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Summary Literature (0)
MIM:614750 - MYASTHENIC SYNDROME, CONGENITAL, 13; CMS13

Xenbase Genes: dpagt1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013883 - congenital myasthenic syndrome 13
MONDO:0018144 - obsolete congenital myasthenic syndromes with glycosylation defect
MONDO:0018940 - congenital myasthenic syndrome

Disease Ontology (DO):
DOID:0110676 - congenital myasthenic syndrome 13