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Summary Literature (2)
MIM:602481 - MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2

Xenbase Genes: atp1a2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011232 - migraine, familial hemiplegic, 2
MONDO:0018925 - familial or sporadic hemiplegic migraine

Disease Ontology (DO):
DOID:0060178 - familial hemiplegic migraine