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Disease Ontology Browser
inclusion body myopathy with Paget disease of bone and frontotemporal dementia (DOID:0050881)
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Synonyms: IBMPFD; inclusion body myopathy with Paget's disease of bone and frontotemporal dementia
Alt IDs: MESH:C563476, OMIM:PS167320, ORDO:52430
Definition: A syndrome that is characterized by progressive proximal muscle weakness, steolytic bone lesions consistent with Paget disease, and frontotemporal dementia and has_material_basis_in mutation in the valosin containing protein.

Disease References using Mouse Models (9)
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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory