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Summary Literature (0)
DOID:0081420 - familial focal epilepsy with variable foci

Disease Ontology Definition:A focal epilepsy that is characterized by focal seizures, with seizure onset in a discrete area of the brain including the temporal, frontal, parietal, and occipital lobes, with focal seizures arising from different cortical regions in different family members.

Synonyms: DEPDC5-related epilepsy,

Xenbase Genes : nprl2, depdc5, scn3a, nprl3



Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), focal epilepsy (is_a)