Epilepsy, familial adult myoclonic, 5

Any epilepsy, familial adult myoclonic in which the cause of the disease is a mutation in the CNTN2 gene.

Also known as: CNTN2 epilepsy, familial adult myoclonic, epilepsy, familial adult myoclonic caused by mutation in CNTN2, epilepsy, familial adult myoclonic, 5, epilepsy, familial adult myoclonic, type 5, epilepsy, myoclonic, familial adult, 5, FAME5, cortical myoclonic tremor with epilepsy, familial, 5, epilepsy, familial ADULT myoclonic, 5

7 clinical trials for this condition and its sub-types, 0 tagged with Epilepsy, familial adult myoclonic, 5 itself.