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DO Term : familial adult myoclonic epilepsy 7 [DOID:0111694] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A familial adult myoclonic epilepsy that has_material_basis_in a heterozygous 5-bp repeat expansion in the RAPGEF2 gene on chromosome 4q32.1.
  • synonyms:
  • FAME7,
  • FCMTE7,
  • benign adult familial myoclonic epilepsy 7,
  • OMIM:618075,
  • BAFME7,
  • familial cortical myoclonic tremor and epilepsy 7,
  • 618075
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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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