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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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Familial cardiomyopathy
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Familial hypertrophic cardiomyopathy
Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies
rare
Identifiers
MONDO:0859372
OMIM:620236
Causal genes
KLHL24
Part of
Familial hypertrophic cardiomyopathy
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