familial adult myoclonic epilepsy 4 Disease Ontology Browser

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Disease Ontology Browser

familial adult myoclonic epilepsy 4 (DOID:0111693)
Alliance: disease page
Synonyms: FAME4; familial cortical myoclonic tremor and epilepsy 4; FCMTE4
Alt IDs: OMIM:615127
Definition: A familial adult myoclonic epilepsy that has_material_basis_in heterozygous mutation in the YEATS2 gene on chromosome 3q27.1.

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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