Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 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.

Also known as HNRNPA2B1 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 type 2, inclusion body myopathy with Paget disease of bone and frontotemporal dementia caused by mutation in HNRNPA2B1 — per MONDO

Also identified as

• DOID 0111384 per MONDO
• OMIM 615422 per MONDO
• UMLS C3809468 per MONDO