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Summary Literature (4)
DOID:0060178 - familial hemiplegic migraine


Disease Ontology Definition:A migraine with aura that is characterized by temporary numbness or weakness, often affecting one side of the body (hemiparesis). Additional features of an aura can include difficulty with speech, confusion, and drowsiness.

Synonyms:

Xenbase Genes : scn1a, cacna1a, atp1a2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000700 - familial hemiplegic migraine

OMIM:
OMIM:141500 - MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1
OMIM:602481 - MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2
OMIM:609634 - MIGRAINE, FAMILIAL HEMIPLEGIC, 3; FHM3

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): migraine with aura (is_a)