| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Distal trisomy 16q (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Mosaic trisomy 10 syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Mosaic trisomy 12 syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Mosaic trisomy 14 syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Distal trisomy 20q syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Distal trisomy 22q syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Distal trisomy 2p |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Distal trisomy 3p (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Distal trisomy 9q |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Encircling double aortic arch |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Familial focal epilepsy with variable foci |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Familial isolated trichomegaly |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Distal 22q11.2 microduplication syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cylindrical spirals myopathy (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Gouty neuritis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Cheilognathoschisis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cheilognathoprosoposchisis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cleft mandible |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cleft of primary palate |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Bilateral cleft of primary palate |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cleft hard palate with cleft lip, bilateral |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Ventricular extrasystoles with syncope, perodactyly and Robin sequence syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Contracture with ectodermal dysplasia and orofacial cleft syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Kapur Toriello syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cleft palate with bilateral cleft lip and bilateral cleft of alveolar process of maxilla |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Bilateral complete cleft lip and bilateral complete cleft of alveolar process of maxilla (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Craniofacial cleft (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Mosaic trisomy 15 syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Mosaic trisomy 16 syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Mosaic trisomy 17 syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Mosaic trisomy 2 syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Mosaic trisomy 20 syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Mosaic trisomy 22 syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Mosaic trisomy 3 syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Mosaic trisomy 4 syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Mosaic trisomy 5 syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Mosaic trisomy 7 syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Autosomal recessive spastic paraplegia type 15 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Autosomal recessive spastic paraplegia type 35 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Tetrasomy 21 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Distal 17p13.3 microdeletion syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Verloove Vanhorick Brubakk syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| syndrome de microduplication 7p22.1 |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| syndrome de duplication Xq12-q13.3 |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| 9p13 microdeletion syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| Progressive external ophthalmoplegia, myopathy, emaciation syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| X-linked agammaglobulinemia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| X-linked agammaglobulinemia with growth hormone deficiency |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Autosomal recessive spastic paraplegia type 21 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Autosomal recessive spastic paraplegia type 43 (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Proximal chromosome 18q deletion syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Branchiootic syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Autosomal recessive myogenic arthrogryposis multiplex congenita (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Autosomal dominant slowed nerve conduction velocity |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Tibial hemimelia, polysyndactyly, triphalangeal thumb syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| myopathie distale précoce type Laing |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Intellectual disability Birk-Barel type |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Microphthalmos co-occurrent with congenital ocular coloboma (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Fundus albipunctatus |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital muscular dystrophy type 1B |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| Congenital myopathy with internal nuclei and atypical cores (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cryptorchidism, arachnodactyly, intellectual disability syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Laubry Pezzi syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| King Denborough syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Intellectual disability, myopathy, short stature, endocrine defect syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Familial thoracic aortic aneurysm and aortic dissection |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Mosaic trisomy 9 syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Muscle filaminopathy |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Myopathy with hexagonally cross-linked tubular arrays |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| trisomie non distale 13q |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Non-distal trisomy 9q |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Membranous ventricular septum defect |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Biallelic RPE65, retinoid isomerohydrolase mutation associated retinal dystrophy (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Autosomal recessive spastic paraplegia type 62 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
2 |
| SURF1, cytochrome c oxidase assembly factor related Charcot-Marie-Tooth disease type 4 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Spheroid body myopathy |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Rolandic epilepsy, speech dyspraxia syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Metastatic malignant neoplasm to ectopic female breast tissue |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Metastatic malignant neoplasm to ectopic male breast tissue |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Ribonucleotide reductase regulatory TP53 inducible subunit M2B-related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with renal tubulopathy (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Congenital retinal aneurysm |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Mosaic trisomy 5 syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Otofaciocervical syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Otofaciocervical syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Mosaic trisomy 9 syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| 9p13 microdeletion syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Right aortic arch and left descending aorta |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Mosaic trisomy 3 syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Connective tissue disorder due to lysyl hydroxylase-3 deficiency |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Incomplete left cleft lip and incomplete cleft of left alveolar process of maxilla |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Oro-facial digital syndrome type 9 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Renal hepatic pancreatic dysplasia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Renal hepatic pancreatic dysplasia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Cleft hard palate with right cleft lip and cleft of right alveolar process of maxilla (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Double aortic arch with both patent |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Double aortic arch with left arch dominant and coarctation of right arch (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Low set ears |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |