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familial or sporadic hemiplegic migraine

^ http://purl.obolibrary.org/obo/MONDO_0018925

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). [ Orphanet:569 ]

Term info

database cross reference
  • GARD:0010768 (MONDO:equivalentTo)
  • ICD9:346.30 (MONDO:i2s)
  • SCTID:59292006 (MONDO:equivalentTo)
  • Orphanet:569 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease

definition

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).

exactMatch

http://identifiers.org/snomedct/59292006, http://purl.obolibrary.org/obo/Orphanet_569

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0015953, http://purl.obolibrary.org/obo/MONDO_0015642

has exact synonym

hemiplegic migraine, familial or sporadic hemiplegic migraine

id

MONDO:0018925

seeAlso

https://rarediseases.info.nih.gov/diseases/10768/hemiplegic-migraine

Term relations

Subclass of: