/inclusion body myopathy with Paget disease of bone and frontotemporal dementia

/inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2

inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2

Rare Disease

MONDO:0014178

Also Known As

HNRNPA2B1 inclusion body myopathy with Paget disease of bone and frontotemporal dementiainclusion body myopathy with Paget disease of bone and frontotemporal dementia caused by mutation in HNRNPA2B1inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia type 2IBMPFD2multisystem Proteinopathy 2

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 HNRNPA2B1 gene.