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Disease Ontology Browser
hypertrophic cardiomyopathy 2 (DOID:0110308)
Alliance: disease page
Synonyms: cardiomyopathy familial hypertrophic 2; CMH2
Alt IDs: OMIM:115195
Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the cardiac troponin-T2 gene (TNNT2).

Disease References using Mouse Models (9)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
06/04/2019
MGI 6.14
The Jackson Laboratory