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Disease Ontology Browser
hypertrophic cardiomyopathy 18 (DOID:0110324)
Synonyms: cardiomyopathy familial hypertrophic 18; CMH18
Alt IDs: OMIM:613874
Definition: A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the gene encoding phospholamban (PLN) on chromosome 6q22.1.


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
08/08/2017
MGI 6.10
The Jackson Laboratory