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Disease Ontology Browser
hypertrophic cardiomyopathy 11 (DOID:0110317)
Alliance: disease page
Synonyms: cardiomyopathy familial hypertrophic 11; CMH11
Alt IDs: OMIM:612098
Definition: A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the ACTC1 gene on chromosome 15q14.

Disease References using Mouse Models (3)

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