familial focal epilepsy with variable foci 1 Disease Ontology Browser

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familial focal epilepsy with variable foci 1 (DOID:0081421)
Alliance: disease page
Alt IDs: OMIM:604364
Definition: A familial focal epilepsy with variable foci that is characterized by focal seizures arising from different cortical regions in different family members and that has_material_basis_in heterozygous mutation in the DEPDC5 gene on chromosome 22q12.

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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