Episodic pain syndrome, familial, 2
MONDO:0014246Any familial episodic pain syndrome in which the cause of the disease is a mutation in the SCN10A gene.
Also known as: SCN10A familial episodic pain syndrome, episodic pain syndrome, familial, 2, episodic pain syndrome, familial, type 2, familial episodic pain syndrome caused by mutation in SCN10A, FEPS2
10 clinical trials for this condition and its sub-types, 0 tagged with Episodic pain syndrome, familial, 2 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.