Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3657413013 | Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3657415018 | Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 767691000241117 | forme symptomatique de la dystrophie musculaire de Duchenne et Becker de la femme porteuse (trouble) | fr | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 901791000172116 | forme symptomatique de la dystrophie musculaire de Duchenne et Becker de la femme porteuse | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3657414019 | Disease with characteristics of variable degrees of muscle weakness due to progressive skeletal myopathy sometimes associated with dilated cardiomyopathy or left ventricle dilation. Duchenne and Becker muscular dystrophies primarily affect males and only a small percentage of female carriers have been reported to manifest these diseases. Symptomatic female carriers usually present later in life, muscle weakness is generally mild to moderate and is usually proximal and asymmetric, some patients present with cardiac manifestations alone. Females with clinical features are usually carriers of X-chromosome rearrangements, display skewed X-inactivation or have Turner syndrome. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier | évolution clinique (attribut) | progressif | true | Inferred relationship | Some | 2 | |
| Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier | morphologie associée (attribut) | Dystrophy (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier | localisation d'une constatation (attribut) | structure de muscle squelettique | true | Inferred relationship | Some | 1 | |
| Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier | est un(e) (attribut) | Manifesting female carrier of X-linked muscular dystrophy | true | Inferred relationship | Some | ||
| Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier | survenue (attribut) | congénital | false | Inferred relationship | Some | 2 | |
| Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier | morphologie associée (attribut) | Developmental abnormality | false | Inferred relationship | Some | 2 | |
| Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier | localisation d'une constatation (attribut) | structure de muscle squelettique | false | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR