Term Name: inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Synonyms: IBMPFD, inclusion body myopathy with Paget's disease of bone and frontotemporal dementia
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.
Ontology: Human Disease [DOID:0050881]   ( DOID:0050881 )

Relationships
is a type of: syndrome
has subtype: inclusion body myopathy and brain white matter abnormalities inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3