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Summary Literature (6)
DOID:0060171 - Dravet syndrome


Disease Ontology Definition:An epilepsy that is characterized by frequent febrile seizures with onset before 1 year.

Synonyms: SMEI, severe myoclonic epilepsy in infancy

In OMIM:
OMIM:607208 - DRAVET SYNDROME; DRVT

In Mondo Disease Ontology:
MONDO:0100135 - Dravet syndrome

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : scn1a, gabrg2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): infancy electroclinical syndrome (is_a)