Myofibrillar myopathy 7

Any myofibrillar myopathy in which the cause of the disease is a mutation in the KY gene.

Also known as: KY myofibrillar myopathy (disease), alpha-b crystalin-related fatal infantile hypertonic myofibrillar myopathy, myofibrillar myopathy (disease) caused by mutation in KY, myopathy, myofibrillar, 7, myopathy, myofibrillar, type 7, MFM7

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