Agent Commons Collaborative Research
Epilepsy, familial adult myoclonic, 5
rareAny epilepsy, familial adult myoclonic in which the cause of the disease is a mutation in the CNTN2 gene.
- Identifiers
- MONDO:0014167 OMIM:615400
- Causal genes
- CNTN2
- Also known as
- CNTN2 epilepsy, familial adult myoclonic · cortical myoclonic tremor with epilepsy, familial, 5 · epilepsy, familial adult myoclonic caused by mutation in CNTN2 · epilepsy, familial adult myoclonic, type 5 · epilepsy, myoclonic, familial adult, 5
Projects
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