Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3448005019 | Immunotactoid glomerulonephritis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3448006018 | Immunotactoid glomerulonephritis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5403529016 | 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. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403530014 | Immunotactoid glomerulopathy (ITG) is a very rare condition characterised by glomerular accumulation of microtubules in the mesangium and the glomerular basement membrane, that mainly presents with proteinuria, micro-haematuria, nephrotic syndrome, renal insufficiency and haematologic malignancy. ITG and non-amyloid fibrillary glomerulopathy are often grouped together as pathogenetically related diseases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3448005019 | Immunotactoid glomerulonephritis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3448006018 | Immunotactoid glomerulonephritis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3448007010 | 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. Etiopathology is unknown. It may arise spontaneously or be associated with lymphoproliferative disorders, hepatitis C virus infection, leukocytoclastic vasculitis and hypocomplementemia. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3448008017 | A very rare condition characterised by glomerular accumulation of microtubules in the mesangium and the glomerular basement membrane, that mainly presents with proteinuria, micro-haematuria, nephrotic syndrome, renal insufficiency and haematologic malignancy. Aetiopathology is unknown. It may arise spontaneously or be associated with lymphoproliferative disorders, hepatitis C virus infection, leucocytoclastic vasculitis and hypocomplementaemia. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403529016 | 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. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403530014 | Immunotactoid glomerulopathy (ITG) is a very rare condition characterised by glomerular accumulation of microtubules in the mesangium and the glomerular basement membrane, that mainly presents with proteinuria, micro-haematuria, nephrotic syndrome, renal insufficiency and haematologic malignancy. ITG and non-amyloid fibrillary glomerulopathy are often grouped together as pathogenetically related diseases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3440061001000116 | Glomerulopathie, immunotaktoide | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6276641000241113 | GN (glomérulonéphrite) immunotactoïde | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6276651000241111 | néphrite glomérulaire immunotactoïde | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6276661000241114 | glomérulonéphrite immunotactoïde | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6276641000241113 | GN (glomérulonéphrite) immunotactoïde | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6276651000241111 | néphrite glomérulaire immunotactoïde | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6276661000241114 | glomérulonéphrite immunotactoïde | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3440061001000116 | Glomerulopathie, immunotaktoide | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
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. | Is a | Glomerulonephritis | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
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. | Associated morphology | inflammation | false | 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 | Glomerulus structure (body structure) | true | 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. | Associated morphology | Inflammatory morphology (morphologic abnormality) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)