Congenital myasthenic syndrome 21

MONDO:0014983

Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the SLC18A3 gene.

Also known as: CMS21, SLC18A3 congenital myasthenic syndrome, congenital myasthenic syndrome caused by mutation in SLC18A3, congenital myasthenic syndrome type 21, myasthenic syndrome, congenital, 21, presynaptic

0 clinical trials for this condition and its sub-types, 0 tagged with Congenital myasthenic syndrome 21 itself.

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↑ Presynaptic congenital myasthenic syndrome (1)

Including sub-types (0) Tagged with Congenital myasthenic syndrome 21 (0)

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