Human genes for inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2
Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 [DOID:0111384]
An inclusion body myopathy with Paget disease of bone and frontotemporal dementia that has_material_basis_in heterozygous mutation in HNRPA2B1 on 7p15.2.
Synonyms: inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2, DOID:0111384, inclusion body myopathy with earlyonset Paget disease of bone with or without frontotemporal dementia 2, IBMPFD2, multisystem proteinopathy 2