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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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Familial visceral myopathy
Visceral myopathy 1
rare
Identifiers
MONDO:0020754
OMIM:155310
Causal genes
ACTG2
Part of
Familial visceral myopathy
Also known as
visceral myopathy · VSCM
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