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Disease Ontology Browser
hypertrophic cardiomyopathy 8 (DOID:0110314)
Alliance: disease page
Synonyms: cardiomyopathy hypertrophic mid-left ventricular chamber type 1; cardiomyopathy, familial hypertrophic, 8
Alt IDs: OMIM:608751
Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in homozygous or heterozygous mutation in the MYL3 gene.

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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last database update
MGI 6.15
The Jackson Laboratory