Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 356845017 | Loss of multiple peroxisomal functions | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 626894014 | Loss of multiple peroxisomal functions (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Loss of multiple peroxisomal functions | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Loss of multiple peroxisomal functions | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Loss of multiple peroxisomal functions | Is a | Disorder of peroxisomal function | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Rhizomelic chondrodysplasia punctata syndrome | Is a | True | Loss of multiple peroxisomal functions | Inferred relationship | Some | |
| Zellweger's-like syndrome | Is a | True | Loss of multiple peroxisomal functions | Inferred relationship | Some | |
| Pseudoinfantile Refsum's disease | Is a | True | Loss of multiple peroxisomal functions | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR