Status: current, Defined. Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4213648012 | Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
4213649016 | EDMD2 - autosomal dominant Emery-Dreifuss muscular dystrophy | en | Synonym | Active | Case sensitive | SNOMED CT core |
4213650016 | Autosomal dominant Emery-Dreifuss muscular dystrophy | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant Emery-Dreifuss muscular dystrophy | Is a | Emery-Dreifuss muscular dystrophy | true | Inferred relationship | Some | ||
Autosomal dominant Emery-Dreifuss muscular dystrophy | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal dominant Emery-Dreifuss muscular dystrophy | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Autosomal dominant Emery-Dreifuss muscular dystrophy | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 1 | |
Autosomal dominant Emery-Dreifuss muscular dystrophy | Clinical course | Progressive | true | Inferred relationship | Some | 2 | |
Autosomal dominant Emery-Dreifuss muscular dystrophy | Is a | Hereditary progressive muscular dystrophy | true | Inferred relationship | Some | ||
Autosomal dominant Emery-Dreifuss muscular dystrophy | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set