WormBase Tree Display for DO_term: DOID:0111691
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| DOID:0111691 | Name | familial adult myoclonic epilepsy 5 | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| 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. | ||||
| Synonym | Exact | FAME5 | |||
| FCMTE5 | |||||
| familial cortical myoclonic tremor and epilepsy 5 | |||||
| Parent | Is_a | DOID:0050737 | |||
| DOID:0111689 | |||||
| DB_info | Database | OMIM | disease | 615400 | |
| Attribute_of | Gene_by_orthology | WBGene00016354 |
