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Disease Ontology Browser
epilepsy (DOID:1826)
Alliance: disease page
Synonyms: epilepsy syndrome; epileptic syndrome
Alt IDs: EFO:0000474, ICD10CM:G40.9, ICD10CM:G40.909, ICD9CM:345.9, MESH:D004827, NCI:C3020, UMLS_CUI:C0014544
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.

Disease References using Mouse Models (106)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
11/05/2019
MGI 6.14
The Jackson Laboratory