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 (0)
MIM:616322 - MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL; CMS3B

Xenbase Genes: chrnd

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014584 - congenital myasthenic syndrome 3B
MONDO:0018940 - congenital myasthenic syndrome
MONDO:0020344 - postsynaptic congenital myasthenic syndrome