Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3302283014 | Autosomal recessive limb girdle muscular dystrophy type 2A (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3302284015 | Autosomal recessive limb girdle muscular dystrophy type 2A | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3302285019 | Primary calpainopathy | en | Synonym | Active | Case insensitive | SNOMED CT core |
3302286018 | Calpain-3 deficiency limb girdle muscular dystrophy type 2A | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3758294015 | Leyden-Möbius muscular dystrophy | en | Synonym | Active | Case sensitive | SNOMED CT core |
3302287010 | A limb girdle muscular dystrophy characterized by symmetrical and selective atrophy and weakness of proximal limb and girdle muscles without cardiac or facial disturbances. | en | Definition | Active | Case sensitive | SNOMED CT core |
3302288017 | A limb girdle muscular dystrophy characterised by symmetrical and selective atrophy and weakness of proximal limb and girdle muscles without cardiac or facial disturbances. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive limb girdle muscular dystrophy type 2A | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2A | Clinical course | Progressive | true | Inferred relationship | Some | 2 | |
Autosomal recessive limb girdle muscular dystrophy type 2A | Is a | Autosomal recessive muscular dystrophy with limb girdle distribution | true | Inferred relationship | Some | ||
Autosomal recessive limb girdle muscular dystrophy type 2A | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2A | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 1 |
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