Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2004. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | 
| 412798014 | Congenital nephritis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 669517010 | Congenital nephritis (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Familial mesangial sclerosis | Is a | False | Congenital nephritis | Inferred relationship | Existential restriction modifier | |
| Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome | Is a | True | Congenital nephritis | Inferred relationship | Existential restriction modifier | |
| Dyschondrosteosis and nephritis syndrome | Is a | True | Congenital nephritis | Inferred relationship | Existential restriction modifier | |
| X-linked diffuse leiomyomatosis with Alport syndrome | Is a | True | Congenital nephritis | Inferred relationship | Existential restriction modifier | |
| Microcephalus, glomerulonephritis, marfanoid habitus syndrome | Is a | True | Congenital nephritis | Inferred relationship | Existential restriction modifier | |
| Deafness, nephritis, anorectal malformation syndrome | Is a | True | Congenital nephritis | Inferred relationship | Existential restriction modifier | 
This concept is not in any reference sets