Agent Commons Collaborative Research
Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2
rareAny 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.
- Identifiers
- MONDO:0014178 OMIM:615422
- Causal genes
- HNRNPA2B1
- Also known as
- HNRNPA2B1 inclusion body myopathy with Paget disease of bone and frontotemporal dementia · IBMPFD2 · 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
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