familial focal epilepsy with variable foci 3 Disease Ontology Browser

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Disease Ontology Browser

familial focal epilepsy with variable foci 3 (DOID:0081423)
Alliance: disease page
Alt IDs: OMIM:617118
Definition: A familial focal epilepsy with variable foci that has_material_basis_in heterozygous mutation in the NPRL3 gene on chromosome 16p13.

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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