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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 hypertrophic cardiomyopathy that hhas_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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.11
The Jackson Laboratory