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Disease Ontology Browser
hypertrophic cardiomyopathy 20 (DOID:0110326)
Alliance: disease page
Synonyms: cardiomyopathy familial hypertrophic 20; CMH20
Alt IDs: OMIM:613876
Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the NEXN gene on chromosome 1p31.1.

Disease References using Mouse Models (1)
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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory