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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
ChildIsDOID:1824
DOID:0050701
DOID:0060281
DOID:0070471
DOID:0070472
DOID:0080768
DOID:0080769
DOID:0080994
DOID:0112122
DOID:11832
DOID:1827
DOID:2234
DOID:2544
Disease_model_annotationWBDOannot00000549
WBDOannot00000550
WBDOannot00000551
WBDOannot00000552
WBDOannot00000553
WBDOannot00000554
WBDOannot00000555
WBDOannot00000556
WBDOannot00000557
WBDOannot00000558
WBDOannot00000559
WBDOannot00000803
WBDOannot00001010
WBDOannot00001011
WBDOannot00001012
WBDOannot00001013
WBDOannot00001014
WBDOannot00001202
WBDOannot00001203
WBDOannot00001204
WBDOannot00001321
WBDOannot00001322
WBDOannot00001323
WBDOannot00001324
Attribute_ofGene_by_biologyWBGene00003829
WBGene00011230
WBGene00011955
WBGene00003239
WBGene00000407
WBGene00002081
WBGene00000962
WBGene00005009
WBGene00004267
WBGene00006784
WBGene00000424
WBGene00003247
WBGene00006762
WBGene00006805
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_variationWBVar00241556
WBVar00146319
WBVar00143616
WBVar00146335
WBVar00143000
WBVar00241515
WBVar00275340
WBVar00090672
WBVar00143186
WBVar00146356
WBVar00000620
WBVar00241532
WBVar00241608
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