(Q3508770)
English
inclusion body myopathy with Paget disease of bone and frontotemporal dementia
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)
- IBMPFD
- inclusion body myopathy with Paget's disease of bone and frontotemporal dementia
- Limb-girdle muscular dystrophy with Paget disease of bone
- Pagetoid neuroskeletal syndrome
- inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia
- Pagetoid amyotrophic lateral sclerosis
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