Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Ulna fibula ray defect and brachydactyly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Ulna fibula ray defect and brachydactyly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Multiple anterior segment anomalies |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Atelosteogenesis type 2 |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Atrioventricular septal defect - ventricular component |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital prolapse of urethra |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Bertolotti's syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Neonatal intestinal perforation co-occurrent and due to intestinal atresia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital pontocerebellar hypoplasia type 5 |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hypospadias and epispadias |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Laryngo-onycho-cutaneous syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Laryngo-onycho-cutaneous syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Dominant dystrophic epidermolysis bullosa, albopapular type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Incomplete ossification of centrum of thoracic vertebra |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital muscular dystrophy |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Microphthalmia with linear skin defect syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Greither type of ectodermal dysplasia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Isolation of left common carotid artery |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Dermatofibrosis lenticularis disseminata |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Congenital hyperplasia of sebaceous glands of lip |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Cortical blindness, intellectual disability, polydactyly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Cortical blindness, intellectual disability, polydactyly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Cortical blindness, intellectual disability, polydactyly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Cloverleaf skull with multiple congenital anomalies syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Cloverleaf skull with multiple congenital anomalies syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Cloverleaf skull with multiple congenital anomalies syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
4 |
Cloverleaf skull with multiple congenital anomalies syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
5 |
Cloverleaf skull with multiple congenital anomalies syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Erythrodermic lamellar ichthyosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Deafness, vitiligo, achalasia syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Deafness, vitiligo, achalasia syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Myelocele with hydrocephalus |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
5 |
Myelocele with hydrocephalus |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Osteochondrodysplasia |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital portal-systemic shunt |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Obstruction of right ventricular outflow tract due to aortico-left ventricular tunnel |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital hypoplasia of cerebrum |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Constricting band of extremity |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Superior to inferior ventricular relationship |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Van den Ende-Gupta syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Van den Ende-Gupta syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Talon cusp |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Osseous syndactyly of toes first web space |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Incomplete ossification of tympanic anulus |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Ectodermal dysplasia trichoodontoonychial type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Ectodermal dysplasia trichoodontoonychial type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Holoanencephaly |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Sacral hemivertebra |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Bipartite ossification of sternebra |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Goniodysgenesis with intellectual disability and short stature syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Vascular ring with left aortic arch and right patent arterial duct |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Vascular ring with left aortic arch and right arterial duct arising from retroesophageal aortic diverticulum |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal recessive ocular albinism |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Accessory ossification center |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Vascular ring with left aortic arch to right descending aorta and right patent arterial duct |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Thoracic spina bifida with hydrocephalus - open |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Vascular ring with left aortic arch and retroesophageal right descending aorta and right arterial duct arising from aortic diverticulum and aberrant right subclavian artery |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Sacral spina bifida with hydrocephalus - open |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
4 |
Infracardiac location of anomalous pulmonary venous connection with two descending veins |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Posterior lenticonus |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Metaphyseal chondrodysplasia, McKusick type with associated immunodeficiency |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Congenital hernia of foramen of Morgagni |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital hernia of foramen of Morgagni |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
German syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Diaphragmatic defect, limb deficiency, skull defect syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Diaphragmatic defect, limb deficiency, skull defect syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Retinal detachment and occipital encephalocele |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
4 |
Localized macrodontia |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Infracardiac location of anomalous pulmonary venous connection to hepatic vein |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Ocular albinism |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hereditary hypotrichosis with recurrent skin vesicles syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Pachyonychia congenita type III of Schafer-Brunauer |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Ocular albinism-lentigines-deafness syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital lipomatous overgrowth, vascular malformation, epidermal nevi, skeletal anomaly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Craniosynostosis Boston type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Congenital venous malformation of skin |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Ocular albinism, type I |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Fetal genitourinary abnormality |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Craniosynostosis Philadelphia type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Vascular ring with left aortic arch to right descending aorta and right arterial ligament |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Microcephalus cardiomyopathy syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Albinism co-occurrent with hematologic disorder |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Aland eye disease and ocular albinism |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Raised birthmark |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital cataract, nephropathy, encephalopathy syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Vascular ring with left aortic arch and right arterial duct ligament arising from retroesophageal aortic diverticulum with aberrant right subclavian artery |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Lumbar spina bifida with hydrocephalus - open |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
5 |
Ocular albinism with late-onset sensorineural deafness |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Pachyonychia congenita type II of Jackson-Lawler |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Deafness, enamel hypoplasia, nail defect syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Familial digital arthropathy and brachydactyly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Nasofrontal encephalocele |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Nasofrontal encephalocele |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Hydrencephalomeningocele |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hydrencephalomeningocele |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Nasopharyngeal encephalocele |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Nasopharyngeal encephalocele |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Autosomal dominant palmoplantar keratoderma and congenital alopecia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Vascular ring with left aortic arch and right arterial duct arising from aberrant retroesophageal brachiocephalic artery |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Vascular ring with left aortic arch and retrotracheal right patent arterial duct |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |