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 |
3318734013 | Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3318735014 | Autosomal dominant limb girdle muscular dystrophy type 1G | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5402300014 | A rare, mild subtype of autosomal dominant limb-girdle muscular dystrophy characterized by a typically adult onset of mild, progressive, proximal weakness of pelvic and shoulder girdle muscles and progressive, permanent finger and toes flexion limitation without flexion contractures. Normal to highly elevated creatine kinase serum levels are observed. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402301013 | A rare, mild subtype of autosomal dominant limb-girdle muscular dystrophy characterised by a typically adult onset of mild, progressive, proximal weakness of pelvic and shoulder girdle muscles and progressive, permanent finger and toes flexion limitation without flexion contractures. Normal to highly elevated creatine kinase serum levels are 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 1G (disorder) | Is a | Autosomal dominant muscular dystrophy with limb girdle distribution | true | Inferred relationship | Some | ||
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | 2 | |
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | 3 | |
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 2 | |
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | Associated morphology | Dystrophy | false | Inferred relationship | Some | 3 | |
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 1 | |
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal dominant limb girdle muscular dystrophy type 1G (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)