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Summary Literature (0)
MIM:117100 - CENTRALOPATHIC EPILEPSY

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007295 - childhood epilepsy with centrotemporal spikes

Disease Ontology (DO):
DOID:3329 - benign epilepsy with centrotemporal spikes