- OMIM ID
-
607876
- OMIM term:
- EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2; FAME2
- Alternative terms:
-
BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 2; BAFME2
CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 2; FCMTE2
CORTICAL MYOCLONUS AND EPILEPSY, AUTOSOMAL DOMINANT; ADCME
- (∗) Location:
- 2p11.1-q12.2
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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