Status: current, Primitive. 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 | Initial character case insensitive | SNOMED CT core |
3318735014 | Autosomal dominant limb girdle muscular dystrophy type 1G | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3318736010 | A mild form of limb girdle muscular dystrophy that has characteristics of limb-girdle weakness, marked proximal amyotrophy and abolished myotatic reflexes, associated with progressive fingers and toes flexion limitation. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant limb girdle muscular dystrophy type 1G | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 1 | |
Autosomal dominant limb girdle muscular dystrophy type 1G | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Autosomal dominant limb girdle muscular dystrophy type 1G | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal dominant limb girdle muscular dystrophy type 1G | Clinical course | Progressive | true | Inferred relationship | Some | 2 | |
Autosomal dominant limb girdle muscular dystrophy type 1G | Is a | Autosomal dominant muscular dystrophy with limb girdle distribution | true | Inferred relationship | Some | ||
Autosomal dominant limb girdle muscular dystrophy type 1G | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | 2 | |
Autosomal dominant limb girdle muscular dystrophy type 1G | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | 3 | |
Autosomal dominant limb girdle muscular dystrophy type 1G | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 2 | |
Autosomal dominant limb girdle muscular dystrophy type 1G | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Autosomal dominant limb girdle muscular dystrophy type 1G | Associated morphology | Dystrophy | false | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set