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Disease Ontology Browser
inclusion body myopathy with Paget disease of bone and frontotemporal dementia (DOID:0050881)
Synonyms: IBMPFD; inclusion body myopathy with Paget's disease of bone and frontotemporal dementia
Alt IDs: OMIM:167320, OMIM:615422, OMIM:615424
Definition: A syndrome that is characterized by progressive proximal muscle weakness, steolytic bone lesions consistent with Paget disease, and frontotemporal dementia and has_physical_basis_in mutation in the valosin containing protein (VCP).

Disease References using Mouse Models (8)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/11/2017
MGI 6.08
The Jackson Laboratory