All diseases

OMIM ID
254800
OMIM term:
MYOCLONIC EPILEPSY OF UNVERRICHT AND LUNDBORG
Alternative terms:
ULD
EPILEPSY, PROGRESSIVE MYOCLONIC 1; EPM1
PROGRESSIVE MYOCLONIC EPILEPSY; PME
BALTIC MYOCLONIC EPILEPSY
EPILEPSY, PROGRESSIVE MYOCLONIC 1A; EPM1A
(∗) Location:
21q22.3  
(†) Associated OMIM genes:
CSTB  
(‡) Associated MGI genes:
Cstb  

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* quick link - http://q.sanger.ac.uk/89vki44v