- OMIM ID
-
601068
- OMIM term:
- EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1; FAME1
- Alternative terms:
-
BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 1; BAFME1
CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 1; FCMTE1
- (∗) Location:
- 8q24
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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