Migraine, familial hemiplegic, 3

MONDO:0012320

Any familial or sporadic hemiplegic migraine in which the cause of the disease is a mutation in the SCN1A gene.

Also known as: SCN1A familial or sporadic hemiplegic migraine, familial or sporadic hemiplegic migraine caused by mutation in SCN1A, migraine, familial hemiplegic, 3, migraine, familial hemiplegic, type 3, FHM3

9 clinical trials for this condition and its sub-types, 0 tagged with Migraine, familial hemiplegic, 3 itself.

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↑ Familial hemiplegic migraine (1)

Including sub-types (9) Tagged with Migraine, familial hemiplegic, 3 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.