migraine, familial hemiplegic, 2

Rare Disease

MONDO:0011232

Also known as:

ATP1A2 familial or sporadic hemiplegic migrainefamilial or sporadic hemiplegic migraine caused by mutation in ATP1A2migraine, familial hemiplegic, 2

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

Genes

Clinical Trials

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Newborn Screening

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Patient Groups

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Companies Active in migraine, familial hemiplegic, 2

1 approved

Organizations with approved therapies for this disease

Oceanside Pharmaceuticals

Other

Approved

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migraine, familial hemiplegic, 2

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Companies Active in migraine, familial hemiplegic, 2

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