Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Nephrotic syndrome, diffuse mesangial proliferative glomerulonephritis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Nephrotic syndrome with proliferative glomerulonephritis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Nephrotic syndrome with membranous glomerulonephritis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Congenital nephrotic syndrome due to congenital infection |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Nephrotic syndrome with membranoproliferative glomerulonephritis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
4 |
Steroid-sensitive nephrotic syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Steroid-resistant nephrotic syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Nephrotic syndrome, minor glomerular abnormality |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Steroid-dependent nephrotic syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Nephrotic syndrome, diffuse membranous glomerulonephritis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Congenital nephrotic syndrome with focal glomerulosclerosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
1 |
Drash syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Nephrotic syndrome, diffuse endocapillary proliferative glomerulonephritis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Nephrotic syndrome due to type 2 diabetes mellitus |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Nephrotic syndrome, diffuse mesangiocapillary glomerulonephritis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Nephrotic syndrome in amyloidosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Nephrotic syndrome, diffuse crescentic glomerulonephritis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Finnish congenital nephrotic syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Nephrotic syndrome associated with another disorder |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Genetic steroid-resistant nephrotic syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Nephrotic syndrome due to diabetes mellitus |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Nephrotic syndrome in malaria |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Sporadic idiopathic steroid-resistant nephrotic syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Nephrotic syndrome in polyarteritis nodosa |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
4 |
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Hereditary cryohydrocytosis with reduced stomatin |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Hereditary cryohydrocytosis with reduced stomatin |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive severe congenital neutropenia due to glucose-6-phosphatase catalytic subunit 3 deficiency |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
1 |
Leigh syndrome with nephrotic syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Pancytopenia due to IKAROS family zinc finger 1 mutations |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
1 |
Pancytopenia due to IKAROS family zinc finger 1 mutations |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Pancytopenia due to IKAROS family zinc finger 1 mutations |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Pancytopenia due to IKAROS family zinc finger 1 mutations |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive severe congenital neutropenia due to colony stimulating factor 3 receptor deficiency |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive severe congenital neutropenia due to jagunal homolog 1 deficiency |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
1 |
Bleeding diathesis due to thromboxane synthesis deficiency |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive severe congenital neutropenia due to C-X-C motif chemokine receptor 2 deficiency |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
1 |
Hereditary thrombocytopenia with normal platelets |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
1 |
Hereditary isolated aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Hereditary isolated aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
5 |
Hereditary isolated aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
4 |
Hereditary isolated aplastic anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Osteopetrosis - intermediate type |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal dominant osteopetrosis type 2 |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Osteopetrosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Osteopenia, intellectual disability, sparse hair syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
4 |
Infantile osteopetrosis with neuroaxonal dysplasia syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Juvenile idiopathic generalized osteoporosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Spondyloocular syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Dysplasia with decreased bone density |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Transient infantile osteopetrosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
X-linked osteoporosis with fractures |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Infantile malignant osteopetrosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
X-linked calvarial hyperostosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Doughnut lesion of calvaria and bone fragility syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Benign autosomal dominant osteopetrosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Skeletal dysplasia with wormian bone, multiple fractures, dentinogenesis imperfecta syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Osteopetrosis with renal tubular acidosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Singleton-Merten syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Osteopetrosis - delayed type |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Menkes kinky-hair syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Osteoporosis and oculocutaneous hypopigmentation syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
4 |
Autosomal recessive cutis laxa type 2B |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
4 |
Familial steroid-resistant nephrotic syndrome with sensorineural deafness |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
1 |
Chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and neutrophilic dermatosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
4 |
Chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and neutrophilic dermatosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
5 |
Adult chronic idiopathic neutropenia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
1 |
Acute nephrotic syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
1 |
Neutropenic sepsis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Pancytopenia caused by immunosuppressant |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Pancytopenia caused by immunosuppressant |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
1 |
Pancytopenia caused by immunosuppressant |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
4 |
Pancytopenia caused by immunosuppressant |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Loss of hypoglycemic warning due to diabetes mellitus |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
1 |
Post hypoglycemic hyperglycemia due to diabetes mellitus |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Existential restriction modifier |
1 |
Hypoglycemic unawareness due to type 1 diabetes mellitus |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
1 |
Nocturnal hypoglycemia due to diabetes mellitus |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
1 |
Hypoglycemia due to diabetes mellitus |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
1 |
Midpelvic contraction |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Contracted pelvis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Generally contracted pelvis - delivered |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Generally contracted pelvis with antenatal problem |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Inlet contraction of pelvis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Outlet pelvic contraction with antenatal problem |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Congenital contracted pelvis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Outlet pelvic contraction - delivered |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Geroderma osteodysplastica |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Hyperphosphatasemia tarda |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
4 |
Pyknodysostosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Sclerosteosis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Outlet contraction of pelvis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Hypoglycemia unawareness due to type 2 diabetes mellitus |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
2 |
Endosteal hyperostoses |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Endosteal hyperostoses with cerebellar hypoplasia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Insulin reactive hypoglycemia due to type 2 diabetes mellitus |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Lenz-Majewski hyperostosis syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Worth disease |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Craniometadiaphyseal dysplasia wormian bone type |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
3 |
Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Existential restriction modifier |
5 |