Migraine, familial hemiplegic, 2

Definition

Any familial or sporadic hemiplegic migraine in which the cause of the disease is a mutation in the ATP1A2 gene.

Also known as ATP1A2 familial or sporadic hemiplegic migraine, familial or sporadic hemiplegic migraine caused by mutation in ATP1A2, migraine, familial hemiplegic, 2, migraine, familial hemiplegic, type 2 — per MONDO

Also identified as

• DOID 0111182 per MONDO
• MESH C537246 per MONDO
• OMIM 602481 per MONDO
• UMLS C1865322 per MONDO