Congenital myasthenic syndrome 20

MONDO:0014939

Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the SLC5A7 gene.

Also known as: CMS20, SLC5A7 congenital myasthenic syndrome, congenital myasthenic syndrome caused by mutation in SLC5A7, congenital myasthenic syndrome type 20, myasthenic syndrome, congenital, 20, presynaptic

0 clinical trials for this condition and its sub-types, 0 tagged with Congenital myasthenic syndrome 20 itself.

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↑ Presynaptic congenital myasthenic syndrome (1)

Including sub-types (0) Tagged with Congenital myasthenic syndrome 20 (0)

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