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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:0000700 - familial hemiplegic migraine |
| MIM:141500 - MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1 |
| MIM:602481 - MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2 |
| MIM:609634 - MIGRAINE, FAMILIAL HEMIPLEGIC, 3; FHM3 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
migraine with aura (is_a)