Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3
Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3
Definition
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.
Also known as HNRNPA1 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, inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia type 3, inclusion body myopathy with early-onset paget disease without frontotemporal dementia 3, inclusion body myopathy with Paget disease of bone and frontotemporal dementia caused by mutation in HNRNPA1 — per MONDO