| 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 |