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Summary Literature (0)
MIM:615120 - MYASTHENIC SYNDROME, CONGENITAL, 8; CMS8

Xenbase Genes: agrn

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014052 - congenital myasthenic syndrome 8
MONDO:0018940 - congenital myasthenic syndrome
MONDO:0020344 - postsynaptic congenital myasthenic syndrome
MONDO:0020345 - presynaptic congenital myasthenic syndrome

Disease Ontology (DO):
DOID:0110657 - congenital myasthenic syndrome 8