About   Help   FAQ
Disease Ontology Browser
inclusion body myopathy with Paget disease of bone and frontotemporal dementia (DOID:0050881)
Alliance: disease page
Synonyms: IBMPFD; inclusion body myopathy with Paget's disease of bone and frontotemporal dementia
Alt IDs: 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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
11/12/2019
MGI 6.14
The Jackson Laboratory