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
- Myoclonic Epilepsy, Juvenile
- Standard Disease Name
- myoclonic epilepsy, juvenile
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- D020190
- OMIM ID
- 254770
- UMLS ID
- C0270853
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:An epilepsy characterized by myoclonic jerks, generalized tonic-clonic seizures, and sometimes absence seizures. It appears during adolescence.|MSH2017_2016_08_12:A disorder characterized by the onset of myoclonus in adolescence, a marked increase in the incidence of absence seizures (see EPILEPSY, ABSENCE), and generalized major motor seizures (see EPILEPSY, TONIC-CLONIC). The myoclonic episodes tend to occur shortly after awakening. Seizures tend to be aggravated by sleep deprivation and alcohol consumption. Hereditary and sporadic forms have been identified. (From Adams et al., Principles of Neurology, 6th ed, p323)
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Ingredients
target disease -> ingredient target8 Ingredients
02
(−)-Alloaromadendrene
No data
03
()-2-Carene
No data
04
()-alpha-Funebrene
No data
05
()-alpha-Longipinene
No data
06
()-Alpha-Terpineol
No data
07
()-Beta-Pinene
No data
08