| Human Disease |
Cardiomyopathy, Infantile Histiocytoid OMIM ID: 500000 |
| Synonyms | Cardiomyopathy, Focal Lipid; Cardiomyopathy, Infantile Xanthomatous; Cardiomyopathy, Oncocytic; Foamy Myocardial Transformation of Infancy |
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Genes and mouse models |
There are currently no human or mouse genes associated with this disease in the MGI database. |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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