Status: current, Defined. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
297608012 | Hereditary progressive muscular dystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
577087018 | Hereditary progressive muscular dystrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary progressive muscular dystrophy | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Hereditary progressive muscular dystrophy | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Hereditary progressive muscular dystrophy | Clinical course | Progressive | true | Inferred relationship | Some | 2 | |
Hereditary progressive muscular dystrophy | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Hereditary progressive muscular dystrophy | Associated morphology | Dystrophy | false | Inferred relationship | Some | 1 | |
Hereditary progressive muscular dystrophy | Is a | Muscular dystrophy | true | Inferred relationship | Some | ||
Hereditary progressive muscular dystrophy | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Hereditary progressive muscular dystrophy | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 1 | |
Hereditary progressive muscular dystrophy | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | 1 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set