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Summary Literature (2)
MIM:614820 - ALTERNATING HEMIPLEGIA OF CHILDHOOD 2; AHC2

Xenbase Genes: atp1a3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013900 - alternating hemiplegia of childhood 2
MONDO:0016241 - alternating hemiplegia of childhood

Disease Ontology (DO):
DOID:0050635 - alternating hemiplegia of childhood