Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
Hydrocephalus with obesity and hypogonadism syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
Infection causing congenital anomaly |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
1 |
Hypertrichosis and acromegaloid facial appearance syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
Hypertrichosis and acromegaloid facial appearance syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
GAPO syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
GAPO syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
4 |
GAPO syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
Hypomandibular faciocranial dysostosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
Hypomandibular faciocranial dysostosis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
5 |
Juberg Hayward syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
Juberg Hayward syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
Juberg Hayward syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
Juberg Marsidi syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Microphthalmia with brain and digit anomaly |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Microphthalmia with linear skin defect syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
Microphthalmia with linear skin defect syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
Congenital microgastria with limb reduction defect syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
Congenital microgastria with limb reduction defect syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
Microduplication Xp11.22p11.23 syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Radioulnar synostosis with developmental delay and hypotonia syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
Radioulnar synostosis with developmental delay and hypotonia syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
Qazi Markouizos syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
Qazi Markouizos syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
Qazi Markouizos syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
6 |
Scalp, ear, nipple syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
4 |
Scalp, ear, nipple syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
Scalp, ear, nipple syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
6 |
Scalp, ear, nipple syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
7 |
Schilbach Rott syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
Schilbach Rott syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
Robinow-like syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
Robinow-like syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
Robinow-like syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
6 |
Cleft hard and soft palate with cleft lip |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Cleft of soft palate and bilateral cleft lip |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Cleft of soft palate and cleft lip |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Hip dysplasia Beukes type |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
Odontochondrodysplasia |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
Odontochondrodysplasia |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
Bilateral microtia with deafness and cleft palate syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
Bilateral microtia with deafness and cleft palate syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
6 |
Bilateral microtia with deafness and cleft palate syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
7 |
Blepharonasofacial malformation syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
BRESEK syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Hypergonadotropic hypogonadism with cataract syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
Hypergonadotropic hypogonadism with cataract syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
Acrofrontofacionasal dysostosis type 2 |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
Acrofrontofacionasal dysostosis type 2 |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
6 |
Acrofrontofacionasal dysostosis type 2 |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
7 |
Acrofrontofacionasal dysostosis type 2 |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
8 |
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
7 |
Joubert syndrome with hepatic defect |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
Joubert syndrome with hepatic defect |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
Joubert syndrome with oculorenal defect |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
Joubert syndrome with orofaciodigital defect |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
5 |
Joubert syndrome with orofaciodigital defect |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
6 |
Joubert syndrome with orofaciodigital defect |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
7 |
Joubert syndrome with orofaciodigital defect |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
8 |
Joubert syndrome with orofaciodigital defect |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
9 |
Say Barber Miller syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
Say Barber Miller syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
4 |
Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
6 |
Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
7 |
Limb mammary syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
4 |
Limb mammary syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
Limb mammary syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
6 |
Limb mammary syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
7 |
Lipodystrophy, intellectual disability, deafness syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
Lipodystrophy, intellectual disability, deafness syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
6 |
Lowry MacLean syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
Lowry MacLean syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
6 |
Lowry MacLean syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
7 |
Lung agenesis with heart defect and thumb anomaly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
Lung agenesis with heart defect and thumb anomaly syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
Lung agenesis with heart defect and thumb anomaly syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
Lymphoedema, atrial septal defect, facial changes syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
Lymphoedema, atrial septal defect, facial changes syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
Lymphoedema, atrial septal defect, facial changes syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
Lymphoedema and cerebral arteriovenous anomaly syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
2 |
Lymphoedema and cerebral arteriovenous anomaly syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
DOORS syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
7 |
DOORS syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
8 |
DOORS syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
9 |
DOORS syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
10 |
Multiple epiphyseal dysplasia tarda type IIIa |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Alymphoid cystic thymic dysgenesis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
Alymphoid cystic thymic dysgenesis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
Multiple mitochondrial dysfunctions syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Thoracic insufficiency syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
2 |
Thoracic insufficiency syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |