasia and dysmorphism (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
9 |
| Hirschsprung disease with nail hypoplasia and dysmorphism (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
10 |
| Holmes Gang syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Hunter McAlpine craniosynostosis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Hydrocephalus with obesity and hypogonadism syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Infection causing congenital anomaly (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| syndrome d'hypertrichose-faciès acromégaloïde |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| syndrome d'hypertrichose-faciès acromégaloïde |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Hypomandibular faciocranial dysostosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Hypomandibular faciocranial dysostosis (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| Juberg Hayward syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Juberg Hayward syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Juberg Hayward syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Juberg Marsidi syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Microphthalmia with brain and digit anomaly (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Microphthalmia with linear skin defect syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Microphthalmia with linear skin defect syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Congenital microgastria with limb reduction defect syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Congenital microgastria with limb reduction defect syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Microduplication Xp11.22p11.23 syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Radioulnar synostosis with developmental delay and hypotonia syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Radioulnar synostosis with developmental delay and hypotonia syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Puerto Rican infant hypotonia syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |