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hypertrophic cardiomyopathy 16 (DOID:0110322)
Alliance: disease page
Synonyms: cardiomyopathy familial hypertrophic 16; CMH16
Alt IDs: OMIM:613838
Definition: A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYOZ2 gene on chromosome 4q26.

Disease References using Mouse Models (2)

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