hypertrophic cardiomyopathy 17 Disease Ontology Browser

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Disease Ontology Browser

hypertrophic cardiomyopathy 17 (DOID:0110323)
Alliance: disease page
Synonyms: cardiomyopathy familial hypertrophic 17; CMH17
Alt IDs: OMIM:613873
Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the junctophilin gene (JPH2) on chromosome 20q12.

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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