All diseases

OMIM ID
610003
OMIM term:
CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT
Alternative terms:
NORTHERN EPILEPSY
EPILEPSY, PROGRESSIVE, WITH MENTAL RETARDATION; EPMR
(∗) Location:
8p23.3  
(†) Associated OMIM genes:
CLN8  
(‡) Associated MGI genes:

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