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68288006: Glomerulus structure (body structure)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
113433013 Glomerulus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
500979011 Glomerulus structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
808106015 Glomerulus structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


23 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Glomerulus structure Is a Renal corpuscle structure true Inferred relationship Some
Glomerulus structure partie de Entire renal corpuscle false Additional relationship Some
Glomerulus structure Laterality Side (qualifier value) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Nephrotic syndrome co-occurrent and due to systemic lupus erythematosus (disorder) Finding site True Glomerulus structure Inferred relationship Some 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 Inferred relationship Some 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 Inferred relationship Some 1
Glomerulonephritis co-occurrent and due to scleroderma (disorder) Finding site False Glomerulus structure Inferred relationship Some 5
Multi-drug resistant nephrotic syndrome (disorder) Finding site True Glomerulus structure Inferred relationship Some 3
Alport syndrome autosomal dominant (disorder) Finding site True Glomerulus structure Inferred relationship Some 1
Alport syndrome autosomal recessive (disorder) Finding site True Glomerulus structure Inferred relationship Some 1
Alport syndrome X-linked (disorder) Finding site True Glomerulus structure Inferred relationship Some 1
A rare constitutional hemolytic anemia that is characterized by the association of Alport syndrome, midface hypoplasia, intellectual deficit and elliptocytosis. It has been described in two families. The syndrome is transmitted as an X-linked trait is caused by a contiguous gene deletion in Xq22.3 involving several genes including COL4A5, FACL4 and AMMECR1. Finding site False Glomerulus structure Inferred relationship Some 6
Glomerulonephritis co-occurrent and due to scleroderma (disorder) Finding site True Glomerulus structure Inferred relationship Some 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 Inferred relationship Some 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 Inferred relationship Some 2
Idiopathic glomerular disease (disorder) Finding site True Glomerulus structure Inferred relationship Some 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 Inferred relationship Some 4
Congenital nephrotic syndrome with evidence of an underlying congenital infection (e.g. syphilis, toxoplasmosis, rubella, hepatitis B). Finding site True Glomerulus structure Inferred relationship Some 2
A rare glomerular disease, histologically characterized 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 Inferred relationship Some 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 Inferred relationship Some 3
Focal and segmental glomerulosclerosis in association with long-term treatment with lithium carbonate, after exclusion of alternative causes. Finding site False Glomerulus structure Inferred relationship Some 3
Focal and segmental glomerulosclerosis in a patient with sickle cell disease. Finding site True Glomerulus structure Inferred relationship Some 3
Glomerulonephritis with electron dense deposits in the glomerular baseement membrane, associated with an infection known to cause membranous nephropath and after exclusion of alternative causes. Finding site True Glomerulus structure Inferred relationship Some 3
A rare, genetic multisystem disorder characterized by a neurodegenerative disorder associating global developmental delay, progressive microcephaly, and progressive cerebral and cerebellar atrophy with extrapyramidal involvement, progressive optic atrophy, and in many patients early-onset steroid-resistant nephrotic syndrome. Finding site False Glomerulus structure Inferred relationship Some 3
syndrome de dyschondrostéose - néphropathie Finding site False Glomerulus structure Inferred relationship Some 3
A rare, genetic multisystem disorder characterized by a neurodegenerative disorder associating global developmental delay, progressive microcephaly, and progressive cerebral and cerebellar atrophy with extrapyramidal involvement, progressive optic atrophy, and in many patients early-onset steroid-resistant nephrotic syndrome. Finding site True Glomerulus structure Inferred relationship Some 2
Glomerular disorder due to non-neuropathic heredofamilial amyloidosis (disorder) Finding site True Glomerulus structure Inferred relationship Some 1
Recurrent hematuria co-occurrent and due to dense deposit disease (disorder) Finding site False Glomerulus structure Inferred relationship Some 1
Recurrent hematuria co-occurrent and due to dense deposit disease (disorder) Finding site False Glomerulus structure Inferred relationship Some 2
Persistent hematuria co-occurrent and due to dense deposit disease (disorder) Finding site False Glomerulus structure Inferred relationship Some 1
Persistent hematuria co-occurrent and due to dense deposit disease (disorder) Finding site False Glomerulus structure Inferred relationship Some 2
Complement component 3 glomerulopathy (disorder) Finding site False Glomerulus structure Inferred relationship Some 3
Complement component 3 glomerulopathy (disorder) Finding site False Glomerulus structure Inferred relationship Some 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 Inferred relationship Some 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 Inferred relationship Some 4
Complement component 3 glomerulonephritis (disorder) Finding site False Glomerulus structure Inferred relationship Some 3
Complement component 3 glomerulonephritis (disorder) Finding site False Glomerulus structure Inferred relationship Some 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 Inferred relationship Some 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 Inferred relationship Some 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 Inferred relationship Some 3
A rare a multisystem disorder characterized by spondyloepiphyseal dysplasia and disproportionate short stature, facial dysmorphism, T-cell immunodeficiency, and progressive, proteinuric steroid-resistant nephropathy. Finding site False Glomerulus structure Inferred relationship Some 5
A rare, congenital glomerular disease due to maternal anti-neutral endopeptidase (NEP) alloimmunization characterized by severe renal failure and nephrotic syndrome at birth, which rapidly improves in the first weeks of life. Finding site True Glomerulus structure Inferred relationship Some 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 Inferred relationship Some 1
A rare renal disease characterized by the association of X-linked Alport syndrome (glomerular nephropathy, sensorineural deafness and ocular anomalies) and benign proliferation of visceral smooth muscle cells along the gastrointestinal, respiratory, and female genital tracts and clinically manifests with dysphagia, dyspnea, cough, stridor, postprandial vomiting, retrosternal or epigastric pain, recurrent pneumonia, and clitoral hypertrophy in females. Finding site True Glomerulus structure Inferred relationship Some 3
Persistent proteinuria (finding) Finding site False Glomerulus structure Inferred relationship Some 2
A rare intellectual disability syndrome characterized by intellectual deficit, marfanoid habitus, microcephaly, and glomerulonephritis. There have been no further reports since 1992. Finding site False Glomerulus structure Inferred relationship Some 4
Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome Finding site True Glomerulus structure Inferred relationship Some 3
Granulomatosis with polyangiitis Finding site False Glomerulus structure Inferred relationship Some 3
Granulomatosis with polyangiitis of gingiva Finding site False Glomerulus structure Inferred relationship Some 3
Limited granulomatosis with polyangiitis Finding site False Glomerulus structure Inferred relationship Some 3
Granulomatosis with polyangiitis with multisystem involvement Finding site False Glomerulus structure Inferred relationship Some 3
Granulomatosis with polyangiitis of nose Finding site False Glomerulus structure Inferred relationship Some 4
Granulomatosis with polyangiitis of larynx Finding site False Glomerulus structure Inferred relationship Some 4
Glomerulonephritis due to granulomatosis with polyangiitis Finding site False Glomerulus structure Inferred relationship Some 5
Glomerulonephritis co-occurrent and due to antineutrophil cytoplasmic antibody positive vasculitis (disorder) Finding site False Glomerulus structure Inferred relationship Some 5
Persistent albuminuria (finding) Finding site True Glomerulus structure Inferred relationship Some 1
Cr51 EDTA clearance study Procedure site - Direct (attribute) True Glomerulus structure Inferred relationship Some 1
Vasculitis with glomerulonephritis Finding site False Glomerulus structure Inferred relationship Some 1
A rare renal disease characterized by glomerular nephropathy with hematuria progressing to end-stage renal disease (ESRD), frequently associated with sensorineural deafness, and occasionally with ocular anomalies. Finding site True Glomerulus structure Inferred relationship Some 1
Nephrotic syndrome in malaria Finding site True Glomerulus structure Inferred relationship Some 1
LAMB2-related infantile-onset nephrotic syndrome Finding site True Glomerulus structure Inferred relationship Some 1
A rare intellectual disability syndrome characterized by intellectual deficit, marfanoid habitus, microcephaly, and glomerulonephritis. There have been no further reports since 1992. Finding site True Glomerulus structure Inferred relationship Some 2
A rare a multisystem disorder characterized by spondyloepiphyseal dysplasia and disproportionate short stature, facial dysmorphism, T-cell immunodeficiency, and progressive, proteinuric steroid-resistant nephropathy. Finding site True Glomerulus structure Inferred relationship Some 2
syndrome de dyschondrostéose - néphropathie Finding site False Glomerulus structure Inferred relationship Some 1
A rare constitutional hemolytic anemia that is characterized by the association of Alport syndrome, midface hypoplasia, intellectual deficit and elliptocytosis. It has been described in two families. The syndrome is transmitted as an X-linked trait is caused by a contiguous gene deletion in Xq22.3 involving several genes including COL4A5, FACL4 and AMMECR1. Finding site True Glomerulus structure Inferred relationship Some 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 Inferred relationship Some 2
A rare, genetic, renal disease characterized by hereditary nephritis leading to nephrotic syndrome and end-stage renal failure associated with sensorineural hearing loss and pretibial skin blistering followed by atrophy. Other reported manifestations include bilateral lacrimal duct stenosis, dystrophic teeth and nails, bilateral cervical ribs, unilateral kidney, distal vaginal agenesis and anemia due to beta-thalassemia minor. Finding site True Glomerulus structure Inferred relationship Some 1
Chronic nephritic syndrome Finding site False Glomerulus structure Inferred relationship Some 1
Nephrotic-nephritic syndrome Finding site False Glomerulus structure Inferred relationship Some 3
Chronic nephritic syndrome, minor glomerular abnormality Finding site True Glomerulus structure Inferred relationship Some 1
Nephritic syndrome Finding site True Glomerulus structure Inferred relationship Some 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 Inferred relationship Some 1
Membranous glomerulonephritis - stage III Finding site True Glomerulus structure Inferred relationship Some 1
Complement component 3 glomerulonephritis (disorder) Finding site False Glomerulus structure Inferred relationship Some 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 Inferred relationship Some 1
Complement component 3 glomerulopathy (disorder) Finding site False Glomerulus structure Inferred relationship Some 1
Acute glomerulonephritis Finding site True Glomerulus structure Inferred relationship Some 1
Microalbuminuric diabetic nephropathy Finding site True Glomerulus structure Inferred relationship Some 1
Microalbuminuria due to type 1 diabetes mellitus Finding site True Glomerulus structure Inferred relationship Some 2
Persistent microalbuminuria due to type 2 diabetes mellitus (disorder) Finding site True Glomerulus structure Inferred relationship Some 3
Microalbuminuria due to type 2 diabetes mellitus (disorder) Finding site True Glomerulus structure Inferred relationship Some 2
Proteinuric nephropathy due to diabetes mellitus (disorder) Finding site True Glomerulus structure Inferred relationship Some 1
Recurrent hematuria co-occurrent and due to dense deposit disease (disorder) Finding site False Glomerulus structure Inferred relationship Some 4
Persistent hematuria co-occurrent and due to dense deposit disease (disorder) Finding site False Glomerulus structure Inferred relationship Some 4
Persistent microalbuminuria due to type 1 diabetes mellitus (disorder) Finding site True Glomerulus structure Inferred relationship Some 3
Proteinuria due to type 1 diabetes mellitus (disorder) Finding site True Glomerulus structure Inferred relationship Some 2
Glomerulopathy due to diabetes mellitus (disorder) Finding site True Glomerulus structure Inferred relationship Some 1
A rare, genetic coenzyme Q10 deficiency characterized by sensorineural deafness and severe, progressive nephrotic syndrome not responding to steroid treatment. Clinical manifestations include early onset proteinuria, hypoalbuminemia and edema, leading to end-stage renal disease. The renal biopsy reveals focal segmental glomerulosclerosis and diffuse mesangial sclerosis. Rarely, seizures, ataxia and dysmorphic features have been described. Finding site True Glomerulus structure Inferred relationship Some 3
Persistent proteinuria due to type 1 diabetes mellitus (disorder) Finding site True Glomerulus structure Inferred relationship Some 3
Acute nephrotic syndrome (disorder) Finding site True Glomerulus structure Inferred relationship Some 4
Acute glomerulonephritis associated with another disorder (disorder) Finding site True Glomerulus structure Inferred relationship Some 3
Proteinuria due to type 2 diabetes mellitus Finding site True Glomerulus structure Inferred relationship Some 2
Persistent proteinuria due to type 2 diabetes mellitus (disorder) Finding site True Glomerulus structure Inferred relationship Some 3
Leigh-Syndrom mit nephrotischem Syndrom Finding site False Glomerulus structure Inferred relationship Some 5
Subacute glomerulonephritis Finding site True Glomerulus structure Inferred relationship Some 1
Immune-complex glomerulonephritis Finding site True Glomerulus structure Inferred relationship Some 1
Glomerulonephritis co-occurrent and due to antineutrophil cytoplasmic antibody positive vasculitis (disorder) Finding site True Glomerulus structure Inferred relationship Some 2
Glomerulitis Finding site True Glomerulus structure Inferred relationship Some 1
Chronic nephritic syndrome Finding site True Glomerulus structure Inferred relationship Some 4
Goodpasture's disease Finding site False Glomerulus structure Inferred relationship Some 1
Mesangial proliferative glomerulonephritis Finding site True Glomerulus structure Inferred relationship Some 1
Glomerulonephritis Finding site True Glomerulus structure Inferred relationship Some 1
Nephrotic-nephritic syndrome Finding site True Glomerulus structure Inferred relationship Some 5
Non-progressive hereditary glomerulonephritis (disorder) Finding site True Glomerulus structure Inferred relationship Some 1

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Reference Sets

Lateralizable body structure reference set (foundation metadata concept)

Anatomy structure and entire association reference set (foundation metadata concept)

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