inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3 (DOID:0111386)
Alliance: disease page
Synonyms: IBMPFD3; MSP3; multisystem proteinopathy 3
Alt IDs: OMIM:615424
Definition: An inclusion body myopathy with Paget disease of bone and frontotemporal dementia that has_material_basis_in heterozygous mutation in the HNRNPA1 gene on chromosome 12q13.13.