Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Nemaline myopathy 6

MONDO:0012237

Any nemaline myopathy in which the cause of the disease is a mutation in the KBTBD13 gene.

Also known as: KBTBD13 nemaline myopathy, nemaline myopathy 6, nemaline myopathy caused by mutation in KBTBD13, nemaline myopathy type 6, NEM6

5 clinical trials for this condition and its sub-types, 1 tagged with Nemaline myopathy 6 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by