All diseases

OMIM ID
609056
OMIM term:
AMISH INFANTILE EPILEPSY SYNDROME
Alternative terms:
EPILEPSY SYNDROME, INFANTILE-ONSET SYMPTOMATIC
GM3 SYNTHASE DEFICIENCY
(∗) Location:
2p11.2  
(†) Associated OMIM genes:
ST3GAL5  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/u4o37kvd