Status: current, Defined. Date: 31-Jan 2015. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3029035014 | Gingival disease due to genetic disorder (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3029102018 | Gingival disease due to genetic defect | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3029171012 | Gingival disease due to genetic disorder | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Gingival disease due to genetic disorder | Due to | Hereditary disease | true | Inferred relationship | Some | 1 | |
| Gingival disease due to genetic disorder | Is a | Gingival disease | true | Inferred relationship | Some | ||
| Gingival disease due to genetic disorder | Finding site | Gingival structure | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Gingival enlargement due to Cowden syndrome | Is a | True | Gingival disease due to genetic disorder | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set