Epilepsy, familial adult myoclonic, 2

Definition

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 — per MONDO

Also identified as

• DOID 0111692 per MONDO
• MESH C564313 per MONDO
• OMIM 607876 per MONDO
• UMLS C1842852 per MONDO