Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3330957018 | Idiopathic membranous glomerulonephritis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3330958011 | Idiopathic membranous glomerulonephritis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3330959015 | Idiopathic membranous nephropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5402835016 | 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. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402836015 | 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. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3330957018 | Idiopathic membranous glomerulonephritis (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3330957018 | Idiopathic membranous glomerulonephritis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3330958011 | Idiopathic membranous glomerulonephritis | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3330958011 | Idiopathic membranous glomerulonephritis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3330959015 | Idiopathic membranous nephropathy | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3330959015 | Idiopathic membranous nephropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3330779019 | Glomerulonephritis with electron dense deposits in the glomerular baseement membrane; after exclusion of membranous nephropathy caused by malignancy, systemic lupus erythematosus, drugs, or infection. Includes membranous nephropathy associated with autoantibodies to the phospholipase A2 receptor1. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3672999011 | Glomerulonephritis with electron dense deposits in the glomerular basement membrane; after exclusion of membranous nephropathy caused by malignancy, systemic lupus erythematosus, drugs, or infection. Includes membranous nephropathy associated with autoantibodies to the phospholipase A2 receptor1. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402835016 | 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. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402836015 | 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. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3416801001000119 | Glomerulonephritis, primäre membranöse | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5483421000241116 | glomérulonéphrite membraneuse idiopathique | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5483421000241116 | glomérulonéphrite membraneuse idiopathique | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3416801001000119 | Glomerulonephritis, primäre membranöse | 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 |
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. | Is a | Membranous glomerulonephritis | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
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. | Is a | Idiopathic glomerulonephritis | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
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. | Clinical course | Chronic (qualifier value) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
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. | Associated morphology | Chronic membranous inflammation (morphologic abnormality) | true | 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 | Glomerulus structure (body structure) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)