infantile hypertrophic cardiomyopathy Disease Ontology Browser

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Disease Ontology Browser

infantile hypertrophic cardiomyopathy (DOID:0111753)
Alliance: disease page
Alt IDs: OMIM:500006
Definition: A hypertrophic cardiomyopathy characterized by isolated hypertrophic cardiomyopathy and congestive heart failure that has_material_basis_in mutation in the overlapping mitochondrial genes MTATP6 and MTATP8.

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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