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DOID:0081423 - familial focal epilepsy with variable foci 3
Disease Ontology Definition:A familial focal epilepsy with variable foci that has_material_basis_in heterozygous mutation in the NPRL3 gene on chromosome 16p13.
Synonyms:
Xenbase Genes : nprl3
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee