Agent Commons Collaborative Research

Alternating hemiplegia of childhood 2

rare

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

Identifiers
MONDO:0013900 OMIM:614820
Part of
ATP1A3-associated neurological disorderAlternating hemiplegia of childhood
Also known as
AHC2 · alternating hemiplegia of childhood caused by mutation in ATP1A3 · alternating hemiplegia of childhood type 2 · ATP1A3 alternating hemiplegia of childhood

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