Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3446263014 | Autosomal dominant myoglobinuria (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3446264015 | Autosomal dominant myoglobinuria | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5403498019 | A rare metabolic myopathy characterized by episodic myalgia with myoglobinuria which is induced by fever, viral or bacterial infection, prolonged exercise or alcohol abuse, and could, on occasion, lead to acute renal failure. Between episodes, patients may be asymptomatic or could present elevated creatine kinase levels and mild muscle weakness. There have been no further descriptions in the literature since 1997. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5403499010 | A rare metabolic myopathy characterised by episodic myalgia with myoglobinuria which is induced by fever, viral or bacterial infection, prolonged exercise or alcohol abuse, and could, on occasion, lead to acute renal failure. Between episodes, patients may be asymptomatic or could present elevated creatine kinase levels and mild muscle weakness. There have been no further descriptions in the literature since 1997. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal dominant myoglobinuria (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Autosomal dominant myoglobinuria (disorder) | Is a | Myoglobinuria | true | Inferred relationship | Some | ||
| Autosomal dominant myoglobinuria (disorder) | Is a | Lipid storage myopathy | true | Inferred relationship | Some | ||
| Autosomal dominant myoglobinuria (disorder) | Interprets | Urine observable | false | Inferred relationship | Some | 2 | |
| Autosomal dominant myoglobinuria (disorder) | Has interpretation | Present | false | Inferred relationship | Some | 3 | |
| Autosomal dominant myoglobinuria (disorder) | Interprets | Myoglobin measurement, urine | true | Inferred relationship | Some | 3 | |
| Autosomal dominant myoglobinuria (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 4 | |
| Autosomal dominant myoglobinuria (disorder) | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 4 | |
| Autosomal dominant myoglobinuria (disorder) | Is a | Abnormal urinary product | true | Inferred relationship | Some | ||
| Autosomal dominant myoglobinuria (disorder) | Has interpretation | Detected | true | Inferred relationship | Some | 3 | |
| Autosomal dominant myoglobinuria (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR