- OMIM ID
-
300672
- OMIM term:
- EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2
- Alternative terms:
-
INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2
RETT SYNDROME, VARIANT, WITH INFANTILE SPASMS
RETT SYNDROME, ATYPICAL, CDKL5-RELATED
- (∗) Location:
- Xp22.13
- (†) Associated OMIM genes:
- CDKL5
- (‡) Associated MGI genes:
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