| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| crise d'anémie falciforme |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Sickling disorder due to hemoglobin S (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Hemoglobin SS disease with crisis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Sickle cell-hemoglobin C disease with crisis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Sickle cell-hemoglobin C disease without crisis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Sickle cell-hemoglobin D disease with crisis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Hereditary hemoglobinopathy (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Hemoglobin SS disease with vasoocclusive crisis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Acute sickle cell splenic sequestration crisis (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Hemoglobin O-Arab trait (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Hemoglobin H constant spring thalassemia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Alpha thalassemia X-linked intellectual disability syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Dominant beta-thalassemia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Beta thalassemia X-linked thrombocytopenia syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Pseudoprogeria syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| Pseudoprogeria syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
6 |
| Pseudoprogeria syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Pseudoprogeria syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
8 |
| Pseudoprogeria syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
9 |
| Exostosis, anetoderma, brachydactyly type E syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
7 |
| Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
8 |
| Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
9 |
| Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
13 |
| Joubert syndrome with Jeune asphyxiating thoracic dystrophy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Joubert syndrome with Jeune asphyxiating thoracic dystrophy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Joubert syndrome with Jeune asphyxiating thoracic dystrophy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Carbohydrate deficient glycoprotein syndrome type 2 due to deficiency of mannosidase alpha class 1B member 1 (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital disorder of glycosylation type 1s |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Long thumb brachydactyly syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Long thumb brachydactyly syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
5 |
| Long thumb brachydactyly syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
6 |
| Long thumb brachydactyly syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
7 |
| Sickle cell trait in mother complicating pregnancy |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Thalassemia in mother complicating pregnancy |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Sickle cell anaemia in mother complicating childbirth |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Sickle cell trait in mother complicating childbirth (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Thalassemia in mother complicating childbirth |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Congenital anomaly of lacrimal system |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital lobulation of kidney |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Ring chromosome 22 syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital duplication of stomach |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital cleft hand |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| Congenital absence of lobe of liver |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| hypercholestérolémie |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Brachycephaly |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital stricture of urethra |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Anomaly of chromosome pair 3 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital anomaly of aortic valve |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Uterus unicornis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital anomaly of urethra |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Buphthalmos |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Preductal coarctation of aorta |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Lenz-Majewski hyperostosis syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Derencephalus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| 12p partial trisomy syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Propionyl-CoA carboxylase deficiency |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Multiple carboxylase deficiency - neonatal onset |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Holocarboxylase synthase deficiency |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Homocystinuria vitamin B12-responsive type III |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Functional defects of methionine synthase |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Homogentisate 1,2-dioxygenase deficiency |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Double renal pelvis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Hypoplastic chondrodystrophy |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Pigmented xerodermoid |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Lipofuscinosis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Hepatic tyrosine aminotransferase deficiency |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Glutaryl-coenzyme A dehydrogenase deficiency (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Doubling of uterus with doubling of cervix and vagina |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Dysplastic ovary |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital ovarian dysplasia |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital epiblepharon-inferior oblique syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Swan's syndrome II |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Brachycephalic dwarfism |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Embedded tooth |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Aganglionosis of Auerbach's plexus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital prolapse of bladder |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital megacolon |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Aganglionosis of colon |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Mesonephric cyst |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Wolffian cyst |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Common atrioventricular canal |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital stenosis of small intestine |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital atresia of jejunum |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Malrotation of the intestine type IIID |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Familial megaloblastic anemia |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| syndrome de Dandy-Walker |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Henck-Assman disease |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Osteopetrosis (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Chondrodysplasia punctata congenita |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Choroideremia with deafness and obesity syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| Choroideremia with deafness and obesity syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Deafness, small bowel diverticulosis, neuropathy syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| Deafness, small bowel diverticulosis, neuropathy syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
6 |
| Deafness, small bowel diverticulosis, neuropathy syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
7 |
| Polydactyly myopia syndrome (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Polydactyly myopia syndrome (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |