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Diseases

Myoclonic Epilepsy, Juvenile

myoclonic epilepsy, juvenile

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

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
01
CACNB4
calcium voltage-gated channel auxiliary subunit beta 4
calcium voltage-gated channel auxiliary subunit beta 4
06
GABRA1
gamma-aminobutyric acid type A receptor subunit alpha1
gamma-aminobutyric acid type A receptor subunit alpha1
08
KCNQ3
potassium voltage-gated channel subfamily Q member 3
potassium voltage-gated channel subfamily Q member 3