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MIM:601462 - MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL; CMS1A
Xenbase Genes: chrna1, chrna1.2, chrnd, chrne, chrnb1
Human Disease Resource: MIM
MONDO:0011088 - congenital myasthenic syndrome 1A |
MONDO:0018940 - congenital myasthenic syndrome |
MONDO:0020344 - postsynaptic congenital myasthenic syndrome |
Disease Ontology (DO):
DOID:0110663 - congenital myasthenic syndrome 1A |