Epilepsy, familial adult myoclonic, 2

Any epilepsy, familial adult myoclonic in which the cause of the disease is a mutation in the ADRA2B gene.

Also known as: ADRA2B epilepsy, familial adult myoclonic, epilepsy, familial adult myoclonic caused by mutation in ADRA2B, epilepsy, familial adult myoclonic, 2, epilepsy, familial adult myoclonic, type 2, FAME2, benign adult familial myoclonic epilepsy 2, cortical myoclonic tremor with epilepsy, familial, 2, cortical myoclonus and epilepsy, autosomal dominant

7 clinical trials for this condition and its sub-types, 0 tagged with Epilepsy, familial adult myoclonic, 2 itself.