Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Syndactyly, polydactyly, ear lobe syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Syndactyly, polydactyly, ear lobe syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Syndactyly, polydactyly, ear lobe syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
4 |
Syndactyly, polydactyly, ear lobe syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Port-wine nevi, mega cisterna magna, hydrocephalus syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Port-wine nevi, mega cisterna magna, hydrocephalus syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Port-wine nevi, mega cisterna magna, hydrocephalus syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
X-linked intellectual disability due to glutamate ionotropic receptor AMPA type subunit 3 mutations |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Conductive hearing loss, malformation of external ear syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Hirschsprung disease, ganglioneuroblastoma syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Hirschsprung disease, ganglioneuroblastoma syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Heart defect, tongue hamartoma, polysyndactyly syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Heart defect, tongue hamartoma, polysyndactyly syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive brachyolmia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive brachyolmia |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Congenital abnormal number of ostium of coronary artery |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Hypertaurodontism |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
External auditory canal atresia, vertical talus, hypertelorism syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
External auditory canal atresia, vertical talus, hypertelorism syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
External auditory canal atresia, vertical talus, hypertelorism syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
External auditory canal atresia, vertical talus, hypertelorism syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
4 |
Tracheoesophageal fistula without atresia of esophagus |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Tracheoesophageal fistula without atresia of esophagus |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Congenital aneurysm of precerebral artery |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital stenosis of pulmonary artery |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital aneurysm of cerebral artery |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Bilateral multicystic renal dysplasia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Spondylometaphyseal dysplasia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Multicystic renal dysplasia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Otopalatodigital syndrome spectrum disorder |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Melnick-Needles syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Lumbar meningomyelocele |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
4 |
Lumbar meningomyelocele |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Lumbar meningomyelocele |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Congenital sacral meningocele with conotruncal heart defect syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Low lumbar myelomeningocele |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Cervical myelocele |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Cervical myelocele |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Lateral meningocele |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital laryngocele |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Congenital meningocele |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital spinal hydromeningocele |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
High lumbar myelomeningocele |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Lumbar myelocele |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Lumbar myelocele |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Thoracic meningomyelocele |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
4 |
Thoracic meningomyelocele |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Thoracic meningomyelocele |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Cervical meningomyelocele |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
4 |
Cervical meningomyelocele |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Cervical meningomyelocele |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Antecubital pterygium syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
X-linked scapuloperoneal muscular dystrophy |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Pulmonary valve agenesis, intact ventricular septum, persistent ductus arteriosus syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Pulmonary valve agenesis, intact ventricular septum, persistent ductus arteriosus syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Craniorhiny |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Craniorhiny |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Craniorhiny |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Potter's facies |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Developmental dislocation of joint of shoulder region |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital single renal cyst |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Ectopic artery |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive cutis laxa type 2A |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal recessive cutis laxa type 2A |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Congenital aneurysm of anterior communicating artery |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Retinal arterial macroaneurysm with supravalvular pulmonic stenosis |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Retinal arterial macroaneurysm with supravalvular pulmonic stenosis |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital aneurysm of aorta |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital peripheral aneurysm |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital aneurysm of systemic artery |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital arterial aneurysm |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital renal artery aneurysm |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Major aortopulmonary collateral artery |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Bronchopulmonary collateral artery |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Posterior fossa arachnoid cyst |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Atrioventricular septal defect with atrioventricular valve regurgitation through right anterosuperior inferior mural commissure |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Atrioventricular septal defect with atrioventricular valve regurgitation through right anterosuperior superior bridging leaflet commissure |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Atrioventricular septal defect with atrioventricular valve regurgitation through right inferior bridging leaflet inferior mural commissure |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Atrioventricular septal defect with atrioventricular valve regurgitation through left septal commissure |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Amelogenesis imperfecta, hypoplastic type with microdontia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Atrioventricular septal defect with atrioventricular valve regurgitation through left superior bridging leaflet lateral mural commissure |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Atrioventricular septal defect with atrioventricular valve regurgitation through right septal commissure |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital vesicoureterorenal reflux, bilateral |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
4 |
Congenital vesicoureterorenal reflux, bilateral |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
Atrioventricular septal defect with atrioventricular valve regurgitation through left inferior bridging leaflet lateral mural commissure |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Atrioventricular septal defect with atrioventricular valve regurgitation |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Multiple congenital anomalies, hypotonia, seizures syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Muscle eye brain disease with bilateral multicystic leukodystrophy |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
Muscle eye brain disease with bilateral multicystic leukodystrophy |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
4 |
Cobblestone lissencephaly without muscular or ocular involvement |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type E |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |