Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
4 |
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Nephrocystin 3-related Meckel-like syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Accessory bilateral ribs |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Accessory bilateral ribs |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Deafness with onychodystrophy syndrome |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
4 |
Deafness with onychodystrophy syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Deafness with onychodystrophy syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Osteopetrosis hypogammaglobulinemia syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Myelocele with hydrocephalus |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
4 |
Congenital failure of fusion between maxillary and mandibular processes |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Radioulnar synostosis of bilateral upper limbs |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Radioulnar synostosis of bilateral upper limbs |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
AT-hook DNA binding motif containing 1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Multiple congenital anomalies, hypotonia, seizures syndrome type 2 |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Pancytopenia with developmental delay syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Piebald trait with neurologic defects syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Peripheral dysostosis |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
4 |
Progeroid and marfanoid aspect, lipodystrophy syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Progeroid and marfanoid aspect, lipodystrophy syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Leukonychia totalis, trichilemmal cysts, ciliary dystrophy syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Sebaceous nevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented nevus syndrome |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Sebaceous nevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented nevus syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Sebaceous nevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented nevus syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Dandy-Walker syndrome with spina bifida |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
6 |
Dandy-Walker syndrome with spina bifida |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
5 |
Congenital retroversion of bilateral femurs |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital retroversion of bilateral femurs |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Intellectual disability, severe speech delay, mild dysmorphism syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital genu varum of left knee |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Brachydactyly of finger of right hand |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Brachydactyly of finger of left hand |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital overriding toes of bilateral feet |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Congenital overriding toes of bilateral feet |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
5 |
Congenital overriding toes of bilateral feet |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Congenital overriding toes of bilateral feet |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital overriding toes of bilateral feet |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
4 |
Congenital overriding toes of right foot |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital overriding toes of right foot |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Congenital overriding toes of right foot |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Brachydactyly of finger of bilateral hands |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Brachydactyly of finger of bilateral hands |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital pes valgo planus of bilateral feet |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Congenital pes valgo planus of bilateral feet |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital genu varum of right knee |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital overriding toes of left foot |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital overriding toes of left foot |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Congenital overriding toes of left foot |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Congenital deformity of bilateral feet |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Congenital deformity of bilateral feet |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital anteversion of left femur |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital deformity of left foot |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital deformity of right foot |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital anteversion of right femur |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital anteversion of bilateral femurs |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital anteversion of bilateral femurs |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Temtamy preaxial brachydactyly syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Temtamy preaxial brachydactyly syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Temtamy preaxial brachydactyly syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
4 |
Congenital pontocerebellar hypoplasia type 9 |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital pontocerebellar hypoplasia type 9 |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Brachytelephalangic chondrodysplasia punctata |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal dominant prognathism of mandible |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Duplication of pituitary gland |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal dominant primary microcephaly |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Fibroblast growth factor receptor 2-related bent bone dysplasia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Fibroblast growth factor receptor 2-related bent bone dysplasia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Didymosis aplasticosebacea |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Didymosis aplasticosebacea |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Didymosis aplasticosebacea |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Severe dermatitis, multiple allergies, metabolic wasting syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Temple syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Blepharophimosis, intellectual disability syndrome, Verloes type |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Ehlers-Danlos syndrome due to tenascin-X deficiency |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Ehlers-Danlos syndrome due to tenascin-X deficiency |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Syndromic multisystem autoimmune disease due to itchy E3 ubiquitin protein ligase deficiency |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Lethal polymalformative syndrome Boissel type |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive cutis laxa type 2B |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal recessive cutis laxa type 2B |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Congenital neutropenia, myelofibrosis, nephromegaly syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Autosomal dominant aplasia and myelodysplasia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Foveal hypoplasia with presenile cataract syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Skin fragility, wooly hair, palmoplantar keratoderma syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |