Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Oct 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4643487015 | Myotonic dystrophy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4643488013 | DM - dystrophia myotonica | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4643489017 | Myotonia dystrophica | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4643490014 | Myotonic dystrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4643491013 | Dystrophia myotonica | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5329621000052115 | myoton dystrofi | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| 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 |
This concept is not in any reference sets
FHIR