Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 356842019 | General loss of peroxisomal function | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 626891018 | General loss of peroxisomal function (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| General loss of peroxisomal function | Is a | Disorder of peroxisomal function | true | Inferred relationship | Existential restriction modifier | ||
| General loss of peroxisomal function | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| General loss of peroxisomal function | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Neonatal adrenoleukodystrophy | Is a | False | General loss of peroxisomal function | Inferred relationship | Existential restriction modifier | |
| Infantile Refsum's disease | Is a | False | General loss of peroxisomal function | Inferred relationship | Existential restriction modifier | |
| Alpha-methylacyl-CoA racemase deficiency disorder | Is a | True | General loss of peroxisomal function | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR