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Disease Ontology Browser
myofibrillar myopathy 7 (DOID:0080098)
Alliance: disease page
Alt IDs: OMIM:617114
Definition: A myofibrillar myopathy that has_material_basis_in homozygous mutation in the KY gene on chromosome 3q22.

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 6.13
The Jackson Laboratory