Human genes for Lennox-Gastaut syndrome
Lennox-Gastaut syndrome [DOID:0050561]
A childhood electroclinical syndrome that is characterized by frequent seizures and intellectual disability that present in early childhood.
Synonyms: Lennox-Gastaut syndrome, DOID:0050561, LennoxGastaut syndrome, Lennox-Gastaut disease, Lennox-Gastaut disorder ...
Linkouts: OMIM