familial focal epilepsy with variable foci 4

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Summary

Literature (0)

DOID:0081424 - familial focal epilepsy with variable foci 4

Disease Ontology Definition:A familial focal epilepsy with variable foci that is characterized by onset of focal seizures in the first years of life and that has_material_basis_in heterozygous mutation in the SCN3A gene on chromosome 2q24.

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: scn3a

MIM:

MIM:617935 - EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 4; FFEVF4

MIM:617935 - EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 4; FFEVF4

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): familial focal epilepsy with variable foci (is_a)