Alternating hemiplegia of childhood 2

Definition

Any alternating hemiplegia of childhood in which the cause of the disease is a mutation in the ATP1A3 gene.

Also known as alternating hemiplegia of childhood 2, alternating hemiplegia of childhood caused by mutation in ATP1A3, alternating hemiplegia of childhood type 2, ATP1A3 alternating hemiplegia of childhood — per MONDO

Also identified as

• OMIM 614820 per MONDO
• UMLS C3553788 per MONDO