Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (3)
OMIM:607208 - DRAVET SYNDROME; DRVT


Xenbase Genes: scn1a, gabrg2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0100079 - epileptic encephalopathy, early infantile, 6

Disease Ontology (DO):
DOID:0060171 - Dravet syndrome
DOID:2481 - infantile epileptic encephalopathy