Epilepsy, familial adult myoclonic, 5

Definition

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 — per MONDO

Also identified as

• DOID 0111691 per MONDO
• OMIM 615400 per MONDO
• UMLS C3809374 per MONDO