Myofibrillar myopathy 7

MONDO:0014922

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

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

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