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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 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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory