Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
Patterson Stevenson Fontaine syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Epiphyseal dysplasia, microcephalus, nystagmus syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Epiphyseal dysplasia, microcephalus, nystagmus syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Aglossia-adactyly syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Vascular ring with left aortic arch and right arterial duct arising from retroesophageal aortic diverticulum and aberrant right subclavian artery (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Double mitral valve |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Fetus with central nervous system malformation unspecified |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Split hand, split foot malformation with sensorineural hearing loss syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Split hand, split foot malformation with sensorineural hearing loss syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
Split hand, split foot malformation with sensorineural hearing loss syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Incomplete ossification of supraoccipital bone |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Multiple malformation syndrome with facial-limb defects as major feature |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Fetus with central nervous system malformation NOS |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Incomplete ossification of centrum of lumbar vertebra |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Pre-eruptive colour change of tooth |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
Fetus with chromosomal abnormality unspecified |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Mesomelic dysplasia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Trigonocephaly with bifid nose and acral anomaly syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Trigonocephaly with bifid nose and acral anomaly syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Trigonocephaly with bifid nose and acral anomaly syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
Spinocerebellar ataxia type 34 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
Alopecia, onychodysplasia, hypohidrosis, deafness ectodermal dysplasia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Fetus with chromosomal abnormality NOS |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Fetus with hereditary disease unspecified |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Junctional epidermolysis bullosa gravis of Herlitz (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Camptodactyly and tall stature with scoliosis and hearing loss syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Camptodactyly and tall stature with scoliosis and hearing loss syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Camptodactyly and tall stature with scoliosis and hearing loss syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
Hypoplasia of corpus callosum and mental retardation with adducted thumbs and spasticity and hydrocephalus syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Roger's disease |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Bone dysplasia lethal Holmgren type (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Thrombocytopathy, asplenia and miosis (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Fetus with hereditary disease NOS |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Auricular abnormality, cleft lip, ocular abnormality syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Auricular abnormality, cleft lip, ocular abnormality syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Fetus with viral damage via mother unspecified |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Fucosidosis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Brittle cornea syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Congenital postural lordosis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
Congenital hypoplasia of cardiac ventricle |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Atrioventricular septal defect - ventricular component under inferior bridging leaflet |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Absent thumb with short stature and immunodeficiency syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Absent thumb with short stature and immunodeficiency syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Persisting fifth aortic arch with atresia of fourth arch (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Congenital fistula between uterus and urinary tract |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
Congenital chorioretinal degeneration |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Incomplete ossification of tarsal bone |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Fetus with viral damage via mother NOS |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Congenital nuclear ophthalmoplegia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Fetus with damage due to other maternal disease unspecified |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Craniodiaphyseal dysplasia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Achondrogenesis, type II |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Grebe syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Vitelline duct polyp (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Sandman-Andra syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Rolland-Debuqois syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Hypoplasia of uterus and cervix |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Fetus with damage due to other maternal disease - delivered |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Fetus with damage due to other maternal disease with antenatal problem |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Supernumerary fused sternebra |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Complete bilateral cleft palate |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Complete bilateral cleft palate |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
brachyolmie autosomique dominante |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
brachyolmie autosomique dominante |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Uterus subseptus (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Inverse junctional epidermolysis bullosa |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Multiple café-au-lait macules due to neurofibromatosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Multiple café-au-lait macules due to neurofibromatosis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Fetus with damage due to other maternal disease NOS |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Tracheal origin of right upper lobe bronchus (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Fetus with drug damage unspecified |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Temtamy syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Temtamy syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
Uterus cordiformis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
syndrome de Kartagener |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
Bilateral renal dysplasia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
syndrome de la maladie cardiaque polyvalvulaire |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Complete situs inversus with dextrocardia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Thanatophoric dysplasia, type 2 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Congenital pericardial defect (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Fetus with drug damage NOS |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Dysplasias with significant membranous bone involvement |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Fetus with radiation damage unspecified |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
Skeletal dysplasia brachydactyly syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Branchial cleft, cyst or fistula; preauricular sinus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
Holoprosencephaly and postaxial polydactyly syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Short tarsus with absence of lower eyelashes syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Congenital pulmonary artery conduit |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Right renal agenesis co-occurrent with left renal hypoplasia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Smith McCort dysplasia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
Radioulnar synostosis with microcephaly and scoliosis syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |