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Summary Literature (0)
MIM:616228 - MYASTHENIC SYNDROME, CONGENITAL, 14; CMS14

Xenbase Genes: alg2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014543 - congenital myasthenic syndrome 14
MONDO:0018144 - obsolete congenital myasthenic syndromes with glycosylation defect
MONDO:0018940 - congenital myasthenic syndrome