Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3316656010 | Autosomal dominant focal dystonia DYT25 type (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 3316657018 | Autosomal dominant focal dystonia DYT25 type | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal dominant focal dystonia DYT25 type | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant focal dystonia DYT25 type | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant focal dystonia DYT25 type | Is a | Focal dystonia | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant focal dystonia DYT25 type | Finding site | Extrapyramidal system structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal dominant focal dystonia DYT25 type | Interprets | Movement | true | Inferred relationship | Existential restriction modifier | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR