# familial hemiplegic migraine

> migraine with aura that is characterized by temporary numbness or weakness, often affecting one side of the body

**Wikidata**: [Q3312899](https://www.wikidata.org/wiki/Q3312899)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Familial_hemiplegic_migraine)  
**Source**: https://4ort.xyz/entity/familial-hemiplegic-migraine


## References

1. Disease Ontology
2. Freebase Data Dumps. 2013
3. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4
4. Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia
5. Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine
6. Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)
8. [OpenAlex](https://docs.openalex.org/download-snapshot/snapshot-data-format)