Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3446315013 | Autosomal recessive limb girdle muscular dystrophy type 2Y (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3446316014 | Autosomal recessive limb girdle muscular dystrophy type 2Y | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3446317017 | Autosomal recessive muscular dystrophy due to LAP1B (lamin-associated protein 1B) deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3446318010 | Autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3446319019 | Muscular dystrophy with progressive weakness, distal contracture and rigid spine | en | Synonym | Active | Case insensitive | SNOMED CT core |
3446320013 | A form of limb-girdle muscular dystrophy presenting in the first or second decades of life with characteristics of slowly progressive proximal and distal muscle weakness and atrophy. Additional manifestations include contractures of the proximal and distal interphalangeal hand joints, rigid spine, restricted pulmonary function and mild cardiomyopathy. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive limb girdle muscular dystrophy type 2Y | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2Y | Clinical course | Progressive | true | Inferred relationship | Some | 2 | |
Autosomal recessive limb girdle muscular dystrophy type 2Y | Is a | Autosomal recessive muscular dystrophy with limb girdle distribution | true | Inferred relationship | Some | ||
Autosomal recessive limb girdle muscular dystrophy type 2Y | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2Y | 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