Alternating hemiplegia of childhood 1

Definition

Any alternating hemiplegia of childhood in which the cause of the disease is a mutation in the ATP1A2 gene.

Also known as alternating hemiplegia of childhood 1, alternating hemiplegia of childhood caused by mutation in ATP1A2, alternating hemiplegia of childhood type 1, ATP1A2 alternating hemiplegia of childhood — per MONDO

Also identified as

• OMIM 104290 per MONDO
• UMLS C3549447 per MONDO