Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 359685013 | Myopathy with abnormality of histochemical fibre type | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 359686014 | Myopathy with abnormality of histochemical fiber type | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 629176019 | Myopathy with abnormality of histochemical fiber type (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Myopathy with abnormality of histochemical fibre type | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Myopathy with abnormality of histochemical fibre type | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
| Myopathy with abnormality of histochemical fibre type | Is a | Congenital anomaly of skeletal muscle | true | Inferred relationship | Some | ||
| Myopathy with abnormality of histochemical fibre type | Finding site | Skeletal muscle system structure | false | Inferred relationship | Some | ||
| Myopathy with abnormality of histochemical fibre type | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | 1 | |
| Myopathy with abnormality of histochemical fibre type | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Myopathy with abnormality of histochemical fibre type | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | 1 | |
| Myopathy with abnormality of histochemical fibre type | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | 1 | |
| Myopathy with abnormality of histochemical fibre type | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
| Myopathy with abnormality of histochemical fibre type | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 2 | |
| Myopathy with abnormality of histochemical fibre type | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | 2 | |
| Myopathy with abnormality of histochemical fibre type | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 1 | |
| Myopathy with abnormality of histochemical fibre type | Is a | Congenital myopathy | false | Inferred relationship | Some | ||
| Myopathy with abnormality of histochemical fibre type | Occurrence | Congenital | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Congenital myopathy with reduced type 2 muscle fibres | Is a | True | Myopathy with abnormality of histochemical fibre type | Inferred relationship | Some | |
| Myopathy with type I hypotrophy | Is a | True | Myopathy with abnormality of histochemical fibre type | Inferred relationship | Some | |
| Congenital myopathy with fibre type disproportion | Is a | True | Myopathy with abnormality of histochemical fibre type | Inferred relationship | Some | |
| Congenital myopathy with uniform fibre type | Is a | True | Myopathy with abnormality of histochemical fibre type | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set
FHIR