familial hemiplegic migraine Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A migraine with aura that is characterized by temporary numbness or weakness, often affecting one side of the body (hemiparesis). Additional features of an aura can include difficulty with speech, confusion, and drowsiness. (Human Disease Ontology, DOID_0060178)
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Genes

4 genes involed in the disease familial hemiplegic migraine from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ATP1A2 ATPase, Na+/K+ transporting, alpha 2 polypeptide
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
PRRT2 proline-rich transmembrane protein 2
SCN1A sodium channel, voltage gated, type I alpha subunit