| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Mowat-Wilson syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Complete ablepharon |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Acrocraniofacial dysostosis |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Acrocraniofacial dysostosis |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Acrocraniofacial dysostosis |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
| Congenital uterovesical fistula |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital uterovesical fistula |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Arteriohepatic dysplasia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Hypoplastic chondrodystrophy |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Hypoplastic chondrodystrophy |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Shprintzen Goldberg omphalocele syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Shprintzen Goldberg omphalocele syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Hydranencephaly with proliferative vasculopathy |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Schisis association syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Acrorenal mandibular syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Acrorenal mandibular syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
| Acrorenal mandibular syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Bifid tongue |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Ocular albinism with late-onset sensorineural deafness |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Interrupted right inferior vena cava |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Ehlers-Danlos syndrome, type 4 |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Ehlers-Danlos syndrome, type 4 |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Hair defect with photosensitivity and intellectual disability syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital anomaly of anterior segment of eye |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital hypoplasia of squamosal bone |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Cleft of soft palate and bilateral cleft lip |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Cleft of soft palate and bilateral cleft lip |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Otopalatodigital syndrome |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Otopalatodigital syndrome |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
4 |
| Otopalatodigital syndrome |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Otopalatodigital syndrome |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
5 |
| Otopalatodigital syndrome |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
| Arteriovenous malformation of stomach |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital short bowel syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Alopecia, progressive neurological defect, endocrinopathy syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Alopecia, progressive neurological defect, endocrinopathy syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
| Alopecia, progressive neurological defect, endocrinopathy syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Hypoplasia of right ventricular outflow tract and trabecular area |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Cornea plana |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Malformation association |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital duplication of aorta |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Hepatic vein to left sided atrium |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Hepatic vein to left sided atrium |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Malrotation of the intestine type IIIB |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Double kidney with double pelvis |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital anomaly of thoracic cage |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Mesocardia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Pierre Robin sequence faciodigital anomaly syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Pierre Robin sequence faciodigital anomaly syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Prelingual non-syndromic genetic deafness |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Spondyloenchondromatosis |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Carpal synostosis |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Right sided atrium connecting to both ventricles |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Neu-Laxova syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Abnormal position of cardiac valve |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital absence of right pulmonary artery |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Malattachment of atrial septum with superior aspect of septum primum to left and posterior |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Crisponi syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
| Crisponi syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Crisponi syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Bicornuate uterus affecting obstetric care |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital pulmonary arteriovenous aneurysm |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital leukonychia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Band of Ladd |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Aortic left ventricular tunnel with right coronary artery from tunnel |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Aortic left ventricular tunnel with right coronary artery from tunnel |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Acromelanosis |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Supernumerary centrum of cervical vertebra |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Diaphanospondylodysostosis |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Microcephalus with brachydactyly and kyphoscoliosis syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Microcephalus with brachydactyly and kyphoscoliosis syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
| Microcephalus with brachydactyly and kyphoscoliosis syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Microcephalus with brachydactyly and kyphoscoliosis syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
4 |
| Microcephalus, lymphedema, chorioretinopathy syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital absence of appendix |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital aneurysm of heart |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Single right ventricle |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Single right ventricle |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital absence of eye bulge |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Atresia of the anterior nares |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital absence of tympanic anulus |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Atrioventricular septal defect with ventricular component under superior bridging leaflet with chords to papillary muscle on right ventricular side septum |
Pathological process |
True |
Pathological developmental process |
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 |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Lethal recessive chondrodysplasia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital maxillary hypoplasia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Simple lymphangioma |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Simple lymphangioma |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Congenital absence of multiple toes |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Familial focal facial dermal dysplasia |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Roberts-SC phocomelia syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Roberts-SC phocomelia syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Congenital dysplasia of cardiac valve |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Isolated optic nerve hypoplasia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Paramedian facial cleft - Tessier cleft 3 |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Axenfeld-Rieger syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Anterior imbrication of teeth |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital malposition of humerus |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital malposition of nasal septum |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital absence of lung fissures |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |