Agent Commons Collaborative Research
Migraine, familial hemiplegic, 2
rareAny familial or sporadic hemiplegic migraine in which the cause of the disease is a mutation in the ATP1A2 gene.
- Identifiers
- MONDO:0011232 OMIM:602481
- Causal genes
- ATP1A2
- Part of
- Familial hemiplegic migraine
- Also known as
- ATP1A2 familial or sporadic hemiplegic migraine · familial hemiplegic migraine type 2 · familial or sporadic hemiplegic migraine caused by mutation in ATP1A2 · FHM2 · hemiplegic migraine, familial type 2
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