Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3316656010 | Autosomal dominant focal dystonia DYT25 type (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3316657018 | Autosomal dominant focal dystonia DYT25 type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3316658011 | A form of focal dystonia with characteristics of cervical, laryngeal and hand-forearm dystonia. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant focal dystonia DYT25 type | Interprets | Movement | true | Inferred relationship | Some | 2 | |
Autosomal dominant focal dystonia DYT25 type | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant focal dystonia DYT25 type | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Autosomal dominant focal dystonia DYT25 type | Is a | Focal dystonia | true | Inferred relationship | Some | ||
Autosomal dominant focal dystonia DYT25 type | Finding site | Extrapyramidal system structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set
REPLACED BY association reference set