Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (1)
MIM:168300 - PARAMYOTONIA CONGENITA; PMC

Xenbase Genes: scn4a

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008195 - paramyotonia congenita of Von Eulenburg

Disease Ontology (DO):
DOID:0111538 - paramyotonia congenita of Von Eulenburg