Migraine, familial hemiplegic, 2

MONDO:0011232

Any familial or sporadic hemiplegic migraine in which the cause of the disease is a mutation in the ATP1A2 gene.

Also known as: ATP1A2 familial or sporadic hemiplegic migraine, familial or sporadic hemiplegic migraine caused by mutation in ATP1A2, migraine, familial hemiplegic, 2, migraine, familial hemiplegic, type 2, FHM2, Mhp2, familial hemiplegic migraine type 2, hemiplegic migraine, familial type 2

9 clinical trials for this condition and its sub-types, 0 tagged with Migraine, familial hemiplegic, 2 itself.

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↑ Familial hemiplegic migraine (1)

Including sub-types (9) Tagged with Migraine, familial hemiplegic, 2 (0)

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