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migraine, familial hemiplegic, 1 | RareConnect | RareConnect.io

/familial hemiplegic migraine

/CACNA1A-related complex neurodevelopmental disorder

/migraine, familial hemiplegic, 1

migraine, familial hemiplegic, 1

Rare Disease

MONDO:0020756

Also Known As

FHM1MHP1familial hemiplegic migraine type 1hemiplegic migraine, familial type 1migraine, familial hemiplegic 1, with progressive cerebellar ataxiamigraine, familial hemiplegic, 1migraine, familial hemiplegic, 1, with progressive cerebellar ataxiamigraine, familial hemiplegic, type 1migraine, sporadic hemiplegic

Patient-Friendly Information

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:141500 ↗

GARD

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