Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3655974016 | Muscle filaminopathy | en | Synonym | Active | Case insensitive | SNOMED CT core |
3655975015 | Muscle filaminopathy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3655797013 | A rare myofibrillar myopathy with characteristics of slowly progressive, proximal skeletal muscle weakness, which is initially more prominent in lower extremities and involves upper extremities with disease progression. Patients present with difficulty climbing stairs, a waddling gait, marked winging of scapula, lower back pain, paresis of limb girdle musculature, hypo or areflexia and/or mild facial muscle weakness in rare cases. Respiratory muscle weakness is common and cardiac anomalies (conduction blocks, tachycardia, diastolic dysfunction, left ventricular hypertrophy) have been reported in some cases. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Muscle filaminopathy | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Muscle filaminopathy | Is a | Congenital disease | true | Inferred relationship | Some | ||
Muscle filaminopathy | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Muscle filaminopathy | Is a | Myofibrillar myopathy | true | Inferred relationship | Some | ||
Muscle filaminopathy | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Muscle filaminopathy | 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