Congenital myasthenic syndrome 16

MONDO:0013620

Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the SCN4A gene.

Also known as: CMS16, SCN4A congenital myasthenic syndrome, congenital myasthenic syndrome caused by mutation in SCN4A, congenital myasthenic syndrome type 16, myasthenic syndrome, congenital, type 16, myasthenic syndrome, congenital, 16, myasthenic syndrome, congenital, Acetazolamide-responsive

38 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by