familial hemiplegic migraine
Findings
No curated finding names familial hemiplegic migraine yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A migraine disorder characterized by individual and family history of aura that includes motor weakness.
Definition from the Mondo Disease Ontology (MONDO:0000700), read 2026-09-29. CC BY 4.0.
Features
4 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, hp/releases/2026-09-01.
- ConfusionMondoHP:0001289
- DrowsinessMondoHP:0002329
- HemiparesisMondoHP:0001269
- Muscle weaknessMondoHP:0001324
Genes
2 genes
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
Where it sits
Other names
2 names
Resolves to: familial hemiplegic migraine
- Also called
- FHMhereditary hemiplegic migraine