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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Hereditary skeletal muscle disorder
/
Myofibrillar myopathy
Myofibrillar myopathy 10
rare
Identifiers
MONDO:0033620
OMIM:619040
Causal genes
SVIL
Part of
Myofibrillar myopathy
Also known as
MFM10
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