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familial or sporadic hemiplegic migraine

Disease Summary
Associated Targets (4)
Tclin

2

Tchem

1

Tbio

1


GARD Rare
Mondo Description Hemiplegic migraine (HM) is a rare variety of migraine with aura characterized by the presence of a motor weakness during the aura. Hemiplegic migraine has two main forms depending on the familial history: patients with at least one first- or second-degree relative who has aura including motor weakness have familial hemiplegic migraine (FHM); patients without such familial history have sporadic hemiplegic migraine (SHM).
Mondo Term and Equivalent IDs
MONDO:0018925:  familial or sporadic hemiplegic migraine
GARD:0010768: 
ICD9:346.30: 
Orphanet:569: 
SCTID:59292006: