| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Familial male-limited precocious puberty (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Benign multiple endocrine neoplasia type 2a |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Malignant multiple endocrine neoplasia type 2a (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Homozygous methylenetetrahydrofolate reductase mutation |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Heterozygous methylenetetrahydrofolate reductase mutation (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Adolescent X-linked adrenoleukodystrophy (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Childhood cerebral X-linked adrenoleukodystrophy |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Hyperuricuria |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Transitory amino acid metabolic disorder |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Longitudinal deficiency of humerus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| syndrome de Beckwith-Wiedemann |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
6 |
| Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Familial isolated hypoparathyroidism (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| 17p11.2 microduplication syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| dysplasie ectodermique tricho-odonto-onychiale |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| dysplasie ectodermique tricho-odonto-onychiale |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| dysplasie ectodermique tricho-odonto-onychiale |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| Chronic diarrhea with villous atrophy syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Wolfram-like syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| Wolfram-like syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
6 |
| Wolfram-like syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
7 |
| Intermediate anorectal malformation (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Isolated congenital megalocornea (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| 49,XYYYY syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Distal 22q11.2 microdeletion syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Distal 22q11.2 microdeletion syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| 12q15q21.1 microdeletion syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| 12q15q21.1 microdeletion syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Incomplete congenital absence of thigh AND leg |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Complete bilateral cleft palate with cleft lip |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Deafness, vitiligo, achalasia syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| SCARF syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| SCARF syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| SCARF syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| SCARF syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
8 |
| Accessory lobe of lung |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Glucocorticoid deficiency with achalasia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Deafness, vitiligo, achalasia syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Paravaginal cyst arising in mesonephric duct |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital cerebellar cortical atrophy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital arteriovenous fistula of kidney |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Total anodontia of permanent and deciduous teeth |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital stenosis of external auditory canal |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital aneurysm of aorta |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Lip hypertrophy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Congenital absence of leg with foot AND toes |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Aortopulmonary window (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Ehlers-Danlos syndrome, type 4 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| 4p partial monosomy syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital eventration of diaphragm |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital absence of uterus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Fibrochondrogenesis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| pili torti |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| hernie diaphragmatique congénitale |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Dextroposition of aorta |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Fetal valproate syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Allantoic cyst |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital clinodactyly |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Double artery |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Ebstein's anomaly with atrial septal defect |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Ectopic thymic tissue |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Fusion of teeth |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Polyorchism |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Atresia of pupil |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Sacralization of lumbar vertebra |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| syndrome d'alpha-thalassémie-déficience intellectuelle associée au chromosome 16 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| syndrome d'alpha-thalassémie-déficience intellectuelle associée au chromosome 16 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| syndrome d'alpha-thalassémie-déficience intellectuelle associée au chromosome 16 |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
7 |
| Pyridoxine-dependent epilepsy (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Pyridoxine-dependent epilepsy (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| Congenital hydrothorax (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Overriding skull bones |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Sclerosteosis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital subluxation of carpus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Bilateral right-sidedness sequence |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Child syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Thoracodidymus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Ostium primum defect |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Acquired megaduodenum |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Anomaly of chromosome pair 13 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Mohr syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Azygos lobe of lung |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Leri-Weill dyschondrosteosis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Cross syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Primary hyperoxaluria |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Tracheo-esophageal fistula without atresia of esophagus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Tracheo-esophageal fistula without atresia of esophagus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Acrokeratosis verruciformis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Trichorhinophalangeal syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital deformity of sacroiliac joint |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Accessory breast |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Progressive supranuclear palsy (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Progressive supranuclear palsy (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Early urethral obstruction sequence |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital duodenal obstruction |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Unstable hemoglobin disease |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Schmitt Gillenwater Kelly syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |