familial focal epilepsy with variable foci 3

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Summary

Literature (0)

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 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

: nprl3

MIM:

MIM:617118 - EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 3; FFEVF3

MIM:617118 - EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 3; FFEVF3

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)