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DO Term : epilepsy [DOID:1826] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • SNOMEDCT_US_2023_03_01:267698007,
  • EFO:0000474,
  • NCI:C3020,
  • epileptic syndrome,
  • epilepsy syndrome,
  • ICD9CM:345.9,
  • UMLS_CUI:C0014544,
  • ICD10CM:G40,
  • MESH:D004827
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents