Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 345288017 | Myoclonic absence epilepsy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5173084011 | Epilepsy with myoclonic absence (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5173085012 | Epilepsy with myoclonic absence | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5173086013 | EMA - epilepsy with myoclonic absence | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5173087016 | Epilepsy with myoclonic absence presents with daily myoclonic absence seizures between 1 to 12 years of age. Other generalised seizure types which may be seen in this syndrome include generalised tonic-clonic seizures, clonic, atonic and typical absence seizures. Developmental impairment may be present at onset of epilepsy and may become more evident with age. The electroencephalogram shows regular three Hz generalised spike-and-wave pattern time-locked with myoclonic jerks, with a normal background. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5173088014 | Epilepsy with myoclonic absence presents with daily myoclonic absence seizures between 1 to 12 years of age. Other generalized seizure types which may be seen in this syndrome include generalized tonic-clonic seizures, clonic, atonic and typical absence seizures. Developmental impairment may be present at onset of epilepsy and may become more evident with age. The electroencephalogram shows regular three Hz generalized spike-and-wave pattern time-locked with myoclonic jerks, with a normal background. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5640931000172119 | épilepsie avec absences myocloniques | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 4143111000172114 | myoklonische absence-epilepsie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Epilepsy with myoclonic absence (disorder) | Is a | épilepsie généralisée cryptogénique | false | Inferred relationship | Some | ||
| Epilepsy with myoclonic absence (disorder) | Finding site | Cerebrum | false | Inferred relationship | Some | 1 | |
| Epilepsy with myoclonic absence (disorder) | Has definitional manifestation | Seizure | false | Inferred relationship | Some | ||
| Epilepsy with myoclonic absence (disorder) | Is a | Absence seizure | false | Inferred relationship | Some | ||
| Epilepsy with myoclonic absence (disorder) | Is a | Generalized epilepsy | false | Inferred relationship | Some | ||
| Epilepsy with myoclonic absence (disorder) | Is a | Myoclonic absence seizure | false | Inferred relationship | Some | ||
| Epilepsy with myoclonic absence (disorder) | Is a | Genetic generalised epilepsy | true | Inferred relationship | Some | ||
| Epilepsy with myoclonic absence (disorder) | Occurrence | Childhood | true | Inferred relationship | Some | 1 | |
| Epilepsy with myoclonic absence (disorder) | Finding site | Brain structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Perioral myoclonia with absences (disorder) | Is a | False | Epilepsy with myoclonic absence (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR