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Human Disease

familial hypertrophic cardiomyopathy

Term ID
DOID:0080326
Synonyms
Definition
A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations. https://ghr.nlm.nih.gov/condition/familial-hypertrophic-cardiomyopathy#genes
References
Ontology
Human Disease   ( DOID:0080326 )
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is a type of
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