Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3737502017 | Myoclonic epilepsy in non-progressive encephalopathy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3737504016 | Myoclonic epilepsy in non-progressive encephalopathy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3737501012 | A rare epilepsy syndrome with characteristics of recurrent, long-lasting myoclonic status in infants and young children with a non-progressive encephalopathy, associated with transient and recurring motor, cognitive and/or behavioral disturbances. | en | Definition | Active | Case sensitive | SNOMED CT core |
| 3737503010 | A rare epilepsy syndrome with characteristics of recurrent, long-lasting myoclonic status in infants and young children with a non-progressive encephalopathy, associated with transient and recurring motor, cognitive and/or behavioural disturbances. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Myoclonic epilepsy in non-progressive encephalopathy | Finding site | Structure of cerebrum | true | Inferred relationship | Some | 1 | |
| Myoclonic epilepsy in non-progressive encephalopathy | Is a | Epileptic encephalopathy | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Queensland allied health clinical finding reference set
Queensland allied health indicator for intervention reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR