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Summary Literature (0)
MIM:608930 - MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B

Xenbase Genes: chrna1, chrna1.2, chrnd, chrne

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012156 - myasthenic syndrome, congenital, 1B, fast-channel
MONDO:0018940 - congenital myasthenic syndrome
MONDO:0020344 - postsynaptic congenital myasthenic syndrome

Disease Ontology (DO):
DOID:0110662 - congenital myasthenic syndrome 1B