| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Nephrotic syndrome, diffuse mesangial proliferative glomerulonephritis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Nephrotic syndrome with proliferative glomerulonephritis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Nephrotic syndrome with membranous glomerulonephritis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Congenital nephrotic syndrome due to congenital infection (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Nephrotic syndrome with membranoproliferative glomerulonephritis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Steroid-sensitive nephrotic syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Steroid-resistant nephrotic syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Nephrotic syndrome, minor glomerular abnormality |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Steroid-dependent nephrotic syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Nephrotic syndrome, diffuse membranous glomerulonephritis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Congenital nephrotic syndrome with focal glomerulosclerosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Drash syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Nephrotic syndrome, diffuse endocapillary proliferative glomerulonephritis (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Nephrotic syndrome due to type 2 diabetes mellitus |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Nephrotic syndrome, diffuse mesangiocapillary glomerulonephritis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Nephrotic syndrome in amyloidosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Nephrotic syndrome, diffuse crescentic glomerulonephritis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Finnish congenital nephrotic syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Nephrotic syndrome associated with another disorder (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Genetic steroid-resistant nephrotic syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Nephrotic syndrome due to diabetes mellitus (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Nephrotic syndrome in malaria |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Sporadic idiopathic steroid-resistant nephrotic syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Nephrotic syndrome in polyarteritis nodosa |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| X-linked dyserythropoietic anemia with abnormal platelets and neutropenia (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| X-linked dyserythropoietic anemia with abnormal platelets and neutropenia (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Hereditary cryohydrocytosis with reduced stomatin |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Hereditary cryohydrocytosis with reduced stomatin |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Autosomal recessive severe congenital neutropenia due to glucose-6-phosphatase catalytic subunit 3 deficiency (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| infantiele subacute necrotiserende encefalopathie met nefrotisch syndroom (aandoening) |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
2 |
| Pancytopenia due to IKZF1 mutations |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Pancytopenia due to IKZF1 mutations |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Pancytopenia due to IKZF1 mutations |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Pancytopenia due to IKZF1 mutations |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Autosomal recessive severe congenital neutropenia due to CSF3R deficiency |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Bleeding diathesis due to thromboxane synthesis deficiency |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Hereditary thrombocytopenia with normal platelets |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Hereditary isolated aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Hereditary isolated aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| Hereditary isolated aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Hereditary isolated aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Osteopetrosis - intermediate type |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Autosomal dominant osteopetrosis type 2 (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Osteopetrosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Osteopenia, intellectual disability, sparse hair syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Infantile osteopetrosis with neuroaxonal dysplasia syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Juvenile idiopathic generalized osteoporosis |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
2 |
| Spondyloocular syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Dysplasia with decreased bone density |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Transient infantile osteopetrosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| X-linked osteoporosis with fractures |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Infantile malignant osteopetrosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| X-linked calvarial hyperostosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Doughnut lesion of calvaria and bone fragility syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| benigne autosomaal dominante osteopetrose |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
2 |
| Skeletal dysplasia with wormian bone, multiple fractures, dentinogenesis imperfecta syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Osteopetrosis with renal tubular acidosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Singleton-Merten syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Osteopetrosis - delayed type |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Menkes kinky-hair syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Osteoporosis and oculocutaneous hypopigmentation syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Autosomal recessive cutis laxa type 2B |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Familial steroid-resistant nephrotic syndrome with sensorineural deafness (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Majeed syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Majeed syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| Adult chronic idiopathic neutropenia (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Acute nephrotic syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Neutropenic sepsis (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Pancytopenia caused by immunosuppressant |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Pancytopenia caused by immunosuppressant |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Pancytopenia caused by immunosuppressant |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Pancytopenia caused by immunosuppressant |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Loss of hypoglycemic warning due to diabetes mellitus |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Somogyi phenomenon |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
1 |
| Hypoglycaemic unawareness due to type 1 diabetes mellitus |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Nocturnal hypoglycemia due to diabetes mellitus |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Hypoglycaemia due to diabetes mellitus |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Midpelvic contraction |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Contracted pelvis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| algemeen vernauwd bekken - bevallen |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
2 |
| Generally contracted pelvis with antenatal problem (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Inlet contraction of pelvis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Outlet pelvic contraction with antenatal problem |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Congenital contracted pelvis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| vernauwing van bekkenuitgang - bevallen |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
2 |
| Geroderma osteodysplastica (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Hyperphosphatasemia tarda |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Pyknodysostosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Sclerosteosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Outlet contraction of pelvis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Hypoglycemia unawareness due to type 2 diabetes mellitus |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Endosteal hyperostoses |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Endosteal hyperostoses with cerebellar hypoplasia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Insulin reactive hypoglycemia due to type 2 diabetes mellitus (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Lenz-Majewski hyperostosis syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Worth disease |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Craniometadiaphyseal dysplasia wormian bone type (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |