Any postsynaptic congenital myasthenic syndrome in which the cause of the disease is a mutation in the CHRNE gene.
Comprehensive, easy-to-understand information about this condition
Checking for content...
No external resources available.
congenital myasthenic syndrome 10
MONDO:0009690
congenital myasthenic syndrome 1A
MONDO:0011088
congenital myasthenic syndrome 4A
MONDO:0011600
congenital myasthenic syndrome 4C
MONDO:0012157
congenital myasthenic syndrome 16
MONDO:0013620
congenital myasthenic syndrome 8
MONDO:0014052