Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Crisponi syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Crisponi syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Crisponi syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Congenital pulmonary arteriovenous aneurysm |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital leukonychia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Aortic left ventricular tunnel with right coronary artery from tunnel |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Acromelanosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Diaphanospondylodysostosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Microcephalus with brachydactyly and kyphoscoliosis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Microcephalus with brachydactyly and kyphoscoliosis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Microcephalus with brachydactyly and kyphoscoliosis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
4 |
Microcephalus with brachydactyly and kyphoscoliosis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Atrioventricular septal defect with ventricular component under superior bridging leaflet with chords to papillary muscle on right ventricular side septum |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Lethal recessive chondrodysplasia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Roberts-SC phocomelia syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Anterior imbrication of teeth |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Right superior vena cava connecting to left atrium and right atrium |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Ectodermal dysplasia with natal teeth Turnpenny type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Thoracic spina bifida with hydrocephalus - closed |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hyperplastic tooth follicle |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hyperplastic tooth follicle |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Disorganized development of cartilaginous and fibrous components of the skeleton |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Uterus bicornuatus vetularum |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Kniest-Stickler dysplasia group |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Multiple congenital articular rigidities |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Simple syndactyly of toes of bilateral feet |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Radial polydactyly Wassel 6 |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Interrupted aortic arch between left subclavian and left common carotid artery |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital abnormality of atrioventricular valves in atrioventricular septal defect |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Septate vagina affecting pregnancy |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Polydactyly of thumb |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Ectodermal dysplasia-ocular malformation syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Epidermolysis bullosa simplex, Ogna type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Lingual thyroid |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Short stature with webbed neck and congenital heart disease syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Short stature with webbed neck and congenital heart disease syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Ichthyosis, oral and digital anomalies syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Ichthyosis, oral and digital anomalies syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Neurocutaneous melanosis sequence |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Isolation of left subclavian artery |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Ectopic liver |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Holoprosencephaly craniosynostosis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Acrocephalosyndactyly type I |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Acrocephalosyndactyly type I |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Macrocephaly, obesity, mental disability, ocular abnormality syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Macrocephaly, obesity, mental disability, ocular abnormality syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Oculoosteocutaneous syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Adult fucosidosis |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Notomelus |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Growth delay with hydrocephalus and lung hypoplasia syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital hereditary facial paralysis with variable hearing loss syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Congenital hereditary facial paralysis with variable hearing loss syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Contracture with ectodermal dysplasia and orofacial cleft syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Contracture with ectodermal dysplasia and orofacial cleft syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Cataract and microcornea syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Fusion of crown of teeth |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital coronary artery fistula to left atrium |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Lethal arthrogryposis co-occurrent with anterior horn cell disease |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Patent ductus arteriosus - delayed closure |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Leri's pleonosteosis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Ichthyosis congenita with biliary atresia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Acrofacial dysostosis Catania type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Laryngeal cleft type I |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Urachal diverticulum |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Spondylocamptodactyly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital corneal opacity not interfering with vision |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Anomalous pulmonary venous drainage to right atrium |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Radioulnar synostosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hypoplasia of right ventricular inflow tract |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hypospadias, hypertelorism, coloboma, deafness syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hypospadias, hypertelorism, coloboma, deafness syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Hypospadias, hypertelorism, coloboma, deafness syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Absent ductus venosus with direct connection of umbilical vein to renal vein |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Absent ductus venosus with direct connection of umbilical vein to renal vein |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Absent ductus venosus with direct connection of umbilical vein to renal vein |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Dominant dystrophic epidermolysis bullosa with absence of skin |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Joubert syndrome with congenital hepatic fibrosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
High assimilation pelvis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital trigger thumb of bilateral hands |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Aorta to right ventricle tunnel |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Duane anomaly, myopathy, scoliosis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Duane anomaly, myopathy, scoliosis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Persistent Gartner's duct |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Melanosis oculi |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Complete cleft hard and soft palate |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Atrioventricular septal defect with ventricular component under free floating superior bridging leaflet and chords to papillary muscle at right ventricular free wall |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hypotrichosis with juvenile macular degeneration syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital retraction of nipple |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Aortic valve overriding ventricular septum |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Lumbar spina bifida with hydrocephalus - closed |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Persisting fifth aortic arch with double barrell arch |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal dominant epidermolysis bullosa simplex |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital diaphragmatic hernia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Cutis laxa, autosomal dominant |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Paravaginal cyst arising in mesonephric duct |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |