Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3318715013 | Autosomal dominant limb girdle muscular dystrophy type 1A (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3318716014 | Autosomal dominant limb girdle muscular dystrophy type 1A | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3318717017 | Limb girdle muscular dystrophy due to myotilin deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3318719019 | Limb-girdle muscular dystrophy 1A myotilin myopathy | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5402294011 | A rare subtype of autosomal dominant limb girdle muscular dystrophy characterized by an adult onset of proximal shoulder and hip girdle weakness (that later progresses to include distal weakness), nasal speech and dysarthria. Other frequent findings include tightened heel cords, reduced deep-tendon reflexes and elevated creatine kinase serum levels. Respiratory failure, as well as mild facial weakness and dysphagia, may also be observed. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402295012 | A rare subtype of autosomal dominant limb girdle muscular dystrophy characterised by an adult onset of proximal shoulder and hip girdle weakness (that later progresses to include distal weakness), nasal speech and dysarthria. Other frequent findings include tightened heel cords, reduced deep-tendon reflexes and elevated creatine kinase serum levels. Respiratory failure, as well as mild facial weakness and dysphagia, may also be observed. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant limb girdle muscular dystrophy type 1A (disorder) | Is a | Autosomal dominant muscular dystrophy with limb girdle distribution | true | Inferred relationship | Some | ||
Autosomal dominant limb girdle muscular dystrophy type 1A (disorder) | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | 2 | |
Autosomal dominant limb girdle muscular dystrophy type 1A (disorder) | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | 3 | |
Autosomal dominant limb girdle muscular dystrophy type 1A (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 2 | |
Autosomal dominant limb girdle muscular dystrophy type 1A (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Autosomal dominant limb girdle muscular dystrophy type 1A (disorder) | Associated morphology | Dystrophy | false | Inferred relationship | Some | 3 | |
Autosomal dominant limb girdle muscular dystrophy type 1A (disorder) | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 1 | |
Autosomal dominant limb girdle muscular dystrophy type 1A (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Autosomal dominant limb girdle muscular dystrophy type 1A (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal dominant limb girdle muscular dystrophy type 1A (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)