Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3450985013 | Autosomal recessive limb girdle muscular dystrophy type 2P (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3450986014 | Autosomal recessive limb girdle muscular dystrophy type 2P | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3450987017 | A form of limb-girdle muscular dystrophy with characteristics of slowly-progressive mainly proximal muscle weakness presenting in early childhood (with difficulties walking and climbing stairs) and mild to severe intellectual disability. Additional manifestations reported include microcephaly, mild increase in thigh or calf muscles and contractures of the ankles. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive limb girdle muscular dystrophy type 2P | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2P | Clinical course | Progressive | true | Inferred relationship | Some | 2 | |
Autosomal recessive limb girdle muscular dystrophy type 2P | Is a | Autosomal recessive muscular dystrophy with limb girdle distribution | true | Inferred relationship | Some | ||
Autosomal recessive limb girdle muscular dystrophy type 2P | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2P | 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