|OBO ID: DOID:1826|
|Term Name:||epilepsy||Search Ontology:|
|Definition:||A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions. (2)|
|Ontology:||Human Disease (DOID:1826)|
|is a type of:||
OTHER epilepsy PAGES
GENES INVOLVED No data available
PHENOTYPE No data available
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