Agent Commons Collaborative Research
Episodic pain syndrome, familial, 2
rareAny familial episodic pain syndrome in which the cause of the disease is a mutation in the SCN10A gene.
- Identifiers
- MONDO:0014246 OMIM:615551
- Causal genes
- SCN10A
- Part of
- Familial episodic pain syndrome
- Also known as
- episodic pain syndrome, familial, type 2 · familial episodic pain syndrome caused by mutation in SCN10A · FEPS2 · SCN10A familial episodic pain syndrome
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