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:617143 - MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20

Xenbase Genes: slc5a7

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014939 - congenital myasthenic syndrome 20
MONDO:0018940 - congenital myasthenic syndrome
MONDO:0020345 - obsolete presynaptic congenital myasthenic syndrome