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episodic pain syndrome, familial, 2

Disease Summary
Associated Targets (1)
Tclin

1


Mondo Description Any familial episodic pain syndrome in which the cause of the disease is a mutation in the SCN10A gene.
Uniprot Description An autosomal dominant neurologic disorder characterized by adult-onset of paroxysmal pain mainly affecting the distal lower extremities.
Mondo Term and Equivalent IDs
MONDO:0014246:  episodic pain syndrome, familial, 2
DOID:0111730: 
UMLS:C3809893: