Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 358178018 | Familial multiple tumor syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 358179014 | Familial multiple tumour syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 627960017 | Familial multiple tumor syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2454541000052117 | familjärt multipelt tumörsyndrom | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| familjärt multipelt tumörsyndrom | Is a | Genodermatosis | false | Inferred relationship | Some | ||
| familjärt multipelt tumörsyndrom | Occurrence | Congenital | false | Inferred relationship | Some | ||
| familjärt multipelt tumörsyndrom | Finding site | Skin structure | false | Inferred relationship | Some | ||
| familjärt multipelt tumörsyndrom | Is a | Familial neoplastic disease | false | Inferred relationship | Some | ||
| familjärt multipelt tumörsyndrom | Associated morphology | kongenital anomali | false | Inferred relationship | Some | ||
| familjärt multipelt tumörsyndrom | Associated morphology | Neoplasm | false | Inferred relationship | Some | ||
| familjärt multipelt tumörsyndrom | Is a | Hereditary cancer-predisposing syndrome | false | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)
FHIR