Centronuclear myopathy

MONDO:0018947

Centronuclear myopathy (CNM) is an inherited neuromuscular disorder characterized by clinical features of a congenital myopathy and centrally placed nuclei on muscle biopsy.

Also known as: CNM, centronuclear myopathy, myopathy, centronuclear, myopathy, myotubular

9 clinical trials for this condition and its sub-types, 2 tagged with Centronuclear myopathy itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Congenital myopathy (75)

Sub-types of Centronuclear myopathy

X-linked myotubular myopathy 4 trials
2 sub-types
- X-linked myotubular myopathy-abnormal genitalia syndrome 0 trials
- Symptomatic form of X-linked centronuclear myopathy in female carriers 0 trials
Autosomal dominant centronuclear myopathy 0 trials
Autosomal recessive centronuclear myopathy 0 trials
2 sub-types
- Myopathy, centronuclear, 2 0 trials
- Myopathy, centronuclear, 5 0 trials
Congenital myopathy with internal nuclei and atypical cores 0 trials
Myopathy, centronuclear, 6, with fiber-type disproportion 0 trials

Including sub-types (9) Tagged with Centronuclear myopathy (2)

Trials to join now! 2

Centronuclear myopathy

Where it sits in the disease tree

Shocking muscles to move: new exercise hope for nerve disease patients

Gene hunt for rare muscle diseases could unlock future treatments