All diseases

OMIM ID
308350
OMIM term:
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1; EIEE1
Alternative terms:
INFANTILE SPASM SYNDROME, X-LINKED 1; ISSX1
WEST SYNDROME, X-LINKED
OHTAHARA SYNDROME, X-LINKED
INFANTILE EPILEPTIC-DYSKINETIC ENCEPHALOPATHY
XMESID
(∗) Location:
Xp21.3  
(†) Associated OMIM genes:
ARX  
(‡) Associated MGI genes:
Arx  

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