Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3451016013 | Autosomal recessive limb girdle muscular dystrophy type 2M (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3451017016 | Autosomal recessive limb girdle muscular dystrophy type 2M | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3451018014 | A form of limb-girdle muscular dystrophy with characteristics of an infantile onset of hypotonia, axial and proximal lower limb weakness (with severe weakness noted after febrile illnesses), cardiomyopathy and normal or reduced intelligence. Hypertrophy of calves, thighs, and triceps have also been reported in some cases. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive limb girdle muscular dystrophy type 2M | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2M | Clinical course | Progressive | true | Inferred relationship | Some | 2 | |
Autosomal recessive limb girdle muscular dystrophy type 2M | Is a | Autosomal recessive muscular dystrophy with limb girdle distribution | true | Inferred relationship | Some | ||
Autosomal recessive limb girdle muscular dystrophy type 2M | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2M | 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