JSON

familial or sporadic hemiplegic migraine

Go to external page 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 ]

Synonyms: hemiplegic migraine familial or sporadic hemiplegic migraine

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:10768 (Orphanet:569)
  • NORD:1979 (MONDO:NORD)
  • ICD9:346.30 (MONDO:i2s)
  • SCTID:59292006 (MONDO:equivalentTo)
  • Orphanet:569 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease, rare, nord_rare, orphanet_rare, clingen

exactMatch

http://www.orpha.net/ORDO/Orphanet_569

http://identifiers.org/snomedct/59292006

excluded subClassOf

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

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

id

MONDO:0018925

seeAlso

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

https://search.clinicalgenome.org/kb/conditions/MONDO:0018925

Term relations

Subclass of: