FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term familial adult myoclonic epilepsy 7 ID (Ontology) DOID:0111694 (Human Disease)
Definition A familial adult myoclonic epilepsy that has_material_basis_in a heterozygous 5-bp repeat expansion in the RAPGEF2 gene on chromosome 4q32.1.
Also Known As "BAFME7" ; "benign adult familial myoclonic epilepsy 7" ; "FAME7" (for all, see Synonyms field below)
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 Genes
 familial adult myoclonic epilepsy 7       1
 for disease ribbon | familial adult myoclonic epilepsy 7       1
 model of | familial adult myoclonic epilepsy 7       1
Spanning Tree (Parents/Children)
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adolescence-adult electroclinical syndrome
 |__familial adult myoclonic epilepsy__
autosomal genetic disease              |
 |__autosomal dominant disease_________|
                                       familial adult myoclonic epilepsy 7  1 rec.
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Is a autosomal dominant disease
familial adult myoclonic epilepsy
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Synonyms
  • "BAFME7" EXACT OMO:0003012
    "benign adult familial myoclonic epilepsy 7" EXACT
    "FAME7" EXACT OMO:0003012
    "familial cortical myoclonic tremor and epilepsy 7" EXACT
    "FCMTE7" EXACT OMO:0003012
Secondary IDs
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MIM:618075