Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). 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 | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 4213649016 | EDMD2 - autosomal dominant Emery-Dreifuss muscular dystrophy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4213650016 | Autosomal dominant Emery-Dreifuss muscular dystrophy | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder) | est un(e) (attribut) | dystrophie musculaire d'Emery-Dreifuss | true | Inferred relationship | Some | ||
| Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder) | morphologie associée (attribut) | Dystrophy (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder) | localisation d'une constatation (attribut) | structure de muscle squelettique | true | Inferred relationship | Some | 1 | |
| Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder) | évolution clinique (attribut) | progressif | true | Inferred relationship | Some | 2 | |
| Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder) | est un(e) (attribut) | Hereditary progressive muscular dystrophy | true | Inferred relationship | Some | ||
| Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder) | est un(e) (attribut) | Autosomal dominant hereditary disorder | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR