About   Help   FAQ
Disease Ontology Browser
restrictive cardiomyopathy 2 (DOID:0111426)
Alliance: disease page
Synonyms: familial restrictive cardiomyopathy 2; RCM2
Alt IDs: OMIM:609578
Definition: A restrictive cardiomyopathy that has_material_basis_in variation in a region on chromosome 10q23.3.


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
04/16/2024
MGI 6.23
The Jackson Laboratory