MeSH Browser

MeSH Supplementary: Hemiplegic migraine, familial type 2
Unique ID: C537246
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537246
Entry Term(s): Familial hemiplegic migraine, type 2; Migraine, familial hemiplegic, 2
Heading Mapped to: *Migraine with Aura
Frequency: 32
Note: An autosomal dominant type of familial hemiplegic migraine (Migraine with Aura) with onset between 6 to 30 years and characterized by hemiparesis or paresthesias, aphasia, headaches, and behavioral changes, with subsequent loss of consciousness. Mutations in the ATP1A2 gene have been identified. OMIM: 602481
Date of Entry: 2010/08/25
Revision Date: 2015/09/26

Hemiplegic migraine, familial type 2 MeSH Supplementary Concept Data 2024