WormBase Tree Display for DO_term: DOID:1826
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DOID:1826 | Name | epilepsy | |
---|---|---|---|
Status | Valid | ||
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. | ||
Synonym | Exact | epilepsy syndrome | |
epileptic syndrome | |||
Parent | Is_a | DOID:936 | |
Child | Is (13) | ||
Disease_model_annotation (24) | |||
Attribute_of | Gene_by_biology (14) | ||
Gene_by_orthology (29) | |||
Disease_model_variation (13) | |||
Disease_model_strain | WBStrain00000001 | ||
Disease_model_genotype | WBGenotype00000119 | ||
Chemical_inducer (3) | |||
Other_inducer | electroshock treatment | ||
Molecule_modifier | WBMol:00005371 | ||
WBMol:00004943 | |||
WBMol:00007971 | |||
WBMol:00007997 |