| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Nephrotic syndrome co-occurrent and due to systemic lupus erythematosus (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| A rare, hereditary nephrotic syndrome characterized by proteinuria, hypoalbuminemia, edema, and hyperlipidemia, with an absence of response to an initial trial of corticosteroids (i.e. steroid-resistant nephrotic syndrome; SRNS) and a generally complicated course. |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Non-amyloid fibrillary glomerulopathy (non-amyloid FGP) is a rare cause of glomerulonephritis (GN) characterized by glomerular accumulation of non-amyloid fibrils in the mesangium and the glomerular (and rarely tubular) basement membrane, that mainly presents with renal insufficiency, micro-hematuria and nephrotic range proteinuria. Non-amyloid FGP and immunotactoid glomerulopathy are often grouped together as pathogenetically related diseases. |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Glomerulonephritis co-occurrent and due to scleroderma (disorder) |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
| Multi-drug resistant nephrotic syndrome (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Alport syndrome autosomal dominant |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Alport syndrome autosomal recessive |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Alport syndrome X-linked (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder) |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
| Glomerulonephritis co-occurrent and due to scleroderma (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| A rare hereditary motor and sensory neuropathy disorder characterized by the typical CMT phenotype (slowly progressive distal muscle weakness and atrophy in upper and lower limbs, distal sensory loss in extremities, reduced or absent deep tendon reflexes and foot deformities) associated with focal segmental glomerulosclerosis (manifesting with proteinuria and progression to end-stage renal disease). Mild or moderate sensorineural hearing loss may also be associated. Nerve biopsy reveals both axonal and demyelinating changes and nerve conduction velocities vary from the demyelinating to axonal range (typically between 25-50m/sec). |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Idiopathic glomerular disease (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Glomerulonephritis with electron dense deposits in the glomerular baseement membrane in a patient with cancer, after exclusion of other possible causes of membranous glomerulonephritis. |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Congenital nephrotic syndrome with evidence of an underlying congenital infection (e.g. syphilis, toxoplasmosis, rubella, hepatitis B). |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| A rare glomerular disease, histologically characterised by thickening of the capillary wall, with immune deposits predominantly containing IgG4 and C3 on the sub-epithelial side, and typically manifesting with nephrotic syndrome. |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Glomerulonephritis with electron dense deposits in the glomerular baseement membrane, associated with treatment with a drug known to be associated with membranous nephropathy and after exclusion of alternative causes. |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Focal and segmental glomerulosclerosis in association with long-term treatment with lithium carbonate, after exclusion of alternative causes. |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Focal segmental glomerulosclerosis due to sickle cell disease |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Membranous glomerulonephritis co-occurrent with infectious disease (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Galloway Mowat syndrome (disorder) |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Dyschondrosteose - Nephritis |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Galloway Mowat syndrome (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Glomerular disorder due to non-neuropathic heredofamilial amyloidosis (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Recurrent hematuria co-occurrent and due to dense deposit disease |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Recurrent hematuria co-occurrent and due to dense deposit disease |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Persistent hematuria co-occurrent and due to dense deposit disease (disorder) |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Persistent hematuria co-occurrent and due to dense deposit disease (disorder) |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Complement component 3 glomerulopathy (disorder) |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Complement component 3 glomerulopathy (disorder) |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits. |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits. |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Complement component 3 glomerulonephritis (disorder) |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Complement component 3 glomerulonephritis (disorder) |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| An extremely rare syndromic lymphedema disorder characterized by early-onset hypotrichosis, childhood-onset lymphedema, and variable telangiectasia, particularly of the palms. |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
| A rare primary glomerular disease characterized by the association of congenital nephrotic syndrome, early onset renal failure and ocular anomalies with microcoria and severe neurodevelopment deficits. |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| A rare primary glomerular disease characterized by the association of congenital nephrotic syndrome, early onset renal failure and ocular anomalies with microcoria and severe neurodevelopment deficits. |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Schimke immuno-osseous dysplasia |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
| Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Immunotactoid glomerulopathy (ITG) is a very rare condition characterized by glomerular accumulation of microtubules in the mesangium and the glomerular basement membrane, that mainly presents with proteinuria, micro-hematuria, nephrotic syndrome, renal insufficiency and hematologic malignancy. ITG and non-amyloid fibrillary glomerulopathy are often grouped together as pathogenetically related diseases. |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| X-linked diffuse leiomyomatosis with Alport syndrome |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Persistent proteinuria (finding) |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Microcephalus, glomerulonephritis, marfanoid habitus syndrome (disorder) |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Wegener's granulomatosis (disorder) |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Granulomatosis with polyangiitis of gingiva (disorder) |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Limited granulomatosis with polyangiitis |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Granulomatosis with polyangiitis with multisystem involvement (disorder) |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Granulomatosis with polyangiitis of nose |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Granulomatosis with polyangiitis of larynx |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Glomerulonephritis due to granulomatosis with polyangiitis |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
| Glomerulonephritis co-occurrent and due to antineutrophil cytoplasmic antibody positive vasculitis |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
| Persistent albuminuria (finding) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Cr51 EDTA clearance study |
Procedure site - Direct (attribute) |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Vasculitis with glomerulonephritis |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Alport syndrome (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Nephrotic syndrome in malaria |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| LAMB2-related infantile-onset nephrotic syndrome |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Microcephalus, glomerulonephritis, marfanoid habitus syndrome (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Schimke immuno-osseous dysplasia |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Dyschondrosteose - Nephritis |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| A rare hereditary motor and sensory neuropathy disorder characterized by the typical CMT phenotype (slowly progressive distal muscle weakness and atrophy in upper and lower limbs, distal sensory loss in extremities, reduced or absent deep tendon reflexes and foot deformities) associated with focal segmental glomerulosclerosis (manifesting with proteinuria and progression to end-stage renal disease). Mild or moderate sensorineural hearing loss may also be associated. Nerve biopsy reveals both axonal and demyelinating changes and nerve conduction velocities vary from the demyelinating to axonal range (typically between 25-50m/sec). |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Chronic nephritic syndrome |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Nephrotic-nephritic syndrome |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Chronic nephritic syndrome, minor glomerular abnormality (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Nephritic syndrome |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Glomerulonephritis with electron dense deposits in the glomerular baseement membrane, associated with treatment with a drug known to be associated with membranous nephropathy and after exclusion of alternative causes. |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Membranous glomerulonephritis - stage III |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Complement component 3 glomerulonephritis (disorder) |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits. |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Complement component 3 glomerulopathy (disorder) |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Acute glomerulonephritis (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Microalbuminuric diabetic nephropathy |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Microalbuminuria due to type 1 diabetes mellitus |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Persistent microalbuminuria due to type 2 diabetes mellitus (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Microalbuminuria due to type 2 diabetes mellitus (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Proteinuric nephropathy due to diabetes mellitus (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Recurrent hematuria co-occurrent and due to dense deposit disease |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Persistent hematuria co-occurrent and due to dense deposit disease (disorder) |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Persistent microalbuminuria due to type 1 diabetes mellitus (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Proteinuria due to type 1 diabetes mellitus (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Glomerulopathy due to diabetes mellitus (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Familial steroid-resistant nephrotic syndrome with sensorineural deafness (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Persistent proteinuria due to type 1 diabetes mellitus (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Acute nephrotic syndrome (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Acute glomerulonephritis associated with another disorder (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Proteinuria due to type 2 diabetes mellitus |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Persistent proteinuria due to type 2 diabetes mellitus (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
| Leigh-Syndrom mit nephrotischem Syndrom |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
| Subacute glomerulonephritis (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Immune-complex glomerulonephritis |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Glomerulonephritis co-occurrent and due to antineutrophil cytoplasmic antibody positive vasculitis |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
| Glomerulitis (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Chronic nephritic syndrome |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
| Goodpasture's disease |
Finding site |
False |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Mesangial proliferative glomerulonephritis |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Glomerulonephritis |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
| Nephrotic-nephritic syndrome |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
| Non-progressive hereditary glomerulonephritis (disorder) |
Finding site |
True |
Glomerulus structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
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