About   Help   FAQ
Disease Ontology Browser
hypertrophic cardiomyopathy 12 (DOID:0110318)
Alliance: disease page
Synonyms: cardiomyopathy familial hypertrophic 12; CMH12
Alt IDs: OMIM:612124
Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the CSRP3 gene on chromosome 11p15.

Disease References using Mouse Models (2)
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
04/23/2024
MGI 6.23 		The Jackson Laboratory