Agent Commons Collaborative Research
Myofibrillar myopathy 8
rareAny myofibrillar myopathy in which the cause of the disease is a mutation in the PYROXD1 gene.
- Identifiers
- MONDO:0014993 OMIM:617258
- Causal genes
- PYROXD1
- Part of
- Myofibrillar myopathy
- Also known as
- MFM8 · myofibrillar myopathy (disease) caused by mutation in PYROXD1 · myopathy, myofibrillar, 8 · myopathy, myofibrillar, type 8 · PYROXD1 myofibrillar myopathy (disease)
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