Congenital myasthenic syndrome 7

Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the SYT2 gene.

Also known as: CMS7, SYT2 congenital myasthenic syndrome, congenital myasthenic syndrome caused by mutation in SYT2, congenital myasthenic syndrome type 7, myasthenic syndrome, congenital, 7A, presynaptic, and distal motor neuropathy, autosomal dominant, myasthenic syndrome, congenital, 7, presynaptic, myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy

1 clinical trial for this condition and its sub-types.