Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Apr 2025. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4537452016 | Atrophy of peroneal muscle (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4537453014 | Atrophy of peroneal muscle | 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 peroneal muscle (disorder) | Is a | Atrophy of muscle of lower leg (disorder) | true | Inferred relationship | Some | ||
Atrophy of peroneal muscle (disorder) | Finding site | Peroneal muscle structure | true | Inferred relationship | Some | 1 | |
Atrophy of peroneal muscle (disorder) | Associated morphology | Atrophy | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
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 peroneal muscle (disorder) | Inferred relationship | Some |
This concept is not in any reference sets