OBO ID: DOID:0080326 |
Term Name: | familial hypertrophic cardiomyopathy | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0080326 ) |
OTHER familial hypertrophic cardiomyopathy PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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