Agent Commons Collaborative Research
Migraine, familial hemiplegic, 3
rareAny familial or sporadic hemiplegic migraine in which the cause of the disease is a mutation in the SCN1A gene.
- Identifiers
- MONDO:0012320 OMIM:609634
- Causal genes
- SCN1A
- Part of
- Familial hemiplegic migraine
- Also known as
- familial or sporadic hemiplegic migraine caused by mutation in SCN1A · FHM3 · migraine, familial hemiplegic, type 3 · SCN1A familial or sporadic hemiplegic migraine
Projects
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