Status: current. Date: 31-Jan 2002
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 356848015 | Loss of single peroxisomal function | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 626897019 | Loss of single peroxisomal function (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Loss of single peroxisomal function | Is a | Disorder of peroxisomal function | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| Loss of single peroxisomal function | Occurrence | Congenital | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Contiguous ABCD1 DXS1357E deletion syndrome (disorder) | Is a | True | Loss of single peroxisomal function | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly |
This concept is not in any reference sets
FHIR