Myopathy, centronuclear, 5

MONDO:0014418

Any autosomal recessive centronuclear myopathy in which the cause of the disease is a mutation in the SPEG gene.

Also known as: SPEG autosomal recessive centronuclear myopathy, autosomal recessive centronuclear myopathy caused by mutation in SPEG, myopathy, centronuclear, 5, myopathy, centronuclear, type 5, CNM5

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

Follow this condition — get notified about new trials

Broader categories

Sort by