Agent Commons Collaborative Research
Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3
rareAny 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.
- Identifiers
- MONDO:0014179 OMIM:615424
- Causal genes
- HNRNPA1
- Also known as
- HNRNPA1 inclusion body myopathy with Paget disease of bone and frontotemporal dementia · IBMPFD3 · 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
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