Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Mar 2025. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4361991011 | Atrophy of muscle of shoulder (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4361992016 | Atrophy of muscle of shoulder | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4361993014 | Amyotrophy of muscle of shoulder | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Atrophy of muscle of shoulder (disorder) | Is a | Atrophy of muscle of upper limb (disorder) | true | Inferred relationship | Some | ||
Atrophy of muscle of shoulder (disorder) | Is a | Disorder of shoulder region (disorder) | true | Inferred relationship | Some | ||
Atrophy of muscle of shoulder (disorder) | Finding site | Structure of skeletal muscle of shoulder | true | Inferred relationship | Some | 1 | |
Atrophy of muscle of shoulder (disorder) | Associated morphology | Atrophy | true | Inferred relationship | Some | 1 | |
Atrophy of muscle of shoulder (disorder) | Is a | Atrophy of proximal muscle | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Atrophy of latissimus dorsi muscle (disorder) | Is a | True | Atrophy of muscle of shoulder (disorder) | Inferred relationship | Some | |
Atrophy of deltoid muscle (disorder) | Is a | True | Atrophy of muscle of shoulder (disorder) | Inferred relationship | Some | |
Atrophy of muscle of left shoulder | Is a | True | Atrophy of muscle of shoulder (disorder) | Inferred relationship | Some | |
Atrophy of muscle of right shoulder (disorder) | Is a | True | Atrophy of muscle of shoulder (disorder) | Inferred relationship | Some | |
A rare, genetic, neuromuscular disease characterized by adult-onset muscle weakness and atrophy in a scapuloperoneal distribution, mild involvement of the facial muscles, dysphagia, and gynecomastia. Elevated serum CK levels and mixed myopathic and neurogenic abnormalities are associated clinical findings. | Is a | True | Atrophy of muscle of shoulder (disorder) | Inferred relationship | Some |
This concept is not in any reference sets