Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2023. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 350249011 | Defect of diaphragm | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 621971011 | Defect of diaphragm (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2118621000005117 | diaphragmadefekt | 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 |
| diaphragmadefekt | Is a | Disorder of diaphragm (disorder) | false | Inferred relationship | Some | ||
| diaphragmadefekt | Finding site | Diaphragm structure | false | Inferred relationship | Some | ||
| diaphragmadefekt | Finding site | Entire body wall | false | Inferred relationship | Some | ||
| diaphragmadefekt | Finding site | Body wall structure | false | Inferred relationship | Some | ||
| diaphragmadefekt | Is a | Lesion of soft tissue (disorder) | false | Inferred relationship | Some | ||
| diaphragmadefekt | Associated morphology | Defekt | false | Inferred relationship | Some | 1 | |
| diaphragmadefekt | Finding site | Diaphragm structure | false | Inferred relationship | Some | 1 | |
| diaphragmadefekt | Is a | Lesion of skeletal muscle (disorder) | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Congenital eventration of diaphragm | Is a | False | diaphragmadefekt | Inferred relationship | Some | |
| Diaphragmatic hernia | Is a | False | diaphragmadefekt | Inferred relationship | Some | |
| Congenital absence of diaphragm | Is a | False | diaphragmadefekt | Inferred relationship | Some | |
| Aplasia of diaphragm (disorder) | Is a | False | diaphragmadefekt | Inferred relationship | Some | |
| A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by diaphragmatic hernia, lung hypoplasia, ossification defect of the skull, and severe limb hypoplasia. Other clinical features may include, syndactyly, clinodactyly, extra spleen, absence of the femur or pelvic bone, partial intestinal malrotation, omphalocele and testicular atrophy. | Is a | False | diaphragmadefekt | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)
FHIR