Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3308304013 | Maternally inherited mitochondrial dystonia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3308305014 | Maternally inherited mitochondrial dystonia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5401480011 | Maternally-inherited mitochondrial dystonia is a rare neurological mitochondrial DNA-related disorder characterized clinically by progressive pediatric-onset dystonia with variable degrees of severity. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5401481010 | Maternally-inherited mitochondrial dystonia is a rare neurological mitochondrial DNA-related disorder characterised clinically by progressive paediatric-onset dystonia with variable degrees of severity. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Maternally inherited mitochondrial dystonia (disorder) | Is a | Dystonia | true | Inferred relationship | Some | ||
| Maternally inherited mitochondrial dystonia (disorder) | Is a | Mitochondrial cytopathy (disorder) | true | Inferred relationship | Some | ||
| Maternally inherited mitochondrial dystonia (disorder) | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Maternally inherited mitochondrial dystonia (disorder) | Finding site | Extrapyramidal system structure | true | Inferred relationship | Some | 1 | |
| Maternally inherited mitochondrial dystonia (disorder) | Interprets | Movement | true | Inferred relationship | Some | 2 | |
| Maternally inherited mitochondrial dystonia (disorder) | Is a | Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder) | true | Inferred relationship | Some | ||
| Maternally inherited mitochondrial dystonia (disorder) | Occurrence | Childhood | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR