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hypertrophic cardiomyopathy 1 (DOID:0110307)
Alliance: disease page
Synonyms: cardiomyopathy, familial hypertrophic 1; CMH1; hypertrophic cardiomyopathy 19
Alt IDs: OMIM:192600, DOID:0110325, DOID:0110325, DOID:0110325, DOID:0110325, DOID:0110325, DOID:0110325, DOID:0110325, DOID:0110325, DOID:0110325, DOID:0110325, DOID:0110325, DOID:0110325, DOID:0110325, DOID:0110325, DOID:0110325, DOID:0110325
Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYH7 gene on chromosome 14q12.


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
10/08/2019
MGI 6.14
The Jackson Laboratory