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Disease Ontology Browser
hypertrophic cardiomyopathy 13 (DOID:0110319)
Synonyms: cardiomyopathy familial hypertrophic 13; CMH13
Alt IDs: OMIM:613243
Definition: A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNC1 gene on chromosome 3p21.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/21/2017
MGI 6.08
The Jackson Laboratory