Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2983256013 | Myopathy with deficiency of iron-sulfur cluster assembly enzyme (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
2983276019 | Myopathy with deficiency of succinate dehydrogenase and aconitase | en | Synonym | Active | Case insensitive | SNOMED CT core |
2983343015 | Myopathy with deficiency of iron-sulphur cluster assembly enzyme | en | Synonym | Active | Case insensitive | SNOMED CT core |
2983346011 | Myoglobinuria due to abnormal glycolysis | en | Synonym | Active | Case insensitive | SNOMED CT core |
2983419019 | Hereditary myopathy with lactic acidosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
2983445011 | Myopathy with exercise intolerance, Swedish type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2983465016 | Myopathy with deficiency of iron-sulfur cluster assembly enzyme | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Myopathy with deficiency of iron-sulfur cluster assembly enzyme | Is a | Disorder of skeletal muscle | true | Inferred relationship | Some | ||
Myopathy with deficiency of iron-sulfur cluster assembly enzyme | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Myopathy with deficiency of iron-sulfur cluster assembly enzyme | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Myopathy with deficiency of iron-sulfur cluster assembly enzyme | 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