Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3311383017 | Autosomal recessive limb girdle muscular dystrophy type 2F (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3311385012 | Autosomal recessive limb girdle muscular dystrophy type 2F | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3311386013 | Limb girdle muscular dystrophy due to delta-sarcoglycan deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
3311387016 | Autosomal recessive limb-girdle muscular dystrophy type 2F (LGMD2F) is a limb-girdle muscular dystrophy with manifestations of limb-girdle weakness, cardiomyopathy and respiratory impairment. LGMD2F is caused by a deficit of a sarcoglycan protein and therefore belongs to a group of disorders named sarcoglycanopathy. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive limb girdle muscular dystrophy type 2F | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2F | Clinical course | Progressive | true | Inferred relationship | Some | 2 | |
Autosomal recessive limb girdle muscular dystrophy type 2F | Is a | Autosomal recessive muscular dystrophy with limb girdle distribution | true | Inferred relationship | Some | ||
Autosomal recessive limb girdle muscular dystrophy type 2F | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2F | 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