Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Incomplete ossification of arch of cervical vertebra |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Oculocutaneous albinoidism |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Familial intestinal malrotation |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Osteogenesis imperfecta type III |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Retinal degeneration, nanophthalmos, glaucoma syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Intellectual disability, developmental delay, contracture syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Intellectual disability, developmental delay, contracture syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Bilateral secondary renal dysplasia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Bilateral secondary renal dysplasia |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Restrictive interatrial communication with obligatory shunt |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Closed ductus venosus |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Diaphragmatic hernia, abnormal face and distal limb anomalies |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Oculocerebral hypopigmentation syndrome of Preus type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Porokeratosis of Mibelli, plaque type |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Nephrosis, deafness, urinary tract, digital malformation syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Scimitar syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Mannosidosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital positive ulnar variant of wrist |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital coxa vara |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Stenosis of systemic to pulmonary artery collateral artery |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
6 |
Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
4 |
Congenital junctional epidermolysis bullosa |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Dysostosis multiplex group |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Osteochondrodysplasia co-occurrent with defects of growth of tubular bones and spine |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Incomplete ossification of premaxilla |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Pseudo-polycoria |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Dacryocystitis and osteopoikilosis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Dacryocystitis and osteopoikilosis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Osteogenesis imperfecta type II |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Multiple congenital anomalies of fetus |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Progressive diaphyseal dysplasia |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Osler hemorrhagic telangiectasia syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital coxa valga |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Achondroplasia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Achondroplasia |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Imperforate pulmonary valve |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Pulmonary venous confluence in horizontal orientation |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Right superior vena cava persisting to coronary sinus and then to right sided atrium |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Right superior vena cava persisting to coronary sinus and then to right sided atrium |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Epidermolysis bullosa simplex with neuromuscular disease |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Otomandibular dysostosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Glycogenosis with glucoaminophosphaturia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Fallot's trilogy |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Fallot's trilogy |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Postaxial polydactyly and intellectual disability syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Craniofacial dyssynostosis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Alopecia, contracture, dwarfism, intellectual disability syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Alopecia, contracture, dwarfism, intellectual disability syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Alopecia, contracture, dwarfism, intellectual disability syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Metaphyseal chondrodysplasia, Spahr type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive faciodigitogenital syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive faciodigitogenital syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Hepatic vein to left atrium and right atrium |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hepatic vein to left atrium and right atrium |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Lumbar hemivertebra - balanced |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Acrofrontofacionasal dysostosis type 2 |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
4 |
Acrofrontofacionasal dysostosis type 2 |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Acrofrontofacionasal dysostosis type 2 |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Acrofrontofacionasal dysostosis type 2 |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Craniometaphyseal dysplasia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Craniometaphyseal dysplasia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal dominant lamellar ichthyosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Spondyloepiphyseal dysplasia with congenital joint dislocations |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hip dysplasia Beukes type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hip dysplasia Beukes type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Dysplasia with defective mineralization |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Triplex ureter |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Lamellar ichthyosis AND trichorrhexis invaginata syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital obstructive defect of renal pelvis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Incomplete ossification of arch of lumbar vertebra |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital leg length discrepancy |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Split hand, obstructive uropathy, spina bifida, diaphragmatic defect syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Split hand, obstructive uropathy, spina bifida, diaphragmatic defect syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
5 |
Split hand, obstructive uropathy, spina bifida, diaphragmatic defect syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
4 |
Split hand, obstructive uropathy, spina bifida, diaphragmatic defect syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Split hand, obstructive uropathy, spina bifida, diaphragmatic defect syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Jawad syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
5 |
Jawad syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
4 |
Bilateral microtia with deafness and cleft palate syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Bilateral microtia with deafness and cleft palate syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Arteriovenous malformation of large intestine |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital arteriovenous malformation of retina |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Bipartite ossification of centrum of thoracic vertebra |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Encephalo-ophthalmic dysplasia |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Juvenile cataract, microcornea, renal glucosuria syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital cataracts, facial dysmorphism and neuropathy |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Microphthalmia with ankyloblepharon and intellectual disability syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Temple Baraitser syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Temple Baraitser syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Frontal encephalocele |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Aplasia of fibula and ectrodactyly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Aplasia of fibula and ectrodactyly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Lutembacher's syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Lutembacher's syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |