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 |
|