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 |
3321124019 | Autosomal recessive limb girdle muscular dystrophy type 2G (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3321125018 | Autosomal recessive limb girdle muscular dystrophy type 2G | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3321126017 | Limb girdle muscular dystrophy due to telethonin deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5402395014 | A mild subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a variable onset (ranging from infancy to adolescence) of progressive proximal upper and lower limb muscle weakness and atrophy. Mild scapular winging, calf hypertrophy, and lack of respiratory and cardiac involvement are also observed. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402396010 | A mild subtype of autosomal recessive limb-girdle muscular dystrophy characterised by a variable onset (ranging from infancy to adolescence) of progressive proximal upper and lower limb muscle weakness and atrophy. Mild scapular winging, calf hypertrophy, and lack of respiratory and cardiac involvement are also observed. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive limb girdle muscular dystrophy type 2G (disorder) | Is a | Autosomal recessive muscular dystrophy with limb girdle distribution | true | Inferred relationship | Some | ||
Autosomal recessive limb girdle muscular dystrophy type 2G (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2G (disorder) | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2G (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2G (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)