| 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 | 
| Leigh syndrome with nephrotic syndrome (disorder) | Has interpretation | True | 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 | True | 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 | 
| Benign autosomal dominant osteopetrosis | 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 | 
| Generally contracted pelvis - delivered | 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 | 
| Outlet pelvic contraction - delivered | 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 |