01
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 24
Basic Information
Grouped by core information, identifiers, and descriptions.
Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
Core Information
- Disease Name
- Epilepsies, Myoclonic
- Standard Disease Name
- epilepsies, myoclonic
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- D004831
- OMIM ID
- MTHU011422|MTHU046868|MTHU002980|MTHU010507
- UMLS ID
- C0014550
- HPO ID
- No data
Description and Extensions
- Description
- MSH2017_2016_08_12: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.).|CSP2006:any form of epilepsy accompanied by myoclonus, shock like contractions of the muscle.