Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Pseudohermaphroditism |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Oto-onycho-peroneal syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Oto-onycho-peroneal syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
4 |
Oto-onycho-peroneal syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Oto-onycho-peroneal syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Spina bifida with hydrocephalus - closed |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Neurofibromatosis Noonan syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Neurofibromatosis Noonan syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Lung agenesis with heart defect and thumb anomaly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Lung agenesis with heart defect and thumb anomaly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Congenital fibrosis of inferior rectus muscle |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Malaligned atrial septum |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Ventricular septal defect with anterior malaligned outlet septum with overriding pulmonary valve |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Lenticonus |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Incomplete ossification of hyoid bone |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Short rib polydactyly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Enlarged parietal foramina |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Male pseudohermaphroditism due to 5-alpha-reductase deficiency |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Scalp, ear, nipple syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Scalp, ear, nipple syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Scalp, ear, nipple syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Distal radioulnar synostosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Cardiospondylocarpofacial syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Salla disease |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Ebstein's anomaly with atrial septal defect |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Midline cleft of lower lip |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Persistent lanugo |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive brachyolmia and amelogenesis imperfecta syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive brachyolmia and amelogenesis imperfecta syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal recessive brachyolmia and amelogenesis imperfecta syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Median nasal dermoid fistula |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Intrauterine amputation of lower limb |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hennekam lymphangiectasia-lymphedema syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Capillary fragility abnormality |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Arthrogryposis multiplex congenita and whistling face syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Arthrogryposis multiplex congenita and whistling face syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Syphilitic saddle nose |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Microhepatia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Posterior lentiglobus |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Ichthyosis cheek eyebrow syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Earpit syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Atrioventricular septal defect with separate atrioventricular orifices |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hooded clitoris |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Central polydactyly of fingers |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Coloboma of eyelid |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Chondrodysplasia punctata congenita |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Capillary malformation-arteriovenous malformation syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Metaphyseal chondromatosis co-occurrent with D-2 hydroxyglutaric aciduria |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Stickler syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital tracheocele |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Fordyce spots of buccal mucosa |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Osteodysplasia |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital ichthyosis with hypotrichosis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Malattachment of atrial septum with posterior aspect of septum primum to left |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Sialic storage disease |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Manus vara |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Lamellar ichthyosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hypohidrosis-diabetes insipidus syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Atrioventricular septal defect with ventricular component and interchordal shunting under superior bridging leaflet |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Familial multiple fibrofolliculoma |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Lethal hemolytic anemia and genital anomaly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Atrioventricular septal defect with ventricular imbalance consisting of dominant left ventricle and hypoplastic right ventricle |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Spondylometaphyseal dysplasia Schmidt type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Camptodactyly |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hemifacial hyperplasia strabismus syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Hemifacial hyperplasia strabismus syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Odonto-onycho-dermal dysplasia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Thumb stiffness, brachydactyly, intellectual disability syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Cerebrofacial dysplasia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital gastrointestinal-urinary tract fistula |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Vertical alopecia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Microcephalic osteodysplastic primordial dwarfism types I and III |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hyperplasia of pancreatic islet beta cell |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Radial polydactyly Wassel 4 |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
8q22.1 microdeletion syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
8q22.1 microdeletion syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Craniosynostosis fibular aplasia syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital abnormality of left atrioventricular valve in double inlet ventricle |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital dislocation of knee with genu recurvatum |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Pseudohypoparathyroidism type I B |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Megalencephaly-capillary malformation syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Familial scaphocephaly syndrome McGillivray type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Localized junctional epidermolysis bullosa |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Female hypospadias |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Skeletal dysplasia with intellectual disability syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Coronary sinus defect in left atrium |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Cyprus facial neuromusculoskeletal syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Cyprus facial neuromusculoskeletal syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Hydrorhachis |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Ichthyosis hystrix Bäfverstedt type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Weissenbacher-Zweymuller syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Arteriovenous angioma |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Constriction ring syndrome of lower limb with amputation |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Multirooted tooth with convergent roots |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Late secondary abnormalities of the central nervous system |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Pierson syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Crowding of anterior maxillary teeth |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Cleft palate with stapes fixation and oligodontia syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Cleft palate with stapes fixation and oligodontia syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Paraplegia, brachydactyly, cone-shaped epiphysis syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Paraplegia, brachydactyly, cone-shaped epiphysis syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |