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Summary Literature (0)
MIM:616326 - MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS11

Xenbase Genes: rapsn

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014588 - congenital myasthenic syndrome 11
MONDO:0018940 - congenital myasthenic syndrome
MONDO:0020344 - postsynaptic congenital myasthenic syndrome

Disease Ontology (DO):
DOID:0110675 - congenital myasthenic syndrome 11