Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3288657017 | Hereditary nephropathy co-occurrent with membranoproliferative glomerulonephritis type III (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3288695010 | Hereditary nephropathy co-occurrent with membranoproliferative glomerulonephritis type III | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 12724231000172114 | maladie héréditaire du rein concomitante d'une néphrite glomérulaire membranoproliférative de type III | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 12724241000172119 | néphropathie héréditaire concomitante d'une glomérulonéphrite membranoproliférative de type III | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 12724251000172117 | affection rénale héréditaire concomitante d'une GN (glomérulonéphrite ) mésangiocapillaire de type III | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 4776421000172110 | erfelijke nierziekte gelijktijdig met mesangiocapillaire glomerulonefritis type III | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 4776431000172113 | hereditaire nefropathie gelijktijdig met MPGN type III | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 4776441000172118 | hereditaire nefropathie gelijktijdig met membranoproliferatieve glomerulonefritis type 3 | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary nephropathy co-occurrent with membranoproliferative glomerulonephritis type III (disorder) | Is a | Hereditary nephritis (disorder) | true | Inferred relationship | Some | ||
| Hereditary nephropathy co-occurrent with membranoproliferative glomerulonephritis type III (disorder) | Is a | Mesangiocapillary glomerulonephritis type III | true | Inferred relationship | Some | ||
| Hereditary nephropathy co-occurrent with membranoproliferative glomerulonephritis type III (disorder) | Clinical course | Chronic | true | Inferred relationship | Some | 1 | |
| Hereditary nephropathy co-occurrent with membranoproliferative glomerulonephritis type III (disorder) | Associated morphology | Chronic proliferative inflammation | true | Inferred relationship | Some | 2 | |
| Hereditary nephropathy co-occurrent with membranoproliferative glomerulonephritis type III (disorder) | Finding site | Structure of glomerular mesangium (body structure) | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR