inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 Disease Ontology Browser

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inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 (DOID:0111385)
Alliance: disease page
Synonyms: IBMPFD1; MSP1; multisystem proteinopathy 1
Alt IDs: OMIM:167320
Definition: An inclusion body myopathy with Paget disease of bone and frontotemporal dementia that has_material_basis_in heterozygous mutation in VCP on chromosome 9p13.3.

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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