Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 359692015 | Myopathy with cytoplasmic inclusions | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 629180012 | Myopathy with cytoplasmic inclusions (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Inclusion body myopathy 2 | Is a | True | Myopathy with cytoplasmic inclusions | Inferred relationship | Some | |
| Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia | Is a | True | Myopathy with cytoplasmic inclusions | Inferred relationship | Some | |
| Desmin related myopathy with Mallory body-like inclusions | Is a | True | Myopathy with cytoplasmic inclusions | Inferred relationship | Some | |
| X-linked myopathy with excessive autophagy | Is a | True | Myopathy with cytoplasmic inclusions | Inferred relationship | Some | |
| Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome | Is a | True | Myopathy with cytoplasmic inclusions | Inferred relationship | Some | |
| Desmin-related myofibrillar myopathy | Is a | True | Myopathy with cytoplasmic inclusions | Inferred relationship | Some | |
| Hereditary inclusion body myopathy type 4 | Is a | True | Myopathy with cytoplasmic inclusions | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set