hypertrophic cardiomyopathy 21 Disease Ontology Browser

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Disease Ontology Browser

hypertrophic cardiomyopathy 21 (DOID:0110311)
Alliance: disease page
Synonyms: cardiomyopathy familial hypertrophic 21; CMH21
Alt IDs: OMIM:614676
Definition: A familial hypertrophic cardiomyopathy associated that has_material_basis_in region 7p12.1-q21 variation.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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