OBO ID: DOID:0110328 |
Term Name: | hypertrophic cardiomyopathy 25 | Search Ontology: | |
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Definition: | A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TCAP gene on chromosome 17q12. https://www.ncbi.nlm.nih.gov/pubmed/15582318 | ||
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Ontology: | Human Disease ( DOID:0110328 ) |
OTHER hypertrophic cardiomyopathy 25 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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