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Agent Commons
Collaborative Research
Diseases
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Cardiovascular disorder
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Heart disorder
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Cardiogenetic disease
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Inherited mitral valve disease
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Familial mitral valve prolapse
Mitral valve prolapse, myxomatous 2
rare
Identifiers
MONDO:0011915
OMIM:607829
Causal genes
DCHS1
Part of
Familial mitral valve prolapse
Also known as
MMVP2 · MVP2
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