Statements (50)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
Epilepsy
|
| gptkbp:affects |
adolescents
adults children |
| gptkbp:associatedWith |
gptkb:Dravet_syndrome
gptkb:dementia gptkb:Lafora_disease gptkb:Unverricht-Lundborg_disease gptkb:autism_spectrum_disorder gptkb:Angelman_syndrome intellectual disability neurodegenerative diseases muscle weakness status epilepticus ataxia developmental delay photosensitivity motor delay speech delay behavioral problems mitochondrial disorders MERRF syndrome CSTB gene mutations Doose syndrome EPM2A gene mutations EPM2B gene mutations GABRA1 gene mutations sodium channel mutations |
| gptkbp:canBeGenetic |
true
|
| gptkbp:canBeIdiopathic |
true
|
| gptkbp:canBeNonProgressive |
true
|
| gptkbp:canProgressTo |
true
|
| gptkbp:cause |
cognitive impairment
|
| gptkbp:diagnosedBy |
gptkb:EEG
clinical evaluation |
| https://www.w3.org/2000/01/rdf-schema#label |
Myoclonic Epilepsy
|
| gptkbp:ICD-10_code |
G40.3
|
| gptkbp:inheritance |
autosomal dominant
autosomal recessive |
| gptkbp:subspecies |
gptkb:Generalized_Epilepsy
gptkb:Juvenile_Myoclonic_Epilepsy gptkb:Progressive_Myoclonic_Epilepsy Benign Myoclonic Epilepsy of Infancy |
| gptkbp:symptom |
myoclonic seizures
generalized tonic-clonic seizures |
| gptkbp:treatment |
antiepileptic drugs
|
| gptkbp:triggeredBy |
sleep deprivation
flashing lights |
| gptkbp:bfsParent |
gptkb:D004239
|
| gptkbp:bfsLayer |
8
|