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DOID:0050881 - inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Disease Ontology 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.
Synonyms: IBMPFD, inclusion body myopathy with Paget's disease of bone and frontotemporal dementia
Xenbase Genes
:
hnrnpa2b1,
hnrnpa1,
vcp
| MONDO:0000507 - inclusion body myopathy with Paget disease of bone and frontotemporal dementia |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
syndrome (is_a)