Status: current, Defined. Date: 31-Jul 2004. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 412798014 | Congenital nephritis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 669517010 | Congenital nephritis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Familial mesangial sclerosis | Is a | False | Congenital nephritis | Inferred relationship | Some | |
| Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome | Is a | True | Congenital nephritis | Inferred relationship | Some | |
| Dyschondrosteosis and nephritis syndrome | Is a | True | Congenital nephritis | Inferred relationship | Some | |
| X-linked diffuse leiomyomatosis with Alport syndrome | Is a | True | Congenital nephritis | Inferred relationship | Some | |
| Microcephalus, glomerulonephritis, marfanoid habitus syndrome | Is a | True | Congenital nephritis | Inferred relationship | Some | |
| Lowe Kohn Cohen syndrome | Is a | True | Congenital nephritis | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set
REPLACED BY association reference set