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DO Term : Lennox-Gastaut syndrome [DOID:0050561] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A childhood electroclinical syndrome that is characterized by frequent seizures and intellectual disability that present in early childhood.

synonyms:
OMIM:606369,
GARD:9912,
MESH:D065768,
606369,
Lennox syndrome,
ORDO:2382

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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