progressive myoclonic epilepsy
GPTKB entity
Statements (22)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
neurological disorder |
| gptkbp:affects |
gptkb:nervous_system
|
| gptkbp:causedBy |
genetic disorder
|
| gptkbp:frequency |
rare
|
| https://www.w3.org/2000/01/rdf-schema#label |
progressive myoclonic epilepsy
|
| gptkbp:ICD-10_code |
G40.4
|
| gptkbp:inheritance |
autosomal dominant
autosomal recessive |
| gptkbp:onset |
childhood
adolescence |
| gptkbp:prognosis |
progressive
|
| gptkbp:subspecies |
gptkb:Lafora_disease
gptkb:Unverricht-Lundborg_disease Neuronal ceroid lipofuscinosis Myoclonic epilepsy with ragged red fibers |
| gptkbp:symptom |
myoclonus
progressive neurological decline epileptic seizures |
| gptkbp:treatment |
antiepileptic drugs
|
| gptkbp:bfsParent |
gptkb:Unverricht-Lundborg_disease
|
| gptkbp:bfsLayer |
8
|