Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Oct 2021. Module: SNOMED CT core
Descriptions:
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Myotonic dystrophy (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Myotonic dystrophy (disorder) | Is a | Hereditary progressive muscular dystrophy | true | Inferred relationship | Some | ||
Myotonic dystrophy (disorder) | Is a | Myotonic disorder | true | Inferred relationship | Some | ||
Myotonic dystrophy (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 2 | |
Myotonic dystrophy (disorder) | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 1 | |
Myotonic dystrophy (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Myotonic dystrophy (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Steinert myotonic dystrophy syndrome | Is a | True | Myotonic dystrophy (disorder) | Inferred relationship | Some | |
Proximal myotonic myopathy (disorder) | Is a | True | Myotonic dystrophy (disorder) | Inferred relationship | Some | |
Cardiomyopathy in myotonic dystrophy | Associated with | True | Myotonic dystrophy (disorder) | Inferred relationship | Some | 1 |
Congenital myotonic dystrophy | Is a | True | Myotonic dystrophy (disorder) | Inferred relationship | Some | |
Dilated cardiomyopathy due to myotonic dystrophy (disorder) | Due to | True | Myotonic dystrophy (disorder) | Inferred relationship | Some | 2 |
Reference Sets
Description inactivation indicator reference set