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Summary Literature (0)
MIM:609634 - MIGRAINE, FAMILIAL HEMIPLEGIC, 3; FHM3

Xenbase Genes: scn1a

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012320 - migraine, familial hemiplegic, 3
MONDO:0018925 - familial or sporadic hemiplegic migraine

Disease Ontology (DO):
DOID:0060178 - familial hemiplegic migraine
DOID:0111183 - familial hemiplegic migraine 3