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General Information
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| Term |
familial adult myoclonic epilepsy 5 |
ID (Ontology) |
DOID:0111691 (Human Disease) |
| Definition |
A familial adult myoclonic epilepsy characterized by onset of seizures in adolescence, followed by the development of cortical myoclonic tremor that has_material_basis_in homozygous or compound heterozygous mutation in the CNTN2 gene on chromosome 1q32.1. |
| Also Known As |
"FAME5" ; "familial cortical myoclonic tremor and epilepsy 5" ; "FCMTE5" |
| Comment |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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familial adult myoclonic epilepsy 5 | 1 | for disease ribbon | familial adult myoclonic epilepsy 5 | 1 | model of | familial adult myoclonic epilepsy 5 | 1 |
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Relationships