All diseases

OMIM ID
300088
OMIM term:
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 9; EIEE9
Alternative terms:
EPILEPSY, FEMALE-RESTRICTED, WITH MENTAL RETARDATION; EFMR
JUBERG-HELLMAN SYNDROME
(∗) Location:
Xq22.1  
(†) Associated OMIM genes:
PCDH19  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/w7c77xm2