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WormBase Tree Display for DO_term: DOID:1826

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Name Class

DOID:1826Nameepilepsy
StatusValid
DefinitionA 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.
SynonymExactepilepsy syndrome
epileptic syndrome
ParentIs_aDOID:936
ChildIs (13)
Disease_model_annotation (24)
Attribute_ofGene_by_biology (14)
Gene_by_orthologyWBGene00000035
WBGene00000036
WBGene00000037
WBGene00000038
WBGene00001137
WBGene00001374
WBGene00002242
WBGene00003376
WBGene00003995
WBGene00003996
WBGene00003997
WBGene00003998
WBGene00003999
WBGene00004000
WBGene00004001
WBGene00004002
WBGene00004003
WBGene00004006
WBGene00004008
WBGene00004800
WBGene00007862
WBGene00010524
WBGene00012185
WBGene00012364
WBGene00012967
WBGene00013258
WBGene00021948
WBGene00022048
WBGene00194737
Disease_model_variation (13)
Disease_model_strainWBStrain00000001
Disease_model_genotypeWBGenotype00000119
Chemical_inducerWBMol:00005371
WBMol:00004251
WBMol:00007997
Other_inducerelectroshock treatment
Molecule_modifierWBMol:00005371
WBMol:00004943
WBMol:00007971
WBMol:00007997