Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3331711016 | Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3331712011 | Congenital nephrotic syndrome due to diffuse mesangial sclerosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3331713018 | Congenital nephrotic syndrome (CNS) due to diffuse mesangial sclerosis | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3331714012 | Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) | est un(e) (attribut) | Hereditary nephropathy (disorder) | true | Inferred relationship | Some | ||
| Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) | est un(e) (attribut) | Congenital disease | true | Inferred relationship | Some | ||
| Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) | a pour interprétation (attribut) | au-dessus de l'étendue de référence | true | Inferred relationship | Some | 1 | |
| Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) | interprète (attribut) | Albumin measurement | true | Inferred relationship | Some | 3 | |
| Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) | interprète (attribut) | Measurement of protein in urine (procedure) | true | Inferred relationship | Some | 1 | |
| Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) | a pour interprétation (attribut) | au-dessous de l'étendue de référence | true | Inferred relationship | Some | 3 | |
| Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) | est un(e) (attribut) | Glomerular disease due to diffuse mesangial sclerosis | true | Inferred relationship | Some | ||
| Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) | Due to | Diffuse mesangial sclerosis | true | Inferred relationship | Some | 4 | |
| Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) | est un(e) (attribut) | Congenital nephrotic syndrome (disorder) | false | Inferred relationship | Some | ||
| Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) | est un(e) (attribut) | Nephrotic syndrome associated with another disorder (disorder) | true | Inferred relationship | Some | ||
| Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 2 | |
| Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) | localisation d'une constatation (attribut) | Glomerulus structure | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR