loading...| Preferred Name | Epilepsies, Myoclonic [Disease/Finding] | |
| Synonyms |
Myoclonic Epilepsy Myoclonic Seizure Disorder Epilepsies, Myoclonic Epilepsy, Myoclonus |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000001130 |
|
| altLabel |
Myoclonic Epilepsy Myoclonic Seizure Disorder Epilepsies, Myoclonic Epilepsy, Myoclonus |
|
| cui |
C0014550 |
|
| May be treated by |
http://purl.bioontology.org/ontology/NDFRT/N0000150370 http://purl.bioontology.org/ontology/NDFRT/N0000164781 http://purl.bioontology.org/ontology/NDFRT/N0000163774 http://purl.bioontology.org/ontology/NDFRT/N0000164779 http://purl.bioontology.org/ontology/NDFRT/N0000164780 http://purl.bioontology.org/ontology/NDFRT/N0000146152 http://purl.bioontology.org/ontology/NDFRT/N0000163776 http://purl.bioontology.org/ontology/NDFRT/N0000150371 http://purl.bioontology.org/ontology/NDFRT/N0000164783 http://purl.bioontology.org/ontology/NDFRT/N0000150372 |
|
| MESH DEFINITION |
A clinically diverse group of epilepsy syndromes characterized either by myoclonic seizures or by myoclonus in association with other seizure types. Myoclonic epilepsy syndromes are divided into three subtypes based on etiology: familial, cryptogenic, and symptomatic (i.e., occurring secondary to known disease processes such as infections, hypoxic-ischemic injuries, trauma, etc.). |
|
| MESH DUI |
D004831 |
|
| MeSH name |
Epilepsies, Myoclonic |
|
| MESH UI |
M0328686 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000001130 |
|
| NUI |
N0000001130 |
|
| prefLabel |
Epilepsies, Myoclonic [Disease/Finding] |
|
| SNOMED CID |
37356005 192992007 |
|
| tui |
T047 |
|
| subClassOf |