Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 356842019 | General loss of peroxisomal function | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 626891018 | General loss of peroxisomal function (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| General loss of peroxisomal function | Finding site | Body system structure | false | Inferred relationship | Some | ||
| General loss of peroxisomal function | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| General loss of peroxisomal function | Is a | Disorder of peroxisomal function | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Alpha-methylacyl-CoA racemase deficiency disorder | Is a | True | General loss of peroxisomal function | Inferred relationship | Some | |
| Neonatal adrenoleucodystrophy | Is a | False | General loss of peroxisomal function | Inferred relationship | Some | |
| Infantile Refsum's disease | Is a | False | General loss of peroxisomal function | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR