Status: retired, Not 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 |
| 170406013 | Malformation defect spectrum | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 576971014 | Malformation defect spectrum (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1822661000005113 | Misdannelsesdefektspektrum | da | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Danish module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Misdannelsesdefektspektrum | Is a | Multiple kongenitte misdannelser | false | Inferred relationship | Some | ||
| Misdannelsesdefektspektrum | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Misdannelsesdefektspektrum | Associated morphology | Kongenit malformation | false | Inferred relationship | Some | ||
| Misdannelsesdefektspektrum | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
| Misdannelsesdefektspektrum | Is a | Congenital malformation syndrome (disorder) | false | Inferred relationship | Some | ||
| Misdannelsesdefektspektrum | Associated morphology | dysgenese | false | Inferred relationship | Some | 1 | |
| Misdannelsesdefektspektrum | Associated morphology | Morphologically abnormal structure | false | Inferred relationship | Some | 1 | |
| Misdannelsesdefektspektrum | Pathological process (attribute) | Pathological developmental process | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Facio-auriculo-vertebral spectrum (disorder) | Is a | False | Misdannelsesdefektspektrum | Inferred relationship | Some | |
| A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandible (hypoglossia, aglossia, micrognathia, glossopalatine ankylosis, cleft palate, and gingival anomalies). | Is a | False | Misdannelsesdefektspektrum | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)
FHIR