All diseases

OMIM ID
600512
OMIM term:
EPILEPSY, FAMILIAL TEMPORAL LOBE, 1; ETL1
Alternative terms:
EPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT; ADLTE
EPILEPSY, PARTIAL, WITH AUDITORY FEATURES; ADPEAF
(∗) Location:
10q23.33  
(†) Associated OMIM genes:
LGI1  
(‡) Associated MGI genes:
Lgi1  

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