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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
| Id | http://purl.bioontology.org/ontology/NDFRT/N0000001130
http://purl.bioontology.org/ontology/NDFRT/N0000001130
|
|---|---|
| Preferred Name | Epilepsies, Myoclonic [Disease/Finding] |
| Synonyms |
Myoclonic Epilepsy
Myoclonic Seizure Disorder
Epilepsies, Myoclonic
Epilepsy, Myoclonus
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
Myoclonic Epilepsy
Myoclonic Seizure Disorder
Epilepsies, Myoclonic
Epilepsy, Myoclonus
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|---|---|
| prefLabel | Epilepsies, Myoclonic [Disease/Finding]
|
| 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
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| MESH UI | M0328686
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| MeSH name | Epilepsies, Myoclonic
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| type | |
| tui | T047
|
| SNOMED CID |
37356005
192992007
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| May be treated by |
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| notation | N0000001130
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| Semantic type UMLS property | |
| NUI | N0000001130
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| cui | C0014550
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| NDFRT kind | DISEASE_KIND
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| subClassOf |
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| No notes to display |