Status: current, Defined. Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1767880010 | Congenital hamartoma (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
1779241016 | Congenital hamartoma | en | Synonym | Active | Case insensitive | SNOMED CT core |
3005817015 | Congenital hamartosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
3005821010 | Hamartomatous disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
3005858010 | Hamartomatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital hamartoma | Pathological process | Pathological developmental process | false | Inferred relationship | Some | 1 | |
Congenital hamartoma | Is a | Hamartoma | true | Inferred relationship | Some | ||
Congenital hamartoma | Is a | Congenital disease | true | Inferred relationship | Some | ||
Congenital hamartoma | Occurrence | Congenital | false | Inferred relationship | Some | ||
Congenital hamartoma | Associated morphology | Hamartoma | false | Inferred relationship | Some | ||
Congenital hamartoma | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital hamartoma | Associated morphology | Hamartoma | true | Inferred relationship | Some | 1 | |
Congenital hamartoma | Is a | Congenital anomaly | false | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Neoplasm and/or hamartoma reference set
Problem/Diagnosis reference set