| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Hypotrichosis and intellectual disability syndrome Lopes type (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Hypotrichosis and intellectual disability syndrome Lopes type (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Midline cleft of lower lip |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Midline cleft of lower lip |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Microcephalic osteodysplastic dysplasia Saul Wilson type (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Microcephalic osteodysplastic dysplasia Saul Wilson type (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Microcephalic osteodysplastic dysplasia Saul Wilson type (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Embryopathy caused by mycophenolate mofetil (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Multinodular goiter, cystic kidney, polydactyly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Multinodular goiter, cystic kidney, polydactyly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| syndrome de lipomes naso-palpébraux-colobome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| syndrome de lipomes naso-palpébraux-colobome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Native American myopathy |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Native American myopathy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| X-linked spastic paraplegia type 2 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Simpson Golabi Behmel syndrome type 2 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Postaxial polydactyly type A (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Postaxial polydactyly type B (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Nephrogenic syndrome of inappropriate antidiuresis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Noonan syndrome-like disorder with loose anagen hair (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Noonan syndrome-like disorder with loose anagen hair (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Polydactyly of index finger (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| syndrome de la maladie cardiaque polyvalvulaire |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| syndrome de la maladie cardiaque polyvalvulaire |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Pigmented paravenous retinochoroidal atrophy (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Pigmented paravenous retinochoroidal atrophy (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Pterygia, heart anomaly, autosomal recessive inheritance, vertebral defect, ear anomaly, radial defect syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Pierre Robin sequence faciodigital anomaly syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Pierre Robin sequence faciodigital anomaly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Revesz syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| Revesz syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
7 |
| Revesz syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
8 |
| Talo-patello-scaphoid osteolysis syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Talo-patello-scaphoid osteolysis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Spondylocostal dysostosis with anal atresia and genitourinary malformation syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Spondylocostal dysostosis with anal atresia and genitourinary malformation syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Spondylocostal dysostosis with anal atresia and genitourinary malformation syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Spondylocostal dysostosis with anal atresia and genitourinary malformation syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| X-linked spastic paraplegia type 2 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Solute carrier family 35 member A1 congenital disorder of glycosylation (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Citrullinemia, late-onset type |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Multinodular goiter, cystic kidney, polydactyly syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Congenital stenosis of larynx |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Accessory left tarsal navicular bone (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Accessory right tarsal navicular bone (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital hypoplasia of ascending aorta |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Revesz syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
6 |
| Congenital rectocloacal fistula |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Clastothrix |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Clastothrix |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Clastothrix |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Pierson syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Pierson syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Autosomal recessive aplasia cutis congenita of limb (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Renier Gabreels Jasper syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Renier Gabreels Jasper syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Retinal degeneration, nanophthalmos, glaucoma syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Retinal degeneration, nanophthalmos, glaucoma syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Trichothiodystrophy (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Trichothiodystrophy (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Trichothiodystrophy (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Thymic, renal, anal, lung dysplasia syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Thymic, renal, anal, lung dysplasia syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Thoracolaryngopelvic dysplasia |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Thoracolaryngopelvic dysplasia |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Steroid dehydrogenase deficiency and dental anomaly syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Steroid dehydrogenase deficiency and dental anomaly syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Split hand, split foot malformation with sensorineural hearing loss syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Split hand, split foot malformation with sensorineural hearing loss syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Split hand, split foot malformation with sensorineural hearing loss syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
8 |
| Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
9 |
| Sialidosis type 1 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Severe generalized recessive dystrophic epidermolysis bullosa (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Sex reversion, kidney, adrenal and lung dysgenesis syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Sex reversion, kidney, adrenal and lung dysgenesis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Sex reversion, kidney, adrenal and lung dysgenesis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Sex reversion, kidney, adrenal and lung dysgenesis syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Transient bullous dermolysis of newborn (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Congenital pes cavus of bilateral feet (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Congenital pes cavus of bilateral feet (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Congenital pes cavus of bilateral feet (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Congenital pes cavus of left foot (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Congenital pes cavus of left foot (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Congenital pes cavus of right foot (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Congenital pes cavus of right foot (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Congenital deformity of left upper limb (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Umbilical hernia with obstruction but no gangrene |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Autosomal dominant spastic paraplegia type 36 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Autosomal dominant spastic paraplegia type 4 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Autosomal recessive spastic paraplegia type 44 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Autosomal recessive spastic paraplegia type 46 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|