familial focal epilepsy with variable foci 4 Disease Ontology Browser

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familial focal epilepsy with variable foci 4 (DOID:0081424)
Alliance: disease page
Alt IDs: OMIM:617935
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.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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