All diseases

OMIM ID
607208
OMIM term:
DRAVET SYNDROME
Alternative terms:
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6; EIEE6
SEVERE MYOCLONIC EPILEPSY OF INFANCY; SMEI
(∗) Location:
2q24.3   5q34  
(†) Associated OMIM genes:
GABRG2   SCN1A   SCN9A  
(‡) Associated MGI genes:
Scn1a  

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