Term Name: inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2
Synonyms: IBMPFD2, MSP2, multisystem proteinopathy 2
Definition: An inclusion body myopathy with Paget disease of bone and frontotemporal dementia that has_material_basis_in heterozygous mutation in HNRPA2B1 on 7p15.2.
Ontology: Human Disease [DOID:0111384]   ( DOID:0111384 )

Relationships
is a type of: autosomal dominant disease inclusion body myopathy with Paget disease of bone and frontotemporal dementia