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DO Term : childhood absence epilepsy [DOID:1825] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A childhood electroclinical syndrome that is characterized by brief and frequent absence seizures in children with age of onset between four and ten years.

synonyms:
UMLS_CUI:C0014553,
MESH:D004832,
petit mal seizure,
pyknolepsy,
NCI:C3023,
absence seizure,
SNOMEDCT_US_2023_03_01:163596002

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

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