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Disease Ontology Browser
Lennox-Gastaut syndrome (DOID:0050561)
Alliance: disease page
Synonyms: Lennox syndrome
Alt IDs: OMIM:606369, MESH:D065768, ORDO:2382
Definition: A childhood electroclinical syndrome that is characterized by frequent seizures and intellectual disability that present in early childhood.

Disease References using Mouse Models (1)
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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Send questions and comments to User Support. 		last database update
04/09/2024
MGI 6.23 		The Jackson Laboratory