| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Aberrant origin of left subclavian artery |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Hypohidrosis-diabetes insipidus syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Hypohidrosis-diabetes insipidus syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
| Hypohidrosis-diabetes insipidus syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Floating-Harbor syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Atrioventricular septal defect with ventricular component and interchordal shunting under superior bridging leaflet |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Atrioventricular septal defect with ventricular component and interchordal shunting under superior bridging leaflet |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Laterality sequence |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital anomaly of myocardium |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital anomaly of peripheral blood vessel |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant hypohidrotic ectodermal dysplasia syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
| Autosomal dominant hypohidrotic ectodermal dysplasia syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant hypohidrotic ectodermal dysplasia syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Congenital absence of thoracic vertebra |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Midline sinus of the upper lip |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Fetal methyl mercury syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital duplication of vagina |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Familial multiple fibrofolliculoma |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Lethal hemolytic anemia and genital anomaly syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
| Duane's syndrome of bilateral eyes |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Duane's syndrome of bilateral eyes |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Duane's syndrome of bilateral eyes |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
| Congenital enlarged nails |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Origin of innominate artery from left side of aortic arch |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Origin of innominate artery from left side of aortic arch |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Sacral dysgenesis |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Sacral dysgenesis |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital malrotation of intestine |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Fetal or neonatal effect of placental or breast transfer of alcohol |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital malposition of gallbladder |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Agenesis of fifth metatarsal |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital hyperextension of limb |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Hypomyelination neuropathy arthrogryposis syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Hypomyelination neuropathy arthrogryposis syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Single ventricular outlet above right ventricle |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Otospondylomegaepiphyseal dysplasia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Otospondylomegaepiphyseal dysplasia |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Congenital abnormal fusion of maxilla |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Atrioventricular septal defect with ventricular imbalance consisting of dominant left ventricle and hypoplastic right ventricle |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Atrioventricular septal defect with ventricular imbalance consisting of dominant left ventricle and hypoplastic right ventricle |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Congenital malformation syndromes involving limbs |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Inferior cava to left of spine with right descending aorta |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital alveolar hyperplasia of mandible |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Spondylometaphyseal dysplasia Schmidt type |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Brachydactyly syndrome type C |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Brachydactyly syndrome type C |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Camptodactyly |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Camptodactyly |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Vascular malformation of the nervous system |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Trichodysplasia xeroderma syndrome |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Trichodysplasia xeroderma syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Hereditary benign acanthosis nigricans |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Hereditary benign acanthosis nigricans |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Hemifacial hyperplasia strabismus syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Hemifacial hyperplasia strabismus syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital pericardial cyst |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Odonto-onycho-dermal dysplasia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Odonto-onycho-dermal dysplasia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Thumb stiffness, brachydactyly, intellectual disability syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Thumb stiffness, brachydactyly, intellectual disability syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Cerebrofacial dysplasia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Cerebrofacial dysplasia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Triphalangeal great toe |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Triphalangeal great toe |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Congenital gastrointestinal-urinary tract fistula |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Congenital gastrointestinal-urinary tract fistula |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Male subcoronal hypospadias |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Male subcoronal hypospadias |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Vertical alopecia |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital anomaly of blood vessel of upper limb |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital anomaly of the pelvis |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Microcephalic osteodysplastic primordial dwarfism types I and III |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Microcephalic osteodysplastic primordial dwarfism types I and III |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Hyperplasia of pancreatic islet beta cell |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Radial polydactyly Wassel 4 |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| 8q22.1 microdeletion syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| 8q22.1 microdeletion syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
3 |
| 8q22.1 microdeletion syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Isolated hypoplasia of cerebellar vermis |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital anomaly of perineum |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital anomaly of carotid artery |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital anomaly of face bones |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Craniosynostosis fibular aplasia syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Craniosynostosis fibular aplasia syndrome |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Congenital abnormality of left atrioventricular valve in double inlet ventricle |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital fusion of ribs |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital anomaly of upper respiratory system |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Systemic to pulmonary collateral artery connecting with central pulmonary arteries |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Systemic to pulmonary collateral artery connecting with central pulmonary arteries |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital dislocation of knee with genu recurvatum |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Congenital dislocation of knee with genu recurvatum |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Pseudohypoparathyroidism type I B |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital torticollis |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital malposition of kidney |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Megalencephaly-capillary malformation syndrome |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
2 |
| Megalencephaly-capillary malformation syndrome |
Pathological process |
False |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital esophageal pouch |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |
| Distal origin of brachiocephalic trunk |
Pathological process |
True |
Pathological developmental process |
Inferred relationship |
Existential restriction modifier |
1 |