Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2023. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5160314014 | Dystonia due to inherited disorder | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 5160315010 | Dystonia due to hereditary disease (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 5160347017 | Dystonia due to hereditary disease | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Dystonia due to hereditary disease | Is a | Dystonia | true | Inferred relationship | Existential restriction modifier | ||
| Dystonia due to hereditary disease | Is a | Central nervous system complication | true | Inferred relationship | Existential restriction modifier | ||
| Dystonia due to hereditary disease | Interprets | Movement | true | Inferred relationship | Existential restriction modifier | 2 | |
| Dystonia due to hereditary disease | Due to | Hereditary disease | true | Inferred relationship | Existential restriction modifier | 3 | |
| Dystonia due to hereditary disease | Finding site | Extrapyramidal system structure | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Dystonia due to hereditary spastic paraplegia | Is a | True | Dystonia due to hereditary disease | Inferred relationship | Existential restriction modifier | |
| Dystonia due to Leigh syndrome | Is a | True | Dystonia due to hereditary disease | Inferred relationship | Existential restriction modifier | |
| Dystonia due to Lesch Nyhan syndrome | Is a | True | Dystonia due to hereditary disease | Inferred relationship | Existential restriction modifier | |
| Dystonia due to GM2 gangliosidosis | Is a | True | Dystonia due to hereditary disease | Inferred relationship | Existential restriction modifier | |
| Dystonia due to atypical pantothenate kinase associated neurodegeneration | Is a | True | Dystonia due to hereditary disease | Inferred relationship | Existential restriction modifier | |
| Dystonia due to ataxia telangiectasia syndrome | Is a | True | Dystonia due to hereditary disease | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR