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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)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory