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Summary Literature (2)
MIM:141500 - MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1

Xenbase Genes: cacna1a

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018925 - familial or sporadic hemiplegic migraine
MONDO:0020756 - migraine, familial hemiplegic, 1

Disease Ontology (DO):
DOID:0060178 - familial hemiplegic migraine
DOID:0111181 - familial hemiplegic migraine 1