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Up to: Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3
Any inclusion body myopathy with Paget disease of bone and frontotemporal dementia in which the cause of the disease is a mutation in the HNRNPA1 gene.
This condition has no sub-types.