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 |
3318731017 | Autosomal dominant limb girdle muscular dystrophy type 1F (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3318732012 | Autosomal dominant limb girdle muscular dystrophy type 1F | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5402298014 | A rare subtype of autosomal dominant limb-girdle muscular dystrophy, with a variable age of onset, characterized by progressive, proximal weakness and wasting of the shoulder and pelvic musculature (with the pelvic girdle, and especially the ileopsoas muscle, being more affected) and frequent association of calf hypertrophy, dysphagia, arachnodactyly with or without finger contractures and/or distal and axial muscle involvement. Additional features include an abnormal gait, exercise intolerance, myalgia, fatigue and respiratory insufficiency. Cardiac conduction defects are typically not observed. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402299018 | A rare subtype of autosomal dominant limb-girdle muscular dystrophy, with a variable age of onset, characterised by progressive, proximal weakness and wasting of the shoulder and pelvic musculature (with the pelvic girdle, and especially the ileopsoas muscle, being more affected) and frequent association of calf hypertrophy, dysphagia, arachnodactyly with or without finger contractures and/or distal and axial muscle involvement. Additional features include an abnormal gait, exercise intolerance, myalgia, fatigue and respiratory insufficiency. Cardiac conduction defects are typically not 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 1F (disorder) | Is a | Autosomal dominant muscular dystrophy with limb girdle distribution | true | Inferred relationship | Some | ||
Autosomal dominant limb girdle muscular dystrophy type 1F (disorder) | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | 2 | |
Autosomal dominant limb girdle muscular dystrophy type 1F (disorder) | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | 3 | |
Autosomal dominant limb girdle muscular dystrophy type 1F (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 2 | |
Autosomal dominant limb girdle muscular dystrophy type 1F (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Autosomal dominant limb girdle muscular dystrophy type 1F (disorder) | Associated morphology | Dystrophy | false | Inferred relationship | Some | 3 | |
Autosomal dominant limb girdle muscular dystrophy type 1F (disorder) | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 1 | |
Autosomal dominant limb girdle muscular dystrophy type 1F (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Autosomal dominant limb girdle muscular dystrophy type 1F (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal dominant limb girdle muscular dystrophy type 1F (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)