Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1770706011 | Inherited pseudoxanthoma elasticum (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1781876017 | Inherited pseudoxanthoma elasticum | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Inherited pseudoxanthoma elasticum (disorder) | Is a | Pseudoxanthoma elasticum | true | Inferred relationship | Some | ||
| Inherited pseudoxanthoma elasticum (disorder) | Finding site | Connective tissue structure | false | Inferred relationship | Some | 1 | |
| Inherited pseudoxanthoma elasticum (disorder) | Associated morphology | Degeneration | false | Inferred relationship | Some | 1 | |
| Inherited pseudoxanthoma elasticum (disorder) | Finding site | Connective tissue structure | true | Inferred relationship | Some | 1 | |
| Inherited pseudoxanthoma elasticum (disorder) | Associated morphology | Degeneration | false | Inferred relationship | Some | 1 | |
| Inherited pseudoxanthoma elasticum (disorder) | Is a | Connective tissue hereditary disorder (disorder) | true | Inferred relationship | Some | ||
| Inherited pseudoxanthoma elasticum (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Autosomal dominant pseudoxanthoma elasticum (disorder) | Is a | True | Inherited pseudoxanthoma elasticum (disorder) | Inferred relationship | Some | |
| Autosomal recessive pseudoxanthoma elasticum (disorder) | Is a | True | Inherited pseudoxanthoma elasticum (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR