Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Non-progressive hereditary glomerulonephritis (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Macroalbuminuric nephropathy due to diabetes mellitus (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Goodpasture's syndrome |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Anti-glomerular basement membrane tubulointerstitial nephritis (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
3 |
Fibrillary glomerulonephritis |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Focal and segmental glomerulosclerosis in association with long-term treatment with lithium carbonate, after exclusion of alternative causes. |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Focal AND segmental proliferative glomerulonephritis |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Vasculitis with glomerulonephritis |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
2 |
Anti-glomerular basement membrane disease (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular fibrosis (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
A primary glomerular disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerulopathy with giant fibrillar deposits (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerulopathy with fibronectin deposits 2 (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
A rare, secondary glomerular disease characterized by proteinuria, dysproteinemias, nephrotic syndrome, and nodular glomerulopathy leading to renal failure, with or without extra-renal manifestations. The renal biopsy shows typical deposits of monoclonal immunoglobulins that do not show a fibrillar organization and are negative for Congo red staining. Associated signs and symptoms depend on the involvement of other organs, liver, heart, nerve fibers, gastrointestinal tract, or skin. |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Pulmonic stenosis and congenital nephrosis |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
2 |
Glomerular disease due to infectious disease (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disease due to parasitic disease (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disease due to Fabry disease |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disorder due to haemolytic uraemic syndrome |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disorder due to thrombotic thrombocytopenic purpura |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
An extremely rare syndromic lymphedema disorder characterized by early-onset hypotrichosis, childhood-onset lymphedema, and variable telangiectasia, particularly of the palms. |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
4 |
Glomerular disease due to neoplastic disease |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disease due to mitochondrial cytopathy |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disease due to Finnish type congenital nephrotic syndrome |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disease due to hematological disease |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disease due to familial hematuria |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disease due to thin basement membrane nephropathy |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Disorder of glomerulus due to double heterozygous sickling disorder (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Disorder of glomerulus due to sickle cell trait (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Idiopathic nodular glomerulosclerosis |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Secondary glomerular disease |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disease due to Alport syndrome |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Nodular glomerulosclerosis due to heavy chain deposition disease |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disease due to action myoclonus renal failure syndrome |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disease due to diffuse mesangial sclerosis |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disease due to familial disease |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disease due to coagulation disorder |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disease due to complement system disorder |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Acute exudative glomerulonephritis (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Exudative glomerulonephritis (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disorder due to infection caused by Schistosoma |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Disorder of glomerulus due to infection caused by Strongyloides (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
A rare disorder with multisystemic involvement and glomerulopathy characterized by progressive steroid-resistant nephrotic syndrome typically associated with focal segmental glomerulosclerosis, as well as primary adrenal insufficiency with adrenal calcifications. Age of onset and disease course are variable, with some cases presenting as severe fetal hydrops, while most patients present in infancy or early childhood and progress to end-stage renal disease within a few years. Additional features include ichthyosis, primary hypothyroidism, hypogonadism, immunodeficiency, and neurological manifestations (such as cognitive impairment, ataxia, sensorineural hearing loss, or seizures). |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
4 |
Glomerular disorder due to amyloidosis |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disorder due to secondary systemic amyloidosis |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disorder due to neuropathic heredofamilial amyloidosis |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Glomerular disorder due to organ-limited amyloidosis |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Transplant glomerulopathy |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
3 |
Transplant glomerulopathy - early form |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
3 |
Transplant glomerulopathy - late form |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
3 |
A rare multiple congenital anomalies/dysmorphic syndrome characterized by profound intellectual disability, choreoathetosis, progressive spastic diplegia, progressive tapetoretinal degeneration with loss of retinal vessels, and glomerulopathy resulting in death late in the first or early in the second decade of life. Absence of the cerebellar granular layer has been reported. There have been no further descriptions in the literature since 1982. |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
7 |
Diffuse proliferative glomerulonephritis (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Recurrent glomerulonephritis following transplantation of kidney (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Hypoxic nephrosis |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
3 |
A rare, idiopathic nephrotic syndrome characterized by the triad of proteinuria, hypoalbuminemia and edema in patients who do not respond, or only partially respond, to the initial trial of corticosteroids. Patients may be multidrug resistant or may be sensitive to second-line immunosuppressive therapy. |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
4 |
A rare idiopathic glomerular clinical syndrome characterized by diffuse renal lesions that are indistinguishable from the lesions observed in systemic lupus erythematosus (SLE) in the absence of circulating autoantibodies and other systemic features necessary to meet the classification criteria for SLE. Patients may present with nephrotic syndrome, abnormal urinary sediment, acute renal insufficiency, progressive glomerulonephritis, and hypertension. Some patients have been reported to develop a progression to SLE over time. |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
A rare, idiopathic nephrotic syndrome characterized by pediatric onset of proteinuria, hypoalbuminemia and edema. Patients respond successfully to the initial standard course of corticosteroids but are resistant to standard therapy for a subsequent relapse and following this relapse remain steroid-resistant. |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
2 |
Disorder of glomerulus caused by Plasmodium malariae (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Focal segmental glomerulosclerosis caused by substance |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Focal segmental glomerulosclerosis with infectious disease (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
A rare non-amyloid monoclonal immunoglobulin deposition disease characterized by production of monoclonal immunoglobulins with truncated heavy chains and no detectable light chains, which are deposited in tissues and cause organ dysfunction, but do not form amyloid beta-pleated sheets or contain an amyloid P component. The condition frequently occurs in association with multiple myeloma. Patients most commonly present with renal involvement (manifesting as hypertension, progressive renal dysfunction, anemia, and nephrotic syndrome with microhematuria), but other organs (such as the liver or skin) may also be affected. Production of IgG1 or IgG3 isotypes results in hypercomplementemia. |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
5 |
Familial interstitial nephritis |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
3 |
Multiple cysts of glomerulus of kidney (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Nephrotic syndrome in amyloidosis |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
3 |
Steroid sensitive nephrotic syndrome of childhood (disorder) |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
1 |
Minimal change nephrotic syndrome |
Finding site |
True |
Glomerulus structure |
Inferred relationship |
Some |
3 |