Congenital myasthenic syndrome 10

MONDO:0009690

Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the DOK7 gene.

Also known as: CMS10, DOK7 congenital myasthenic syndrome, congenital muscular dystrophy merosin-positive, congenital myasthenic syndrome 10, congenital myasthenic syndrome caused by mutation in DOK7, congenital myasthenic syndrome type 10, myasthenic syndrome, congenital, type 10, CMS Ib

8 clinical trials for this condition and its sub-types, 3 tagged with Congenital myasthenic syndrome 10 itself.

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Where it sits in the disease tree

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Part of

↑ Congenital muscular dystrophy (10) ↑ Postsynaptic congenital myasthenic syndrome (3)

Including sub-types (8) Tagged with Congenital myasthenic syndrome 10 (3)

Trials to join now! 1 Not yet recruiting 1 Not yet finished but already full! 1

Researchers track rare muscle disease to uncover its secrets

Knowledge-focused Recruiting now

This study is for people with a rare genetic muscle condition called congenital myasthenic syndrome (CMS). It does not test any new drug or treatment. Instead, researchers will collect information from up to 100 participants over 4 visits to better understand how the disease affe…

Sponsor: argenx • Aim: Knowledge-focused

Last updated Jul 24, 2026 00:00 UTC

Congenital myasthenic syndrome 10

Where it sits in the disease tree

Researchers track rare muscle disease to uncover its secrets