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