Myofibrillar myopathy 8

MONDO:0014993

Any myofibrillar myopathy in which the cause of the disease is a mutation in the PYROXD1 gene.

Also known as: PYROXD1 myofibrillar myopathy (disease), myofibrillar myopathy (disease) caused by mutation in PYROXD1, myofibrillar myopathy 8, myopathy, myofibrillar, 8, myopathy, myofibrillar, type 8, MFM8

4 clinical trials for this condition and its sub-types, 0 tagged with Myofibrillar myopathy 8 itself.

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Part of

↑ Myofibrillar myopathy (3)

Including sub-types (4) Tagged with Myofibrillar myopathy 8 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.