Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3737504016 | Myoclonic epilepsy in non-progressive encephalopathy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | 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 | Entire term case sensitive (core metadata concept) | 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 | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Myoclonic epilepsy in non-progressive encephalopathy | Finding site | Cerebrum | false | Inferred relationship | Some | 1 | |
Myoclonic epilepsy in non-progressive encephalopathy | Is a | Epileptic encephalopathy (disorder) | false | Inferred relationship | Some | ||
Myoclonic epilepsy in non-progressive encephalopathy | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Myoclonic epilepsy in non-progressive encephalopathy | Finding site | Brain structure | true | Inferred relationship | Some | 2 | |
Myoclonic epilepsy in non-progressive encephalopathy | Is a | Developmental and epileptic encephalopathy | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets