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Disease Ontology Browser
familial hypertrophic cardiomyopathy (DOID:0080326)
Alliance: disease page
Alt IDs: MESH:D024741, NCI:C84773, OMIM:PS192600, ORDO:217569, UMLS_CUI:C0949658
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.

Disease References using Mouse Models (68)

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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last database update
03/19/2024
MGI 6.23
The Jackson Laboratory