DISEASES

Disease-gene associations mined from literature

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