Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2871257019 | Mitochondrial disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 359706019 | Mitochondrial myopathy | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 359707011 | Mitochondrial cytopathy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 629193019 | Mitochondrial cytopathy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Mitochondrial cytopathy | Is a | Metabolic disease | true | Inferred relationship | Some | ||
| Mitochondrial cytopathy | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | ||
| Mitochondrial cytopathy | Is a | Metabolic myopathy | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Combined oxidative phosphorylation defect type 2 | Is a | True | Mitochondrial cytopathy | Inferred relationship | Some | |
| Combined oxidative phosphorylation defect type 4 | Is a | True | Mitochondrial cytopathy | Inferred relationship | Some |
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Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR