Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Paravaginal cyst arising in mesonephric duct |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Pili torti-deafness syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Acral dystrophic epidermolysis bullosa |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Functionally congenital single lung |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Rothmund-Thomson syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Micromelic spondyloepimetaphyseal dysplasia |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Abnormal course of aortic arch and descending aorta |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Incomplete ossification of lacrimal bone |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Isolation of right subclavian artery |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Dwarfism, alopecia, pseudoanodontia, cutis laxa |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Trigonocephaly |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Bilateral congenital absence of fallopian tube |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Spondylometaphyseal dysplasia - Sutcliffe type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Rachischisis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Spina bifida aperta of cervical spine |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Spina bifida aperta of cervical spine |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Atrichia congenita |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Macrocolon |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Cooks syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Athabaskan brainstem dysgenesis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Catel Manzke syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital rhabdomyoma of heart |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Mesotaurodontism |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Total anomalous pulmonary venous return |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Pseudoprogeria syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Pseudoprogeria syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Pseudoprogeria syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Pseudoprogeria syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
4 |
Congenital diverticulosis of small intestine |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Overriding skull bones |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital pulmonary vein confluence |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Laryngeal cleft type II |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Albinism with deafness syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal dominant spondylocostal dysostosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Chondrodysplasia punctata Toriello type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Oculocerebrofacial syndrome Kaufman type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Oculocerebrofacial syndrome Kaufman type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Heart defect and limb shortening syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Heart defect and limb shortening syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
German syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
German syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Incomplete anencephaly |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hypoplasia of right ventricular outflow tract |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Coronal hypospadias |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Double uterus affecting pregnancy |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Craniometadiaphyseal dysplasia wormian bone type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
12q14 microdeletion syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
12q14 microdeletion syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
12q14 microdeletion syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Derodidymis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Acropectorovertebral dysplasia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Acropectorovertebral dysplasia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Acropectorovertebral dysplasia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal recessive amelia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Diaphragmatic defect, limb deficiency, skull defect syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Diaphragmatic defect, limb deficiency, skull defect syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
4 |
Dextrocardia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Overriding left ventriculoarterial valve |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hypotrichosis and intellectual disability syndrome Lopes type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Hypotrichosis and intellectual disability syndrome Lopes type |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Holorachischisis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Microcephaly, microphthalmia, ectrodactyly of lower limbs and prognathism syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Microcephaly, microphthalmia, ectrodactyly of lower limbs and prognathism syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Anencephalus |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
6 |
Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
4 |
Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Acrofrontofacionasal dysostosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Acrofrontofacionasal dysostosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Doubling of uterus with doubling of cervix and vagina with obstruction |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Acrootoocular syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Sacral spina bifida with hydrocephalus - closed |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Atrioventricular septal defect with ventricular component and interchordal shunting under inferior bridging leaflet |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital vertical mandibular hypoplasia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Dysmorphism, short stature, deafness, disorder of sex development syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Dysmorphism, short stature, deafness, disorder of sex development syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Pseudochondroplasia |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Manus plana |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Persistent left posterior cardinal vein |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Persistent left posterior cardinal vein |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Radial polydactyly Wassel 7 |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital abnormality of iris and ciliary body |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Increased anogenital distance |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Megacalycosis |
Occurrence |
False |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Incomplete ossification of mandible |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Brachygnathism |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital cataract ichthyosis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Neurocutaneous syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Weaver Williams syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Spinocerebellar ataxia dysmorphism syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Spinocerebellar ataxia dysmorphism syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Spinocerebellar ataxia dysmorphism syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
4 |
Spinocerebellar ataxia dysmorphism syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
3 |
Spina bifida without hydrocephalus - open |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
2 |
Congenital hypertrichosis lanuginosa |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital cervicoaural fistula |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |
Congenital arteriovenous fistula stenosis |
Occurrence |
True |
Congenital |
Inferred relationship |
Existential restriction modifier |
1 |