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Summary Literature (3)
MIM:607208 - DRAVET SYNDROME; DRVT

Xenbase Genes: scn1a, gabrg2

Human Disease Resource: OMIM

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

Disease Ontology (DO):
DOID:0060171 - obsolete Dravet syndrome
DOID:0080422 - Dravet syndrome
DOID:2481 - infantile epileptic encephalopathy