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Disease Ontology Browser
hypertrophic cardiomyopathy 3 (DOID:0110309)
Alliance: disease page
Synonyms: cardiomyopathy familial hypertrophic 3; CMH3
Alt IDs: OMIM:115196
Definition: A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22.

Disease References using Mouse Models (12)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.11
The Jackson Laboratory