| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Hemoglobin SS disease without crisis (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Sickle cell-hemoglobin D disease without crisis (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Hemoglobin S sickling disorder without crisis (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Hereditary hemoglobin S (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Sickle cell-hemoglobin E disease with crisis (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Sickle cell-hemoglobin E disease without crisis (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Sickle cell-thalassemia disease with crisis (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
4 |
| Sickle cell-thalassemia disease without crisis (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
4 |
| Hemoglobin S sickling disorder with crisis (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Sickling disorder due to hemoglobin S (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Hemoglobin SS disease with crisis (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Sickle cell-hemoglobin C disease with crisis (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Sickle cell-hemoglobin C disease without crisis (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Sickle cell-hemoglobin D disease with crisis (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Hereditary hemoglobinopathy (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Hemoglobin SS disease with vasoocclusive crisis (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Acute sickle cell splenic sequestration crisis (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Hemoglobin O-Arab trait (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Hemoglobin H constant spring thalassemia (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Alpha thalassemia X-linked intellectual disability syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Dominant beta-thalassemia (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Beta thalassemia X-linked thrombocytopenia syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Pseudoprogeria syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
5 |
| Pseudoprogeria syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
6 |
| Pseudoprogeria syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
7 |
| Pseudoprogeria syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
8 |
| Pseudoprogeria syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
9 |
| Exostosis, anetoderma, brachydactyly type E syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
7 |
| Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
8 |
| Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
9 |
| Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
13 |
| Joubert syndrome with Jeune asphyxiating thoracic dystrophy |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
| Joubert syndrome with Jeune asphyxiating thoracic dystrophy |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
| Joubert syndrome with Jeune asphyxiating thoracic dystrophy |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
6 |
| Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
| Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
6 |
| Carbohydrate deficient glycoprotein syndrome type 2 due to deficiency of mannosidase alpha class 1B member 1 (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Congenital disorder of glycosylation type 1s |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Long thumb brachydactyly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
4 |
| Long thumb brachydactyly syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
| Long thumb brachydactyly syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
6 |
| Long thumb brachydactyly syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
7 |
| Sickle cell trait in mother complicating pregnancy |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Thalassemia in mother complicating pregnancy |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Sickle cell anaemia in mother complicating childbirth |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Sickle cell trait in mother complicating childbirth (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Thalassemia in mother complicating childbirth |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Choroideremia with deafness and obesity syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
1 |
| Choroideremia with deafness and obesity syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Deafness, small bowel diverticulosis, neuropathy syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
5 |
| Deafness, small bowel diverticulosis, neuropathy syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
6 |
| Deafness, small bowel diverticulosis, neuropathy syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
7 |
| Polydactyly myopia syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Polydactyly myopia syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
| Preaxial polydactyly, colobomata, intellectual disability syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Preaxial polydactyly, colobomata, intellectual disability syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
| Spastic paraplegia, nephritis, deafness syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
7 |
| Spastic paraplegia, nephritis, deafness syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
9 |
| syndrom med mikrocefali, digital anomali och intellektuell funktionsnedsättning |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
2 |
| syndrom med mikrocefali, digital anomali och intellektuell funktionsnedsättning |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
| Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
| Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
| Dandy-Walker malformation with postaxial polydactyly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
5 |
| Dandy-Walker malformation with postaxial polydactyly syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
7 |
| Skeletal dysplasia brachydactyly syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Skeletal dysplasia brachydactyly syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
| Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
| Van den Bosch syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
5 |
| Van den Bosch syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
6 |
| Van den Bosch syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
7 |
| Congenital disorder of glycosylation type 1w (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Congenital disorder of glycosylation type 1x |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Hypogonadotropic hypogonadism retinitis pigmentosa syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Hypogonadotropic hypogonadism retinitis pigmentosa syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
4 |
| Hypogonadotropic hypogonadism retinitis pigmentosa syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
5 |
| Congenital disorder of glycosylation type 1y |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Aniridia, renal agenesis, psychomotor retardation syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Aniridia, renal agenesis, psychomotor retardation syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
| Thumb stiffness, brachydactyly, intellectual disability syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Thumb stiffness, brachydactyly, intellectual disability syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
| Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
| Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
11 |
| Acrocephalopolysyndactyly type IV (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
3 |
| Acrocephalopolysyndactyly type IV (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
4 |
| 16p11.2p12.2 microduplication syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| 17q12 microdeletion syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| 17q12 microdeletion syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
| 20q13.33 microdeletion syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| 20q13.33 microdeletion syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
| Distal 16p11.2 microdeletion syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
2 |
| Distal 16p11.2 microdeletion syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
| Megalocornea with intellectual disability syndrome |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
| Spastic paraplegia, nephritis, deafness syndrome (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
6 |
| Isolated hereditary congenital facial paralysis (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
| Dandy-Walker malformation with postaxial polydactyly syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
9 |