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Congenital myasthenic syndrome 15

MONDO:0014542

Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the ALG14 gene.

Also known as: ALG14 congenital myasthenic syndrome, CMS15, congenital myasthenic syndrome caused by mutation in ALG14, congenital myasthenic syndrome type 15, myasthenic syndrome, congenital, 15, without tubular aggregates, myasthenic syndrome, congenital, type 15, myasthenic syndrome, congenital, 15, myasthenic syndrome, congenital, without tubular aggregates

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

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Broader categories

Disease (618) Nervous system disorder (217) Metabolic disease (215) Hereditary disease (172) Neuromuscular disease (98) Inborn errors of metabolism (42) Syndromic disease (24) Human disease (14) Congenital disorder of glycosylation (6) Hereditary neurological disease (5)
Trials to join now! 14 Not yet recruiting 4 Not yet finished but already full! 3 Completed 6
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