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Summary Literature (0)
MIM:614417 - EPILEPSY, FAMILIAL TEMPORAL LOBE, 5; ETL5

Xenbase Genes: cpa6

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013741 - familial temporal lobe epilepsy 5
MONDO:0015586 - obsolete benign familial mesial temporal lobe epilepsy

Disease Ontology (DO):
DOID:0060752 - familial temporal lobe epilepsy 5